Department of Chemistry and Biochemistry, The University of North Carolina at Greensboro, Greensboro, NC.
Department of Chemistry, University of Kentucky, Lexington, KY.
Photochem Photobiol. 2020 Mar;96(2):327-339. doi: 10.1111/php.13174. Epub 2019 Dec 6.
A series of strained Ru(II) complexes were studied for potential anticancer activity in hypoxic tissues. The complexes were constructed with methylated ligands that were photolabile and an imidizo[4,5-f][1,10]phenanthroline ligand that contained an appended aromatic group to potentially allow for contributions of ligand-centered excited states. A systematic variation of the size and energy of the aromatic group was performed using systems containing 1-4 fused rings, and the photochemical and photobiological behaviors of all complexes were assessed. The structure and nature of the aromatic group had a subtle impact on photochemistry, altering environmental sensitivity, and had a significant impact on cellular cytotoxicity and photobiology. Up to 5-fold differences in cytotoxicity were observed in the absence of light activation; this rose to 50-fold differences upon exposure to 453 nm light. Most significantly, one complex retained activity under conditions with 1% O , which is used to induce hypoxic changes. This system exhibited a photocytotoxicity index (PI) of 15, which is in marked contrast to most other Ru(II) complexes, including those designed for O -independent mechanisms of action.
一系列紧张的 Ru(II) 配合物被研究用于缺氧组织的潜在抗癌活性。这些配合物是由光不稳定的甲基化配体和咪唑并[4,5-f][1,10]菲咯啉配体构建而成,后者带有附加的芳基基团,可能允许配体中心激发态的贡献。使用含有 1-4 个稠合环的系统,系统地改变了芳基基团的大小和能量,评估了所有配合物的光化学和光生物学行为。芳基基团的结构和性质对光化学有细微的影响,改变了环境敏感性,并对细胞毒性和光生物学有显著影响。在没有光激活的情况下,观察到细胞毒性差异高达 5 倍;而在暴露于 453nm 光下,差异增加到 50 倍。最重要的是,一个配合物在 1%O 2 的条件下保持活性,O 2 用于诱导缺氧变化。该系统表现出 15 的光细胞毒性指数(PI),与大多数其他 Ru(II) 配合物形成鲜明对比,包括那些设计用于 O 2 独立作用机制的配合物。