Gao Enjun, Zhu Mingchang, Yin Hongxi, Liu Lei, Wu Qiong, Sun Yaguang
Laboratory of Coordination Chemistry, Shenyang Institute of Chemical Technology, Shenyang 110142, China.
J Inorg Biochem. 2008 Oct;102(10):1958-64. doi: 10.1016/j.jinorgbio.2008.07.011. Epub 2008 Jul 29.
The dinuclear complexes [Pd(2)(L)(2)(bipy)(2)] (1), [Pd(2)(L)(2)(phen)(2)] (2), [Pt(2)(L)(2)(bipy)(2)] (3) and [Pt(2)(L)(2)(phen)(2)] (4), where bipy=2,2'-bipyridine, phen=1,10-phenanthroline and L=2,2'-azanediyldibenzoic dianion) dibridged by H(2)L ligands have been synthesized and characterized. The binding of the complexes with fish sperm DNA (FS-DNA) were investigated by fluorescence spectroscopy. The results indicate that the four complexes bound to DNA with different binding affinity, in the order complex 4>complex 3>complex 2>complex 1, and the complex 3 binds to DNA in both coordination and intercalative mode. Gel electrophoresis assay demonstrates the ability of the complexes to cleave the pBR 322 plasmid DNA. The cytotoxic activity of the complexes was tested against four different cancer cell lines. The four complexes exhibited cytotoxic specificity and significant cancer cell inhibitory rate.
已合成并表征了双核配合物[Pd₂(L)₂(bipy)₂] (1)、[Pd₂(L)₂(phen)₂] (2)、[Pt₂(L)₂(bipy)₂] (3) 和 [Pt₂(L)₂(phen)₂] (4),其中bipy = 2,2'-联吡啶,phen = 1,10-菲咯啉,L = 2,2'-氮杂二亚基二苯甲酸二价阴离子,它们由H₂L配体双桥连。通过荧光光谱研究了这些配合物与鱼精DNA (FS-DNA) 的结合。结果表明,这四种配合物与DNA的结合亲和力不同,顺序为配合物4>配合物3>配合物2>配合物1,并且配合物3以配位和插入两种模式与DNA结合。凝胶电泳分析证明了这些配合物切割pBR 322质粒DNA的能力。测试了这些配合物对四种不同癌细胞系的细胞毒性活性。这四种配合物表现出细胞毒性特异性和显著的癌细胞抑制率。