Prakash Govindan, Manikandan Rajendran, Viswanathamurthi Periasamy, Velmurugan Krishnaswamy, Nandhakumar Raju
Department of Chemistry, Periyar University, Salem 636011, Tamil Nadu, India.
Department of Chemistry, Periyar University, Salem 636011, Tamil Nadu, India.
J Photochem Photobiol B. 2014 Sep 5;138:63-74. doi: 10.1016/j.jphotobiol.2014.04.019. Epub 2014 May 14.
New Ru(III) isothiosemicarbazone complexes [RuCl(EPh3)L(1-4)] (E=P or As) were obtained from the reactions between [RuCl3(EPh3)3] and bis(salicylaldehyde)-S-methylisothiosemicarbazone (H2L(1-3))/bis(2-hydroxy-naphthaldehyde)-S-methylisothiosemicarbazone (H2L(4)) ligands. The new complexes were characterized by using elemental analyses and various spectral (UV-Vis, IR, (1)H NMR, FAB-Mass and EPR) methods. The redox properties of the complexes were studied by using cyclic voltammetric method. The new complexes were subjected to various biological investigations such as antioxidant assays involving DPPH radical, hydroxyl radical, nitric oxide radical and hydrogen peroxide, DNA/protein interaction studies and in vitro cytotoxic studies against human breast cancer cell line (MCF-7). New complexes showed excellent free radicals scavenging ability and could bind with DNA via intercalation. Protein binding studies using fluorescence spectroscopy showed that the new complexes could bind strongly with bovine serum albumin (BSA). Photo cleavage experiments using DNA of E-coli bacterium exhibited the DNA cleavage ability of the complexes. Further, the in vitro anticancer activity studies on the new complexes against MCF-7 cell line exhibited the ability of Ru(III) isothiosemicarbazone complexes to suppress the development of malignant neoplastic disease cells.
新型钌(III)异硫代半卡巴腙配合物[RuCl(EPh3)L(1 - 4)](E = P或As)是通过[RuCl3(EPh3)3]与双(水杨醛)-S-甲基异硫代半卡巴腙(H2L(1 - 3))/双(2-羟基萘甲醛)-S-甲基异硫代半卡巴腙(H2L(4))配体反应得到的。通过元素分析和各种光谱(紫外可见光谱、红外光谱、1H核磁共振光谱、快原子轰击质谱和电子顺磁共振光谱)方法对新型配合物进行了表征。采用循环伏安法研究了配合物的氧化还原性质。对新型配合物进行了各种生物学研究,如涉及二苯基苦味酰基自由基、羟基自由基、一氧化氮自由基和过氧化氢的抗氧化测定、DNA/蛋白质相互作用研究以及对人乳腺癌细胞系(MCF - 7)的体外细胞毒性研究。新型配合物表现出优异的自由基清除能力,并且可以通过插入作用与DNA结合。利用荧光光谱进行的蛋白质结合研究表明,新型配合物可以与牛血清白蛋白(BSA)强烈结合。使用大肠杆菌DNA进行的光裂解实验展示了配合物的DNA裂解能力。此外,对新型配合物针对MCF - 7细胞系的体外抗癌活性研究表明,钌(III)异硫代半卡巴腙配合物具有抑制恶性肿瘤疾病细胞发展的能力。