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自乳化药物传递系统:一种新的药物传递方法。

Self-emulsifying drug delivery systems: a novel approach to deliver drugs.

机构信息

Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.

出版信息

Drug Deliv. 2022 Dec;29(1):1811-1823. doi: 10.1080/10717544.2022.2083724.

DOI:10.1080/10717544.2022.2083724
PMID:35666090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9176699/
Abstract

Self-emulsifying drug delivery systems (SEDDS) are a proven method for poorly soluble substances works by increasing the solubility and bioavailability. SEDDS and isotropic mixtures, are composed of oils, surfactants, and occasionally cosolvents. The ability of these formulations and methods to produce microemulsions or fine oil-in-water (o/w) emulsions after moderate stirring and dilution by water phase along the GI tract might be a promising technique for lipophilic agents with dissolution rate-limited absorption. This review provides an outline of SEDDS's numerous advances and biopharmaceutical elements, types, manufacturing, characterization, limitations, and future prospects. The evaluation of SEDDS and its applications are also discussed, focusing on the advances of SEDDS's solid self-emulsifying delivery mechanism and dosage form. By integrating suitable polymer into the formulation, SEDDS may be studied for the creation of a formulation with sustained drug release. This technology's improvement might lead to a new application in the field of medicine delivery. SEDDS has been demonstrated to be quite efficient in increasing oral bioavailability of lipophilic products. SEDDS is one of the promising methods for controlling the characteristics of medications that are not great choices for oral delivery. It is also worth mentioning that SEDDS may be made in variety of solid dosage forms that are acceptable for both oral and parenteral administration.

摘要

自乳化药物传递系统 (SEDDS) 是一种已被证实的方法,可用于增加脂溶性物质的溶解度和生物利用度。SEDDS 和各向同性混合物由油、表面活性剂和偶尔的助溶剂组成。这些配方和方法在适度搅拌和水相稀释后,能够在胃肠道中产生微乳液或精细的油包水 (o/w) 乳液,这可能是一种有前途的技术,可用于具有溶解速率限制吸收的亲脂性药物。本文综述了 SEDDS 的许多进展和生物制药要素、类型、制造、特性、局限性和未来前景。还讨论了 SEDDS 的评价及其应用,重点介绍了 SEDDS 的固体自乳化传递机制和剂型的进展。通过将合适的聚合物整合到配方中,SEDDS 可用于研究具有持续药物释放的制剂。这项技术的改进可能会在药物输送领域带来新的应用。SEDDS 已被证明在提高脂溶性产品的口服生物利用度方面非常有效。SEDDS 是控制口服给药不理想的药物特性的有前途的方法之一。值得一提的是,SEDDS 可以制成多种固体剂型,既可以口服也可以肠胃外给药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a7a/9176699/9d15aaa8d30e/IDRD_A_2083724_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a7a/9176699/708153d2aef7/IDRD_A_2083724_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a7a/9176699/9d15aaa8d30e/IDRD_A_2083724_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a7a/9176699/708153d2aef7/IDRD_A_2083724_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a7a/9176699/9d15aaa8d30e/IDRD_A_2083724_F0002_B.jpg

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