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用于蛋白质和肽类药物持续递送的脂质和聚乳酸-羟基乙酸共聚物微粒

Lipid and PLGA Microparticles for Sustained Delivery of Protein and Peptide Drugs.

作者信息

Wu Chengyu, Mu Huiling

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, DK 2100, Copenhagen, Denmark.

出版信息

Pharm Nanotechnol. 2020;8(1):22-32. doi: 10.2174/2211738507666191029160944.

Abstract

Solid lipid particles have a great potential in sustained drug delivery, the lipid excipients are solid at room temperature with a slow degradation rate. Poly (D, L-lactic-coglycolic acid) (PLGA) has been successfully clinically applied for the sustained delivery of peptide drugs. A recent study showed the advantage of hybrid PLGA-lipid microparticles (MPs) over PLGA MPs for the sustained delivery of peptide drug in vivo. In this paper, we briefly present PLGA MPs, solid lipid MPs and PLGA lipid hybrid MP prepared by the double emulsion method and the spray drying method and discuss the effects of excipients on encapsulation efficiency of protein and peptide drugs in the MPs. The pros and cons of PLGA MPs, solid lipid MPs and PLGA lipid hybrid MP as carriers for sustained delivery of protein and peptide drugs are also discussed.

摘要

固体脂质颗粒在药物持续递送方面具有巨大潜力,脂质辅料在室温下为固体,降解速率缓慢。聚(D,L-乳酸-乙醇酸)(PLGA)已成功临床应用于肽类药物的持续递送。最近的一项研究表明,PLGA-脂质混合微粒(MPs)在体内持续递送肽类药物方面优于PLGA MPs。在本文中,我们简要介绍了通过双乳液法和喷雾干燥法制备的PLGA MPs、固体脂质 MPs和PLGA-脂质混合MP,并讨论了辅料对MPs中蛋白质和肽类药物包封效率的影响。还讨论了PLGA MPs、固体脂质 MPs和PLGA-脂质混合MP作为蛋白质和肽类药物持续递送载体的优缺点。

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