光动力疗法
光敏剂
激进的
化学
光化学
活性氧
氧气
生物物理学
双光子激发显微术
超氧化物
生物化学
荧光
有机化学
生物
酶
物理
量子力学
作者
Shi Kuang,Lingli Sun,Xianrui Zhang,Xinxing Liao,Thomas W. Rees,Leli Zeng,Yu Chen,Xiting Zhang,Liang‐Nian Ji,Hui Chao,Liangnian Ji,Hui Chao
标识
DOI:10.1002/anie.202009888
摘要
Abstract The efficacy of photodynamic therapy is typically reliant on the local concentration and diffusion of oxygen. Due to the hypoxic microenvironment found in solid tumors, oxygen‐independent photosensitizers are in great demand for cancer therapy. We herein report an iridium(III) anthraquinone complex as a mitochondrion‐localized carbon‐radical initiator. Its emission is turned on under hypoxic conditions after reduction by reductase. Furthermore, its two‐photon excitation properties ( λ ex =730 nm) are highly desirable for imaging. Upon irradiation, the reduced form of the complex generates carbon radicals, leading to a loss of mitochondrial membrane potential and cell death (IC 50 light =2.1 μ m , IC 50 dark =58.2 μ m , PI=27.7). The efficacy of the complex as a PDT agent was also demonstrated under hypoxic conditions in vivo. To the best of our knowledge, it is the first metal‐complex‐based theranostic agent which can generate carbon radicals for oxygen‐independent two‐photon photodynamic therapy.
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