Development of an In situ Gel Polymer Composite for Local and Sustained Delivery of Drugs in Vaginal Cavity

Q2 Pharmacology, Toxicology and Pharmaceutics
S. S. Boregowda, Sadanand R. Maggidi, Rajamma A. Jayaramu, Nethravathi Puttegowda, Nikhat Parbin
{"title":"Development of an In situ Gel Polymer Composite for Local and Sustained Delivery of Drugs in Vaginal Cavity","authors":"S. S. Boregowda, Sadanand R. Maggidi, Rajamma A. Jayaramu, Nethravathi Puttegowda, Nikhat Parbin","doi":"10.2174/2210303109666190226152857","DOIUrl":null,"url":null,"abstract":"\n\nThe present research work is aimed at the development of an in situ gel polymer\ncomposite to provide local and sustained delivery of therapeutic agents in the vaginal cavity. Administration\nof medicated gel into a vaginal cavity is very complicated, inconvenient and needs expert assistance.\nThere is a chance of expulsion of liquid formulation from site of application, leads to poor therapeutic\nefficacy. The effective drug delivery system for the vaginal cavity should be of liquid for application\nand gel to reside in the cavity.\n\n\n\nIn situ gel composed of chitosan (0.8%) cross-linked with β-glycerol phosphate (15%) and\nglutaraldehyde treated guar gum (0.2%) was developed. Gel was characterized for in situ gelling properties.\nIn vitro drug release pattern of the gel was tested on a nutrient agar medium containing attenuated\nE. coli and B. Subtilis. In vitro diffusion pattern of gel was tested using KC-diffusion cell with\nSimulated Vaginal Fluid (SVF) (pH 4.2) as the diffusion medium.\n\n\n\n In situ gel exhibited sharpest sol-gel transition at 35±2°C, at pH 5.4 in 62±1.31sec. The viscosity\nof polymer composite is 51.25±3.68 CPs at 20±2°C and 328.56±4.16 CPs at 35±2°C. The gelation\ntime of gel was found to be decreasing as the concentration of cross-linking agent β-GP increased.\nFormulations exhibited a shear thinning property. Drug release from this polymeric composite was\nfound to be highly linear and follows non-fickian diffusion mechanism.\n\n\n\n This advanced thermosensitive in situ gel is convenient to apply and reside in the vaginal\ncavity for a prolonged period of time. The gel is mucoadhesive, biodegradable and suitable for controlled\ndrug delivery in the cavity.\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":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Delivery Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2210303109666190226152857","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 2

Abstract

The present research work is aimed at the development of an in situ gel polymer composite to provide local and sustained delivery of therapeutic agents in the vaginal cavity. Administration of medicated gel into a vaginal cavity is very complicated, inconvenient and needs expert assistance. There is a chance of expulsion of liquid formulation from site of application, leads to poor therapeutic efficacy. The effective drug delivery system for the vaginal cavity should be of liquid for application and gel to reside in the cavity. In situ gel composed of chitosan (0.8%) cross-linked with β-glycerol phosphate (15%) and glutaraldehyde treated guar gum (0.2%) was developed. Gel was characterized for in situ gelling properties. In vitro drug release pattern of the gel was tested on a nutrient agar medium containing attenuated E. coli and B. Subtilis. In vitro diffusion pattern of gel was tested using KC-diffusion cell with Simulated Vaginal Fluid (SVF) (pH 4.2) as the diffusion medium. In situ gel exhibited sharpest sol-gel transition at 35±2°C, at pH 5.4 in 62±1.31sec. The viscosity of polymer composite is 51.25±3.68 CPs at 20±2°C and 328.56±4.16 CPs at 35±2°C. The gelation time of gel was found to be decreasing as the concentration of cross-linking agent β-GP increased. Formulations exhibited a shear thinning property. Drug release from this polymeric composite was found to be highly linear and follows non-fickian diffusion mechanism. This advanced thermosensitive in situ gel is convenient to apply and reside in the vaginal cavity for a prolonged period of time. The gel is mucoadhesive, biodegradable and suitable for controlled drug delivery in the cavity.
用于阴道局部和持续给药的原位凝胶聚合物复合材料的研制
目前的研究工作旨在开发一种原位凝胶聚合物复合物,以在阴道中提供局部和持续的治疗剂递送。将药物凝胶注入阴道非常复杂、不方便,需要专家协助。液体制剂有可能从应用部位排出,导致疗效不佳。用于阴道腔的有效药物递送系统应该是用于应用的液体和驻留在腔中的凝胶。开发了由壳聚糖(0.8%)与β-甘油磷酸酯(15%)交联和戊二醛处理的瓜尔胶(0.2%)组成的原位凝胶。对凝胶的原位胶凝性能进行了表征。在含有衰减E的营养琼脂培养基上测试凝胶的体外药物释放模式。大肠杆菌和枯草芽孢杆菌。采用KC扩散池,以pH4.2的模拟阴道液(SVF)为扩散介质,对凝胶的体外扩散模式进行了测试。原位凝胶在35±2°C、pH 5.4和62±1.31秒内表现出最明显的溶胶-凝胶转变。聚合物复合材料的粘度在20±2°C.为51.25±3.68 CPs,在35±2中为328.56±4.16 CPs。随着交联剂β-GP浓度的增加,凝胶的凝胶化时间逐渐缩短。制剂表现出剪切稀化特性。发现这种聚合物复合物的药物释放是高度线性的,并遵循非菲克扩散机制。这种先进的热敏原位凝胶易于涂抹并在阴道腔中长时间停留。该凝胶具有粘性,可生物降解,适合在腔内进行药物控释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Drug Delivery Letters
Drug Delivery Letters Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.70
自引率
0.00%
发文量
30
×
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