| Literature DB >> 32735748 |
Shi Kuang1, Lingli Sun1, Xianrui Zhang1, Xinxing Liao1, Thomas W Rees1, Leli Zeng1, Yu Chen1, Xiting Zhang2, Liangnian Ji1, Hui Chao1,3.
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 (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 (IC50 light =2.1 μm, IC50 dark =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.Entities:
Keywords: bioinorganic chemistry; carbon radicals; medicinal inorganic chemistry; metals in medicine; photodynamic therapy
Year: 2020 PMID: 32735748 DOI: 10.1002/anie.202009888
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336