Cytotoxicity of Pd(ii) and Pt(ii) complexes of 2′,6′-di(thiazol-2-yl)-2,4′-bipyridine: insights into the mode of cell death and cell cycle arrest†

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY RSC Advances Pub Date : 2025-04-16 DOI:10.1039/D5RA00647C
Ahmed M. Mansour, Krzysztof Radacki, Ola R. Shehab, Gamal A. E. Mostafa, Essam A. Ali and Mahmoud T. Abo-Elfadl
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Abstract

Square-planar complexes were synthesized by the reaction of 2′,6′-di(thiazol-2-yl)-2,4′-bipyridine with either Na2[PdCl4] or K2[PtCl4], and these were thoroughly structurally characterized using some analytical and spectroscopic techniques. Density functional theory computations, including natural bond orbital analysis, were used to complement the experimental work to gain insight into the natural charge and electronic arrangement of the metal ion, as well as the strength of the metal–ligand bonds. The Pd(II) complex exhibited exceptional cytotoxicity against the A549 and HCT-116 cell lines with IC50 values of 60.1 ± 3.45 and 23.8 ± 1.48 μM, respectively. Unfortunately, the Pd(II) complex was harmful to the Vero normal cell line with an IC50 value of 24.5 ± 2.13 μM. The Pt(II) complex is unstable and has a high likelihood of exchanging the chlorido ligand for solvent molecules such as DMSO. The fluorescent-stain photos of the treated HCT-116 cells with the Pd(II) complex showed increased apoptotic bodies, indicating both early (18%) and late apoptosis (32%), as well as a necrosis ratio of about 10%. Flow cytometric analysis demonstrated that a cell arrest was induced by the Pd(II) complex on HCT-116 cells in the G2/M phase.

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2 ',6 ' -二(噻唑-2-基)-2,4 ' -联吡啶的Pd(ii)和Pt(ii)配合物的细胞毒性:对细胞死亡模式和细胞周期阻滞的见解
用Na2[PdCl4]或K2[PtCl4]与2′,6′-二(噻唑-2-基)-2,4′-联吡啶反应合成了方形平面配合物,并利用分析和光谱技术对其结构进行了表征。密度泛函理论计算,包括自然键轨道分析,被用来补充实验工作,以深入了解金属离子的自然电荷和电子排列,以及金属-配体键的强度。Pd(II)复合物对A549和HCT-116细胞系的IC50值分别为60.1±3.45 μM和23.8±1.48 μM。不幸的是,Pd(II)复合物对Vero正常细胞系的IC50值为24.5±2.13 μM。Pt(II)配合物是不稳定的,并且很有可能将氯基配体交换为溶剂分子,如DMSO。Pd(II)复合物处理的HCT-116细胞的荧光染色照片显示凋亡小体增加,表明早期(18%)和晚期(32%)凋亡,坏死比例约为10%。流式细胞术分析表明,Pd(II)复合物在G2/M期诱导HCT-116细胞阻滞。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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