前药
联合疗法
光热治疗
药理学
细胞毒性T细胞
光动力疗法
药品
靶向治疗
生物相容性材料
材料科学
癌症研究
纳米技术
靶向给药
细胞色素c
组合化学
肿瘤细胞
细胞毒性
线粒体
药物输送
纳米医学
酶
精密医学
放射治疗
细胞凋亡
癌症治疗
癌症治疗
抗癌药
癌症医学
医学
癌症
作者
Hongyu Wang,Tao Zhang,Shaojin Lu,Tingting Sun,Zhigang Xie,Xuesi Chen
标识
DOI:10.1002/adma.202412376
摘要
Precision medicine is characterized by high accuracy and safety, showing robust superiority and significant potential in clinical applications. Organelle-targeting therapies are important tactics for precision medicine, allowing for efficient tumor treatment and reduced off-target toxicity. Herein, a mitochondria-targeting and hypoxia-activatable nanoprodrug (POPZ NPs) is prepared. The N-oxide groups of POPZ NPs can successfully target mitochondria and are reduced to tertiary amines by Cytochrome P450 enzymes (CYP450s), which are highly expressed in hypoxic tumors and located in the inner mitochondrial membranes. Biocompatible POPZ NPs can become cytotoxic and produce type-I photodynamic activities and enhance photothermal properties after reduction by CYP450s. The tumor-specific activatable prodrug reveals potent efficacy for tumor elimination without causing systemic toxicity. This work may provide a paradigm for achieving precision medicine as well as more convenient and feasible tumor combination therapy.
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