光动力疗法
光敏剂
电子转移
金属有机骨架
卟啉
单线态氧
化学
光诱导电子转移
体内
活性氧
材料科学
纳米技术
光化学
氧气
生物化学
有机化学
生物
生物技术
吸附
作者
Jiahao Zhuang,Shitai Liu,Bowen Li,Zhiyao Li,Chongzhi Wu,Duo Xu,Weidong Pan,Zhen Li,Xiaogang Liu,Bin Liu
标识
DOI:10.1002/anie.202420643
摘要
Photodynamic therapy (PDT), a minimally invasive and effective local treatment, heavily depends on photosensitizer (PS) performance and oxygen availability. Despite the use of PS‐based metal‐organic frameworks (MOFs) to address the solubility and aggregation issues of PSs, the inherent hypoxic intolerance of mainstream Type II PDT remains challenging. Herein, we report an electron transfer strategy for the fabrication of hypoxia‐tolerant Type I MOFs by encapsulating thymoquinone (TQ) into existing Type II MOFs. With TQ serving as an effective electron transfer mediator, it facilitates the electron transfer process from the MOF ligand PS to oxygen, establishing the Type I pathway and attenuating the original Type II pathway. Four representative porphyrin‐based MOFs are synthesized to demonstrate the proposed strategy. Our findings reveal that TQ@MOF‐1 nanoparticles (NPs) exhibit enhanced anticancer activity under hypoxic conditions and superior in vivo antitumor efficacy compared to parent MOF‐1 NPs. This work offers an effective and universal strategy to modulate ROS generation in PS‐based MOFs, endowing hypoxic tolerance with improved PDT performance against solid tumors.
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