乳液界面反应法制备壳聚糖负载萘普生纳米颗粒及其性能评价

Q2 Pharmacology, Toxicology and Pharmaceutics Drug Delivery Letters Pub Date : 2019-05-15 DOI:10.2174/2210303109666190211150117
A. Sailaja, J. Banu
{"title":"乳液界面反应法制备壳聚糖负载萘普生纳米颗粒及其性能评价","authors":"A. Sailaja, J. Banu","doi":"10.2174/2210303109666190211150117","DOIUrl":null,"url":null,"abstract":"\n\nThe aim of this investigation was to develop and characterize naproxen loaded chitosan\nnanoparticles by emulsion interfacial reaction method.\n\n\n\nFor emulsion interfacial reaction method chitosan was used as a polymer. In this\nmethod, eight formulations were prepared by varying drug to polymer concentration.\n\n\n\nOut of eight formulations prepared using emulsion interfacial reaction method EI8 formulation\nwas found to be the best formulation. The drug content was observed as 94.4%, entrapment efficiency\nand loading capacity were found to be 87.5% and 75%, respectively. The mean particle diameter\nwas measured as 324.6nm and the Zeta potential value was found to be -42.4mv. In vitro drug release\ndata showed 97.2% of drug release rate sustained up to 12hrs.\n\n\n\nThe results clearly reveal that EI8 formulation having the highest amount of drug was\nconsidered as the best formulation because of its small mean particle diameter, good entrapment efficiency,\nand stability.\n","PeriodicalId":11310,"journal":{"name":"Drug Delivery Letters","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation and Evaluation of Chitosan Loaded Naproxen Nanoparticles by Emulsion Interfacial Reaction Method\",\"authors\":\"A. Sailaja, J. Banu\",\"doi\":\"10.2174/2210303109666190211150117\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nThe aim of this investigation was to develop and characterize naproxen loaded chitosan\\nnanoparticles by emulsion interfacial reaction method.\\n\\n\\n\\nFor emulsion interfacial reaction method chitosan was used as a polymer. In this\\nmethod, eight formulations were prepared by varying drug to polymer concentration.\\n\\n\\n\\nOut of eight formulations prepared using emulsion interfacial reaction method EI8 formulation\\nwas found to be the best formulation. The drug content was observed as 94.4%, entrapment efficiency\\nand loading capacity were found to be 87.5% and 75%, respectively. The mean particle diameter\\nwas measured as 324.6nm and the Zeta potential value was found to be -42.4mv. In vitro drug release\\ndata showed 97.2% of drug release rate sustained up to 12hrs.\\n\\n\\n\\nThe results clearly reveal that EI8 formulation having the highest amount of drug was\\nconsidered as the best formulation because of its small mean particle diameter, good entrapment efficiency,\\nand stability.\\n\",\"PeriodicalId\":11310,\"journal\":{\"name\":\"Drug Delivery Letters\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Delivery Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2210303109666190211150117\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Delivery Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2210303109666190211150117","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: 0

摘要

采用乳化液界面反应法制备了萘普生负载壳聚糖颗粒,并对其进行了表征。采用壳聚糖作为聚合物进行乳液界面反应。在该方法中,通过改变药物与聚合物的浓度,制备了8种制剂。采用乳液界面反应法制备的8个配方中,EI8为最佳配方。所得样品中药物含量为94.4%,包封率为87.5%,载药量为75%。平均粒径为324.6nm, Zeta电位值为-42.4mv。体外释药数据显示,97.2%的释药率持续时间长达12小时。结果表明,EI8平均粒径小,包封效率好,稳定性好,给药量最高,为最佳配方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Preparation and Evaluation of Chitosan Loaded Naproxen Nanoparticles by Emulsion Interfacial Reaction Method
The aim of this investigation was to develop and characterize naproxen loaded chitosan nanoparticles by emulsion interfacial reaction method. For emulsion interfacial reaction method chitosan was used as a polymer. In this method, eight formulations were prepared by varying drug to polymer concentration. Out of eight formulations prepared using emulsion interfacial reaction method EI8 formulation was found to be the best formulation. The drug content was observed as 94.4%, entrapment efficiency and loading capacity were found to be 87.5% and 75%, respectively. The mean particle diameter was measured as 324.6nm and the Zeta potential value was found to be -42.4mv. In vitro drug release data showed 97.2% of drug release rate sustained up to 12hrs. The results clearly reveal that EI8 formulation having the highest amount of drug was considered as the best formulation because of its small mean particle diameter, good entrapment efficiency, and stability.
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
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
期刊最新文献
In-vitro and In-silico Examinations on Baicalein-loaded Solid Lipid Nanoparticles for Neurodegeneration D-Optimal Mixture Design Enabled Development of Lyophilized Nanoemulsifying Drug Delivery System of Paliperidone Intranasal Route an Alternative Approach for Systemic Drug Delivery: Recent Strategies and Progression Revolutionizing Nitrofurantoin Delivery: Unraveling Challenges and Pioneering Solutions for Enhanced Efficacy in UTI Treatment Hot Melt Extrusion Technique for Developing Pharmaceutical Co-crystals: A Review
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1