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
标识
DOI:10.1002/anie.202009888
摘要
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 (λex =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 (IC50light =2.1 μm, IC50dark =58.2 μm, 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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