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溶剂辅助一锅法形成钌(III)和钌(II)腙配合物,具有潜在的体外细胞毒性以及增强的乳酸脱氢酶、一氧化氮和活性氧释放。

Solvent assisted formation of ruthenium(III) and ruthenium(II) hydrazone complexes in one-pot with potential in vitro cytotoxicity and enhanced LDH, NO and ROS release.

作者信息

Jayanthi Eswaran, Kalaiselvi Sivalingam, Padma Viswanatha Vijaya, Bhuvanesh Nattamai S P, Dharmaraj Nallasamy

机构信息

Inorganic & Nanomaterials Research Laboratory, Department of Chemistry, Bharathiar University, Coimbatore - 641 046, India.

Department of Biotechnology, Bharathiar University, Coimbatore 641 046, India.

出版信息

Dalton Trans. 2016 Jan 28;45(4):1693-707. doi: 10.1039/c5dt03849a.

Abstract

A set each of new bivalent and trivalent ruthenium complexes, [Ru(III)(HL)Cl2(EPh3)2] and [Ru(II)(L)(CO)(EPh3)2] (E = P (complexes and ) or As (complexes and )) were synthesised from the reactions of [Ru(III)Cl3(EPh3)3] with 2-hydroxynaphthaldehyde benzoic acid hydrazone (H2L) in methanol-chloroform and characterized by elemental analysis, spectral data and XRD study. A suitable mechanism to account for the formation of bivalent ruthenium carbonyl complexes from the corresponding trivalent precursors is provided by considering the role of added base in the reaction. Interaction of complexes with CT-DNA/bovine serum albumin was analysed with absorption and emission spectral titration studies. In vitro cytotoxic potential of the above ruthenium hydrazone complexes assayed against the A549 cell line revealed a significant growth inhibition. The test complexes added in IC50 concentration into the cell culture medium enhanced the release of lactate dehydrogenase, NO and reactive oxygen species in comparison with the control. Cell death induced by the complexes was studied using a propidium iodide staining assay and showed noticeable changes in the cell morphology which resembled apoptosis.

摘要

合成了一组新的二价和三价钌配合物,即[Ru(III)(HL)Cl2(EPh3)2]和[Ru(II)(L)(CO)(EPh3)2](E = P(配合物 和 )或As(配合物 和 )),它们是由[Ru(III)Cl3(EPh3)3]与2-羟基萘甲醛苯甲酸腙(H2L)在甲醇-氯仿中反应制得,并通过元素分析、光谱数据和X射线衍射研究进行了表征。通过考虑反应中添加碱的作用,提供了一种合适的机理解释从相应三价前体形成二价钌羰基配合物的过程。通过吸收和发射光谱滴定研究分析了配合物与CT-DNA/牛血清白蛋白的相互作用。对上述钌腙配合物针对A549细胞系的体外细胞毒性潜力进行测定,结果显示出显著的生长抑制作用。与对照相比,以IC50浓度添加到细胞培养基中的测试配合物增强了乳酸脱氢酶、一氧化氮和活性氧的释放。使用碘化丙啶染色试验研究了配合物诱导的细胞死亡,结果显示细胞形态发生了明显变化,类似于细胞凋亡。

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