Self-Emulsifying Drug Delivery System (SEDDS) and its Pharmaceutical Applications

Sankha Bhattacharya
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引用次数: 3

Abstract

Poor aqueous solubility, oral bioavailability, inter, and inter-subject variability, and physical stability have always been a concern for pharmaceutical formulation scientists while formulating an oral dosage form. Self-Emulsifying Drug Delivery System (SEDDS) is a promising new approach to mitigating those potential problems. The main advantages of SEDDS are that it increases the solubility and decreases the bio-degradation of lipophilic drugs. Mostly BCS II & IV Class drugs are preferable. SEDDS is an admixture of drugs, oil, surfactants, cosolvents, and stabilizers. With little energy input, they form (o/w) microemulsion within the G.I. lumen. The present review discusses the various formulations of SEDDS, selection criteria for surfactants, oils, Patentable SEDDS dosage forms, solidification technique, characterization, and future approaches.
自乳化给药系统(SEDDS)及其制药应用
水溶性差、口服生物利用度、个体间和个体间的可变性以及物理稳定性一直是药物制剂科学家在制定口服剂型时所关注的问题。自乳化给药系统(SEDDS)是缓解这些潜在问题的一种很有前途的新方法。SEDDS的主要优点是增加了亲脂性药物的溶解度,减少了其生物降解。首选BCS II和iv类药物。SEDDS是药物、油、表面活性剂、共溶剂和稳定剂的混合物。在很少的能量输入下,它们在胃肠道腔内形成(0 /w)微乳剂。本综述讨论了SEDDS的各种配方,表面活性剂的选择标准,油,可申请专利的SEDDS剂型,固化技术,表征和未来的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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