药物输送
背景(考古学)
细胞外小泡
药品
纳米技术
聚乙二醇
计算生物学
胞外囊泡
核酸
计算机科学
生化工程
化学
生物
药理学
材料科学
细胞生物学
生物化学
工程类
微泡
古生物学
小RNA
基因
作者
Coline Ducrot,Stanislas Loiseau,Christophe Wong,Elise Madec,Jeanne Volatron,Max Piffoux
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2023-02-24
卷期号:558: 216107-216107
被引量:60
标识
DOI:10.1016/j.canlet.2023.216107
摘要
Extracellular vesicles (EVs) are expected to serve as interesting drug delivery vectors as they may offer unique and new properties for drug delivery. Their natural origin, protein and nucleic acid composition, and intrinsic pleiotropic therapeutic effects could enable new possibilities in the field of drug delivery. Here, we aimed to review the methods used to produce Hybrid EVs, a recently emerged type of EV-based vector made from both EVs and synthetic vectors to exploit their respective properties. Hybrid EV/synthetic objects can be obtained by incubation, electrostatic interactions, polyethylene glycol (PEG)-mediated fusion, co-extrusion, freeze-thawing, or simple EV surface modification, leading to different types of objects. We also opted to review the properties of these vectors, and specifically compared them with those of other drug delivery vectors. It has to be noticed that only a limited number of study report loading metrics that allow cross article comparison. Based on this critical analysis, we attempted to draw the pith and marrow from these relatively difficult-to-compare studies and integrate them into the more general context of opportunities in drug delivery and drug development, with a particular focus on oncology.
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