Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization

Naga Sai D, K. V, C. Sb, B. B
{"title":"Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization","authors":"Naga Sai D, K. V, C. Sb, B. B","doi":"10.46624/ajptr.2019.v9.i3.015","DOIUrl":null,"url":null,"abstract":"Please cite this article as: Bhavani B et al., Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization. American Journal of PharmTech Research 2019. Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization Naga Sai D, Krishna Veni V, Chandra Sekhar SB, Bhavani B* 1.Koringa College of Pharmacy, Tallarevu, East Godavari 2.Drug Testing Laboratory, Karnataka ABSTRACT Donepezil HCl is an anti Alzheimer’s drug of the acetylcholinesterase class. It is widely used in treatment of Alzheimer’s disease and to control dementia. Orodispersable Tablets (ODTs) containing Donepezil HCl was prepared using super-disintegrant (croscarmellose sodium) by direct compression method using solid dispersion technique to mask the taste of the drug. Three types of excipient were used to mask the taste namely Mannitol, PEG 6000 and PVP K 30 in three different ratios (i.e. 1:1, 1:2, 1:3) using solvent evaporation method in solid dispersion technique. The optimized formulation shows the minimum disintegration time of 50 sec and release maximum amount of drug in 10 min. Short term stability studies indicated no significant changes in hardness, friability, in vitro disintegration time, drug content and in vitro drug release.","PeriodicalId":7701,"journal":{"name":"American Journal of PharmTech Research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of PharmTech Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46624/ajptr.2019.v9.i3.015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Please cite this article as: Bhavani B et al., Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization. American Journal of PharmTech Research 2019. Solid Dispersion Method for Design of Donepezil Orodispersible Tablets: Formulation & Characterization Naga Sai D, Krishna Veni V, Chandra Sekhar SB, Bhavani B* 1.Koringa College of Pharmacy, Tallarevu, East Godavari 2.Drug Testing Laboratory, Karnataka ABSTRACT Donepezil HCl is an anti Alzheimer’s drug of the acetylcholinesterase class. It is widely used in treatment of Alzheimer’s disease and to control dementia. Orodispersable Tablets (ODTs) containing Donepezil HCl was prepared using super-disintegrant (croscarmellose sodium) by direct compression method using solid dispersion technique to mask the taste of the drug. Three types of excipient were used to mask the taste namely Mannitol, PEG 6000 and PVP K 30 in three different ratios (i.e. 1:1, 1:2, 1:3) using solvent evaporation method in solid dispersion technique. The optimized formulation shows the minimum disintegration time of 50 sec and release maximum amount of drug in 10 min. Short term stability studies indicated no significant changes in hardness, friability, in vitro disintegration time, drug content and in vitro drug release.
多奈哌齐口腔分散片的固体分散设计:配方与表征
请引用这篇文章:Bhavani B et al.,固体分散法设计多奈哌齐口服分散片:配方与表征。美国医药技术研究杂志2019。多奈哌齐口腔分散片的固体分散法设计:处方与表征科林加药学院,塔拉雷乌,东戈达瓦里盐酸多奈哌齐是一种抗阿尔茨海默病的乙酰胆碱酯酶类药物。它被广泛用于治疗阿尔茨海默病和控制痴呆症。采用固体分散技术,采用超崩解剂(交联棉糖钠)直接压缩法制备盐酸多奈哌齐口腔分散片。采用固体分散技术中的溶剂蒸发法,以甘露醇、PEG 6000和PVP K 30三种不同的配比(1:1、1:2、1:3)掩盖味。优化后的处方最短崩解时间为50秒,最大释药量为10 min。短期稳定性研究表明,其硬度、脆度、体外崩解时间、药物含量和体外释药量均无明显变化。
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
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