应用化学

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阿司匹林铜(Ⅱ)配合物的合成、晶体结构和抗肿瘤活性

刘涛1,魏冬1,姜波1,徐国永1,周双生1,2*   

  1. (1.安徽中医药大学 合肥 230031;2.安徽大学现代科学实验技术中心 合肥 230039)
  • 收稿日期:2013-04-24 修回日期:2013-07-15 出版日期:2014-03-10 发布日期:2014-03-10
  • 通讯作者: 周双生,教授; Tel:0551-65169291; E-mail:zshuangsheng@126.com; 研究方向:药物设计与合成
  • 基金资助:
    国家自然科学基金(21071001)和安徽省自然科学基金(1208085MH273)资助项目

Synthesis,Characterization and Antitumor Activitiesof of Cu(Ⅱ)-Aspirin Complex

LIU Tao1, WEI Dong1, JIANG Bo1, XU Guoyong1, ZHOU Shuangsheng1,2*   

  1. (1.Department of Pharmacy,Anhui College of Traditional Chinese Medicine,Hefei 230031,China;
    2.Center of Modern Experimental Technology,Anhui University,Hefei 230039,China)
  • Received:2013-04-24 Revised:2013-07-15 Published:2014-03-10 Online:2014-03-10
  • Supported by:

    Supported by the National Natural Science Foundation(21071001) and The Natural Science Foundation Of Anhui Province(1208085MH273)

摘要: 合成了阿司匹林铜(Ⅱ)配合物,通过红外、X射线单晶衍射对其结构进行了表征。 配合物属单斜晶系,P21/n空间群,晶胞参数为a=8.211(5) nm,b=10.419(5) nm,c=21.003(5) nm,β=98.021(5)°,V=1779.2(14) nm3,Z=4。 采用紫外光谱和荧光光谱法及循环伏安法研究了配合物与小牛胸腺DNA(ct-DNA)的相互作用。 采用MTT法测定了配合物对体外培养人乳腺癌MCF-7和胃癌MGC-803细胞的抑制活性。 当配合物浓度为120 μmol/L时,对2种细胞增殖的抑制率分别为80.01%和70.16%。

关键词: 阿司匹林铜(Ⅱ)配合物, 晶体结构, 抗肿瘤活性, ct-DNA, 相互作用

Abstract: A Cu(Ⅱ)-aspirin complex has been synthesized and characterized by IR spectroscopy and single crystal X-ray diffraction analyses. The complex crystallizes in monoclinic space group P21/n with cell parameters of a=8.211(5) nm, b=10.419(5) nm, c=21.003(5) nm, β=98.021(5)°, V=1779.2(14) nm3, Z=4. The interactions of the complex with ct-DNA were studied by UV, fluorescence spectroscopy and cyclic voltammetry method. At the same time, the antitumor activities of the complex against MCF-7 and MGC-803 cell lines were tested by MTT assay. The in vitro inhibitory ratios against two tumor cell lines are 80.01% and 70.16% at concentration of 120 μmol/L, respectively.

Key words: Cu(Ⅱ)-aspirin complex, crystal structure, antitumor activity, ct-DNA, interaction

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