光动力疗法
卟啉
细胞器
化学
双层
金属
对偶(语法数字)
纳米技术
图层(电子)
生物化学
组合化学
材料科学
光化学
有机化学
艺术
文学类
作者
Taokun Luo,Yingjie Fan,Jianming Mao,Xiaomin Jiang,Luciana Albano,Eric Yuan,Tomas Germanas,Wenbin Lin
标识
DOI:10.1002/anie.202301910
摘要
Abstract The efficacy of photodynamic therapy (PDT) depends on the subcellular localization of photosensitizers. Herein, we report a dual‐organelle‐targeted nanoparticle platform for enhanced PDT of cancer. By grafting 5‐aminolevulinic acid (ALA) to a Hf 12 ‐based nanoscale metal‐organic layer (Hf‐MOL) via carboxylate coordination, ALA/Hf‐MOL enhanced ALA delivery and protoporphyrin IX (PpIX) synthesis in mitochondria, and trapped the Hf‐MOL comprising 5,15‐di‐p‐benzoatoporphyrin (DBP) photosensitizers in lysosomes. Light irradiation at 630 nm simultaneously excited PpIX and DBP to generate singlet oxygen and rapidly damage both mitochondria and lysosomes, leading to synergistic enhancement of the PDT efficacy. The dual‐organelle‐targeted ALA/Hf‐MOL outperformed Hf‐MOL in preclinical PDT studies, with a 2.7‐fold lower half maximal inhibitory concentration in cytotoxicity assays in vitro and a 3‐fold higher cure rate in a colon cancer model in vivo.
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