纳米载体
纳米纤维
谷胱甘肽
胶束
两亲性
内化
线粒体
癌细胞
生物物理学
药物输送
化学
纳米技术
生物化学
材料科学
癌症
细胞
共聚物
生物
水溶液
酶
聚合物
有机化学
遗传学
作者
Jingbo Wang,Qinghao Zhou,Xiang Li,Debabrata Dutta,Zhishen Ge
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2022-04-01
卷期号:11 (4): 543-548
被引量:10
标识
DOI:10.1021/acsmacrolett.2c00059
摘要
Nanofibers self-assembled from peptides have attracted much attention to inhibit cancer cells. However, there are still some disadvantages, including high concentration for self-assembly and incapability to load drugs, which limit their applications. In this report, we rationally integrate self-assembled peptides, glutathione-sensitive disulfide bonds, and mitochondrial targeting moieties into the amphiphilic block copolymer to construct the nanocarriers, which can be used to load anticancer drug doxorubicin (DOX). After cellular internalization, the nanocarriers can reassemble from micelles to nanofibers under the trigger by glutathione and locate in mitochondria. The released DOX and nanofibers induce mitochondrial dysfunction and activate the apoptosis pathway to synergistically inhibit tumor cells. This organelle-specific drug delivery system with reassembly capability from micelles to nanofibers shows great potential for effectively killing cancer cells.
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