Synthesis, characterization and in vitro antitumor activities of a biimidazole-chelated Ir(III) complex

IF 0.4 4区 化学 Q4 CHEMISTRY, ORGANIC
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Abstract

In this paper, a new cyclometalated iridium(III) complex [Ir(ppy)2(mbiim)]Cl (Ir3) (in which mbiim = 1-Methyl-2,2'-biimidazole, ppy = 2-phenylpyridine) has been successfully synthesized and characterized by ESI-MS, UV-Vis spectroscopy and 1H NMR. The fluorescence properties of Ir3 have been studied in different pH value conditions. The fluorescence properties show that the fluorescence intensity of Ir3 decreases with the increase of pH in the experiment range, which is due to the protonation/deprotonation of active hydrogen of the imidazole ring on the imidazole ligand. Moreover, the photodynamic antitumor activities in vitro of three Ir(III) complexes have been investigated by MTT assay against four cell lines (HeLa, A549, A549R and LO2). These complexes exhibit low dark toxicity and high phototoxicity in three tumor cells. To our excitement, Ir3 has achieved satisfactory photodynamic therapy effects on cisplatin-resistant tumor cell lines A549R, while its toxicity towards normal cells is relatively lower. The results indicate that Ir3 is a relatively ideal photosensitizer, which may be developed into a new potential photodynamic therapy reagent against tumor.
双咪唑螯合Ir(III)配合物的合成、表征及体外抗肿瘤活性研究
本文成功合成了一种新的环金属化铱(III)配合物[Ir(ppy)2(mbiim)]Cl (Ir3)(其中mbiim = 1-甲基-2,2'-双咪唑,ppy = 2-苯基吡啶),并用ESI-MS、UV-Vis光谱和1h - NMR对其进行了表征。研究了Ir3在不同pH值条件下的荧光性质。荧光性质表明,在实验范围内,Ir3的荧光强度随着pH的增加而降低,这是由于咪唑配体上咪唑环上活性氢的质子化/去质子化所致。此外,采用MTT法研究了3种Ir(III)复合物对4种细胞系(HeLa、A549、A549R和LO2)的体外光动力抗肿瘤活性。这些复合物在三种肿瘤细胞中表现出低暗毒性和高光毒性。令人兴奋的是,Ir3对顺铂耐药肿瘤细胞系A549R取得了满意的光动力治疗效果,而对正常细胞的毒性相对较低。结果表明,Ir3是一种较为理想的光敏剂,有可能发展成为一种新的有潜力的肿瘤光动力治疗试剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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