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铜与烟酸和8-羟基喹啉配合物的电化学行为及与DNA的相互作用     被引量:2

Electrochemical Property of Ternary Copper Complex with Nicotinic Acid and 8-Hydroxyquinoline and Its Interaction with DNA

文献类型:期刊文献

中文题名:铜与烟酸和8-羟基喹啉配合物的电化学行为及与DNA的相互作用

英文题名:Electrochemical Property of Ternary Copper Complex with Nicotinic Acid and 8-Hydroxyquinoline and Its Interaction with DNA

作者:李小芳[1];冯小强[1];马乐[1];杨声[2];朱元成[1]

第一作者:李小芳

机构:[1]天水师范学院化学工程与技术学院,甘肃天水741001;[2]定西师范高等专科学校,甘肃定西743000

第一机构:天水师范学院化学工程与技术学院,甘肃天水741001

年份:2016

卷号:32

期号:6

起止页码:861

中文期刊名:分析科学学报

外文期刊名:Journal of Analytical Science

收录:CSTPCD;;北大核心:【北大核心2014】;CSCD:【CSCD2015_2016】;

基金:国家自然科学基金(No.51063006);天水师范学院"青蓝"人才工程

语种:中文

中文关键词:烟酸;8-羟基喹啉;Cu2+;鲱鱼精DNA;相互作用

外文关键词:Nicotinic acid ; 8 Hydroxyquinoline ; Cu2+ ; DNA ; Interaction

摘要:采用循环伏安法研究了铜与烟酸和8-羟基喹啉配合物(Cu(Hq)(NA)0.5(Hq=8-羟基喹啉,NA=烟酸))的电化学行为。此外,以鲱鱼精DNA为靶点,采用紫外吸收光谱、DNA粘度滴定和差分脉冲伏安法,从分子水平研究了该配合物与DNA的键合方式。结果发现:配合物的中心Cu^(2+)在循环伏安图上呈现明显的氧化还原峰,峰电流随扫描速度的增加呈增加趋势,并且与扫描速度成正比。配合物的吸收峰强度随着DNA的加入减色显著,氧化还原峰电流也随之减小,式量电位发生正移;粘度实验结果发现DNA的相对比粘度随配合物的加入而增大。这些结果表明配合物与DNA通过嵌插方式发生作用。
The electrochemical behavior of the complex of Cu (Hq)(NA)0.5(Hq = 8 hydroxyquinoline, NA-- Nicotinic acid) was studied by cyclic voltammetry. In addition,the interaction between the complex and Herring sperm DNA as biomolecular target was studied by UV spectroscopy, DNA viscosity titration experiment and differential pulse voltammetry(DPV). The results showed that two pairs of well-defined quasi reversible redox peaks of Cu2+ of complex have been obtained. The peak current significantly increased with the increase of scanning rate and was proportional to the scanning rate. UV absorption peaks of complex was red-shifted and the intensity was weakened with the addition of DNA. In addition, the peak current decreased significantly and potential moved positively. Viscosity titration experiment vertified that the complex increased the relative viscosity of DNA. All of the above results illustrated that the complex and DNA binded by the mode of intercalation,and it is very important for the design of DNA-targeting drugs in the hereditary engineering.

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