A mitochondrial-targeting iridium(iii) complex for H2O2-responsive and oxidative stress amplified two-photon photodynamic therapy. Issue 23 (12th October 2021)

• Record Type: Journal Article
• Authors: Liao, Xinxing; Shen, Jinchao; Wu, Weijun; Kuang, Shi; Lin, Mingwei; Karges, Johannes; Tang, Zilong; Chao, Hui
• Is Part Of: Inorganic chemistry frontiers. Volume 8:Issue 23(2021)
• Page Start: 5045
• Page End: 5053
• Publication Date: 2021-10-12
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d1qi01038g
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : The mitochondrial-targeting iridium(iii ) complex Ir–B(OH)2 is activated in the presence of endogenous H2 O2 to release the two-photon photosensitizer Ir–OH and the GSH scavenger methylquinone for amplified two-photon photodynamic therapy. Abstract : High amounts of glutathione in tumour cells are able to decrease the effectiveness of cancer treatments by capturing the therapeutically necessary reactive oxygen species during the photodynamic therapy (PDT) process. In addition, many photosensitizers for PDT are limited by the light tissue penetration depth, which hinders the application of these compounds to treat deep seated or large tumors. To overcome the aforementioned drawbacks, herein, the use of a mitochondrial-targeting iridium(iii ) prodrug Ir–B(OH)2 which is responsive to the tumour microenvironment (H2 O2 rich) and able to release two-photon photosensitizers (Ir–OH ) for PDT and methylquinone as a glutathione scavenger for disrupting the mitochondrial redox homeostasis is presented. Based on the reduction of glutathione, the cancerous cells were more vulnerable to oxidative stress caused by two-photon photodynamic therapy. Upon two-photon laser irradiation (730 nm), a strong and amplified phototoxic effect towards human gastric adenocarcinoma (AGS) cellular and animal models was observed.