Synthesis, X-ray crystal structure, DNA/BSA binding, DNA cleavage and cytotoxicity studies of phenanthroline based copper(II)/zinc(II) complexes

被引:21
|
作者
Wang, Qingming [1 ]
Mao, Han [2 ]
Wang, Wenling [1 ]
Zhu, Huimin [1 ]
Dai, Lihui [1 ]
Chen, Yanli [1 ]
Tang, Xinhui [1 ,2 ]
机构
[1] Yancheng Teachers Univ, Jiangsu Prov Key Lab Coastal Wetland Bioresources, Sch Pharm, Yancheng 224051, Jiangsu, Peoples R China
[2] Nanjing Univ Technol, Coll Biotechnol & Pharmaceut Engn, Nanjing 210009, Peoples R China
关键词
Potential anticancer agents; DNA binding; Bull serum albumin (BSA) binding; DNA cleavage; Binding modes; Metals complexes; BOVINE SERUM-ALBUMIN; BIOLOGICAL EVALUATION; PLATINUM(II) COMPLEXES; NICKEL(II) COMPLEXES; ANTICANCER ACTIVITY; ACID STRUCTURE; COPPER; CISPLATIN; INHIBITION; REACTIVITY;
D O I
10.1007/s10534-017-0028-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Research on copper(II) 1,10-phenanththroline (phen) derivatives continues to attract interest in the context of structure and biological properties. In this paper, two metal complexes [Cu-2(phen)(2)(mu-Cl)(2)]Cl-2 (1), [Zn(phen)(2)(H2O)Cl]Cl center dot 4H(2)O (2) were synthesized and characterized. The crystal structures of 1 and 2 were determined by X-ray diffraction. In order to investigate the biological properties of the prepared complexes, spectroscopic and biological studies were performed. Results of X-ray diffraction showed that 1 and 2 form two types of crystal structures in a given system: dinuclear and mono-nuclear complex. The preliminary study on the DNA cleavage activity has shown that 1 under study behaved as the chemical nucleases. The DNA binding interaction of 1 & 2 with CT-DNA has been investigated by UV-Visible and fluorescence emission spectrometry and the apparent binding constant (K-app) values are 5.1 x 10(4) and 1.2 x 10(4) M-1, respectively. In addition, fluorescence spectrometry of bovine serum albumin (BSA) with 1 & 2 showed that the quenching mechanism might be a static quenching procedure with one binding sites for BSA. In addition, the cytotoxicity of 1 in vitro on tumor cells lines (MCF-7, HepG2 and HT29) was examined by MTT and showed better antitumor effect on the tested cells.
引用
收藏
页码:575 / 587
页数:13
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