Enhancing Targeted Drug Delivery through Cell-Specific Endosomal Escape

被引:3
|
作者
Chen, Pengwen [1 ]
Cabral, Horacio [1 ]
机构
[1] Univ Tokyo, Dept Bioengn, 7-3-1 Hongo,Bunkyo-ku, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
Endosomal escape; drug delivery; stimuli-responsive nanocarrier; nanomedicine; CATHEPSIN-B; POLYMERIC MICELLES; BUBBLE LIPOSOMES; GENE-TRANSFER; CANCER; NANOPARTICLES; PH; ACIDIFICATION; PROTEASES; THERAPY;
D O I
10.1002/cmdc.202400274
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Endosome is a major barrier in the intracellular delivery of drugs, especially for biologics, such as proteins, peptides, and nucleic acids. After being endocytosed, these cargos will be trapped inside the endosomal compartments and finally degraded in the lysosomes. Thus, various strategies have been developed to facilitate the escape of cargos from the endosomes to improve the intracellular delivery efficiency. While the majority of the studies are focusing on strengthening the endosomal escape capability to maximize the delivery outcome, recent evidence suggests that a careful control of the endosomal escape process could provide opportunity for targeted drug delivery. In this concept review, we examined current delivery systems that can sense intra-endosomal factors or external stimuli for controlling endosomal escape toward a targeted intracellular delivery of cargos. Furthermore, the prospects and challenges of such strategies are discussed. Controlling the endosomal escape provides opportunity for enhancing targeted drug delivery. Delivery systems sensing internal or external stimuli can be designed to conduct endosomal escape only in target cells rather than non-target cells to reach a delivery with high specificity. image
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收藏
页数:9
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