吡啶-2,6-二羧酸两种Gd(III), Ce(IV)配合物的合成、表征、晶体结构、理论研究及体外细胞毒性评价

Mina Zohrevani, S. Abdolmaleki, M. Ghadermazi, Yasin Gholiee, A. Aliabadi, Elham Motieiyan, M. Hakimi, D. Marabello
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引用次数: 0

摘要

本文报道了吡啶-2,6-二羧酸(pydcH2)、菲罗啉和2-氨基吡啶与Gd(NO3)3.6H2O和Ce (NO3)3.6H2O金属盐通过一锅反应合成了两种配合物。用光谱学方法鉴定了新的配位配合物C1和C2。用x射线晶体学对配合物进行了表征。利用NBO和EDA-NOCV分析从理论上研究了金属与配体相互作用的性质。结果表明,两种配合物中静电相互作用的贡献都明显大于轨道相互作用。然而,轨道相互作用在[CeL3]2 -中的贡献大于[GdL3]3 -中的贡献(28.8%比21.8%)。接下来,我们以奥沙利铂为标准,在体外研究了合成复合物对人乳腺癌(MCF7)、人结肠癌(HT29)和人淋巴细胞(HL60)三种癌细胞系的细胞毒作用。C1 (IC50=80.7 μM,活力抑制率为83.41%)和C2 (IC50=98.3 μM,活力抑制率为77.19%)对MCF7细胞株的抑制作用最显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization, Crystallographic Structure, Theoretical Studies, and in Vitro Cytotoxicity Assessment of Two Gd(III), Ce(IV) Complexes of Pyridine-2,6-Dicarboxylic Acid
This paper reports the synthesis of two complexes through one-pot reactions of pyridine-2,6-dicarboxylic acid (pydcH2), phenanthroline, and 2-aminopyridine, with Gd(NO3)3.6H2O and Ce (NO3)3.6H2O metal salts. The new coordination complexes C1 and C2 have been identified by spectroscopic methods. The complexes were characterized by X-ray crystallography. The nature of metal-ligand interactions was studied theoretically using NBO and EDA-NOCV analyses. The results showed that the contribution of electrostatic interactions in both complexes is considerably larger than orbital. However, the contribution of orbital interactions in [CeL3]2–, is more than that in [GdL3]3– (28.8% vs. 21.8%). In following, the cytotoxic effect of synthetic complexes was investigated in vitro using oxaliplatin as a standard against three cancer cell lines including human breast cancer (MCF7), human colon adenocarcinoma (HT29), and human lymphocyte (HL60). The most significant inhibition activity was observed by both C1 (IC50=80.7 μM, Viability inhibition=83.41%) and C2 (IC50=98.3 μM, Viability inhibition=77.19%) toward the MCF7 cell line.
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