School of Chemistry and Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, The University of Dublin, Dublin 2, Ireland.
Advanced Materials and BioEngineering Research (AMBER) Centre, Trinity College Dublin, The University of Dublin, Dublin 2, Ireland.
ACS Appl Bio Mater. 2021 Sep 20;4(9):6664-6681. doi: 10.1021/acsabm.1c00284. Epub 2021 Aug 19.
A family of six Ru(II) polypyridyl complexes (-) which contain phenanthroline-based ligands functionalized with alkyl chains of different lengths (one methyl group, 10 and 21 carbon alkyl chains) and either 1,10-phenanthroline (phen) or 1,4,5,8-tetraazaphenanthrene (TAP) as ancillary ligands have been synthesized and characterized. The influence of the alkyl chain length on their photophysical and photochemical properties as well as in their photobiological applications has been elucidated by monitoring the changes in their MLCT-centered absorption and emission bands. The presence of one methyl group or 10 carbon alkyl chains does not seem to significantly affect the photophysical and photochemical properties of the resulting Ru(II) complexes when compared to the well-known [Ru(phen)] and [Ru(TAP)phen]. However, an effect on their emission properties and in their ability to photosensitize singlet oxygen is observed for the Ru(II) complexes containing 21 carbon alkyl chains. The binding of these complexes to salmon testes DNA (stDNA) was investigated by observing the changes in the photophysical properties. Complexes , , , and all showed changes in their MLCT bands that could be analyzed using conventional fitting methods, such as the Bard equation. In contrast, complexes and , possessing long aliphatic chains, gave rise to nonclassic behavior. In addition to these analyses, both thermal denaturation and circular dichroism studies of - were carried out in the presence of stDNA which confirmed that these complexes bind to DNA. Confocal microscopy and viability studies in HeLa cervical cancer cells reveal an alkyl chain-length dependence on the cellular uptake and cytotoxicity of the resulting Ru(II) complexes due to an enhancement of their lipophilicity with increasing alkyl chain length. Thus, complexes containing 10 and 21 carbon alkyl chains are rapidly taken up into HeLa cells and, in particular, those with 21 carbon alkyl chains show a significant phototoxicity against the same cell line. Therefore, this study provides further insight into the possible modulation of the photophysical, photochemical, and photobiological properties of Ru(II) polypyridyl complexes by varying the length of the alkyl chains attached to the polypyridyl ligands coordinated to the Ru(II) center and the nature of the auxiliary groups, which we show has a significant effect on photophysical and biological properties.
已经合成并表征了六个 Ru(II) 多吡啶配合物(-),它们包含基于菲咯啉的配体,这些配体带有不同长度的烷基链(一个甲基、10 个和 21 个碳烷基链),并且带有辅助配体 1,10-菲咯啉(phen)或 1,4,5,8-四氮杂菲(TAP)。通过监测其 MLCT 中心吸收和发射带的变化,阐明了烷基链长度对其光物理和光化学性质以及在光生物应用中的影响。与知名的[Ru(phen)]和[Ru(TAP)phen]相比,当存在一个甲基或 10 个碳烷基链时,似乎不会显著影响所得 Ru(II)配合物的光物理和光化学性质。然而,对于含有 21 个碳烷基链的 Ru(II)配合物,观察到其发光性质和产生单线态氧的能力发生了变化。通过观察光物理性质的变化,研究了这些配合物与鲑鱼睾丸 DNA(stDNA)的结合。配合物 、 、 、 和 都表现出 MLCT 带的变化,这些变化可以使用常规拟合方法(如 Bard 方程)进行分析。相比之下,带有长脂肪链的配合物 和 产生了非经典行为。除了这些分析之外,还在 stDNA 存在的情况下进行了 - 的热变性和圆二色性研究,证实这些配合物与 DNA 结合。共聚焦显微镜和 HeLa 宫颈癌细胞的活力研究揭示,由于疏水性随烷基链长度的增加而增强,所得 Ru(II)配合物的细胞摄取和细胞毒性存在烷基链长度依赖性。因此,含有 10 和 21 个碳烷基链的配合物被迅速摄取到 HeLa 细胞中,特别是含有 21 个碳烷基链的配合物对同一细胞系表现出显著的光毒性。因此,本研究进一步深入了解通过改变与 Ru(II)中心配位的多吡啶配体上附着的烷基链的长度和辅助基团的性质,可能对 Ru(II)多吡啶配合物的光物理、光化学和光生物性质进行调制,我们表明这对光物理和生物学性质有重大影响。