利巴米胺负载胃保留藻酸盐基黏附微球的研究:配方及体外、体内评价

Pooja Kashid, R. Doijad, A. Shete, Sachin Sajane, Abhimanyu Bhagat
{"title":"利巴米胺负载胃保留藻酸盐基黏附微球的研究:配方及体外、体内评价","authors":"Pooja Kashid, R. Doijad, A. Shete, Sachin Sajane, Abhimanyu Bhagat","doi":"10.5530/PHM.2016.7.20","DOIUrl":null,"url":null,"abstract":"Introduction: Oral route is the most common and convenient route to deliver the drug. Many oral drug delivery systems were developed to improve drug bio availability; gastro retentive drug delivery system is one of them. Gastroretentive drug delivery system is the system in which a drug can remain in the gastric region for several hours in order to prolong its gastric residence time. The purpose of this work was to develop and evaluate rebamipide loaded gastro retentive alginate based muco adhesive beads. Materials and Methods: Rebamipide loaded alginate beads were prepared by ionotropic gelation and polyelectrolyte complexation method. Prepared beads were characterized for IR, DSC, SEM and evaluated for dissolution and stability studies. Results: The FTIR spectra revealed that there were no interaction between drug and excipients. The particle size analysis showed that beads with 3% of sodium alginate were spherical in shape. The mucoadhesion study reveals that as concentration of alginate and carbopol 934 increases percentage of mucoadhesion also increases. Conclusion: From in-vivo study it was concluded that the prepared formulation showed better control on ulcer than that of pure rebamipide. Rebamipide was successfully formulated as gastroretentive floating and mucoadhesive alginate beads by using ionotropic gelation and polyelectrolyte complexation method. Key words: Rebamipide, Gastroretentive, Alginate beads, Mucoadhesion and Carbopol 934.","PeriodicalId":19960,"journal":{"name":"Pharmaceutical Methods","volume":"15 40 1","pages":"132-138"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Studies on Rebamipide Loaded Gastroretentive Alginate Based Mucoadhesive Beads: Formulation & In-vitro, In-vivo Evaluation\",\"authors\":\"Pooja Kashid, R. Doijad, A. Shete, Sachin Sajane, Abhimanyu Bhagat\",\"doi\":\"10.5530/PHM.2016.7.20\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Oral route is the most common and convenient route to deliver the drug. Many oral drug delivery systems were developed to improve drug bio availability; gastro retentive drug delivery system is one of them. Gastroretentive drug delivery system is the system in which a drug can remain in the gastric region for several hours in order to prolong its gastric residence time. The purpose of this work was to develop and evaluate rebamipide loaded gastro retentive alginate based muco adhesive beads. Materials and Methods: Rebamipide loaded alginate beads were prepared by ionotropic gelation and polyelectrolyte complexation method. Prepared beads were characterized for IR, DSC, SEM and evaluated for dissolution and stability studies. Results: The FTIR spectra revealed that there were no interaction between drug and excipients. The particle size analysis showed that beads with 3% of sodium alginate were spherical in shape. The mucoadhesion study reveals that as concentration of alginate and carbopol 934 increases percentage of mucoadhesion also increases. Conclusion: From in-vivo study it was concluded that the prepared formulation showed better control on ulcer than that of pure rebamipide. Rebamipide was successfully formulated as gastroretentive floating and mucoadhesive alginate beads by using ionotropic gelation and polyelectrolyte complexation method. Key words: Rebamipide, Gastroretentive, Alginate beads, Mucoadhesion and Carbopol 934.\",\"PeriodicalId\":19960,\"journal\":{\"name\":\"Pharmaceutical Methods\",\"volume\":\"15 40 1\",\"pages\":\"132-138\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmaceutical Methods\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5530/PHM.2016.7.20\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/PHM.2016.7.20","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8

摘要

口服给药是最常见、最方便的给药途径。许多口服给药系统的开发是为了提高药物的生物利用度;胃保留给药系统就是其中之一。胃保留性给药系统是指药物在胃内停留数小时以延长其在胃内停留时间的系统。本工作的目的是开发和评价利巴米胺负载的胃保留藻酸盐基粘液粘附珠。材料与方法:采用离子化凝胶法和聚电解质络合法制备了负载雷巴米胺的海藻酸盐微球。用IR、DSC、SEM对制备的微球进行了表征,并对其溶出度和稳定性进行了评价。结果:FTIR光谱显示药物与辅料无相互作用。粒径分析表明,添加3%海藻酸钠的微球呈球形。黏附研究表明,随着藻酸盐和卡泊酚934浓度的增加,黏附率也随之增加。结论:体内实验表明,该制剂对溃疡的控制效果优于纯利巴米胺。采用亲离子凝胶法和聚电解质络合法制备雷巴米胺为胃保留型浮黏藻酸盐微球。关键词:利巴米胺,胃保留剂,海藻酸盐珠,黏附,卡波波尔934
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on Rebamipide Loaded Gastroretentive Alginate Based Mucoadhesive Beads: Formulation & In-vitro, In-vivo Evaluation
Introduction: Oral route is the most common and convenient route to deliver the drug. Many oral drug delivery systems were developed to improve drug bio availability; gastro retentive drug delivery system is one of them. Gastroretentive drug delivery system is the system in which a drug can remain in the gastric region for several hours in order to prolong its gastric residence time. The purpose of this work was to develop and evaluate rebamipide loaded gastro retentive alginate based muco adhesive beads. Materials and Methods: Rebamipide loaded alginate beads were prepared by ionotropic gelation and polyelectrolyte complexation method. Prepared beads were characterized for IR, DSC, SEM and evaluated for dissolution and stability studies. Results: The FTIR spectra revealed that there were no interaction between drug and excipients. The particle size analysis showed that beads with 3% of sodium alginate were spherical in shape. The mucoadhesion study reveals that as concentration of alginate and carbopol 934 increases percentage of mucoadhesion also increases. Conclusion: From in-vivo study it was concluded that the prepared formulation showed better control on ulcer than that of pure rebamipide. Rebamipide was successfully formulated as gastroretentive floating and mucoadhesive alginate beads by using ionotropic gelation and polyelectrolyte complexation method. Key words: Rebamipide, Gastroretentive, Alginate beads, Mucoadhesion and Carbopol 934.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信