Eudragit NE30D Based Metformin/Gliclazide Extended Release Tablets: Formulation, Characterisation and in Vitro Release Studies

Metformin/Gliclazide extended release tablets were formulated with Eudragit NE30D by wet granulation technique. Two batches were prepared in order to study influence of drug polymer ratio on the tablet formation and in vitro drug release. The formulated tablets were characterized by disintegration t...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 2002, Vol.50(11), pp.1495-1498
Hauptverfasser: Arno, Enose Appavoo, Anand, Prithiviraj, Bhaskar, Kesavan, Ramachandran, Somasundaram, Saravanan, Muniyandy, Vinod, Radhakrishnan
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container_end_page 1498
container_issue 11
container_start_page 1495
container_title Chemical & pharmaceutical bulletin
container_volume 50
creator Arno, Enose Appavoo
Anand, Prithiviraj
Bhaskar, Kesavan
Ramachandran, Somasundaram
Saravanan, Muniyandy
Vinod, Radhakrishnan
description Metformin/Gliclazide extended release tablets were formulated with Eudragit NE30D by wet granulation technique. Two batches were prepared in order to study influence of drug polymer ratio on the tablet formation and in vitro drug release. The formulated tablets were characterized by disintegration time, hardness, friability, thickness, weight variation, and in vitro drug release. The percentage of polymer, with respect to Metformin/Gliclazide, required to produce tablets with acceptable qualities was 9 to 13.45. The percentage of polymer below this range released the drug immediately and above this range produced granules not suitable for tablet formation. The quantity of Metformin/Gliclazide present in the tablets and the release medium were estimated by a validated HPLC method. The formulated tablets had acceptable physicochemical characters and released the drug over 6—8 h. The data obtained from in vitro release studies were fitted with various kinetic models and was found to follow Higuchi kinetics.
doi_str_mv 10.1248/cpb.50.1495
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Pharm. Bull.</addtitle><description>Metformin/Gliclazide extended release tablets were formulated with Eudragit NE30D by wet granulation technique. Two batches were prepared in order to study influence of drug polymer ratio on the tablet formation and in vitro drug release. The formulated tablets were characterized by disintegration time, hardness, friability, thickness, weight variation, and in vitro drug release. The percentage of polymer, with respect to Metformin/Gliclazide, required to produce tablets with acceptable qualities was 9 to 13.45. The percentage of polymer below this range released the drug immediately and above this range produced granules not suitable for tablet formation. The quantity of Metformin/Gliclazide present in the tablets and the release medium were estimated by a validated HPLC method. The formulated tablets had acceptable physicochemical characters and released the drug over 6—8 h. 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Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymethacrylic Acids - pharmacokinetics</topic><topic>release kinetic</topic><topic>Tablets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arno, Enose Appavoo</creatorcontrib><creatorcontrib>Anand, Prithiviraj</creatorcontrib><creatorcontrib>Bhaskar, Kesavan</creatorcontrib><creatorcontrib>Ramachandran, Somasundaram</creatorcontrib><creatorcontrib>Saravanan, Muniyandy</creatorcontrib><creatorcontrib>Vinod, Radhakrishnan</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arno, Enose Appavoo</au><au>Anand, Prithiviraj</au><au>Bhaskar, Kesavan</au><au>Ramachandran, Somasundaram</au><au>Saravanan, Muniyandy</au><au>Vinod, Radhakrishnan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Eudragit NE30D Based Metformin/Gliclazide Extended Release Tablets: Formulation, Characterisation and in Vitro Release Studies</atitle><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>50</volume><issue>11</issue><spage>1495</spage><epage>1498</epage><pages>1495-1498</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><coden>CPBTAL</coden><abstract>Metformin/Gliclazide extended release tablets were formulated with Eudragit NE30D by wet granulation technique. Two batches were prepared in order to study influence of drug polymer ratio on the tablet formation and in vitro drug release. The formulated tablets were characterized by disintegration time, hardness, friability, thickness, weight variation, and in vitro drug release. The percentage of polymer, with respect to Metformin/Gliclazide, required to produce tablets with acceptable qualities was 9 to 13.45. The percentage of polymer below this range released the drug immediately and above this range produced granules not suitable for tablet formation. 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source MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects Biological and medical sciences
Chemistry, Pharmaceutical
Delayed-Action Preparations - pharmacokinetics
Eudragit NE30D
extended release tablets
General pharmacology
Gliclazide - pharmacokinetics
HPLC
Medical sciences
Metformin - pharmacokinetics
Metformin/Gliclazide
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Polymethacrylic Acids - pharmacokinetics
release kinetic
Tablets
title Eudragit NE30D Based Metformin/Gliclazide Extended Release Tablets: Formulation, Characterisation and in Vitro Release Studies
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