<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">A. R. Tekade</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">P. P. Bhattad</style></author><author><style face="normal" font="default" size="100%">Senthamarai. R</style></author><author><style face="normal" font="default" size="100%">Ismail. A. M</style></author><author><style face="normal" font="default" size="100%">G. S. Talele</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potentiality of a newer oral antihyperglycemic combination therapy over conventional one</style></title><secondary-title><style face="normal" font="default" size="100%">The IXth World Conference on Clinical Pharmacology and Therapeutics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diabetes Mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycosylated hemoglobin</style></keyword><keyword><style  face="normal" font="default" size="100%">HbA1c</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 July 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Quebec, Canada.</style></pub-location><abstract><style face="normal" font="default" size="100%">Potentiality of a Newer Oral Antihyperglycemic Combination Therapy over
Conventional One
P. V. Ingle, V. G. Kuchake, A. R. Tekade, P. H. Patil, S. J. Surana,
P. P. Bhattad, Senthamarai. R., Ismail. A. M., G. S. Talele.
1R. C. Patel College of Pharmacy, Shirpur, India, 2Periyar College of Pharmaceutical
Sciences for Girl’s, Tiruchirappalli, India, 3Jalgaon Zillha Medicine Dealers Society’s
College of Pharmacy, Mamurabad, India
The Aim of this study is to perceive the “Potentiality of a newer oral antihyperglycemic
combination therapy over conventional ones” &amp; “aid and assist” the people with type 2
diabetes mellitus. Main objective is to compare efficacy of newer oral antihyperglycemic
combination therapy over conventional ones in the therapy of type 2 diabetes mellitus by
finding out the effect of these two varied combinations on glycemic control by monitoring
fasting plasma glucose (FPG), glycosylated haemoglobin (HbA1c), the Lipid Profile and
the body mass index (BMI). Major Findings - In the glibenclamide plus metformin
combination therapy (n = 23) group FPG &amp; HbA1c decreased during the therapy
significantly up to − 49.06 mg/dL &amp; − 0.90 % respectively during the 4 months of study
period. In the glimepiride plus metformin combination therapy group (n = 15) FPG &amp;
HbA1c decreased during the therapy significantly up to − 55.44 mg/dL &amp; − 1.28 %
respectively during the 4 months of study period. It was found that combination therapy
with metformin plus glimepiride is more effective than glibenclamide plus metformin in
improving glycemic control in type 2 diabetes mellitus and is a beneficial adjunct to
diet/exercise in management of type 2 diabetes mellitus. At the end of the study period in
glimepiride combination therapy more patients were observed to have ≤ 8% of HbA1c
(60.00 %) as compared to glibenclamide combination therapy (39.13 %). Reduction in
BMI and in total and LDL cholesterol level were not too significant.</style></abstract><notes><style face="normal" font="default" size="100%">Got Travel Grant $1,000.00 CAD from “Canadian Society for Clinical Pharmacology AND National Research Council of Canada”, for attending the “THE IXth WORLD CONFERENCE ON CLINICAL PHARMACOLOGY AND THERAPEUTICS” going to be held at QUEBEC, CANADA. 2008 July 27- August 01.</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karthikeyan. D</style></author><author><style face="normal" font="default" size="100%">Mithun. B</style></author><author><style face="normal" font="default" size="100%">Pandey. V. P</style></author><author><style face="normal" font="default" size="100%">Sengottuvelu</style></author><author><style face="normal" font="default" size="100%">Nandakumar</style></author><author><style face="normal" font="default" size="100%">T. SIVAKUMAR</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Design and evaluation of extended release Ofloxacin ocular inserts for once a day therapy</style></title><secondary-title><style face="normal" font="default" size="100%">Research Journal of Pharmacy and Technology (www.rjptonline.org)</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S. B. Kosalge</style></author><author><style face="normal" font="default" size="100%">P. O. Patil</style></author><author><style face="normal" font="default" size="100%">P. K. Deshmukh</style></author><author><style face="normal" font="default" size="100%">R. A. Fursule</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Marketing of medicinal plants of satpuda hills</style></title><secondary-title><style face="normal" font="default" size="100%">international journal of plant sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. O. Patil</style></author><author><style face="normal" font="default" size="100%">B. D. Shewale</style></author><author><style face="normal" font="default" size="100%">P. K. Deshmukh</style></author><author><style face="normal" font="default" size="100%">Fursule R. A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of hydroxypropyl-β-cyclodextrin on Solubility and Stability of Telmisartan</style></title><secondary-title><style face="normal" font="default" size="100%">international journal of chemical sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>36</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Virendra Gajbhiye</style></author><author><style face="normal" font="default" size="100%">P. Vijayaraj Kumar</style></author><author><style face="normal" font="default" size="100%">N. K. Jain</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Novel PEGylated Nanoparticulate Architectures for Sustained Delivery of H2 Receptor Antagonist</style></title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>34</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zambre, V. P</style></author><author><style face="normal" font="default" size="100%">A. Y. Deshpande</style></author><author><style face="normal" font="default" size="100%">R. R. Punde</style></author><author><style face="normal" font="default" size="100%">A. Mungantiwar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Determination of pregabalin in human plasma by LC-MS/MS and pharmacokinetic application.</style></title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>34</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. R.,Sathesh Babu</style></author><author><style face="normal" font="default" size="100%">Biswajit,Basu</style></author><author><style face="normal" font="default" size="100%">Kevin Garala</style></author><author><style face="normal" font="default" size="100%">Manojkumar Tyagi,</style></author><author><style face="normal" font="default" size="100%">G. L. ,Prabhushankar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">FORMULATION AND IN VITRO EVALUATION OF PERIODONTAL FILMS CONTAINING METRONIDAZOLE</style></title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bhagavan P S. B. Pharm, Former Deputy Director Pharmacy, Ministrtry of Health &amp; FW, Governemnt of Karnataka, India</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hospital  pharmacy series</style></title><secondary-title><style face="normal" font="default" size="100%">Hospital pharmacy for students of pharmacy</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">Hospital</style></tertiary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">5Cs</style></keyword><keyword><style  face="normal" font="default" size="100%">Choultry to Hospital</style></keyword><keyword><style  face="normal" font="default" size="100%">Classification</style></keyword><keyword><style  face="normal" font="default" size="100%">First hospital in INdia</style></keyword><keyword><style  face="normal" font="default" size="100%">Health management</style></keyword><keyword><style  face="normal" font="default" size="100%">Hospitality</style></keyword><keyword><style  face="normal" font="default" size="100%">Medical management</style></keyword><keyword><style  face="normal" font="default" size="100%">National Health care programs</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates><publisher><style face="normal" font="default" size="100%">None</style></publisher><pages><style face="normal" font="default" size="100%">On going writ up</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">A. C. Pawar</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">A. H. Sharma</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Study of Prescribing Pattern of Antibiotics in the Intensive Care Unit of Private Hospital</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal Of Hospital Pharmacy</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">A. C. Pawar</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Evaluation of various pattern of anemia in patient  with chronic renal disease and renal failure by using RDW and biochemical Test”</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Medical  Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">M. S. Pardeshi</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">APPLICATION OF ACUPUNCTURE THERAPY IN PATIENTS WITH DIABETES MELLITUS</style></title><secondary-title><style face="normal" font="default" size="100%">JOURNAL OF CLINICAL EPIDEMIOLOGY</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">R. D. Shimpi</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">P. N. Dighore</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">COMPARISON OF EFFECT OF METFORMIN IN COMBINATION WITH GLIMEPIRIDE AND GLIBENCLAMIDE ON GLYCAEMIC CONTROL IN PATIENT WITH TYPE 2 DIABETES MELLITUS</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Pharmtech</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates><abstract><style face="normal" font="default" size="100%">The aim of the present study was to compare the effect of metformin in combination with Glimepiride and Glibenclamide In patient with type 2 Diabetes Mellitus. Subjects and method: This is an open-label, randomized study carried out to study the effect of metformin when it is given in combination with either glimepiride or glibenclamide on glycaemic control in patient with type 2 Diabetes Mellitus. Patients with Glycosylated Hemoglobin more than 7% were included in the study. 31 patients were randomly assigned for treatment based on metformin-glibenclamide 1000/10 mg tablets or metformin-glimepiride1000/2mg for 12 weeks. The comparisons were conducted between these two groups for HbA1C, FPG, PPG and lipid profile. Result: At week 12, the significant reductions in HbA1c were found in both groups but the patients treated with metformin-glimepiride resulted in significantly greater reductions in HbA1C (-1.4%) than metformin-glibenclamide (-1.2%). Also the greater significant reductions were observed in case of FPG, total cholesterole, serum triglyceride and LDL cholesterole in patient with metformin-glimepiride group. Conclusion: Metformin-glimepiride tablets resulted in significantly greater reductions in HbA1C and fasting plasma glucose compared with metformin plus glibenclamide in patients with type 2 diabetes mellitus.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">D. A. Satpute</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">P. N. Dighore</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ASSESSMENT OF IMPACT OF PATIENT COUNSELLING, NUTRTION AND EXERCISE IN PATIENT WITH TYPE 2 DIABETES MELLITUS.</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Pharmtech</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Counseling</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes Mellitus-2</style></keyword><keyword><style  face="normal" font="default" size="100%">Diet / Nutrition</style></keyword><keyword><style  face="normal" font="default" size="100%">Exercise / Physical activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Life Style Modification</style></keyword><keyword><style  face="normal" font="default" size="100%">Patient Education.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates><abstract><style face="normal" font="default" size="100%">ABSTRACT:
Aim &amp; Objective: Assessment of impact of patient counseling, Nutrition and Exercise in patients with Type-2 Diabetes Mellitus. The prevalence of type-2 diabetes, especially in India and devolving countries has grown over the past decade. We performed a study to determine whether a patient counseling for Diabetes patients regarding Disease, Medication, Diet/ Nutrition and Exercise can improve Glycemic control &amp; Lipid profile and associated complications. Research design and methods: A total of 35 patients with type-2 diabetes, mean age 55 ± 1.4, 54 ± 2.2 &amp; 55 ± 2.4 years, were randomly assigned in to three groups. All these received basic diabetes education, counseling regarding Disease, Medication, Diet and Exercise for three months at each visit. Glycosylated hemoglobin (HbA1c), Fasting plasma glucose, PPG, total cholesterol, triglyceride, HDL, LDL and BMI were measured at baseline and the end of the study. Results: In the 12 months present study, the significant reductions were found in HbA1c in Group-I by 1.0 ± 0.2 %, in Group-II by 1.3 ± 1.71% and in Group-III by 1.2 ± 0.13% after 3 month as impact of patient counseling. Also the greater significant reductions were observed in case of FPG, total cholesterol, serum triglyceride and LDL cholesterol in all groups after 3 month. Conclusions: Glycemic control of type-2 diabetic patients can be improved through patient counseling regarding disease, medication, personal hygiene, diet and exercise. This study provides an economically feasible model for programs that aim to improve the health status of people with type-2 diabetes.
	
KEY WORDS: Diabetes Mellitus-2, Counseling, Diet / Nutrition, Exercise / Physical activity, Life Style Modification, Patient Education. 
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Vijayaraj Kumar</style></author><author><style face="normal" font="default" size="100%">ajay sharma</style></author><author><style face="normal" font="default" size="100%">Abhinav Agarwal</style></author><author><style face="normal" font="default" size="100%">Abhay Asthana</style></author><author><style face="normal" font="default" size="100%">NARENDRA KUMAR JAIN</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">DENDRIMERIC NANOARCHITECTURES MEDIATED TRANSDERMAL AND ORAL DELIVERY OF BIOACTIVES</style></title></titles><dates><year><style  face="normal" font="default" size="100%">In Press</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K.Venkateshkumar</style></author><author><style face="normal" font="default" size="100%">K.Punith</style></author><author><style face="normal" font="default" size="100%">N.Arunkumar</style></author><author><style face="normal" font="default" size="100%">PRP Verma</style></author><author><style face="normal" font="default" size="100%">P.Siva</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Dissolution enhancement of olanzapine by solid dispersions</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Pharmagenesis</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">In Press</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Magdum, C. S</style></author><author><style face="normal" font="default" size="100%">D. S. Ghodke</style></author><author><style face="normal" font="default" size="100%">R. R. Shah</style></author><author><style face="normal" font="default" size="100%">P. D. Nakhat</style></author><author><style face="normal" font="default" size="100%">P. G. Yeole</style></author><author><style face="normal" font="default" size="100%">N. S. Naikwade</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation and characterization of domperidone inclusion complexes of with cyclodextrin: influence of preparation methods</style></title><secondary-title><style face="normal" font="default" size="100%">Iranian Journal of Pharmaceutical Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">In Press</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Basniwal</style></author><author><style face="normal" font="default" size="100%">P, Kumar</style></author><author><style face="normal" font="default" size="100%">Vinesh</style></author><author><style face="normal" font="default" size="100%">Gupta</style></author><author><style face="normal" font="default" size="100%">Madan M.</style></author><author><style face="normal" font="default" size="100%">Khunteta</style></author><author><style face="normal" font="default" size="100%">Alok</style></author><author><style face="normal" font="default" size="100%">Rathore Garvendra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sunrise Technology of 21st Century; The Promise of Biotechnology</style></title><secondary-title><style face="normal" font="default" size="100%">The Indian Pharmacist</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">In Press</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. P. Vyas, V. L. Ghori, K. R. Chaudhari, M. R. Dabhi, N. R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Delivery Across the Blood-Brain Barrier Using the Corvus Peptide</style></title><secondary-title><style face="normal" font="default" size="100%">Recent Advances in Conventional Pharmaceutical Dosage Forms</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">6th &amp; 7th Feb 09</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360005, Gujarat, India.</style></publisher><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shah S. D. , Pathak P. K. , Namasha V. A. , Dabhi M. R. , Raval M. K. , Sheth N. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanoedge Drug Delivery Solves the Problem of Poorly Soluble Drugs</style></title><secondary-title><style face="normal" font="default" size="100%">Recent Advances in Conventional Pharmaceutical Dosage Forms</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">6th &amp; 7th Feb 09</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360005, Gujarat, India.</style></publisher><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. S. Khodakiya, A. P. Vyas, V. L. Ghori, M. R. Dabhi, M. K. Raval, N. R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">BIOROD: Bioadhesive Based Oral System for Targeted Delivery</style></title><secondary-title><style face="normal" font="default" size="100%">Recent Advances in Conventional Pharmaceutical Dosage Forms</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">6th &amp; 7th Feb 09</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360005, Gujarat, India.</style></publisher><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chauhan N. P. , Satapara V. P. , Dabhi M. R. , Raval M. K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mouth Dissolving Tablet: As a Patient Complience Dosage Form</style></title><secondary-title><style face="normal" font="default" size="100%">Recent Advances in Conventional Pharmaceutical Dosage Forms</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">6th &amp; 7th Feb 09</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360005, Gujarat, India.</style></publisher><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nitalikar M. M. , Jadhav P. A*. , Mane S. R</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Superdisintegrant Behavior of Water Soluble Chitosan Chlorhydrate </style></title><secondary-title><style face="normal" font="default" size="100%">International Herbal Conference-2009 </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26, 28/02/2009</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Banglore</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle, R.  D. Shimpi, P. H. Patil, V. G. Kuchake, , S. J. Surana, P. N. Dighore</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Comparison of effect of metformin in combination with glimepiride and glibenclamide on glycemic control in patient with type 2 diabetes mellitus”</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of PharmTech Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2009 Jan-Mar</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">50</style></section><volume><style face="normal" font="default" size="100%">01</style></volume><pages><style face="normal" font="default" size="100%">50-61</style></pages><abstract><style face="normal" font="default" size="100%">The aim of the present study is to compare the effect of metformin in combination
with Glimepiride and Glibenclamide In patient with type 2 Diabetes Mellitus.
Subjects and method: This is an open-label, randomized study carried out to study the
effect of metformin when it is given in combination with either glimepiride or
glibenclamide on glycaemic control in patient with type 2 Diabetes Mellitus. Patients
with Glycosylated Hemoglobin more than 7% were included in the study. 31 patients
were randomly assigned for treatment based on metformin-glibenclamide 1000/10 mg
tablets or metformin-glimepiride1000/2mg for 12 weeks. The comparisons were
conducted between these two groups for HbA1C, FPG, PPG and lipid profile. Result:
At week 12, the significant reductions in HbA1c were found in both groups but the
patients treated with metformin-glimepiride resulted in significantly greater
reductions in HbA1C (-1.4%) than metformin-glibenclamide (-1.2%). Also the greater
significant reductions were observed in case of FPG, total cholesterole, serum
triglyceride and LDL cholesterole in patient with metformin-glimepiride group.
Conclusion: Metformin-glimepiride tablets resulted in significantly greater reductions
in HbA1C and fasting plasma glucose compared with metformin plus glibenclamide in
patients with type 2 diabetes mellitus.
Keywords: combination therapy, glimepiride, glibenclamide, metformin, type 2
diabetes mellitus.</style></abstract><issue><style face="normal" font="default" size="100%">01</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle, D. A. Satpute, P. H. Patil, V. G. Kuchake, S. J. Surana, P. N. Dighore</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Assessment of impact of patient counseling, nutrition and exercise in patient with type 2 diabetes mellitus”</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of PharmTech Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Counseling</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes Mellitus-2</style></keyword><keyword><style  face="normal" font="default" size="100%">Diet / Nutrition</style></keyword><keyword><style  face="normal" font="default" size="100%">Exercise / Physical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2009 Jan- Mar</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">01</style></section><volume><style face="normal" font="default" size="100%">01</style></volume><pages><style face="normal" font="default" size="100%">01-21</style></pages><abstract><style face="normal" font="default" size="100%">Aim &amp; Objective: Assessment of impact of patient counseling, Nutrition and Exercise
in patients with Type-2 Diabetes Mellitus. The prevalence of type-2 diabetes,
especially in India and devolving countries has grown over the past decade. We
performed a study to determine whether a patient counseling for Diabetes patients
regarding Disease, Medication, Diet/ Nutrition and Exercise can improve Glycemic
control &amp; Lipid profile and associated complications. Research design and methods:
A total of 35 patients with type-2 diabetes, mean age 55 ± 1.4, 54 ± 2.2 &amp; 55 ± 2.4
years, were randomly assigned in to three groups. All these received basic diabetes
education, counseling regarding Disease, Medication, Diet and Exercise for three
months at each visit. Glycosylated hemoglobin (HbA1c), Fasting plasma glucose,
PPG, total cholesterol, triglyceride, HDL, LDL and BMI were measured at baseline
and the end of the study. Results: In the 12 months present study, the significant
reductions were found in HbA1c in Group-I by 1.0 ± 0.2 %, in Group-II by 1.3 ±
1.71% and in Group-III by 1.2 ± 0.13% after 3 month as impact of patient counseling.
Also the greater significant reductions were observed in case of FPG, total
cholesterol, serum triglyceride and LDL cholesterol in all groups after 3 month.
Conclusions: Glycemic control of type-2 diabetic patients can be improved through
patient counseling regarding disease, medication, personal hygiene, diet and exercise.
This study provides an economically feasible model for programs that aim to improve
the health status of people with type-2 diabetes.</style></abstract><issue><style face="normal" font="default" size="100%">01</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ghodke DS</style></author><author><style face="normal" font="default" size="100%">Nakhat PD</style></author><author><style face="normal" font="default" size="100%">Yeole PG</style></author><author><style face="normal" font="default" size="100%">Chaulang GM</style></author><author><style face="normal" font="default" size="100%">Patel P</style></author><author><style face="normal" font="default" size="100%">Patil K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and evaluation of rapid-dissolving tablet of poorly soluble drug domperidone.</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Parenteral &amp; Pharmaceutical Sciences </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2009</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">56-60</style></section><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">5</style></pages><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hamza Hariz</style></author><author><style face="normal" font="default" size="100%">Prajith P</style></author><author><style face="normal" font="default" size="100%">Sajith S</style></author><author><style face="normal" font="default" size="100%">Thomas, Dixon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Booster Effect of Seminar on Drug Abuse for Pharmacy Students</style></title><secondary-title><style face="normal" font="default" size="100%">3rd IAPST Annual National Convention 2009</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">15/11/2009</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">MCOPS</style></publisher><pub-location><style face="normal" font="default" size="100%">Manipal</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chaturvedi. M.</style></author><author><style face="normal" font="default" size="100%">Dwivedi S.</style></author><author><style face="normal" font="default" size="100%">Dwivedi. A.</style></author><author><style face="normal" font="default" size="100%">Barpete. P. K.</style></author><author><style face="normal" font="default" size="100%">Sachan. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and Evaluation of Polyherbal Anthelmintic Preparation</style></title><secondary-title><style face="normal" font="default" size="100%">Ethnobotanical Leaflets  </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">15 February </style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">329</style></section><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">329-31</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stefan M. Hailey</style></author><author><style face="normal" font="default" size="100%">Brian P. Mahon</style></author><author><style face="normal" font="default" size="100%">Darneisha N. Reed</style></author><author><style face="normal" font="default" size="100%">Malcolm J. D’Souza</style></author><author><style face="normal" font="default" size="100%">Dennis N. Kevill</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Kinetics and Mechanism of Thiolesters</style></title><secondary-title><style face="normal" font="default" size="100%">237th National ACS Meeting</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">03/2009</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Salt Lake City, Utah</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Narayan P. Gavatia, Narendra Vyas, B. K. Gupta, Mukul Tailang, A. K. Pathak</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Antioxidant activity of Psidium Guajava Linn</style></title><secondary-title><style face="normal" font="default" size="100%">13 national convention of Indian society of Pharmacognopsy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant acticvity</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH Method</style></keyword><keyword><style  face="normal" font="default" size="100%">Psidium Guajava</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2009</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.bubhopal.nic.in</style></url></web-urls></urls><pub-location><style face="normal" font="default" size="100%">Bhopal</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Narayan P. Gavatia, Narendra Vyas, B. K. Gupta, Mukul Tailang, A. K. Pathak</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Antioxidant activity of Psidium Guajava Linn</style></title><secondary-title><style face="normal" font="default" size="100%">13 national convention of Indian society of Pharmacognopsy</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant acticvity</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH Method</style></keyword><keyword><style  face="normal" font="default" size="100%">Psidium Guajava</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">02/2009</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Bhopal</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Verma A. M. L. , Misra U, Mishra N. , Bhardwaj P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Liposomes as Carrier Systems</style></title><secondary-title><style face="normal" font="default" size="100%">InPharm Communique</style></secondary-title><short-title><style face="normal" font="default" size="100%">Liposomes as Carrier Systems</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2009</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">20</style></section><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">20-24</style></pages><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Janugade B. U. 1, Patil S. S. , Patil S. V. , Lade P. D.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of PVP concentration on lag time of press-coated Montelukast sodium tablet</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pharmacy Research </style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ethylcellulose</style></keyword><keyword><style  face="normal" font="default" size="100%">lag time</style></keyword><keyword><style  face="normal" font="default" size="100%">low-substituted hydroxypropylcellulose</style></keyword><keyword><style  face="normal" font="default" size="100%">Press-coated tablet</style></keyword><keyword><style  face="normal" font="default" size="100%">pulsatile drug.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">502-506</style></pages><abstract><style face="normal" font="default" size="100%">An oral press-coated tablet was prepared by using direct compression and wet granulation methods to achieve the predetermined lag time. This press-coated tablet containing montelukast sodium in the inner core was formulated with an outer barrier layer by different compositions of hydrophobic polymer ethylcellulose and hydrophilic polymer low-substituted
hydroxypropylcellulose. The effect of concentration of polyvinyl pyrolidone on the lag time and drug release was investigated.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Janugade B. U, Patil S. S. , Patil S. V. , Lade P. D.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pulsatile drug delivery system for chronopharmacological disorders: an overview</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pharmacy Research Vol.2.Issue 1. January 2009</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Asthma</style></keyword><keyword><style  face="normal" font="default" size="100%">Chronobiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Chronotherapeutics</style></keyword><keyword><style  face="normal" font="default" size="100%">Circadian rhythm</style></keyword><keyword><style  face="normal" font="default" size="100%">Pulsatile drug delivery</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">133-143.</style></pages><abstract><style face="normal" font="default" size="100%">Pulsatile systems are gaining a lot of interest as they deliver the drug at the right site of action at the right time and in the right amount, thus providing spatial and temporal delivery thus increasing patient compliance. These systems are designed
according to the circadian rhythm of the body. Chronotherapeutics is the discipline concerned with the delivery of drugs
according to inherent activities of a disease over a certain period of time. It is becoming increasingly more evident that the
specific time that patients take their medication may be even more significant than was recognized in the past. The tradition of prescribing medication at evenly spaced time intervals throughout the day, in an attempt to maintain constant drug levels throughout a 24-hour period, may be changing as researcher’s report that some medications may work better if their administration is coordinated with day-night patterns and biological rhythms. The potential benefits of ronotherapeutics have been demonstrated in the management of a number of diseases. In particular there is a great deal of interest in how chronotherapy can particularly benefit patients suffering from allergic rhinitis, rheumatoid arthritis and related disorders, asthma, cancer, cardiovascular diseases, and peptic ulcer disease.</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dwivedi S.</style></author><author><style face="normal" font="default" size="100%">Dwivedi A.</style></author><author><style face="normal" font="default" size="100%">Barpete P. K.</style></author><author><style face="normal" font="default" size="100%">Pandey S.</style></author><author><style face="normal" font="default" size="100%">Kapadia R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Polyherbal formulation used in the treatment of jaundice</style></title><secondary-title><style face="normal" font="default" size="100%">Ethnobotanical Leaflets</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">73-78</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Swati C Jagdale, Tejas P Shah, Bhanudas S Kuchekar, Aniruddha R Chabukswar, Dhiraj T Baviskar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cancer nanotechnology</style></title><secondary-title><style face="normal" font="default" size="100%">Asian journal of Pharmaceutics</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">4 - 8</style></pages><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">DWIVEDI. A</style></author><author><style face="normal" font="default" size="100%">ARGAL. A.</style></author><author><style face="normal" font="default" size="100%">SACHAN. R</style></author><author><style face="normal" font="default" size="100%">PARIHAR P. S.</style></author><author><style face="normal" font="default" size="100%">MISHRA. R</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">FOLK USES OF SOME PLANTS USED IN THE TREATMENT OF ANIMAL DISORDERS</style></title><secondary-title><style face="normal" font="default" size="100%">Farmavita.Net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. P. Choudhari</style></author><author><style face="normal" font="default" size="100%">D.Patel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous determination of Finasteride and Tamsulosin in pharmaceutical preparations by ratio derivative spectroscopy</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pharmacy Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">1065-1067</style></pages><issue><style face="normal" font="default" size="100%">6</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Janugade B. U. , Patil S. S. , Patil S. V. , Lade P. D.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and evaluation of press coated montelukast sodium tablet for pulsatile drug delivery system</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of ChemTech Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ethylcellulose</style></keyword><keyword><style  face="normal" font="default" size="100%">lag time</style></keyword><keyword><style  face="normal" font="default" size="100%">low-substituted hydroxypropylcellulose</style></keyword><keyword><style  face="normal" font="default" size="100%">Press-coated tablet</style></keyword><keyword><style  face="normal" font="default" size="100%">Pulsatile drug delivery</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">690-695</style></pages><abstract><style face="normal" font="default" size="100%">An oral press-coated tablet was prepared by using direct compression and wet granulation methods to achieve
the predetermined lag time. This press-coated tablet containing montelukast sodium in the inner core was formulated with an outer barrier layer by different compositions of hydrophobic polymer ethylcellulose and hydrophilic polymer low-substituted hydroxypropylcellulose. The effect of formulation composition on the barrier layer comprising both hydrophobic and
hydrophilic excipients on the lag time of drug release was investigated. It was observed that lag time decreases with increasing concentration of low-substituted hydroxypropylcellulose. Press coated tablets coated by dry mixing and by wet granulation showed variations in lag time. As compared to dry mixed blend method wet granulation method gives less lag time.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S. Ruhil, V. Kumar</style></author><author><style face="normal" font="default" size="100%">P. Rathee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Umbilical Cord Stem Cell: An Overview</style></title><secondary-title><style face="normal" font="default" size="100%">Current Pharmaceutical Biotechnology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">bone marrow</style></keyword><keyword><style  face="normal" font="default" size="100%">cell based therapy</style></keyword><keyword><style  face="normal" font="default" size="100%">Human umbilical cord blood</style></keyword><keyword><style  face="normal" font="default" size="100%">non-hematopoietic diseases</style></keyword><keyword><style  face="normal" font="default" size="100%">stem cell</style></keyword><keyword><style  face="normal" font="default" size="100%">therapeutic uses</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">327-334</style></pages><abstract><style face="normal" font="default" size="100%">In recent years, human umbilical cord blood (HUCB) has emerged as an attractive tool for cell-based therapy.
Although at present the clinical application of human umbilical cord blood is limited to the fields of hematology and oncology, a rising number of studies show potential for further application in the treatment of non-hematopoietic diseases.
Stem cells (SC) from umbilical cord blood (UCB) are now a new reliable alternative to treat different blood diseases, if
the samples are frozen at the moment of birth. This procedure is an easy and safe way to preserve genetic materials for future therapeutic uses. It can be used as alternative to bone marrow. Human umbilical cord blood, with its real abundance, simple collection procedure and no serious ethical dilemmas, represents a valuable alternative to the use of other stem cell sources. The aim of this article is to review the literature on human umbilical cord blood (HUCB) and to assess its eventual usability in the treatment of diseases</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amit P. Kandikurwar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Review on granulation technique</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">granulation techniques discussed here</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Denis N. Kevill</style></author><author><style face="normal" font="default" size="100%">Stefan M. Hailey</style></author><author><style face="normal" font="default" size="100%">Brian P. Mahon</style></author><author><style face="normal" font="default" size="100%">Malcolm J. D'Souza</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mechanistic Trends Observed with Sulfur-for-Oxygen Substitution in Chloroformate Esters</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">THOMAS DIXON</style></author><author><style face="normal" font="default" size="100%">Joseph J,</style></author><author><style face="normal" font="default" size="100%">Francis B,</style></author><author><style face="normal" font="default" size="100%">MOHANTA G P</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of patient counseling on quality of life of hemodialysis patients in India. </style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacy Practice</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">181-184</style></pages><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Das J.K.,</style></author><author><style face="normal" font="default" size="100%">Chatterjee P.,</style></author><author><style face="normal" font="default" size="100%">Md. Azaharruddin,</style></author><author><style face="normal" font="default" size="100%">Mondal A,</style></author><author><style face="normal" font="default" size="100%">Sarkar N,</style></author><author><style face="normal" font="default" size="100%">Adhikary S.,</style></author><author><style face="normal" font="default" size="100%">Kandar C.C.</style></author><author><style face="normal" font="default" size="100%">Choudhury S</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies On The Antimicrobial Potential Of Hygrophylla Spinosa (Acanthaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Natural Products – An Indian Journal </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">In Press</style></volume></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Srinivasula Reddy</style></author><author><style face="normal" font="default" size="100%">Manoj Kharkar</style></author><author><style face="normal" font="default" size="100%">Kushal Manudhane</style></author><author><style face="normal" font="default" size="100%">Sandeep Kale</style></author><author><style face="normal" font="default" size="100%">Abijar Bhori,</style></author><author><style face="normal" font="default" size="100%">Arvind Lali</style></author><author><style face="normal" font="default" size="100%">P. Dubey</style></author><author><style face="normal" font="default" size="100%">K. Janar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparative Chromatography Technique in the Removal of Isostructural Genotoxic Impurity in Rizatriptan: Use of Physicochemical Descriptors of Solute and Adsorbent</style></title><secondary-title><style face="normal" font="default" size="100%">Organic Process Research &amp; Development</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromatography</style></keyword><keyword><style  face="normal" font="default" size="100%">impurities</style></keyword><keyword><style  face="normal" font="default" size="100%">Rizatriptan</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">683-689</style></pages><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">concept</style></work-type></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>34</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Harsh P Pandya</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Hemil A Shah</style></author></secondary-authors><tertiary-authors><author><style face="normal" font="default" size="100%">Dr. K. Vishwanath</style></author></tertiary-authors><translated-authors><author><style face="normal" font="default" size="100%">Dr. Bala Prabhakar</style></author></translated-authors></contributors><titles><title><style face="normal" font="default" size="100%">modern advances in insulin delivery system</style></title><secondary-title><style face="normal" font="default" size="100%">Modern advances in insulin delivery system</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diabetes</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin inhalers and insulin mouth spray</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin pen</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin Pump</style></keyword><keyword><style  face="normal" font="default" size="100%">Jet injectors</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><abstract><style face="normal" font="default" size="100%">A huge population in the world is suffering from diabetes mellitus, out of which around 6%-12% are suffering from type-1 while the remaining 85%-90% with type-2. Insulin is available as subcutaneous injections which may be considered as invasive. Insulin drug delivery is essential in type-1 while it is required in type-2 but at the later stage. The main objectives for developing new non-invasive methods are to reduce the pain and to improve the patient compliance associated with hypoglycemic injections. The inhalational system EXUBERA® has been available in U.S and Europe for the patients as non –invasive insulin drug delivery system. </style></abstract><work-type><style face="normal" font="default" size="100%">Review article</style></work-type></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. Praveen Kumar</style></author><author><style face="normal" font="default" size="100%">Y. Rajendra Prasad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A 'Healthy' Hot Cuppa</style></title><secondary-title><style face="normal" font="default" size="100%">ASIAN JOURNAL OF CHEMISTRY</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">21</style></volume></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. K. CHATURVEDI</style></author><author><style face="normal" font="default" size="100%">R. SHARMA*</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">development and validation of RP-HPLC method for simultaneous analysis of three component tablet formulation containing metformin hydrochloride, pioglitazone hydrochloride and glibenclamide</style></title><secondary-title><style face="normal" font="default" size="100%">Acta Chromatographica</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">september 2008</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">451</style></section><publisher><style face="normal" font="default" size="100%">Akadémiai Kiadó</style></publisher><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">11</style></pages><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yogesh S Gattani</style></author><author><style face="normal" font="default" size="100%">Durgacharan A Bhagwat</style></author><author><style face="normal" font="default" size="100%">Akhil P Maske</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and evaluation of intragastric fl oating drug delivery system of diltiazem hydrochloride</style></title><secondary-title><style face="normal" font="default" size="100%">Asia Pharmaceutics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">diltiazem hydrochloride</style></keyword><keyword><style  face="normal" font="default" size="100%">Floating drug delivery system</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro drug release</style></keyword><keyword><style  face="normal" font="default" size="100%">Microsphere</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October-December</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.asiapharmaceutics.info/temp/AsianJPharm24228-3667795_101117.pdf</style></url></web-urls></urls><section><style face="normal" font="default" size="100%">228</style></section><pages><style face="normal" font="default" size="100%">228-231</style></pages><abstract><style face="normal" font="default" size="100%">The present study is aimed towards formulation and evaluation of floating multiparticulate oral drug delivery system
of diltiazem hydrochloride, which can provide sustained release. The work also aims to study various parameters
affecting the behavior of floating multiparticulate in oral dosage form. Floating microspheres were prepared by non-aqueous
emulsification solvent evaporation technique, using ethyl cellulose and Eudragit RS-100 as the rate controlling polymer. The
in vitro performance was evaluated by the usual pharmacopoeial and other tests such as drug-polymer compatibility, (%)
yield, particle size analysis, drug entrapment efficiency, surface topography, in vitro floatability and release studies. Results
show that the mixing ratio of components in the organic phase affected the size, size distribution (199-320 μm), drug content
(59-84%), %yield (57-77%) and drug release of microsphere (45-99% after 12 h) and floating time &gt;12 h. The best results
were obtained at the ratio of drug: polymer Eudragit RS-100 (1:3). In most cases, good in vitro floating behavior was observed
and broad variety of drug release pattern could be achieved by variation of the polymer ratio, which was optimized to match
target release profile. Stability studies showed no significant change in the drug content in the formulation even after 3
months. The data obtained in this study thus suggest that a micro particulate floating dosage form of diltiazem hydrochloride
can be successfully designed to give controlled delivery and improved oral bioavailability.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K N Jayaveera</style></author><author><style face="normal" font="default" size="100%">Sanjay P. Umachigi</style></author><author><style face="normal" font="default" size="100%">C. K. Ashok Kumar</style></author><author><style face="normal" font="default" size="100%">G S Kumar</style></author><author><style face="normal" font="default" size="100%">M. Mallikarjuna</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Hibiscus syriacus L. flowers for wound healing activity in rats</style></title><secondary-title><style face="normal" font="default" size="100%">National Conference on Recent Advances in Chemical Sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 3-5, 2008.</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Bikaner</style></pub-location><pages><style face="normal" font="default" size="100%">Acceptance of research paper for poster presentation on 4th Oct, 2008</style></pages><abstract><style face="normal" font="default" size="100%">Wound healing is the process of repair that follows injury to the skin and other soft tissues. Following injury, an inflammatory response occurs and the cells below the dermis begin to increase collagen production. Later, the epithelial tissue is regenerated
Wound care and maintenance involve a number of measures such as dressing and 
Administration of painkillers, anti-inflammatory agents, healing promoting drugs etc. It
Runs through a number of phases such as coagulation, inflammation, granulation, fibroplasias, collagenation, would contraction and epithelization. Hibiscus syriacus L. (Malvaceae) well known drug in the system of Ayurveda system of Medicine. The search of Ayurvedic literature revealed the uses of Hibiscus syriacus L in wound healing. It is reported to possess diverse physiological properties. The leaves are diuretic, expectorant and stomachic. A decoction of the flowers is diuretic, ophthalmic and stomachic. It is also used in the treatment of itch and other skin diseases, dizziness and bloody stools accompanied by much gas. The bark contains several medically active constituents, including mucilage, carotenoids, sesquiterpenes and anthocyanidins. A decoction of the root bark is antiphlogistic, demulcent, emollient, febrifuge, haemostatic and vermifuge. It is used in the treatment of diarrhoea, dysentery, abdominal pain, leucorrhoea, dysmenorrhoea and dermaphytosis. . Since inflammation precedes the process of healing, drugs affecting inflammation are known to slow down the healing.
Since inflammation precedes the process of healing, drugs affecting inflammation are known to slow down the healing. A treatment could influence the healing of wound by intervening into anyone of many phases of wound healing. Conventional treatment includes keeping the wound clean, dry and covered. The present study was planned to assess the efficacy of this indigenous drug on some biochemical parameters related to wound healing in rats.
</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sanjay P. Umachigi</style></author><author><style face="normal" font="default" size="100%">Jayaveera K. N</style></author><author><style face="normal" font="default" size="100%">C. K. Ashok Kumar</style></author><author><style face="normal" font="default" size="100%">G. S. Kumar,</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of In-Vivo wound healing activity of Anthocephalus cadamba leaf extract on different wound model</style></title><secondary-title><style face="normal" font="default" size="100%">Society for Economic Botany</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Wound healing; Nitrofurazone; Ointment;</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 1-5</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.econbot.org/_organization_/07_annual_meetings/meetings_by_year/2008/SEB2008_Scientific_Program_withabstracts.pdf </style></url></web-urls></urls><pub-location><style face="normal" font="default" size="100%">Durham, North Carolina</style></pub-location><abstract><style face="normal" font="default" size="100%">Introduction
Anthocephalus cadamba (Roxb.) Miq. Syn A. chinensis (Lamk) A. Rich (Rubiaceae) is widely distributed throughout the greater part of India and is used as a folk medicine in the treatment of fever, anemia, uterine complaints, blood
diseases, skin diseases. leprosy, dysentery as antidiuretic, and for improvement of semen quality, leaves is recommended as a gargle in cases of stomatitis. The major constituents of bark are triterpenes, tripernoid glycosides, saponins, indole
alkaloids cadambine, 3a-dihydrocadambine, cadamine, isocadamine and isodihydrocadambine
Objectives
The aim of the present study was to investigate the in-vivo wound healing activity of Anthocephalus cadamba leaf extract on different wound models in rats
Methods
The methanol extract of Anthocephalus cadamba leaves were investigated for the evaluation of their wound healing potential on different experimental models of wounds in rats. The methanol extract of leaves in the form of an ointment with two different concentrations (5% and 10% w/w ointment of leaf extract in simple ointment base) was evaluated for wound healing potential in an excision wound model and an incision wound model in rats.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. M. Nitalikar*, S. M. Nitalikar, Gunjotikar G. A. , Aragade P. D</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spirulina: Nature’s Greatest All Round Food</style></title><secondary-title><style face="normal" font="default" size="100%">INDIAN DRUGS </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Feb. 2008, </style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">77-83</style></section><volume><style face="normal" font="default" size="100%">45</style></volume><pages><style face="normal" font="default" size="100%">7</style></pages><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">J. Thimmasetty</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">P. R. Sathesh Babu</style></author><author><style face="normal" font="default" size="100%">M. A. Maulik</style></author><author><style face="normal" font="default" size="100%">B. A. Viswanath</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solubility Behavior of Primozide in Polar and Non-polar Solvents:  Partial Solubility Parameters Approach</style></title><secondary-title><style face="normal" font="default" size="100%">J. Sol. Chem</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Pimozide - Solubility parameter - Partial solubility parameters - Solubility behavior - Extended Hansen’s approach - Flory-Huggins size correction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 6th 2008</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.springerlink.com/content/fgj17474n6x30714</style></url></web-urls></urls><abstract><style face="normal" font="default" size="100%">The solubility behavior of pimozide in individual solvents ranging from nonpolar to highly polar was studied. For understanding the solute-solvent interactions, the partial solubility parameters concept was utilized. Solutions containing excess drug were shaken in a water bath for 72 hours at 25 Â°C. After the solutions attained equilibrium, they were filtered and analyzed for drug content. A multiple regression method, using extended Hansen’s partial solubility parameters, was applied to verify the solubilities of pimozide in pure polar and nonpolar solvents and to predict its solubility in untested solvents. The three-parameter approach and the Flory-Huggins size correction term ‘B’ give predictions of solubilities with correlations up to 97%. The four-parameter approach involving proton-donor and proton-acceptor parameters was also used in fitting the solubility data. The correlations are appreciable (94%). Further, the ‘B’ term coupled with four-parameter approach was examined in order to improve the data representation, and resulted in a 1% improvement (98%) in the correlation when compared to the Flory-Huggins size-correction method. The solubility parameter obtained by this method is 10.43 H which is closer to the values obtained by theoretical methods, such as Fedors’ and Hoy’s. The resulting partial solubility parameters are δ 2d =8.85 H, δ 2p =2.17 H, δ 2a =3.15 H, and δ 2b =4.08 H, which give insights into the interaction capability of pimozide and are consistent with its chemical structure. Pimozide is a Lewis base as its δ 2b &gt;δ 2a . The total solubility parameter of pimozide is assigned at 10.43 H. This work demonstrates for the first time the validity of the four-parameter approach coupled with the Flory-Huggins size-correction term and therefore the result is interesting</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Suresh Kumar *</style></author><author><style face="normal" font="default" size="100%">Sandhya Bawa</style></author><author><style face="normal" font="default" size="100%">Sushma Drabu</style></author><author><style face="normal" font="default" size="100%">B. P. Panda</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In-vitro antifungal activity of newly synthesized 2-chloro-3-(substituted phenyl/cyclohexyl/butylamino) methylquinolines.</style></title><secondary-title><style face="normal" font="default" size="100%">AICTE Sponsored National Seminar on Recent Advances in Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antifungal activity</style></keyword><keyword><style  face="normal" font="default" size="100%">quinoline</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">7-9/08/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">MSIP, Janakpuri, New Delhi</style></pub-location><abstract><style face="normal" font="default" size="100%">A series of 2-chloro-3-(substituted phenyl/cyclohexyl/butylamino)methylquinolines (4a-n) was synthesized and tested for in-vitro antifungal activity against Aspergillus niger (MTCC, 281), Aspergillus flavus (MTCC,277), Monascus purpureus (MTCC,369) and Penicillium citrinum (NCIM, 768)  and antibacterial activity against Escherichia coli (MTCCB, 1610), Staphylococcus aureus (MTCCB, 96) and Pseudomonas aeruginosa (MTCCB, 741) by serial plate dilutions method. Results of the preliminary screening revealed that some of the compounds mainly those with electron withdrawing groups in the phenyl ring showed promising antifungal activity. However these compounds were moderately active against bacterial strains.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">M. S. Pardeshi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Application of acupuncture  therapy in diabetes mellitus patients”</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 May 22 </style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ingle P. V</style></author><author><style face="normal" font="default" size="100%">Satyanna N. N</style></author><author><style face="normal" font="default" size="100%">Nilak R. S</style></author><author><style face="normal" font="default" size="100%">Patil C. R</style></author><author><style face="normal" font="default" size="100%">Kuchake V. G</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Clinical Trial - The Risk Assessment</style></title><secondary-title><style face="normal" font="default" size="100%">In “Third Indo-Canadian Symposium” held at Govt. college of Pharmacy, Aurangabad, Maharashtra</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Mar 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Aurangabad, Maharashtra, INDIA.</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ingle P. V</style></author><author><style face="normal" font="default" size="100%">Maheshwari O. D</style></author><author><style face="normal" font="default" size="100%">Ajay Kumar</style></author><author><style face="normal" font="default" size="100%">Kuchake V. G</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">&quot;Difference between Clinical Trials and Postmarketing Use&quot;</style></title><secondary-title><style face="normal" font="default" size="100%"> “Third Indo-Canadian Symposium” held at Govt. college of Pharmacy, Aurangabad, Maharashtra</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Mar 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Aurangabad, Maharashtra, INDIA.</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">G. S. Talele</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Clinical importance of Glycosylated hemoglobin (HbA1c) in diabetes mellitus patients</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Mar 21</style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">D. A. Satpute</style></author><author><style face="normal" font="default" size="100%">R. D. Shimpi</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Nutritional and exercise advice for diabetic patients”</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Mar 19</style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">A. C. Pawar</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">A. Sharma.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Study of Prescribing pattern of Antibiotics in the Intensive Care Unit of Niramaya Hospital Pune”</style></title><secondary-title><style face="normal" font="default" size="100%">In “The International Conference on Drug Discovery and Nanotechnology” Organized by: Dept. of Chemistry, Sponsored by: University Grants Commission, New Delhi, Dept. of Science &amp; Technology, Govt. of India, New Delhi, held at Nanded, Maharashtra.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Jan 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Nanded, Maharashtra, INDIA</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">N. N. Satyanna</style></author><author><style face="normal" font="default" size="100%">S. D. Kute</style></author><author><style face="normal" font="default" size="100%">A. R. Tekade</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“NANOMEDICINE - A PROMISE TO LIFE SCIENCES”</style></title><secondary-title><style face="normal" font="default" size="100%">In ''The International Conference on Drug Discovery and Nanotechnology” Organized by: Dept. of Chemistry, Sponsored by: University Grants Commission, New Delhi, Dept. of Science &amp; Technology, Govt. of India, New Delhi, held at Nanded, Maharashtra. </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Jan 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Nanded, Maharashtra, INDIA</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">Malesh M Thakare</style></author><author><style face="normal" font="default" size="100%">D. A. Satpute</style></author><author><style face="normal" font="default" size="100%">V. F. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“NANOTECHNOLOGY: CHALLENGES AND OPPORTUNITIES IN HLBS DISORDERS”</style></title><secondary-title><style face="normal" font="default" size="100%">In “The International Conference on Drug Discovery and Nanotechnology” Organized by: Dept. of Chemistry, Sponsored by: University Grants Commission, New Delhi, Dept. of Science &amp; Technology, Govt. of India, New Delhi, held at Nanded, Maharashtra. </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Jan 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Nanded, Maharashtra, INDIA</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">K. D. Gandhi</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">S D Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“NANOMEDICINE: PHI29 DNA-PACKAGING MOTOR”</style></title><secondary-title><style face="normal" font="default" size="100%">In “The International Conference on Drug Discovery and Nanotechnology” Organized by: Dept. of Chemistry, Sponsored by: University Grants Commission, New Delhi, Dept. of Science &amp; Technology, Govt. of India, New Delhi, held at Nanded, Maharashtra. </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Jan 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Nanded, Maharashtra, INDIA</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. K. Lathi</style></author><author><style face="normal" font="default" size="100%">K. D. Gandhi</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“NANOMEDICINES: THE DRUG TRANSPORTER IN RESPIRATORY DISEASES”</style></title><secondary-title><style face="normal" font="default" size="100%">In “The International Conference on Drug Discovery and Nanotechnology” Organized by: Dept. of Chemistry, Sponsored by: University Grants Commission, New Delhi, Dept. of Science &amp; Technology, Govt. of India, New Delhi, held at Nanded, Maharashtra. </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Jan 27</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Nanded, Maharashtra, INDIA</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">Malesh M Thakare</style></author><author><style face="normal" font="default" size="100%">Sandip M Munot</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Clinical trials of vitamin E in coronary artery disease: It is time to reconsider the low-density lipoprotein oxidation hypothesis” </style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates><abstract><style face="normal" font="default" size="100%">A wide range of structurally unrelated antioxidants inhibit atherosclerosis in animal models of hypercholesterolemia, implicating oxidation of low-density lipoprotein (LDL) in the pathogenesis of atherosclerosis. However, most prospective, randomized trials of one proposed antioxidant, vitamin E, have failed to demonstrate any reduction in cardiovascular events in humans with established coronary artery disease. Recent clinical studies suggest that vitamin E is also ineffectual in the primary prevention of atherosclerosis. These observations have led many to question the relevance of LDL oxidation to the pathogenesis of human cardiovascular disease. However, vitamin E’s ineffectiveness in clinical trials might result from its failure to act as a physiologically relevant antioxidant. Indeed, vitamin E does not consistently inhibit atherosclerosis in hypercholesterolemic animals, and there is remarkably little evidence that clinically relevant doses of vitamin E result in inhibition of lipid peroxidation in vivo. Collectively, these observations indicate that there is little rationale for using vitamin E to prevent coronary artery disease in humans. They also strongly suggest that it will be critically important to establish that compounds with antioxidant activity in vitro actually prevent oxidative reactions in vivo before embarking on any new clinical trials. 

In contrast to other lipid-soluble antioxidants, vitamin E at doses that fail to lower cholesterol levels has not consistently inhibited atherosclerosis in hypercholesterolemic
animals. It is important to note that LDL isolated from the animals was protected from oxidation ex vivo, implying that vitamin E was incorporated effectively into the lipoprotein. A key issue raised by these studies is whether vitamin E is able to inhibit LDL oxidation in the artery wall. Two recent studies provided convincing evidence that very high levels of dietary vitamin E (0.2% of the diet; approximately 8 IU/d per mouse and approximately 10,000 IU/d per human) inhibit atherosclerosis in mice deficient in apolipoprotein E. Importantly, the intervention also lowered tissue levels of isoprostanes , which are sensitive and specific markers of lipid peroxidation . These observations emphasize the importance of documenting that a proposed antioxidant intervention actually inhibits oxidative reactions in vivo. Studies of mice with genetically engineered vitamin E deficiency also suggest that vitamin E has little impact on atherosclerosis. In animals with targeted disruption of the α-tocopherol transport protein, plasma vitamin E levels were less than 10% of those in wild-type mice. Despite the marked decline in plasma levels of vitamin E, the genetically altered animals exhibited only 30% more atherosclerosis and a moderate twofold increase in tissue levels of F2-isoprostanes, markers of lipid oxidation. Collectively, these observations suggest that vitamin E is not a potent inhibitor of atherogenesis in animal models of atherosclerosis. They also raise major questions regarding the ability of vitamin E at clinically relevant levels of dietary supplementation to inhibit lipid peroxidation and LDL oxidation in the artery wall.
</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">Kinnari D Gandhi</style></author><author><style face="normal" font="default" size="100%">Malesh M Thakare</style></author><author><style face="normal" font="default" size="100%">S D Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Melatonin as Antioxidant Under Pathological Process” </style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates><abstract><style face="normal" font="default" size="100%">Many are the diseases which course with free radical formation. These disorders cover a great range of fields such as neurodegenerative, immune, inflammatory and mitochondrial-related diseases. Melatonin is the main pineal gland product and it functions as “time-giver” in the regulation of circadian rhythms, among others. But the actions of melatonin are not only restricted to the neuroendocrine physiology. In fact, it has been known as a radical scavenger, a role that has been deeply studied in all those conditions where free radicals aregenerated.Furthermore, melatonin has been shown to act as an indirect antioxidant, since it is able to increase the activity and expression of the main antioxidant enzymes, the machinery for the glutathione synthesis, and many others direct or indirectly implicated in the free radical removal. Melatonin can also diminish the activity or expression of enzymes or factors that are considered as prooxidants. Thus, researchers have paid attention to the possible actions of melatonin in the attenuation of those processes where free radical overproduction is implicated. This review summarizes some of the proposed melatonin mechanisms for different free radical-dependent pathological situations, as well as some patents on melatonin significance recently reported for the
treatment of attention deficit, hyperactivity disorders, stress-related diseases, Chronic fatigue syndrome, diabetes,
Parkinson’s disease. Alzheimer’s disease, age associated cognitive dysfunction and cancer.
</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Antioxidant Vitamins and Prevention Of Cardiovascular Disease: Laboratory, Epidemiological and Clinical Trial Data”</style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates><abstract><style face="normal" font="default" size="100%">Naturally occurring antioxidants like vitamin E, beta-carotene, and vitamin C can inhibit the oxidative modification of low-density lipoproteins. This action could positively influence the atherosclerotic process and, as a consequence, the progression of coronary heart disease. A wealth of experimental studies provides a sound biological rationale for the mechanisms of action of antioxidants, whereas epidemiological studies strongly sustain the ‘antioxidant hypothesis'. To data, however, clinical trials with beta-carotene supplements have been disappointing and their use as a preventive intervention for cancer and coronary heart disease should be discouraged. Only scant data from clinical trials are available for vitamin C. As for vitamin E, discrepant results have been obtained by the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study with a low-dose vitamin E supplementation (50 mg daily) and the Cambridge Heart Antioxidant Study (400–800 mg daily). Currently ongoing are several large-scale clinical trials that will help in clarifying the role of vitamin E in the prevention of atherosclerotic coronary disease. </style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Antioxidant Vitamins and Prevention Of Cardiovascular Disease: Laboratory, Epidemiological and Clinical Trial Data”</style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Antioxidant Vitamins and Prevention Of Cardiovascular Disease: Laboratory, Epidemiological and Clinical Trial Data”</style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">S. M. Munot</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Antioxidants and prevention of hormonally   regulated cancer” </style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">All India Institute of Medical Sciences (AIIMS) New Delhi. </style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">S. M. Munot</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Alcohol vitamin A and Cancer” </style></title><secondary-title><style face="normal" font="default" size="100%">In Satellite Meeting of “Society for Free Radical Research - India (SFRR – India)” Organized by: Department of Biochemistry, theme based on “Free Radicals and Antioxidants in Human Health, Gene Regulation and Signal Transduction” held at All India Institu</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 11</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">All India Institute of Medical Sciences (AIIMS) New Delhi. </style></pub-location><abstract><style face="normal" font="default" size="100%">Chronic and excessive alcohol intake is associated with an increased risk of a variety of cancers (e.g., oral cavity, larynx, esophagus, liver, lung, colorectal, and breast). Retinoids (vitamin A and its derivatives) are known to exert profound effects on cellular growth, cellular differentiation, and apoptosis, thereby controlling carcinogenesis. Lower hepatic vitamin A levels have been well documented in alcoholics. Substantial research has been done, investigating the mechanisms by which excessive alcohol interferes with retinoid metabolism. More specifically, alcohol acts as a competitive inhibitor of vitamin A oxidation to retinoic acid involving alcohol dehydrogenases and acetaldehyde dehydrogenases; alcohol-induced cytochrome P450 enzymes (CYP), particularly CYP2E1, enhance catabolism of vitamin A and retinoic acid; and alcohol alters retinoid homeostasis by increasing vitamin A mobilization from liver to extra hepatic tissues. As a consequence, long-term and excessive alcohol intake results in impaired status of retinoic acid, the most active derivative of vitamin A and a ligand for both retinoic acid receptors and retinoid X receptors. Moreover, this alcohol-impaired retinoic acid homeostasis interferes with retinoic acid signaling (e.g., down-regulates retinoid target gene expression) and retinoic acid “cross-talk” with the mitogen-activated protein kinase [(MAPK), including Jun N-terminal kinase, extracellular signal-regulated kinase, and p38 kinase] signaling pathway. In addition, restoration of retinoic acid homeostasis by retinoic acid supplementation restored the normal status of both retinoid and MAPK signaling, thereby maintaining normal cell proliferation and apoptosis in alcohol-fed animals. These observations would have implications for the prevention of alcohol-promoted liver (and peripheral tissue) carcinogenesis. However, a better understanding of the alcohol–retinoid interaction and the molecular mechanisms involved is needed before retinoids can be pursued in the prevention of alcohol-related carcinogenesis in human beings, particularly regarding the detrimental effects of polar metabolites of vitamin A. </style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">C. R. Patil</style></author><author><style face="normal" font="default" size="100%">A. R. Tekade,</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Review on Medication Errors”</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 Feb 06 </style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author><author><style face="normal" font="default" size="100%">G. S. Talele</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Body mass index and diabetes - An Overview” </style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2008 April 04</style></date></pub-dates></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jhade DN, Jain R, Dheeraj Ahirwar, Padmaa M Paarakh</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Prof P. R. vavia</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation of active constituent from Chenopodium album</style></title><secondary-title><style face="normal" font="default" size="100%">60 th IPC New Delhi</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">PG-342</style></tertiary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chenopodium album</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12/12/2008</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">2</style></url></web-urls></urls><edition><style face="normal" font="default" size="100%">1</style></edition><publisher><style face="normal" font="default" size="100%">Netaji subhas institute of technology</style></publisher><pub-location><style face="normal" font="default" size="100%">New Delhi, India</style></pub-location><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">1</style></pages><isbn><style face="normal" font="default" size="100%">1</style></isbn><abstract><style face="normal" font="default" size="100%">ISOLATION OF ACTIVE CONSTITUENT FROM Chenopodium album linn..
Jhade DNS., Jain R, Dheeraj Ahirwar, Padmaa M.Paarakh
School of Pharmacy, Chouksey Engineering College,
Lalkhadan, Bilaspur, Chhattisgarh, India 495009

Plants have an almost limitless ability to synthesize aromatic substances, most of which are phenols or their oxygen-substituted derivatives. Most are secondary metabolites, of which at least 12,000 have been isolated, a number estimated to be less than 10% of the total. In many cases, these substances serve as plant defense mechanisms against predation by microorganisms, insects, and herbivores, such as terpenoids, give plants their odors, quinones and tannins are responsible for plant pigment.
 In the present study extraction of dried aerial part of the plant C. album linn was done by successive solvent extraction three compound were isolated viz 3-hydroxynonadecyl henicosanoate, Beta-sitosterol and Lupeol.
	Successive extraction of the aerial part of the plant was done by soxhlation. The petroleum ether precipitate was chosen for isolation of different chemical constituent. Isolation was done by column chromatography method. Three compounds were isolation which are purified by crystallization method. Characterization by NMR, FT-IR and LC-MS Spectroscopy method.
After interpretation compound I is found as 3-hydroxynonadecyl henicosanoate. compound II is lupeol and compound III is Beta-sitosterol.  The compound I and II were isolated from the plant for first time and reported.
</style></abstract><accession-num><style face="normal" font="default" size="100%">1</style></accession-num><call-num><style face="normal" font="default" size="100%">PG-342</style></call-num><notes><style face="normal" font="default" size="100%">M.Pharma Project work</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">R. A. Ughreja</style></author><author><style face="normal" font="default" size="100%">A. P. Dhingani</style></author><author><style face="normal" font="default" size="100%">M. R. Dabhi</style></author><author><style face="normal" font="default" size="100%">M. K. Raval</style></author><author><style face="normal" font="default" size="100%">N. K. Patel</style></author><author><style face="normal" font="default" size="100%">N. R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Drug Nanocrystals: An Approach for Bioavailability Enhancement of Poorly Soluble Drugs</style></title><secondary-title><style face="normal" font="default" size="100%">Microparticulate systems: A Potential Approach to Drug Delivery</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12/08/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">S. K. Patel College of Pharmaceutical Education and Research, Ganpat University, Kherva, Mehsana, Gujarat</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. P. Dhingani</style></author><author><style face="normal" font="default" size="100%">R. A. Ughreja</style></author><author><style face="normal" font="default" size="100%">M. R. Dabhi</style></author><author><style face="normal" font="default" size="100%">M. K. Raval</style></author><author><style face="normal" font="default" size="100%">A. V. Dudhrejiya</style></author><author><style face="normal" font="default" size="100%">N. R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Resealed Erythrocytes: A Novel Approach to Target ‘Res’</style></title><secondary-title><style face="normal" font="default" size="100%">Microparticulate systems: A Potential Approach to Drug Delivery</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12/08/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">S. K. Patel College of Pharmaceutical Education and Research, Ganpat University, Kherva, Mehsana, Gujarat</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N. R. Samdani</style></author><author><style face="normal" font="default" size="100%">P. V. Ingle</style></author><author><style face="normal" font="default" size="100%">M. M. Thakare</style></author><author><style face="normal" font="default" size="100%">V. G. Kuchake</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidants and prevention of hormonally   regulated cancer</style></title><secondary-title><style face="normal" font="default" size="100%">Society for Free Radical Research - India (SFRR – India)</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">11-12/02/2008  .</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">All India Institute of Medical Sciences (AIIMS) New Delhi.</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. Iovu, G. Dumais,</style></author><author><style face="normal" font="default" size="100%">P. du Souich</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-inflammatory activity of chondroitin sulphate</style></title><secondary-title><style face="normal" font="default" size="100%">Osteoarthritis and Cartilage</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">10/2008</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">S14-S18</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. Praveen Kumar</style></author><author><style face="normal" font="default" size="100%">Y. Rajendra Prasad</style></author><author><style face="normal" font="default" size="100%">N. R. kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Antimicrobial Activity of 6,7,8,9-Tetrahydro - 5 (H) - 5 - nitrophenylthiazolo [2,3-b] - quinazoline - 3(2H)- one Derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antimicrobial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenylhydrazine</style></keyword><keyword><style  face="normal" font="default" size="100%">Quinazolines</style></keyword><keyword><style  face="normal" font="default" size="100%">Synthesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">10/2008</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">5161-5165</style></pages><issue><style face="normal" font="default" size="100%">7</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aparna. S:Shanthi Priya. P</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%"> TRANSFEROSOMES: A NOVEL APPROACH FOR ENHANCED TRANSDERMAL DRUG DELIVERY</style></title><secondary-title><style face="normal" font="default" size="100%">FUSION</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2008</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.pharmainfo.net/aparna</style></url></web-urls></urls><pub-location><style face="normal" font="default" size="100%">JNTU, Ananthapur,AP,INDIA.</style></pub-location><abstract><style face="normal" font="default" size="100%">      Transdermal delivery is limited by the barrier properties of the skin. To overcome the barrier properties of the skin various approaches like permeation enhancers, vesicular systems have been developed. But they succeeded to certain extent. Transferosomes offer a novel mode to increase the permeation of vesicles. These have been reported for enhanced transdermal delivery of drugs. Transferosomes are complex, vesicular aggregates optimized to attain extremely flexible and self regulating membranes, which makes the vesicles very deformable. These self optimized aggregates are able to deliver the drug reproducibly either in to or through the skin with high efficiency. Transferosomes consists of mainly of natural; amphipathic compounds suspended in water based solution, sometimes containing biocompatible surfactants, and are meant for enhanced delivery of drugs.
</style></abstract><notes><style face="normal" font="default" size="100%">INTRODUCTION:

        The concept of transferosomes was developed, as recent tool for effective transdermal drug delivery, by Ceve and coworkers in 1992. These are modified forms of the liposomes. These has greater deformability than the standard liposomes and well suitable for skin permeation. Transferosomes overcome the skin permeation difficulty by squeezing themselves along the intracellular sealing lipids of the stratum corneum. Flexibility of transferosomes membrane is achieved by mixing suitable surface active components in the proper ratios.

These has greater advantages

1.These shows greater permeation of the drugs through the skin because of its flexible membranes.
2.These serves as carrier for both small and large molecular weight drugs.
3.In transferosomes percentage of the drug entrapment is more.
4.Protect the entrapped drug from atmospheric degradation.
5.These are biocompatible and biodegradable as they are prepared with natural phospholipids.
	By selecting the suitable composition and administration mode we can site specific therapy.
</style></notes></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sajal Kumar Jha, Venkatesh D P, Geethalakshmi. A, Roopa Karki</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microemulsions: Advancement in Drug Delivery</style></title><secondary-title><style face="normal" font="default" size="100%">THE PHARMA REVIEW</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2008</style></date></pub-dates></dates><pages><style face="normal" font="default" size="100%">68-71</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ankit P. Vyas</style></author><author><style face="normal" font="default" size="100%">Nilesh K. Patel</style></author><author><style face="normal" font="default" size="100%">Shailesh A Shah</style></author><author><style face="normal" font="default" size="100%">Mahesh R. Dabhi</style></author><author><style face="normal" font="default" size="100%">Navin R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photodegradation kinetic study of aceclofenac by HPTLC</style></title><secondary-title><style face="normal" font="default" size="100%">Preformulation: An important regulatory aspect in dosage form design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">08/11/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location><pages><style face="normal" font="default" size="100%">OP-13, Page-14</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. A. Namasha</style></author><author><style face="normal" font="default" size="100%">P. K. Pathak</style></author><author><style face="normal" font="default" size="100%">A. N. Bhatt</style></author><author><style face="normal" font="default" size="100%">M. R. Dabhi</style></author><author><style face="normal" font="default" size="100%">N. R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Transferosomes- New vesicular carrier system for effective transdermal drug delivery</style></title><secondary-title><style face="normal" font="default" size="100%">Preformulation: An important regulatory aspect in dosage form design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">08/11/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location><pages><style face="normal" font="default" size="100%">P-02, Page-22</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Parmar K. R</style></author><author><style face="normal" font="default" size="100%">Dabhi M. R</style></author><author><style face="normal" font="default" size="100%">Raval M. K</style></author><author><style face="normal" font="default" size="100%">Shah S. R</style></author><author><style face="normal" font="default" size="100%">Upadhyay P. H</style></author><author><style face="normal" font="default" size="100%">Sheth N. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Consideration of monitoring and controlling solid polymorphism in abbreviated new drug applications (ANDAs)</style></title><secondary-title><style face="normal" font="default" size="100%">Preformulation: An important regulatory aspect in dosage form design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">08/11/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location><pages><style face="normal" font="default" size="100%">P-66, Page-54</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Akruti S. Khodakiya</style></author><author><style face="normal" font="default" size="100%">Ankit P. Vyas</style></author><author><style face="normal" font="default" size="100%">Mahesh R. Dabhi</style></author><author><style face="normal" font="default" size="100%">Mihir K. Raval</style></author><author><style face="normal" font="default" size="100%">Navin R. Sheth</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A review: preparation of the magnetic colloids</style></title><secondary-title><style face="normal" font="default" size="100%">Preformulation: An important regulatory aspect in dosage form design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">08/11/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Department of Pharmaceutical Sciences, Saurashtra University, Rajkot-360 005, Gujarat, India</style></pub-location><pages><style face="normal" font="default" size="100%">P-71, Page-57</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dr. G. D. Gupta</style></author><author><style face="normal" font="default" size="100%">Shailesh Sharma</style></author><author><style face="normal" font="default" size="100%">Sudhir Bhardwaj</style></author><author><style face="normal" font="default" size="100%">K. Gaurave</style></author><author><style face="normal" font="default" size="100%">P. S. Naruka</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fast Dissolving Tablet: A Novel Approach for Delivery of Diclofenac Sodium</style></title><secondary-title><style face="normal" font="default" size="100%">PHARMANEXT</style></secondary-title><short-title><style face="normal" font="default" size="100%">FDT of Diclofenac Sodium</style></short-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diclofenac Sodium</style></keyword><keyword><style  face="normal" font="default" size="100%">FAST RELEASE</style></keyword><keyword><style  face="normal" font="default" size="100%">FDT</style></keyword><keyword><style  face="normal" font="default" size="100%">STABILITY STUDIES</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">06/2008</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">16</style></section><publisher><style face="normal" font="default" size="100%">Harish Pal, Delhi</style></publisher><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">16-20</style></pages><abstract><style face="normal" font="default" size="100%">Fast dissolving drug delivery system offer a solution for those patients having difficulty in swallowing tablet or capsule etc. Diclofenac Sodium, a non steroidal anti-inflammatory drug with analgesic and anti-inflammatory property was selected as the model drug. The poor aqueous solubility of the drug results in variable dissolution rate and hence poor bioavailability. In the present study, an attempt has been made to prepare fast dissolving tablet of the drug using sugars i.e. Sorbitol, Mannitol and polymers like HPMC, PVP by direct compression technique. The fast dissolving tablets were prepared by pure drug as well as solid dispersion of drug and beta-cyclodextrin.  The tablets were evaluated for hardness, friability, weight variation, In-Vitro Dispersion time and In-Vitro Dissolution study.  The stability studies showed no significant variations in all the parameters and were found to be stable. It was concluded that the fast dissolving tablet of poorly soluble drug can be made by direct compression technique using selective super disintegrates and solid dispersion showing enhanced dissolution and hence better patient compliance and effective therapy. </style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ingle P. V</style></author><author><style face="normal" font="default" size="100%">Kuchake V. G</style></author><author><style face="normal" font="default" size="100%">Tekade A. R</style></author><author><style face="normal" font="default" size="100%">Sakthivel K</style></author><author><style face="normal" font="default" size="100%">Surana S. J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Reduction of medication errors – a focus on patient care approach”</style></title><secondary-title><style face="normal" font="default" size="100%">Indian  Pharmacist</style></secondary-title><short-title><style face="normal" font="default" size="100%">Fcus on Patient Care Approach</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%"> Aug 2008</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">19-22</style></section><volume><style face="normal" font="default" size="100%">VII</style></volume><pages><style face="normal" font="default" size="100%">04</style></pages><issue><style face="normal" font="default" size="100%">74</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amsa P</style></author><author><style face="normal" font="default" size="100%">Pandey GK</style></author><author><style face="normal" font="default" size="100%">Bhowmick M</style></author><author><style face="normal" font="default" size="100%">Sonkar S</style></author><author><style face="normal" font="default" size="100%">Karthikeyan D</style></author><author><style face="normal" font="default" size="100%">Shiva Kumar T</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Scope of Web-based Clinical Research in Pharmacy</style></title><secondary-title><style face="normal" font="default" size="100%">Research Journal of Pharmacy and Technology (www.rjptonline.org)</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karthikeyan. D</style></author><author><style face="normal" font="default" size="100%">Sonkar. S</style></author><author><style face="normal" font="default" size="100%">Pandey. V. P</style></author><author><style face="normal" font="default" size="100%">Nandakumar. J</style></author><author><style face="normal" font="default" size="100%">Sengottuvelu. S</style></author><author><style face="normal" font="default" size="100%">Bhowmick. M</style></author><author><style face="normal" font="default" size="100%">Sivakumar. T</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development and characterization of modified ocular inserts with improved ocular compatibility</style></title><secondary-title><style face="normal" font="default" size="100%">Research Journal of Pharmacy and Technology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karthikeyan. D</style></author><author><style face="normal" font="default" size="100%">vijakumar. S</style></author><author><style face="normal" font="default" size="100%">Pandey. V. P</style></author><author><style face="normal" font="default" size="100%">Nandakumar. J</style></author><author><style face="normal" font="default" size="100%">Sengottuvelu. S</style></author><author><style face="normal" font="default" size="100%">Sivakumar. T</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation and evaluation of ocular inserts for controlled delivery of ciprofloxacin hydrochloride</style></title><secondary-title><style face="normal" font="default" size="100%">Research Journal of Pharmacy and Technology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>12</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Alok Kumar</style></author><author><style face="normal" font="default" size="100%">Bhushan P. Hatwar</style></author><author><style face="normal" font="default" size="100%">Arunabha Mallik</style></author><author><style face="normal" font="default" size="100%">Shobhit Shrivastava</style></author><author><style face="normal" font="default" size="100%">Ashish Jain</style></author><author><style face="normal" font="default" size="100%">Satish Nayak</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Dementia (Alzheimer's Disease) And Aluminium In Drinking Water : May Be A</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">R. A. Fursule</style></author><author><style face="normal" font="default" size="100%">Ch. N. Patra</style></author><author><style face="normal" font="default" size="100%">J. R. Amrutkar</style></author><author><style face="normal" font="default" size="100%">R. L. Bakal</style></author><author><style face="normal" font="default" size="100%">P. O. Patil</style></author><author><style face="normal" font="default" size="100%">P. K. Deshmukh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Study of Multiperticulate Floating Drug Delivery System Prepared by Emulsion Gelation Method</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Pharmaceutical and Clinical Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><section><style face="normal" font="default" size="100%">60</style></section><volume><style face="normal" font="default" size="100%">1</style></volume><pages><style face="normal" font="default" size="100%">4</style></pages><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Modi K. P. , Patel N. M.</style></author><author><style face="normal" font="default" size="100%">Goyal R. K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Estimation of L-Dopa from Mucuna pruriens Linn and formulation s Containing M. Pruriens by HPTLC method</style></title><secondary-title><style face="normal" font="default" size="100%">Chem. Pharm. Bull</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><section><style face="normal" font="default" size="100%">357</style></section><volume><style face="normal" font="default" size="100%">56</style></volume><pages><style face="normal" font="default" size="100%">5</style></pages><issue><style face="normal" font="default" size="100%">(3) </style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Somani Rakesh. R</style></author><author><style face="normal" font="default" size="100%">Shirodkar Prabhakar</style></author><author><style face="normal" font="default" size="100%">Toraskar Mrunmayee. P</style></author><author><style face="normal" font="default" size="100%">Kadam Vilasrao. J</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and biological evaluation of 2-5-disubstituted-1,3,4-oxadiazole analogues</style></title><secondary-title><style face="normal" font="default" size="100%">IJPER,</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. Patel</style></author><author><style face="normal" font="default" size="100%">N. Dand</style></author><author><style face="normal" font="default" size="100%">A. Somwanshi</style></author><author><style face="normal" font="default" size="100%">R S Hirlekar</style></author><author><style face="normal" font="default" size="100%">V J Kadam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Design and Evaluation of a Sustained Release Gastroretentive Dosage Form of Captopril: A Technical Note”</style></title><secondary-title><style face="normal" font="default" size="100%">AAPS PharmSciTech</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. D. Patel</style></author><author><style face="normal" font="default" size="100%">N. Dand</style></author><author><style face="normal" font="default" size="100%">R S Hirlekar</style></author><author><style face="normal" font="default" size="100%">V J Kadam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Resealed Erythrocytes: As a Novel Drug Delivery Carrier</style></title><secondary-title><style face="normal" font="default" size="100%">Current Pharmaceutical Design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">63-70</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>12</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G S Kumar</style></author><author><style face="normal" font="default" size="100%">K N Jayaveera</style></author><author><style face="normal" font="default" size="100%">C. K. Kumar Ashok</style></author><author><style face="normal" font="default" size="100%">T. Bharathi</style></author><author><style face="normal" font="default" size="100%">Sanjay P. Umachigi</style></author><author><style face="normal" font="default" size="100%">Swamy Vrushabendra:</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of antioxidant and antiacne properties of terpenoidal fraction of Hemidesmus indicus (Indian sarsaparilla)</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ispub.com/ostia/index.php?xmlPrinter=true&xmlFilePath=journals/ijaam/vol1n1/indicus.xml</style></url></web-urls></urls><abstract><style face="normal" font="default" size="100%">The present study was undertaken to evaluate the effect of terpenoidal fraction of the roots of Hemidesmus indicus roots (TFHI) on several in vitro antioxidant and antiacne activity. The in vitro antioxidant potential of TFHI was evaluated by various antioxidant assays, including DPPH radical scavenging, superoxide radical scavenging in riboflavin/light/ NBT, and nitric oxide (NO) scavenging activity in sodium nitroprusside/Greiss reagent system. Antiacne activity of TFHI was tested by disc diffusion and broth dilution methods against Propionibacterium acnes and Staphylococcus epidermidis which have been recognized as pus-forming bacteria triggering an inflammation in acne which are etiologic agents of acne vulgaris. Further, preliminary phytochemical analysis and TLC finger print profile of TFHI was established to characterize the terpenoidal fraction which showed antioxidant and antiacne properties. The TFHI was found to have different levels of antioxidant properties in the models tested. In scavenging DPPH and superoxide radicals, its activity was intense (EC50 = 18.7 and 19.3 µg/ml respectively) while scavenging NO radical was moderate. Based on a broth dilution method, the TFHI had the greatest antiacne properties. The MIC values were the same 38 µg/ml for both bacterial species and the MBC values were 38 and 46 µg/ml against Propionibacterium acnes and Staphylococcus epidermidis respectively. The antioxidant and antiacne activity could be attributed to non-polar terpenoidal fraction.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G S Kumar</style></author><author><style face="normal" font="default" size="100%">K N Jayaveera</style></author><author><style face="normal" font="default" size="100%">C. K. Ashok Kumar</style></author><author><style face="normal" font="default" size="100%">Sanjay P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Antiacne Activity of Alkaloidal Fraction of Coscinium fenestratum</style></title><secondary-title><style face="normal" font="default" size="100%">SEB 49TH ANNUAL MEETING 2008 </style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acne vulgaris</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Indian medicinal plant</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.econbot.org/_organization_/07_annual_meetings/meetings_by_year/2008/SEB2008_Scientific_Program_withabstracts.pdf -</style></url></web-urls></urls><abstract><style face="normal" font="default" size="100%">Introduction
Acne vulgaris is a skin disease whose inflammatory component is produced by the host response by Propionibacterium
acnes and Staphylococcus epidermidis have been recognized as pus-forming bacteria triggering an inflammation in acne,
occurring in specialized pilosebaceous units on the face back, and trunk
Objectives
To evaluate antiacne activity of alkaloidal fraction of Coscinium fenestratum (Gaertn) Colebr., an Indian Medicinal
Plant
Methods
Alkaloidal fraction of stems of Coscinium fenestratum was evaluated by antimicrobial susceptibility by disc diffusion
and broth dilution methods against selected bacteria. High Performance Thin Layer Chromatographic profile of
Alkaloidal fraction was established and berberine content was quantified which showed potent antiacne activity.
Results
Alkaloidal fraction of stems of Coscinium fenestratum showed maximum antiacne activity the Minimum Inhibitory
Concentration values were the same (0.039 mg/ml) for both bacterial species and the Minimum Bactericidal
Concentration values were 0.039 and 0.265 mg/ml against Propionibacterium acnes, and Staphylococcus epidermidis
respectively. Detection and quantification were performed by densitometry at » 415 nm. The content of berberine was
found to be 0.375%.
Conclusion
The mechanism of action of highly aromatic planar quaternary alkaloids such as berberine is attributed to their ability to intercalate with DNA It is possible that alkaloidal fraction containing berberine in Coscinium fenestratum may act in the
same mechanism to inhibit Propionibacterium acnes and Staphylococcus epidermidis. Therefore, the active component of the Alkaloidal Fraction could be of interest for further development as an alternative treatment for acne.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Y. Rajendra Prasad, A. Lakshmana Rao, P. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">R. Kasi Viswanadh.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">IN VITRO ANTIOXIDANT ACTIVITY AND SCAVENGING EFFECTS OF SOME NEW 1,3,5-TRIPHENYL- 2-PYRAZOLINES AND 3-(2''-HYDROXY NAPHTHALEN-1''-YL)-1,5-DIPHENYL-2-PYRAZOLINES</style></title><secondary-title><style face="normal" font="default" size="100%">Saudi Pharmaceutical Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">205-212</style></pages><issue><style face="normal" font="default" size="100%">3-4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. V. Chopde</style></author><author><style face="normal" font="default" size="100%">A. A. Phatak</style></author><author><style face="normal" font="default" size="100%">P. S. Bhide</style></author><author><style face="normal" font="default" size="100%">S. B. Jadhav</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">TO STUDY THE USE OF CATECHU FORMULATION IN ORAL HEALTH</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Pharmaceutics</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><abstract><style face="normal" font="default" size="100%">ABSTRACT
Acacia catechu has been in use since long period in India as dyeing agent. But most important uses of black catechu are as an anti-microbial and strong astringent. It can be used in the form of mouthwash in pharyngitis, laryngitis, gingivitis and stomatitis. In this study the aqueous extract of black catechu has been taken and is evaluated for its anti-microbial property against the streptococcus species of microorganism, which are found in oral cavity and are responsible for possible dental disorders due to their growth in dental plaque. The concentrated aqueous extract prepared from black catechu was found to have strong anti microbial activity. The possible mechanism for this action is strong astringent effect of catechu, which may result into precipitation of proteins. This extract is incorporated into the different mouthwash bases. The mouthwash prepared with 10% v/v concentration of extract shown more inhibition of growth of streptococcus species than that prepared with 5%v/v of aqueous extract. The preparation was also evaluated for its physical characteristics and has found good consistency for the use as mouthwash.     
</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shamkant S. Patil, P. N. Dhabale</style></author><author><style face="normal" font="default" size="100%">B. S. Kuchekar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometric Estimation of Pantoprazole in Tablet Dosage Form</style></title><secondary-title><style face="normal" font="default" size="100%">international journal of chemical sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">6</style></volume><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shamkant S. Patil, P. N. Dhabale</style></author><author><style face="normal" font="default" size="100%">B. S. Kuchekar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometric Estimation of Pantoprazole in Tablet Dosage Form</style></title><secondary-title><style face="normal" font="default" size="100%">International journal of chemical sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">6</style></volume><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K. P. R. Chowdary</style></author><author><style face="normal" font="default" size="100%">srinivas. p</style></author><author><style face="normal" font="default" size="100%">veeraiah enturi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation and Evaluation of Ethyl Cellulose Coated Microencapsulation of Gliclazide for Controlled Release</style></title><secondary-title><style face="normal" font="default" size="100%">ASIAN JOURNAL OF CHEMISTRY</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">gliclazide ethyl cellulose controlled release</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">20</style></volume><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K. P. R. Chowdary</style></author><author><style face="normal" font="default" size="100%">srinivas. p</style></author><author><style face="normal" font="default" size="100%">veeraiah enturi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Olibanum Resin Coated Microcapsules of Gliclazide:Preparation and Evaluation For Controlled Release</style></title><secondary-title><style face="normal" font="default" size="100%">ASIAN JOURNAL OF CHEMISTRY</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">20</style></volume><abstract><style face="normal" font="default" size="100%">gliclazide olibanum resin controlled release</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>34</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K. P. R. Chowdary</style></author><author><style face="normal" font="default" size="100%">srinivas. p</style></author><author><style face="normal" font="default" size="100%">veeraiah enturi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Comparative Evaluation of Permeability and Drug Release Kinetics of Olibanum Resin and Ethyl Cellulose Coated Microcapsules of Gliclazide</style></title></titles><keywords><keyword><style  face="normal" font="default" size="100%">controlled release</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethyl cellulose</style></keyword><keyword><style  face="normal" font="default" size="100%">gliclazide</style></keyword><keyword><style  face="normal" font="default" size="100%">olibanum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shamkant S. Patil, P. N. Dhabale</style></author><author><style face="normal" font="default" size="100%">B. S. Kuchekar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometric Estimation of Pantoprazole in Tablet Dosage Form</style></title><secondary-title><style face="normal" font="default" size="100%">International journal of chemical sciences</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">6</style></volume><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N. R. Jaiswal</style></author><author><style face="normal" font="default" size="100%">T. D. Nandgude</style></author><author><style face="normal" font="default" size="100%">R. T. Thube</style></author><author><style face="normal" font="default" size="100%">Kiran Bhise</style></author><author><style face="normal" font="default" size="100%">V. K. Chatap</style></author><author><style face="normal" font="default" size="100%">M. S. Rathore</style></author><author><style face="normal" font="default" size="100%">P. T. Deshmukh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and Evaluation of Thermoreversible in-situ Nasal Gel of Salbutamol Sulphate (Communicated)</style></title><secondary-title><style face="normal" font="default" size="100%">Ind. J. of Pharm. Sci.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nandgude T. D</style></author><author><style face="normal" font="default" size="100%">Bhise K. S</style></author><author><style face="normal" font="default" size="100%">Deshmukh P. T</style></author><author><style face="normal" font="default" size="100%">Shete R. V.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Formulation Study of Diphenhydramine HCl and Tannate Salts (Communicated)</style></title><secondary-title><style face="normal" font="default" size="100%">Ind. J. of Pharm. Edu. Res.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.ijper.com</style></url></web-urls></urls></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">shanti bhushan mishra, B. sangameswaran, kiran prajapati. singh D, Dubey P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical and Preliminary Phytochemical Studies of Leaves of Tridax procumbens L.</style></title><secondary-title><style face="normal" font="default" size="100%">Ethnobotanical Leaflets</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Asteraceae.</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Tridax procumbens L</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ethnoleaflets.com/leaflets/tridax2.htm</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1283-89</style></pages><abstract><style face="normal" font="default" size="100%">Pharmacognostical parameters for the leaves of Tridax procumbens L were studied with the aim of drawing the pharmacopoeial standards for this species. Macroscopical and microscopical characters, physico-chemical constants, extractive values, fluorescence analysis of dry powder and its reaction after treatment with chemical reagents under visible light and UV light at 254 nm and 366 nm were studied. The determination of these characters will aid future investigators in their Pharmacological analyses of this species.
</style></abstract><issue><style face="normal" font="default" size="100%">15</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sajal Kumar Jha, Vijayalakshmi. P, Roopa Karki, Divakar Goli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and evaluation of melt-in-mouth tablets of haloperidol</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Pharmaceutics</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><pages><style face="normal" font="default" size="100%">256-260</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D. P. Venkatesh, Sajal Kumar Jha, Roopa Karki</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Forumlation Development and Evaulation of Taste Masked ORO-dispersible tablets of anti-emetic drug</style></title><secondary-title><style face="normal" font="default" size="100%">JOURNAL OF PHARMACY RESEARCH</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>32</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">SAJAL KUMAR JHA</style></author><author><style face="normal" font="default" size="100%">Vijayalakshmi. P</style></author><author><style face="normal" font="default" size="100%">Roopa Karki</style></author><author><style face="normal" font="default" size="100%">Divakar Goli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Melt-in-Mouth tablets for an Antipsychotic Drug </style></title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rajesh S Jadon</style></author><author><style face="normal" font="default" size="100%">Rajeev K Tyagi</style></author><author><style face="normal" font="default" size="100%">Neeraj Mishra</style></author><author><style face="normal" font="default" size="100%">Amit K Goyal</style></author><author><style face="normal" font="default" size="100%">S. P Vyas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">pH sensitive liposomes enhances immunogenicity of 19 kDa carboxyl-terminal fragment of Plasmodium falciparum</style></title><secondary-title><style face="normal" font="default" size="100%">International Juornal of pharmaceutical scineces and nanotechnology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Reddy, B. P. , K. R. N. Reddy, M. Subba Rao</style></author><author><style face="normal" font="default" size="100%">K. S. Rao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of Antimicrobial Metabolites of Pseudomonas fluorescens Against Rice Fungal Pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">Current Trends in Biotechnology and Pharmacy,</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">Vol.2(1) </style></volume><pages><style face="normal" font="default" size="100%">178-182</style></pages><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. K. CHATURVEDI</style></author><author><style face="normal" font="default" size="100%">R. Sharma</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous Spectrophotometric Estimation and Validation of Three Component Tablet Formulation Containing Pioglitazone Hydrochloride, Metformin Hydrochloride and Glibenclamide </style></title><secondary-title><style face="normal" font="default" size="100%">Analytical Letters </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><publisher><style face="normal" font="default" size="100%">taylor and francis</style></publisher><volume><style face="normal" font="default" size="100%">42</style></volume><issue><style face="normal" font="default" size="100%">12</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rathee Permender</style></author><author><style face="normal" font="default" size="100%">Nagori B. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometric method for the estimation of Tizanidine in Bulk and Tablet dosage forms</style></title><secondary-title><style face="normal" font="default" size="100%">The Indian pharmacist</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">59-62</style></pages><abstract><style face="normal" font="default" size="100%">A simple, sensitive and reproducible spectrophotometric method was developed for quantitative determination of tizanidine hydrochloride in bulk and pharmaceutical formulations using factorial design for optimization of reaction parameter. In this method, tizanidine hydrochloride was made to react with p-dimethylaminobenzaldehyde (PDAB) reagent to give products including Schiffs bases that were oxidized by ferric ions to give yellow coloured species. The absorbance was   measured at 425 nm. Regression analysis of Beer’s plots showed good correlation in the concentration range of 5-50g / ml. The method was validated according to ICH guidelines</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>36</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Virendra Gajbhiye</style></author><author><style face="normal" font="default" size="100%">P. Vijayaraj Kumar</style></author><author><style face="normal" font="default" size="100%">ajay sharma</style></author><author><style face="normal" font="default" size="100%">N. K. Jain</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Novel PEGylated PPI Dendritic Nanostructures for Sustained Delivery of Anti-Inflammatory Agent</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nayak S</style></author><author><style face="normal" font="default" size="100%">Dhongade H</style></author><author><style face="normal" font="default" size="100%">Ghode P</style></author><author><style face="normal" font="default" size="100%">Tripathi A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Estimation of Levocetirizine by UV- spectrophotometry in tablet dosage form</style></title><secondary-title><style face="normal" font="default" size="100%">The Pharmacist</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D. A. Dube</style></author><author><style face="normal" font="default" size="100%">S. V. Deshpande</style></author><author><style face="normal" font="default" size="100%">V. S. Soundale</style></author><author><style face="normal" font="default" size="100%">P. R. Mahaparale</style></author><author><style face="normal" font="default" size="100%">R. S. Telekone</style></author><author><style face="normal" font="default" size="100%">A. S. Kulkarni.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sports Injuries and Effective Treatment- An Overview</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. K. Chatap</style></author><author><style face="normal" font="default" size="100%">D. K. Sharma</style></author><author><style face="normal" font="default" size="100%">P. T. Deshmukh</style></author><author><style face="normal" font="default" size="100%">V. B. Gupta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Taste Masking Property of Ion Exchange Resin</style></title><secondary-title><style face="normal" font="default" size="100%">Pharma Times</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. R. Sathesh Babu</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">K. Valliappan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solubility Bahaviour of Rofecoxib in Individual Solvents using the Concept of Partial Solubility Parameters</style></title><secondary-title><style face="normal" font="default" size="100%">Ind J. Pharm. Educ. Res.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><section><style face="normal" font="default" size="100%">161</style></section><volume><style face="normal" font="default" size="100%">42</style></volume><pages><style face="normal" font="default" size="100%">9</style></pages><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. P. Basavarajappa</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">A. R. Annamalai</style></author><author><style face="normal" font="default" size="100%">J. Thimmasetty</style></author><author><style face="normal" font="default" size="100%">P. R. Sathesh Babu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mutual Interactions of Norfloxacin and Methlyxanthines at Molecular Level – Its Implications in Pharmacotherapy</style></title><secondary-title><style face="normal" font="default" size="100%">Biomed</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><section><style face="normal" font="default" size="100%">73</style></section><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">14</style></pages><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kannur D. 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S. Naruka</style></author><author><style face="normal" font="default" size="100%">Dr. G. D. 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V. Ingle</style></author><author><style face="normal" font="default" size="100%">A. C. Pawar</style></author><author><style face="normal" font="default" size="100%">P. H. Patil</style></author><author><style face="normal" font="default" size="100%">S. J. Surana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">“Evaluation of various pattern of anemia in patient  with chronic renal disease and renal failure by using RDW and biochemical Test” </style></title><secondary-title><style face="normal" font="default" size="100%">In National seminar on “Emerging Trends in Advanced Drug Delivery System” (Sponsored by AICTE), held at Sharad Pawar College of Pharmacy, Nagpur, Maharashtra¬¬¬¬¬</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007 Dec 08</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Sharad Pawar College of Pharmacy, Nagpur, Maharashtra¬¬¬¬¬</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jayaveera K. N</style></author><author><style face="normal" font="default" size="100%">Sanjay. P Umachigi</style></author><author><style face="normal" font="default" size="100%">Vrushabendra Swamy B. M</style></author><author><style face="normal" font="default" size="100%">Kumar G. S</style></author><author><style face="normal" font="default" size="100%">Yashoda Krishna J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Wound healing activity of medicinal plants formulated in Pluronic F127 in rats</style></title><secondary-title><style face="normal" font="default" size="100%">I. International Medicinal and Aromatic Plants Conference on Culinary Herbs in Antalya, Turkey </style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Medicinal Plants.</style></keyword><keyword><style  face="normal" font="default" size="100%">Pluronics</style></keyword><keyword><style  face="normal" font="default" size="100%">wound healing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">(29 April-04 May</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Antalya, Turkey </style></pub-location><abstract><style face="normal" font="default" size="100%">The wound healing effect of the aqueous extracts of Anthocephalus chinesis, Hemidesmus indicus, Quercus infectoria, and the oil of Hibiscus syriacus and Ximenia americana dispersed in water, were examined. The 10% (w/w) Pluronic F127 (PF127) was added to the applied preparations, in order to modify the aqueous extracts viscosity and to stabilize the oil dispersion. Pluronic polyols, a family of widely used surfactants, in very low dosages may be beneficial in early post-surgical wound healing by facilitating early attachment. Synthetic non-ionic surfactants composed of poly (ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) or (PEO–PPO–PEO) tri-block polymer, widely used in the pharmaceutical formulations. In the present study, Pluronic is used as a vehicle mainly due to its thermogelling property where the vehicle viscosity increases after application to the wound area and preventing its loss by flowing. Pluronic, as a surfactant, also improved the dispersion of the plant extracts/oil in water. A full thickness wound was made in the dorsal area of the rats. The wounds were treated with the different preparations with 12 h intervals for four times in two successive days. For 16 days, the wounds were visually observed, photographically documented and the wound area was calculated by dividing each wound area by the average control wound area measured at the same day. After day 16, the animals were sacrificed and the histology of the wound area was examined. In conclusion, while plant based traditional medicine has been used throughout generations, the efficacy of such treatments requires experimental backup and scientific verification. The best wound healing activity was observed with the extract of Anthocephalus chinesis, followed by Ximenia americana, Hemidesmus indicus, Quercus infectoria, and the least active extract was that of Hibiscus syriacus. </style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G S Kumar</style></author><author><style face="normal" font="default" size="100%">K N Jayaveera</style></author><author><style face="normal" font="default" size="100%">C K Kumar</style></author><author><style face="normal" font="default" size="100%">U P Sanjay</style></author><author><style face="normal" font="default" size="100%">B M Swamy</style></author><author><style face="normal" font="default" size="100%">D V Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimicrobial effects of Indian medicinal plants against acne-inducing bacteria </style></title><secondary-title><style face="normal" font="default" size="100%">Tropical Journal of Pharmaceutical Research </style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">www.tjpr.org/vol6_no2/626Kumar.pdf </style></url></web-urls></urls><section><style face="normal" font="default" size="100%">717</style></section><volume><style face="normal" font="default" size="100%">Vol. 6 </style></volume><pages><style face="normal" font="default" size="100%">717-723 </style></pages><abstract><style face="normal" font="default" size="100%">Propionibacterium acnes and Staphylococcus epidermidis have been recognized as pus-forming bacteria triggering an inflammation in acne. The present study was conducted to evaluate antimicrobial activities of Indian medicinal plants against these etiologic agents of acne vulgaris. Ethanolic extracts of Hemidesmus indicus (roots), Eclipta alba (fruits), Coscinium fenestratum (stems), Curcubito pepo (seeds), Tephrosia purpurea (roots), Mentha piperita (leaves), Pongamia pinnata (seeds), Symplocos racemosa (barks), Euphorbia hirta (roots), Tinospora cordyfolia (roots), Thespesia populnea (roots), and Jasminum officinale (flowers) were tested for antimicrobial activities by disc diffusion and broth dilution methods. The results from the disc diffusion method showed that 07 medicinal plants could inhibit the growth of Propionibacterium acnes. Among those Hemidesmus indicus, Coscinium fenestratum, Tephrosia purpurea, Euphorbia hirta, Symplocos racemosa, Curcubito pepo and Eclipta alba had strong inhibitory effects. Based on a broth dilution method, the Coscinium fenestratum extract had the greatest antimicrobial effect. The MIC values were the same (0.049 mg/ml) for both bacterial species and the MBC values were 0.049 and 0.165 mg/ml against Propionibacterium acnes and Staphylococcus epidermidis, respectively. In bioautography assay, the Coscinium fenestratum extract produced strong inhibition zones against Propionibacterium acnes. Phytochemical screening of Coscinium fenestratum revealed the presence of alkaloid which could be responsible for activity. Taken together, our data indicated that Coscinium fenestratum had a strong inhibitory effect on Propionibacterium acnes and Staphylococcus epidermidis. 
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VRUSHABENDRA SWAMY</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">WOUND HEALING POTENTIAL OF VERBENA OFFICINALIS METHANOLIC EXTRACT IN RATS</style></title><secondary-title><style face="normal" font="default" size="100%">Internationl journal of Chemical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Collagen.</style></keyword><keyword><style  face="normal" font="default" size="100%">Tribal medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Verbena officinalis</style></keyword><keyword><style  face="normal" font="default" size="100%">wound healing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><section><style face="normal" font="default" size="100%">1295</style></section><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">1295-1300</style></pages><abstract><style face="normal" font="default" size="100%">The methanolic extract of the bark of Verbena officinalis (Verbenaceage) topically tested at doses of 100 and 200 mg/kg exerted significant wound healing effect in Staphylococcus aureus induced excision wound in rats.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rajendra Y. 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D 1</style></author><author><style face="normal" font="default" size="100%">Chaudhari S. P</style></author><author><style face="normal" font="default" size="100%">Lanke S. D</style></author><author><style face="normal" font="default" size="100%">Patel Nakul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Invitro evaluation of taste masked orodispersible dosage form of levocetirizine dihydrochloride</style></title><secondary-title><style face="normal" font="default" size="100%">Indian journal of pharmaceutical education and research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shailesh Sharma</style></author><author><style face="normal" font="default" size="100%">G. D. Gupta</style></author><author><style face="normal" font="default" size="100%">C. P. Jain</style></author><author><style face="normal" font="default" size="100%">P. S. Naruka</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development and Evaluation of Carvedilol Fast Dissolving Tablets Using Superdisintigrates and Solid Dispersion Technique</style></title><secondary-title><style face="normal" font="default" size="100%">Pharma Review</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><publisher><style face="normal" font="default" size="100%">Kongposh publication</style></publisher><volume><style face="normal" font="default" size="100%">Oct 2007</style></volume><pages><style face="normal" font="default" size="100%">159</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>12</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G. D. Gupta</style></author><author><style face="normal" font="default" size="100%">C. P. Jain</style></author><author><style face="normal" font="default" size="100%">Shailesh Sharma</style></author><author><style face="normal" font="default" size="100%">A. S. Deora</style></author><author><style face="normal" font="default" size="100%">C. S. Chauhan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ion Exchange Resin Complexes: An Approach to Mask the Taste of Bitter Drugs</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmainfo.net</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://pharmainfo.net/reviews/ion-exchange-resin-complexes-approach-mask-taste-bitter-drugs</style></url></web-urls></urls><abstract><style face="normal" font="default" size="100%">Worst the taste of the medication, the cure&quot; was once the prevailing attitude1.
Today this trend has changed and great importance is given to the organoleptic characteristics of pharmaceutical products i.e. mainly appearance, odor and taste2. Masking of the unpleasant taste of a drug improves the compliance of the patient and product value3
</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Buchi N. Nalluri</style></author><author><style face="normal" font="default" size="100%">K. P. R. Chowdary</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author><author><style face="normal" font="default" size="100%">G. Becket</style></author><author><style face="normal" font="default" size="100%">Peter A Croooks</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tablet Formulation Studies on Nimesulide and Meloxicam-Cyclodextrin Binary Systems</style></title><secondary-title><style face="normal" font="default" size="100%">AAPS PharmSciTech</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cyclodextrin Binary Systems</style></keyword><keyword><style  face="normal" font="default" size="100%">Meloxicam</style></keyword><keyword><style  face="normal" font="default" size="100%">Nimesulide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.aapspharmscitech.org</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">8</style></volume><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Polshettiwar S A, M.S. wani and Dr. P.G.Yeole</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Heavy metal, pestcide residue and total microbial count of different brands of chavanprash</style></title><secondary-title><style face="normal" font="default" size="100%">The Bioscan</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">40-44</style></pages><issue><style face="normal" font="default" size="100%">5</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">H.R., Patel G.N.</style></author><author><style face="normal" font="default" size="100%">Venkateshvara S.V.Rao</style></author><author><style face="normal" font="default" size="100%">Patel R.B.</style></author><author><style face="normal" font="default" size="100%">Patel R.P.</style></author><author><style face="normal" font="default" size="100%">Patel M.M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of bile salt on permeation characterics of the oral Mucosal Dosage from of Diltiazem Hydrochloride</style></title><secondary-title><style face="normal" font="default" size="100%">Ethio Pharma Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">29-34</style></pages><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Deshmukh P. K. , Gattani S. G. , Surana S. J. , Belgamwar V. S.</style></author><author><style face="normal" font="default" size="100%">Yeole P. G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular properties of  Gatifloxacin -  Indion 204 complexes</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Pharmaceutical Excipients</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. D. Lokhande , K. R. Gawai , K. M. Kodam , B. S. Kuchekar , A. R. Chabukswar</style></author><author><style face="normal" font="default" size="100%">S. C. Jagdale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial Activity of Extracts of Piper longum </style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pharmacology and Toxicology </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">574-579</style></pages><issue><style face="normal" font="default" size="100%">6</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zambre, Ajit P</style></author><author><style face="normal" font="default" size="100%">Padhye Subhash B</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Vithal M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper Conjugates of Knoevenagel Condensates of Curcumin and their Schiff Base Derivatives: Synthesis, Spectroscopy, Magnetism, ESR, and Electrochemistry</style></title><secondary-title><style face="normal" font="default" size="100%">Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">copper(II) complexes</style></keyword><keyword><style  face="normal" font="default" size="100%">curcumin</style></keyword><keyword><style  face="normal" font="default" size="100%">Knoevenagel condensation</style></keyword><keyword><style  face="normal" font="default" size="100%">redox properties</style></keyword><keyword><style  face="normal" font="default" size="100%">thiosemicarbazones</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><abstract><style face="normal" font="default" size="100%">Novel copper(II) complexes of curcumin Knoevenagel condensates and their Schiff bases have been synthesized and characterized. All copper complexes possess distorted square-planar geometries with 1:1 metal to ligand stoichiometry capable of stabilizing Cu2+/Cu1+ redox couples in the range 0.34 to 0.40 V. ESR spectral features are consistent with g‖&gt;g⊥&gt;2.0 suggesting monomeric nature of copper complexes having dx2 -y2 ground state</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zambre, Ajit P</style></author><author><style face="normal" font="default" size="100%">Ganure, Ashok L.</style></author><author><style face="normal" font="default" size="100%">Shinde, Devanand B.</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Vithal M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Perspective Assessment of COX-1 and COX-2 Selectivity of Nonsteroidal Anti-Inflammatory Drugs from Clinical Practice: Use of Genetic Function Approximation</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Chemical Information and Modeling</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/cgi-bin/article.cgi/jcisd8/2007/47/i02/pdf/ci6004367.pdf</style></url></web-urls></urls><abstract><style face="normal" font="default" size="100%">The beneficial action of nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with the inhibition of cyclooxygenase-2 (COX-2), whereas their harmful side effects are associated with the inhibition of COX-1. In order to understand a meaningful comparison of both classical NSAIDs and newer COX-2 drugs, a series of molecules from varied classes of COX-2 inhibitors was studied by the application of three-dimensional quantitative structure-activity relationships (3D-QSAR) using molecular descriptors obtained by genetic function approximation. The features responsible for the dual inhibition of COX-1 and COX-2 and the selective inhibition of COX-2 with factors contributing to the maintenance of optimum selectivity were identified. The QSAR models revealed the importance of thermodynamic, electronic, structural, and molecular shape analysis parameters, which can reasonably modulate the selectivity pattern to avoid unsolicited side effects. An improved understanding to rationalize the COX-1 and COX-2 binding profiles could be gained to develop safe drug design methods.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kunte, Dhananjay</style></author><author><style face="normal" font="default" size="100%">Padhye, Subhash</style></author><author><style face="normal" font="default" size="100%">Zambre, Ajit P</style></author><author><style face="normal" font="default" size="100%">Jamadar, Abeda</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Vithal M.</style></author><author><style face="normal" font="default" size="100%">Wali, Ramesh</style></author><author><style face="normal" font="default" size="100%">Koetsier, Jennifer</style></author><author><style face="normal" font="default" size="100%">Roy, Hemant.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potentiation of Colorectal Cancer (CRC) Chemoprevention through Novel Cyclooxygenase (COX)-Lipooxygenase (LOX) Inhibitors</style></title><secondary-title><style face="normal" font="default" size="100%">Digestive Disease Week, to be held on 19 - 24 May 2007 in Washington D.C.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zambre, Ajit P</style></author><author><style face="normal" font="default" size="100%">Adsule, Shreelekha</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Vithal M.</style></author><author><style face="normal" font="default" size="100%">Sarkar, Fazlul</style></author><author><style face="normal" font="default" size="100%">Sinn, Ekkehard</style></author><author><style face="normal" font="default" size="100%">Padhye Subhash.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper conjugates of Schiff bases of 3,5-di-tert-butyl phenols as cyclooxygenase enzyme inhibitors for anticancer activity</style></title><secondary-title><style face="normal" font="default" size="100%">American Chemical Society’s 233rd National Meeting &amp; Exposition, March 25-29, 2007 Chicago, IL USA.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kunte, Dhananjay</style></author><author><style face="normal" font="default" size="100%">Padhye, Subhash</style></author><author><style face="normal" font="default" size="100%">Zambre, Ajit P</style></author><author><style face="normal" font="default" size="100%">Jamadar, Abeda</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Vithal M.</style></author><author><style face="normal" font="default" size="100%">Wali, Ramesh</style></author><author><style face="normal" font="default" size="100%">Koetsier, Jennifer</style></author><author><style face="normal" font="default" size="100%">Roy, Hemant.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potentiation of Colorectal Cancer (CRC) Chemoprevention through Novel Cyclooxygenase (COX)-Lipooxygenase (LOX) Inhi</style></title><secondary-title><style face="normal" font="default" size="100%">Digestive Disease Week, held on 19 - 24 May 2007 in Washington D.C.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Virendra Gajbhiye</style></author><author><style face="normal" font="default" size="100%">P. Vijayaraj Kumar</style></author><author><style face="normal" font="default" size="100%">Rakesh Kumar Tekade</style></author><author><style face="normal" font="default" size="100%">N. K. Jain</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmaceutical and Biomedical Potential of PEGylated Dendrimers</style></title><secondary-title><style face="normal" font="default" size="100%">Current Pharmaceutical Design</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. R. Satihesh Babu</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">J. Thimmasetty</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">K. Valliappan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solubility of Meloxicam in Mixed Solvent Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Eth. Pharm. J.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><section><style face="normal" font="default" size="100%">23</style></section><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">6</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. R. Sathesh Babu</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">J. Thimmasetty</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">K. Valliappan, K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solubilization of Rofecoxib Through Cosolvency</style></title><secondary-title><style face="normal" font="default" size="100%">Biomed</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><section><style face="normal" font="default" size="100%">84</style></section><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">7</style></pages><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. R. Sathesh Babu</style></author><author><style face="normal" font="default" size="100%">C. V. S. Subrahmanyam</style></author><author><style face="normal" font="default" size="100%">J. Thimmasetty</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">K. Valliappan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Extended Hansen’s Solubility Approach: Meloxicam in Individual Solvents</style></title><secondary-title><style face="normal" font="default" size="100%">Pak. J. Pharm. Sci.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><section><style face="normal" font="default" size="100%">311</style></section><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">6</style></pages><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">C. P. Jain</style></author><author><style face="normal" font="default" size="100%">Shailesh Sharma</style></author><author><style face="normal" font="default" size="100%">A. S. Deora</style></author><author><style face="normal" font="default" size="100%">Dr. G. D. 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Becket</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inclusion Complexation and Dissolution Properties of Nimesulide and Meloxicam–hydroxypropyl-b-cyclodextrin Binary Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Inclusion Phenomena and Macrocyclic Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">HP-beta-cyclodextrin Binary Systems</style></keyword><keyword><style  face="normal" font="default" size="100%">Inclusion Complexation</style></keyword><keyword><style  face="normal" font="default" size="100%">Meloxicam</style></keyword><keyword><style  face="normal" font="default" size="100%">Nimesulide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><volume><style face="normal" font="default" size="100%">53</style></volume><abstract><style face="normal" font="default" size="100%">The purpose of the work is physicochemical characterization of nimesulide (NI) and meloxicam (ME}-hydroxypropyl-β-cyclodextrin (HP- β -CD) binary systems both in solution and solid states and to improve the pharmaceutical properties of NI and ME via inclusion complexation with HP- β -CD. Binary systems of NI and ME with HP- β -CD have been characterized both in solution and solid state by different physicochemical methods. Three types of drug-HP- β -CD binary systems. namely physical mixtures (PM), kneaded systems (KS) and co evaporated systems (CS) in 1:1 and 1:2 molar ratios (1:1 and 1:2 M) were prepared. Phase solubility and H-NMR spectroscopic studies in solution state revealed 1:1 M complexation of NI and ME with HP-p-CD. A partial inclusion of NI with HP- β -CD at both molar ratios of kneaded and co evaporated systems and a true inclusion of ME with HP- β-CD at both molar ratios of co evaporated systems in solid state was confirmed by differential scanning calorimetry (DSC), powder X-ray diffractometry (powder X-RD) and scanning electron microscopy (SEM) studies. Dissolution properties of NI and ME-HP- β -CD binary systems were superior when compared to corresponding pure drugs. The aqueous solubility and dissolution properties of NI and ME can be improved by inclusion complexation with HP- β -CD.</style></abstract><issue><style face="normal" font="default" size="100%">103</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D. GOWRISANKAR*,S. KALYANSUMANTH,A. K. M. PAWAR P. V. MADHAVILATHA</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">UV Spectrophotometric Determination of Clopidogrel·aild Repaglinide</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D. GoWRISANKAR*</style></author><author><style face="normal" font="default" size="100%">A. K. M. PAWAR</style></author><author><style face="normal" font="default" size="100%">S. KALYANSUMAN</style></author><author><style face="normal" font="default" size="100%">P. V. MADHAVI LATIlA</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometric Determination of Repaglinide and Ezetamibe</style></title><secondary-title><style face="normal" font="default" size="100%">Asian Journal of Chemisitry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Y. Rajendra Prasad</style></author><author><style face="normal" font="default" size="100%">P. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">A. Lakshmana Rao</style></author><author><style face="normal" font="default" size="100%">L. Prasoona</style></author><author><style face="normal" font="default" size="100%">Murali</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Antidepressant activity of some New 1,3,5-triphenyl- 2-pyrazolines and 3-(2''-hydroxynaphthalen-1''-yl)-1,5-diphenyl-2-Pyrazolines</style></title><secondary-title><style face="normal" font="default" size="100%">Bioorganic and Medicinal Chemistry Letters</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">anti-depressant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Pyrazolines</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><section><style face="normal" font="default" size="100%">5030</style></section><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">5030-34</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vyawahare, N. S</style></author><author><style face="normal" font="default" size="100%">Gandhi, S. V</style></author><author><style face="normal" font="default" size="100%">N. Iyer</style></author><author><style face="normal" font="default" size="100%">Zambre, V. P</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ideal Class Seminars: Development of Communication Skills and Subject Knowledge </style></title><secondary-title><style face="normal" font="default" size="100%">Indian journal of pharmaceutical education and research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Class Seminar</style></keyword><keyword><style  face="normal" font="default" size="100%">Communication Skills</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><section><style face="normal" font="default" size="100%">163</style></section><volume><style face="normal" font="default" size="100%">39</style></volume><pages><style face="normal" font="default" size="100%">163-165</style></pages><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">1)	J. B. Perianayagam</style></author><author><style face="normal" font="default" size="100%">S. Narayanan</style></author><author><style face="normal" font="default" size="100%">G. Gnanasekar</style></author><author><style face="normal" font="default" size="100%">A. Pandurangan</style></author><author><style face="normal" font="default" size="100%">S. Raja</style></author><author><style face="normal" font="default" size="100%">K. Rajagopal</style></author><author><style face="normal" font="default" size="100%">R. Rajesh</style></author><author><style face="normal" font="default" size="100%">P. Vijayarajkumar</style></author><author><style face="normal" font="default" size="100%">S. G. Vijayakumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of antidiarrheal Potential of Emblica officinalis.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmaceutical Biology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><section><style face="normal" font="default" size="100%">373</style></section><volume><style face="normal" font="default" size="100%">43</style></volume><pages><style face="normal" font="default" size="100%">5</style></pages><abstract><style face="normal" font="default" size="100%">Abstract
The antidiarrheal potential of the methanol extract of the fruit of Emblica officinalis Gaertn. (Euphorbiaceae) was evaluated using several experimental models of diarrhea in Wistar albino rats. The methanol extract showed a significant inhibitory effect on rats with diarrhea induced by castor oil and magnesium sulfate. The methanol extract produced a significant reduction in gastrointestinal motility in charcoal meal tests in rats. It also significantly inhibited PGE2-induced enteropooling as compared to control animals. The results obtained establish the efficacy and substantiate the use of this herbal remedy as a nonspecific treatment for diarrhea in folk medicine.

Keywords: Antidiarrheal, Emblica officinalis, Euphorbiaceae,
gastrointestinal motility, intestinal secretion.</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>32</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">THOMAS DIXON</style></author><author><style face="normal" font="default" size="100%">JOSEPH JOHN</style></author><author><style face="normal" font="default" size="100%">FRANCIS BABU</style></author><author><style face="normal" font="default" size="100%">MOHANTA G P</style></author><author><style face="normal" font="default" size="100%">Manavalan . R</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">IMPACT OF PATIENT COUNSELING IN AWARENESS, QUALITY OF LIFE AND PATIENT VIEW POINT FOR ESRD (HEMODIALYSIS) PATIENTS</style></title><secondary-title><style face="normal" font="default" size="100%">PHARMACY PRACTICE</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><publisher><style face="normal" font="default" size="100%">ANNAMALAI UNIVERSITY</style></publisher><pub-location><style face="normal" font="default" size="100%">CHIDAMBARAM</style></pub-location><pages><style face="normal" font="default" size="100%">70</style></pages><work-type><style face="normal" font="default" size="100%">M. PHARM</style></work-type></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">T. Satyanarayana</style></author><author><style face="normal" font="default" size="100%">E. Hemalatha</style></author><author><style face="normal" font="default" size="100%">P. Mallikarjuna Rao</style></author><author><style face="normal" font="default" size="100%">B. Madhu Katyayani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preliminary studies on anti-inflammatory effects of Thespesia populnea</style></title><secondary-title><style face="normal" font="default" size="100%">JMAPS</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Athawale R. B.</style></author><author><style face="normal" font="default" size="100%">Singh K. 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P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spectrophotometer Method for the Estimation of Aceclofenac in Tablets.</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Drugs </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>13</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rajeswara Rao P, Routhu KV.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cardioprotective actions of Indian Herbal Drugs in ischemia-reperfusion induced myocardial infarction in rats.</style></title><secondary-title><style face="normal" font="default" size="100%">APTI Annual National Convention, 2004 </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2–4th October</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Visakhapatnam, India,</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N. P. Chotai, V. A. Patel,  B. G. Patel, H. V. Patel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">  Growth of Pharmacy Education in Gujarat as Compared to other Selected States.  </style></title><secondary-title><style face="normal" font="default" size="100%">THE INDIAN JOURNAL OF TECHNICAL EDU., </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2004</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">VOL. 27,</style></volume><pages><style face="normal" font="default" size="100%">, 96-98.</style></pages><issue><style face="normal" font="default" size="100%">NO. 1,</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N. 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Hima Sankar</style></author><author><style face="normal" font="default" size="100%">G. V. Murali Mohan Babu</style></author><author><style face="normal" font="default" size="100%">P. S. S. Krishna Babu</style></author><author><style face="normal" font="default" size="100%">L. Narasinga Rao</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on the Solid Dispersion Systems of Glipizide</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glipizide</style></keyword><keyword><style  face="normal" font="default" size="100%">Solid Dispersion</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2002</style></date></pub-dates></dates><section><style face="normal" font="default" size="100%">433</style></section><volume><style face="normal" font="default" size="100%">64</style></volume><pages><style face="normal" font="default" size="100%">433</style></pages><abstract><style face="normal" font="default" size="100%">Solid dispersions of glipizide were prepared using water-soluble carriers such as polyvinylpyrrolidone and polyethylene glycol by common solvent method in an attempt to increase the dissolution rate of glipizide, a practically insoluble drug in water. Differential scanning calorimetry, x-ray difiractometry and in vitro dissolution studies were used to characterize the solid dispersions. No chemical interaction was found between glipizide and polyvinylpyrrolidone/polyethylene glycol. The results from Differential scanning calorimetry and x-ray diffractometry studies show that polyvinylpyrrolidone/polyethylene glycol inhibits the crystallization of glipizide. The solid dispersions prepared in this study were found to have higher dissolution rates compared to intact glipizide and physical mixtures of polyvinylpyrrolidone/polyethylene glycol and glipizide. It was found that the optimum weight ratio for glipizide:carrier is 1:5 for polyvinylpyrrolidone and 1:7 for polyethylene glycol.</style></abstract></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>25</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. C. Gohel</style></author><author><style face="normal" font="default" size="100%">P. Brahmbhatt</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Process for preparation of directly compressible adjuvant of sodium bi carbonate </style></title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2002</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>25</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. Gohel</style></author><author><style face="normal" font="default" size="100%">S. P. Adeshara</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A novel method of preparation of mouth dissolve tablets of nimesulide from granules prepared by eutectic blend</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2002</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">L. M. College of Pharmacy</style></publisher><pub-location><style face="normal" font="default" size="100%">India</style></pub-location></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. P. Pandey</style></author><author><style face="normal" font="default" size="100%">A. Phanindrudu</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">J. Livingston.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Vitro Study on Capsules Formulations of Omeprazole Containing Enteric Coated Granules.</style></title><secondary-title><style face="normal" font="default" size="100%">Boll. Chim. Farmac-Anno</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V. P. Pandey</style></author><author><style face="normal" font="default" size="100%">N. Kannappan</style></author><author><style face="normal" font="default" size="100%">R. Manavalan</style></author><author><style face="normal" font="default" size="100%">T. Subburaj.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sustaining Pattern of Phenformin Hydrochloride Using Various Polymers and Waxes. </style></title><secondary-title><style face="normal" font="default" size="100%">Boll. Chim. Farmac-Anno</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>19</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. S. Kawtikwar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation of Miconazole Nitrate in Chewable Drug Delivery System using Chewing Gum Base and its Evaluation</style></title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. Annapurna</style></author><author><style face="normal" font="default" size="100%">V. Krishna Kumar</style></author><author><style face="normal" font="default" size="100%">P. Murali Mohan Rao</style></author><author><style face="normal" font="default" size="100%">K. Someswara Rao</style></author><author><style face="normal" font="default" size="100%">J. Rajasekhar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Multiple sclerosis: the disease and its treatment.</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmacology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates><section><style face="normal" font="default" size="100%">3</style></section><volume><style face="normal" font="default" size="100%">34</style></volume><pages><style face="normal" font="default" size="100%">13</style></pages></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P. S. Kawtikwar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development of Technology for Microcrystalline Cellulose from Bagasse and its evaluation for Pharmaceutical use</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Pharmaceutical Excipients</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vyawahare</style></author><author><style face="normal" font="default" size="100%">N. S.</style></author><author><style face="normal" font="default" size="100%">Bhandari</style></author><author><style face="normal" font="default" size="100%">S. V.</style></author><author><style face="normal" font="default" size="100%">Zambre</style></author><author><style face="normal" font="default" size="100%">A. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Do Not Let Your Profession Be Disrupted</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmaceutical Education</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N. R. Jadhav.</style></author><author><style face="normal" font="default" size="100%">R. B. Limzerwala</style></author><author><style face="normal" font="default" size="100%">S. C. Jagdale</style></author><author><style face="normal" font="default" size="100%">A. P. Pawar</style></author><author><style face="normal" font="default" size="100%">A. R. Paradkar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Crystallo-Co-Agglomerarion Technique in Bromhexine Hydrochloride. Controlled Release</style></title><secondary-title><style face="normal" font="default" size="100%">4th Controlled Release Society arranged, International Symposium on advances in Technology &amp; Business Potential of New Drug Delivery Systems at Mumbai </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Athawale R. B</style></author><author><style face="normal" font="default" size="100%">Singh K. K.</style></author><author><style face="normal" font="default" size="100%">Gude R. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solid lipid nanoparticles as drug delivery for anticancer agent</style></title><secondary-title><style face="normal" font="default" size="100%">4th International Symposium Controlled Release Society Indian Chapter</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">B. Sreenivasa Rao</style></author><author><style face="normal" font="default" size="100%">A. Seshasayana</style></author><author><style face="normal" font="default" size="100%">S. V. Pardha Saradhi</style></author><author><style face="normal" font="default" size="100%">N. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">Cheruvu. P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correlation of In Vitro Release and In Vivo Absorption Characteristics of Rifampicin from Ethylcellulose Coated Nonpareil Beads</style></title><secondary-title><style face="normal" font="default" size="100%">International journal of Pharmaceutics</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ethylcellulose Coated Nonpareil Beads</style></keyword><keyword><style  face="normal" font="default" size="100%">Rifampicin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">230</style></volume><issue><style face="normal" font="default" size="100%">1</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G. V. Murali Mohan Babu</style></author><author><style face="normal" font="default" size="100%">Ch. D. S. Prasad</style></author><author><style face="normal" font="default" size="100%">K. Hima Sankar</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Gum Karaya as Carrier in the Design of Oral Controlled Release Hydrophilic Matrix Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Acta Pharmaceutica</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gum Karaya</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">51</style></volume><issue><style face="normal" font="default" size="100%">273</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G. V. Murali Mohan Babu</style></author><author><style face="normal" font="default" size="100%">Ch. D. S. Prasad</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">New System for Microencapsulation of Diclofenac Sodium by using Gum Karaya and Chitosan</style></title><secondary-title><style face="normal" font="default" size="100%">Saudi Pharmaceutical Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chitosan</style></keyword><keyword><style  face="normal" font="default" size="100%">Diclofenac Sodium</style></keyword><keyword><style  face="normal" font="default" size="100%">Gum Karaya</style></keyword><keyword><style  face="normal" font="default" size="100%">Microencapsulation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">9</style></volume><issue><style face="normal" font="default" size="100%">169</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G. V. Murali Mohan Babu</style></author><author><style face="normal" font="default" size="100%">K. Hima Sankar</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Controlled Release of Diclofenac Sodium by Gum Karaya – Chitosan Complex Coacervate: In Vivo Evaluation</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">controlled release</style></keyword><keyword><style  face="normal" font="default" size="100%">Diclofenac Sodium</style></keyword><keyword><style  face="normal" font="default" size="100%">Gum Karaya – Chitosan Complex Coacervate</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">63</style></volume><issue><style face="normal" font="default" size="100%">408</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">B. Sreenivasa Rao</style></author><author><style face="normal" font="default" size="100%">A. Seshasayana</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. Sai Sudha</style></author><author><style face="normal" font="default" size="100%">S. V. Pardhasaradhi</style></author><author><style face="normal" font="default" size="100%">N. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on Release of Rifampicin from Sintered Matrix Tablets</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Rifampicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Sintered Matrix Tablets</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">63</style></volume><issue><style face="normal" font="default" size="100%">371</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A. Seshasayana</style></author><author><style face="normal" font="default" size="100%">B. Sreenivasa Rao</style></author><author><style face="normal" font="default" size="100%">Y. Prasanna Raju</style></author><author><style face="normal" font="default" size="100%">Cheruvu. P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on Release of Rifampicin from Modified Pulsin Cap Technique</style></title><secondary-title><style face="normal" font="default" size="100%">Indian journal of Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Modified Pulsin Cap Technique</style></keyword><keyword><style  face="normal" font="default" size="100%">Rifampicin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">63</style></volume><issue><style face="normal" font="default" size="100%">337</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">B. Sreenivasa Rao</style></author><author><style face="normal" font="default" size="100%">A. Seshasayana</style></author><author><style face="normal" font="default" size="100%">S. V. Pardhasaradhi</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">G. Rambabu</style></author><author><style face="normal" font="default" size="100%">P. Surendra Kumar</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Studies on Two Methods of Preparation of Chitosan Matrix Tablets of Rifampicin</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chitosan Matrix Tablets</style></keyword><keyword><style  face="normal" font="default" size="100%">Rifampicin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">63</style></volume><issue><style face="normal" font="default" size="100%">306</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">B. Sreenivasa Rao</style></author><author><style face="normal" font="default" size="100%">N. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">K. Madhuri</style></author><author><style face="normal" font="default" size="100%">Cheruvu P. S. Narayan</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Historic Development – An Overview: Osmotic Drug Delivery Systems</style></title><secondary-title><style face="normal" font="default" size="100%">The Eastern Pharmacist</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Osmotic Drug Delivery Systems</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><section><style face="normal" font="default" size="100%">21</style></section><volume><style face="normal" font="default" size="100%">44</style></volume><issue><style face="normal" font="default" size="100%">521</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G. V. Murali Mohan Babu</style></author><author><style face="normal" font="default" size="100%">Thaer Abdel Ghani</style></author><author><style face="normal" font="default" size="100%">N. Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">P. Ellaiah</style></author><author><style face="normal" font="default" size="100%">K. V. Ramana Murthy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-Microbial Activity of Gum Karaya: Emerging Pharmaceutical Excipient</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Drugs</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-Microbial Activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Emerging Pharmaceutical Excipient</style></keyword><keyword><style  face="normal" font="default" size="100%">Gum Karaya</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">38</style></volume><abstract><style face="normal" font="default" size="100%">A study was undertaken to find out the viscosity changes of aqueous solution of an emerging pharmaceutical excipient Gum karaya (GK) and modified form of GK (mGK) in comparison with that of guar gum (GG) on long-term storage. It was found that GK and mGK showed no significant changes in their respective viscosities. However, the viscosities of GG aqueous solutions were significantly decreased on long-term storage. Viable count and anti-microbial activity studies confirmed the antimicrial activity of GK and mGK. Aqueous solution of GK exhibited high~st anti-microbial activity and low viable count among the studied excipients. The order of anti-microbial activity is GK&gt;mGK&gt;GG.</style></abstract><issue><style face="normal" font="default" size="100%">153</style></issue></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Athawale R. B</style></author><author><style face="normal" font="default" size="100%">Singh K. K.</style></author><author><style face="normal" font="default" size="100%">Gude R. 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