Pooja D. Vaghela
{"title":"Effect of Polymers in the Design and Characterization of Sustained Release Aceclofenac Microspheres","authors":"Pooja D. Vaghela","doi":"10.35652/igjps.2022.12020","DOIUrl":null,"url":null,"abstract":"Purpose:Theaim of present work was to design and characterize sustained release Aceclofenac, model drug, microspheres by emulsion solvent evaporation technique.Methods:Aceclofenac microspheres were prepared by emulsion solvent evaporation process by using Ethyl cellulose and Hydroxy propyl methyl cellulose as polymers. The microspheres were evaluated by drug release study, drug content, drug loading and encapsulation efficiency, and determination of percentage yield.Results:The present study shows that as the polymer concentration increases the percentage encapsulation efficiency, and drug content in the microsphere formulation also increases. The microspheres of all the formulated batches were spherical, discrete and free flowing. Increasing the polymer concentration in microsphere formulation decreases the rate of drug release dramatically.Conclusions:It might be concluded that drug loaded microspheres appear to be a suitable delivery system for a model drug, Aceclofenac, and may help to reduce dose of drug andfrequency of administration. Sustained release of Aceclofenac microspheres could be formulated by using ethyl cellulose and HPMC as a release retardant by emulsion solvent evaporation technique.©2022iGlobal Research and PublishingFoundation. All rights reserved","PeriodicalId":13366,"journal":{"name":"Indo Global Journal of Pharmaceutical Sciences","volume":"217 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indo Global Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35652/igjps.2022.12020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
高分子材料对乙酰氯芬酸缓释微球设计与表征的影响
目的:采用乳化液溶剂蒸发法设计并表征模型药乙酰氯芬酸缓释微球。方法:以乙基纤维素和羟丙基甲基纤维素为聚合物,采用乳液溶剂蒸发法制备乙酰氯芬酸微球。通过药物释放、药物含量、载药量、包封率、收率等指标对微球进行评价。结果:本研究表明,随着聚合物浓度的增加,微球制剂的包封率和药物含量也随之增加。各配方批次的微球均为球形、离散、自由流动。增加微球制剂中聚合物的浓度可显著降低药物的释放速度。结论:载药微球可能是模型药物乙酰氯芬酸的一种合适的给药系统,并可能有助于减少给药剂量和给药频率。以乙基纤维素和HPMC为缓释剂,采用乳液溶剂蒸发法制备醋酸氯芬酸缓释微球。©2022全球研究与出版基金会。版权所有
本文章由计算机程序翻译,如有差异,请以英文原文为准。