自乳化给药系统的新方法及近期专利综述

A. Deep, Rimmy, S. Tahlan
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引用次数: 0

摘要

目前的主要目的是建立一种革命性的自纳米乳化给药系统,以提高必要的生物利用度,提高口服给药的临床疗效。本研究的主要目标是开发一种新型的自纳米乳化药物递送系统(SNEDDS),用于口服给药,水溶性差的药物。SNEDDS用于强化弱水溶性或亲脂性药物。SNEDDS用于强化弱水溶性或亲脂性药物。它含有一种微或纳米乳液的油携带药物,自发地搅拌水介质。为了提高亲脂性药物的溶解度,SNEDDS在生物制药分类系统[BCS类]II和IV类药物中应用最为广泛。sndds能明显提高溶解速率,防止界面张力。在含水介质中,如胃肠道液体,SNEDDS稀释后产生稳定的乳液。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Approaches of Self Emulsifying Drug Delivery Systems and recent patents: A Comprehensive Review
The main aim of the current work is to set up a revolutionary Self Nano-emulsifying drug delivery system to improve the necessary bio-availability and to boost clinical efficacy when administered orally. This study's main target is to develop a novel self-nano emulsifying drug delivery system (SNEDDS) for orally administered, poorly water-soluble medicines. SNEDDS is designed to intensify weakly water dissolvable or lipophilic drugs. SNEDDS is designed to intensify weakly water dissolvable or lipophilic drugs. It contains a micro- or nano-emulsion of oil carrying medicament that spontaneously agitates an aqueous medium. For enhancing the solubility of lipophilic medicines, SNEDDS is the most significantly used in biopharmaceutics classification system [BCS class] II and IV pharmaceuticals. The improved rate of dissolution and prevention of interfacial tension are clearly demonstrated by SNEDDS. In aqueous mediums, such as gastrointestinal fluid, SNEDDS produces a stable emulsion after dilution.
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