Ruthenium-Based Photoactivated Chemotherapy

被引:109
作者
Bonnet, Sylvestre [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2333 CC Leiden, Netherlands
关键词
INTERSTITIAL PHOTODYNAMIC THERAPY; SINGLET-OXYGEN; PHOTOSUBSTITUTION REACTIONS; RED-LIGHT; LIGAND PHOTOSUBSTITUTION; TEMPERATURE-DEPENDENCE; MACHINE PROTOTYPES; RU(II) COMPLEXES; EXCITED-STATES; HYPOXIC CELLS;
D O I
10.1021/jacs.3c01135
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ruthenium-(II) polypyridyl complexes form a vast family of molecules characterized by their finely tuned photochemical and photophysical properties. Their ability to undergo excited-state deactivation via photosubstitution reactions makes them quite unique in inorganic photochemistry. As a consequence, they have been used, in general, for building dynamic molecular systems responsive to light but, more particularly, in the field of oncology, as prodrugs for a new cancer treatment modality called photoactivated chemotherapy (PACT). Indeed, the ability of a coordination bond to be selectively broken under visible light irradiation offers fascinating perspectives in oncology: it is possible to make poorly toxic agents in the dark that become activated toward cancer cell killing by simple visible light irradiation of the compound inside a tumor. In this Perspective, we review the most important concepts behind the PACT idea, the relationship between ruthenium compounds used for PACT and those used for a related phototherapeutic approach called photodynamic therapy (PDT), and we discuss important questions about real-life applications of PACT in the clinic. We conclude this Perspective with important challenges in the field and an outlook.
引用
收藏
页码:23397 / 23415
页数:19
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