4.2 Article

Effect of Alkyl Chain Length on the Photophysical, Photochemical and Photobiological Properties of Ruthenium(II) Polypyridyl Complexes for Their Application as DNA-Targeting, Cellular-Imaging, and Light-Activated Therapeutic Agents

期刊

ACS APPLIED BIO MATERIALS
卷 4, 期 9, 页码 6664-6681

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.1c00284

关键词

ruthenium(II); polypyridyl complexes; luminescence; lipophilicity; anticancer; cellular imaging

资金

  1. Science Foundation Ireland (SFI PI Awards) [10/45 IN, 1/B2999, 13/IA/1865]
  2. Marie Sklodowska-Curie actions (MSCA)
  3. Trinity College Dublin (TCD)

向作者/读者索取更多资源

A family of six Ru(II) polypyridyl complexes with different lengths of alkyl chains have been synthesized and characterized, showing an influence on their photophysical and photochemical properties. The complexes with 21 carbon alkyl chains exhibited changes in emission properties and photosensitization abilities. The study also revealed that the complexes bind to DNA and demonstrated a length-dependent cellular uptake and cytotoxicity in cancer cells.
A family of six Ru(II) polypyridyl complexes (1-6) 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)(3)](2+) and [Ru(TAP)(2)phen](2+). 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 1, 2, 4, and 5 all showed changes in their MLCT bands that could be analyzed using conventional fitting methods, such as the Bard equation. In contrast, complexes 3 and 6, possessing long aliphatic chains, gave rise to nonclassic behavior. In addition to these analyses, both thermal denaturation and circular dichroism studies of 1-6 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.

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