{"title":"FORMULATION AND CHARACTERIZATION OF CROSS LINK CHITOSAN MICROSPHERE: APPLICATION AS A MUCOADHESIVE DRUG DELIVERY OF NIFEDIPINE","authors":"N. Pandya, R. R. Jivani, N. P. Jivani","doi":"10.1234/JGPT.V4I11.415","DOIUrl":null,"url":null,"abstract":"The purpose of this research was to formulate and systematically evaluate in vitro performance of mucoadhesive microspheres of nifedipine. Cross-linking Nifedipine microspheres containing chitosan were prepared by simple emulsification phase separation technique using glutaraldehyde as a cross-linking agent. A simple lattice design was employed to study the effect of independent variables, volume of cross-linking agent (X1), cross-linking time (X2) and total stirring time (X3) on dependent variables percentage mucoadhesion, drug entrapment efficiency and release of nifedipine. Results of preliminary trials indicate that volume of cross-linking agent, time for cross-linking and total stirring time affected characteristics of microspheres. Microspheres were discrete, spherical, and free flowing. The microspheres exhibited good mucoadhesive property in the in vitro wash-off test and also showed high percentage drug entrapment efficiency. From the statistical evaluation, best batch found showed 60.47 % mucoadhesion after 1 hour, 60 % drug entrapment efficacy and desired drug release profile upto 12 hours by taking 3.2 ml of cross-linking agent, 3 hours of crosslinking time and 3.8 hours of total stirring time. This statistically optimized batch was repeated to validate the results.","PeriodicalId":15889,"journal":{"name":"Journal of Global Pharma Technology","volume":"152 1","pages":"01-07"},"PeriodicalIF":0.0000,"publicationDate":"2012-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Global Pharma Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1234/JGPT.V4I11.415","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The purpose of this research was to formulate and systematically evaluate in vitro performance of mucoadhesive microspheres of nifedipine. Cross-linking Nifedipine microspheres containing chitosan were prepared by simple emulsification phase separation technique using glutaraldehyde as a cross-linking agent. A simple lattice design was employed to study the effect of independent variables, volume of cross-linking agent (X1), cross-linking time (X2) and total stirring time (X3) on dependent variables percentage mucoadhesion, drug entrapment efficiency and release of nifedipine. Results of preliminary trials indicate that volume of cross-linking agent, time for cross-linking and total stirring time affected characteristics of microspheres. Microspheres were discrete, spherical, and free flowing. The microspheres exhibited good mucoadhesive property in the in vitro wash-off test and also showed high percentage drug entrapment efficiency. From the statistical evaluation, best batch found showed 60.47 % mucoadhesion after 1 hour, 60 % drug entrapment efficacy and desired drug release profile upto 12 hours by taking 3.2 ml of cross-linking agent, 3 hours of crosslinking time and 3.8 hours of total stirring time. This statistically optimized batch was repeated to validate the results.