光敏剂
化学
上睑下垂
活性氧
光动力疗法
膜
共价键
体内
组合化学
生物物理学
单线态氧
癌细胞
光毒性
光热治疗
纳米载体
血卟啉
水溶液
过氧化氢
血浆药物
和厚朴酚
苯并咪唑
作者
Bingbing Zheng,Fapu Wu,Qian Ma,Xinyu Qiu,Yuexia Yang,Bin Zhou,Yanyan Wang,Yuehua Chen,T Wang,Hu Xiong
出处
期刊:Small
[Wiley]
日期:2026-05-20
卷期号:22 (39): e73892-e73892
摘要
The development of precise and stable membrane-anchoring photosensitizers is important but challenging for pyroptosis-mediated antitumor therapy. Here, we report a tumor cell membrane-anchored BODIPY photosensitizer (TPMS) capable of inducing plasma membrane rupture via the pyroptosis pathway. Its modular structure integrates a BODIPY core and phenothiazine unit to boost reactive oxygen species (ROS) generation, a quaternary ammonium salt for membrane anchoring, and a disulfide bridge for covalent immobilization. In aqueous solution, TPMS self-assembles into nanoaggregates with intense absorption at 658 nm and efficient type-I ROS production. Notably, TPMS was covalently immobilized on plasma membranes with a prolonged retention time of at least 2 h and effectively induced pyroptosis of cancer cells upon light irradiation. Furthermore, in vivo studies confirmed its potent tumor eradication efficacy with minimal systemic toxicity. This work not only provides a rational molecular strategy for constructing long-term membrane-localized photosensitizers but also highlights the potential of pyroptosis-mediated anticancer treatment.
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