Metal-based compounds: Synthesis and characterization of new thiazole-based iridium and palladium complexes with potential anticancer and other biological activities

IF 2.4 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Polyhedron Pub Date : 2024-08-30 DOI:10.1016/j.poly.2024.117211
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Abstract

Thiazoles and their derivatives are one of the most active classes of compounds known for their wide spectrum of bioactivity. Metal complexes, based on them, show antitumor potential that is attractive for investigations. Herein, we report 6 new biologically active thiazole-based complexes have been synthesized. The iridium- and palladium-based coordination compounds obtained by the precipitation method were characterized using elemental analysis (EA), Fourier-transform infrared spectroscopy (FTIR), magnetic measurements, thermogravimetric analysis coupled with mass spectrometry (TGA-MS), and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX). Spectroscopic data helped to propose the formulas of the complexes and indicated that all ligands acted in a monodentate manner. Water molecules were identified by thermal analysis and FTIR spectroscopy. Mathematical analysis and evaluation of thermodynamic parameters including entropy (ΔS), Gibbs free energy (ΔG), and activation energy (E) were performed using the Coats–Redfern method for all complexes. The biological potential (anticancer, antibacterial, and antifungal properties) of compounds was analyzed by biological evaluation studies. Investigated CT-DNA studies revealed that the prepared compounds were intercalatively bound to the DNA. Cytotoxicity analyses showed that complexation with Ir(III) increased the toxicity of L2 towards both tested cell lines (LN-229 and MDA-MB-231), while complexation of L3 with Pd(II) significantly increased cytotoxic activity against LN-229. Due to this, the further biological studies, such as apoptosis/necrosis detection, cell cycle analysis and JC-1 fluorescence measurements were performed on this pair of compounds.

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金属基化合物:具有潜在抗癌和其他生物活性的新型噻唑基铱和钯配合物的合成与表征
噻唑及其衍生物是生物活性最强的一类化合物,具有广泛的生物活性。以它们为基础的金属复合物显示出抗肿瘤潜力,具有很强的研究吸引力。在此,我们报告了 6 种新的具有生物活性的噻唑基配合物的合成。我们使用元素分析法(EA)、傅立叶变换红外光谱法(FTIR)、磁性测量法、热重分析与质谱法(TGA-MS)以及扫描电子显微镜与能量色散 X 射线光谱法(SEM-EDX)对沉淀法获得的铱基和钯基配位化合物进行了表征。光谱数据有助于提出复合物的分子式,并表明所有配体都以单齿方式发挥作用。通过热分析和傅立叶变换红外光谱鉴定了水分子。使用 Coats-Redfern 方法对所有配合物进行了数学分析和热力学参数评估,包括熵(ΔS)、吉布斯自由能(ΔG)和活化能(E)。通过生物评价研究分析了化合物的生物潜力(抗癌、抗菌和抗真菌特性)。CT-DNA 研究表明,所制备的化合物与 DNA 相互结合。细胞毒性分析表明,与 Ir(III) 复合物会增加 L2 对两种受测细胞系(LN-229 和 MDA-MB-231)的毒性,而 L3 与 Pd(II) 复合物会显著增加对 LN-229 的细胞毒性活性。因此,对这对化合物进行了进一步的生物学研究,如细胞凋亡/坏死检测、细胞周期分析和 JC-1 荧光测量。
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来源期刊
Polyhedron
Polyhedron 化学-晶体学
CiteScore
4.90
自引率
7.70%
发文量
515
审稿时长
2 months
期刊介绍: Polyhedron publishes original, fundamental, experimental and theoretical work of the highest quality in all the major areas of inorganic chemistry. This includes synthetic chemistry, coordination chemistry, organometallic chemistry, bioinorganic chemistry, and solid-state and materials chemistry. Papers should be significant pieces of work, and all new compounds must be appropriately characterized. The inclusion of single-crystal X-ray structural data is strongly encouraged, but papers reporting only the X-ray structure determination of a single compound will usually not be considered. Papers on solid-state or materials chemistry will be expected to have a significant molecular chemistry component (such as the synthesis and characterization of the molecular precursors and/or a systematic study of the use of different precursors or reaction conditions) or demonstrate a cutting-edge application (for example inorganic materials for energy applications). Papers dealing only with stability constants are not considered.
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