Lakshminarayana Reddy Golamaru, K. Rajnarayana, K. Jayaveera
{"title":"硝唑昔尼缓释片的研制及体外评价","authors":"Lakshminarayana Reddy Golamaru, K. Rajnarayana, K. Jayaveera","doi":"10.7439/IJPR.V6I2.3017","DOIUrl":null,"url":null,"abstract":"Objective: The objective of the present investigation was to develop a sustained release (SR) tablet formulation of Nitazoxanide.Methods: Nitazoxanide Tablets were prepared by employing wet granulation methods and hydrophilic polymers used as drug release retardants. The dissolution data also evaluated for the drug release mechanism and kinetics. The optimized formulation was subjected for in vivo studies in rabbits.Results: Based on data obtained from the in vitro drug release studies 5%w/w of Methocel K100M was selected as a release retardant. The drug release followed first order kinetics and fickian diffusion.Conclusion: Present investigation indicates that the developed formulation was able to sustain the drug release.","PeriodicalId":14194,"journal":{"name":"International Journal of Pharmacological Research","volume":"4 1","pages":"75-80"},"PeriodicalIF":0.0000,"publicationDate":"2016-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Development and in vitro- in vivo evaluation of Nitazoxanide sustained release tablets\",\"authors\":\"Lakshminarayana Reddy Golamaru, K. Rajnarayana, K. Jayaveera\",\"doi\":\"10.7439/IJPR.V6I2.3017\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: The objective of the present investigation was to develop a sustained release (SR) tablet formulation of Nitazoxanide.Methods: Nitazoxanide Tablets were prepared by employing wet granulation methods and hydrophilic polymers used as drug release retardants. The dissolution data also evaluated for the drug release mechanism and kinetics. The optimized formulation was subjected for in vivo studies in rabbits.Results: Based on data obtained from the in vitro drug release studies 5%w/w of Methocel K100M was selected as a release retardant. The drug release followed first order kinetics and fickian diffusion.Conclusion: Present investigation indicates that the developed formulation was able to sustain the drug release.\",\"PeriodicalId\":14194,\"journal\":{\"name\":\"International Journal of Pharmacological Research\",\"volume\":\"4 1\",\"pages\":\"75-80\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Pharmacological Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7439/IJPR.V6I2.3017\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmacological Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7439/IJPR.V6I2.3017","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Development and in vitro- in vivo evaluation of Nitazoxanide sustained release tablets
Objective: The objective of the present investigation was to develop a sustained release (SR) tablet formulation of Nitazoxanide.Methods: Nitazoxanide Tablets were prepared by employing wet granulation methods and hydrophilic polymers used as drug release retardants. The dissolution data also evaluated for the drug release mechanism and kinetics. The optimized formulation was subjected for in vivo studies in rabbits.Results: Based on data obtained from the in vitro drug release studies 5%w/w of Methocel K100M was selected as a release retardant. The drug release followed first order kinetics and fickian diffusion.Conclusion: Present investigation indicates that the developed formulation was able to sustain the drug release.