光毒性
化学
苯并噻唑
赫拉
光动力疗法
立体化学
苯并咪唑
光敏剂
癌细胞
铱
程序性细胞死亡
光化学
生物物理学
细胞
细胞凋亡
体外
癌症
生物化学
有机化学
内科学
催化作用
生物
医学
作者
Jana Kašpárkova,Alba Hernández-García,Hana Kostrhunová,Marta Goicuría,Vojtěch Novohradský,Delia Bautista,Lenka Marková,M. Dolores Santana,Viktor Brabec,José Ruiz
标识
DOI:10.1021/acs.jmedchem.3c01978
摘要
A second-generation series of biscyclometalated 2-(5-aryl-thienyl)-benzimidazole and -benzothiazole Ir(III) dppz complexes [Ir(C^N)2(dppz)]+, Ir1–Ir4, were rationally designed and synthesized, where the aryl group attached to the thienyl ring was p-CF3C6H4 or p-Me2NC6H4. These new Ir(III) complexes were assessed as photosensitizers to explore the structure–activity correlations for their potential use in biocompatible anticancer photodynamic therapy. When irradiated with blue light, the complexes exhibited high selective potency across several cancer cell lines predisposed to photodynamic therapy; the benzothiazole derivatives (Ir1 and Ir2) were the best performers, Ir2 being also activatable with green or red light. Notably, when irradiated, the complexes induced leakage of lysosomal content into the cytoplasm of HeLa cancer cells and induced oncosis-like cell death. The capability of the new Ir complexes to photoinduce cell death in 3D HeLa spheroids has also been demonstrated. The investigated Ir complexes can also catalytically photo-oxidate NADH and photogenerate 1O2 and/or •OH in cell-free media.
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