喜树碱
前药
线粒体
癌细胞
药物输送
细胞凋亡
活性氧
体内
生物物理学
细胞内
材料科学
生物化学
细胞生物学
癌症研究
药理学
化学
生物
癌症
纳米技术
生物技术
遗传学
作者
Yajun Wang,Tian Zhang,Chunmei Hou,Menghang Zu,Yi Lu,Xianbin Ma,Die Jia,Peng Xue,Yuejun Kang,Zhigang Xu
标识
DOI:10.1021/acsami.9b10211
摘要
Mitochondria-targeting cancer therapies have achieved unprecedented advances attributed to their superior ability for improving drug delivery efficiency and producing an enhanced therapeutic effect. Herein, we report a mitochondria-targeting camptothecin (CPT) polyprodrug system (MCPS) covalently decorated with a high-proportioned CPT content, which can realize drug release specifically responsive to a tumor microenvironment. The nonlinear structure of MCPS can form water-soluble unimolecular micelles with high micellar stability and improved drug accumulation in tumoral cells/tissues. Furthermore, a classical mitochondria-targeting agent, triphenylphosphonium bromide, was tethered in this prodrug system, which causes mitochondrial membrane potential depolarization and mediates the transport of CPT into mitochondria. The disulfide bond in MCPS can be cleaved by an intracellular reductant such as glutathione, leading to enhanced destruction of mitochondria DNA and cell apoptosis induced by a high level of reactive oxygen species. The systematic analyses both in vitro and in vivo indicated the excellent tumor inhibition effect and biosafety of MCPS, which is believed to be an advantageous nanoplatform for subcellular organelle-specific chemotherapy of cancer.
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