{"title":"尼扎替丁胃保留漂浮生物黏合剂的处方及体外因子评价","authors":"V. Sabale, Hardikkumar Chaudhari, P. Sabale","doi":"10.2174/2210303109666190221155353","DOIUrl":null,"url":null,"abstract":"\n\nThe aim of the present study was to formulate and evaluate floating bioadhesive\ntablets of Nizatidine which is a competitive, reversible H2-receptor antagonist. Floatingbioadhesive\ndrug delivery system exhibiting a unique combination of floatation and bioadhesion to prolong\ngastric residence time was prepared.\n\n\n\nPolymers used were Hydroxy Propyl Methyl Cellulose (HPMC) K15M as matrix forming\nwater swellable release retarding polymer and carbopol 934P as bioadhesive polymer. The gas generating\nagents used were sodium bicarbonate and citric acid. The prepared floating bioadhesive tablets of\nNizatidine were optimized by 32 factorial design to study independent variable X1 (concentration of CP\n934P) and X2 (concentration of HPMC K15M) and dependent variables as floating lag time, cumulative\npercentage drug release at 12h and swelling index. Tablets were evaluated for various parameters\nsuch as hardness, friability, drug content, swelling behavior, floating lag time, bioadhesive strength,\ndrug release profile and stability.\n\n\n\nAll the formulations passed the test for weight variation, hardness, content uniformity and\nshowed acceptable results with respect to drug content (97.93 ± 0.57) and % friability. The tablet containing\n25% HPMC K15M and 13.75 % Carbopol 934P was selected as optimized formulation which\nshowed the floating lag time of 74.34±2.08 seconds, drug release of 97.03±0.55% at 12 h (R12h,%), S.I\nas 79.24±0.87 at 9 h and bioadhesive strength as 10.0023±21.47 g. Stability of the formulation was\nproved using stability study.\n\n\n\nThe formulated tablets have a potential for controlled release of the drug through floatation\nand bioadhesion.\n","PeriodicalId":11310,"journal":{"name":"Drug Delivery Letters","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Formulation and In vitro Evaluation of Gastroretentive Floating Bioadhesive Tablets of Nizatidine using Factorial Design\",\"authors\":\"V. Sabale, Hardikkumar Chaudhari, P. Sabale\",\"doi\":\"10.2174/2210303109666190221155353\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nThe aim of the present study was to formulate and evaluate floating bioadhesive\\ntablets of Nizatidine which is a competitive, reversible H2-receptor antagonist. Floatingbioadhesive\\ndrug delivery system exhibiting a unique combination of floatation and bioadhesion to prolong\\ngastric residence time was prepared.\\n\\n\\n\\nPolymers used were Hydroxy Propyl Methyl Cellulose (HPMC) K15M as matrix forming\\nwater swellable release retarding polymer and carbopol 934P as bioadhesive polymer. The gas generating\\nagents used were sodium bicarbonate and citric acid. The prepared floating bioadhesive tablets of\\nNizatidine were optimized by 32 factorial design to study independent variable X1 (concentration of CP\\n934P) and X2 (concentration of HPMC K15M) and dependent variables as floating lag time, cumulative\\npercentage drug release at 12h and swelling index. Tablets were evaluated for various parameters\\nsuch as hardness, friability, drug content, swelling behavior, floating lag time, bioadhesive strength,\\ndrug release profile and stability.\\n\\n\\n\\nAll the formulations passed the test for weight variation, hardness, content uniformity and\\nshowed acceptable results with respect to drug content (97.93 ± 0.57) and % friability. The tablet containing\\n25% HPMC K15M and 13.75 % Carbopol 934P was selected as optimized formulation which\\nshowed the floating lag time of 74.34±2.08 seconds, drug release of 97.03±0.55% at 12 h (R12h,%), S.I\\nas 79.24±0.87 at 9 h and bioadhesive strength as 10.0023±21.47 g. Stability of the formulation was\\nproved using stability study.\\n\\n\\n\\nThe formulated tablets have a potential for controlled release of the drug through floatation\\nand bioadhesion.\\n\",\"PeriodicalId\":11310,\"journal\":{\"name\":\"Drug Delivery Letters\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Delivery Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2210303109666190221155353\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Delivery Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2210303109666190221155353","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
Formulation and In vitro Evaluation of Gastroretentive Floating Bioadhesive Tablets of Nizatidine using Factorial Design
The aim of the present study was to formulate and evaluate floating bioadhesive
tablets of Nizatidine which is a competitive, reversible H2-receptor antagonist. Floatingbioadhesive
drug delivery system exhibiting a unique combination of floatation and bioadhesion to prolong
gastric residence time was prepared.
Polymers used were Hydroxy Propyl Methyl Cellulose (HPMC) K15M as matrix forming
water swellable release retarding polymer and carbopol 934P as bioadhesive polymer. The gas generating
agents used were sodium bicarbonate and citric acid. The prepared floating bioadhesive tablets of
Nizatidine were optimized by 32 factorial design to study independent variable X1 (concentration of CP
934P) and X2 (concentration of HPMC K15M) and dependent variables as floating lag time, cumulative
percentage drug release at 12h and swelling index. Tablets were evaluated for various parameters
such as hardness, friability, drug content, swelling behavior, floating lag time, bioadhesive strength,
drug release profile and stability.
All the formulations passed the test for weight variation, hardness, content uniformity and
showed acceptable results with respect to drug content (97.93 ± 0.57) and % friability. The tablet containing
25% HPMC K15M and 13.75 % Carbopol 934P was selected as optimized formulation which
showed the floating lag time of 74.34±2.08 seconds, drug release of 97.03±0.55% at 12 h (R12h,%), S.I
as 79.24±0.87 at 9 h and bioadhesive strength as 10.0023±21.47 g. Stability of the formulation was
proved using stability study.
The formulated tablets have a potential for controlled release of the drug through floatation
and bioadhesion.