采用循环伏安法(CV)和差分脉冲伏安法(DPV)，研究了甲啶铂在多壁碳纳米管-离子液体怱饰玻碳电极(MWNTs-[ODMIM]PF6/GCE)上的电化学行为，建立了甲啶铂的测定方法；以紫外-可见光谱法和电化学方法相结合，研究了甲啶铂与 DNA 的嵌插结合作用。结果表明：甲啶铂在MWNTs-[ODMIM]PF6/GCE上有一对氧化还原峰，氧化峰电位Epa与还原峰电位Epc分别为-0.07 V、-0.36 V，峰电位之差为?E=0.29 V，Ipa/Ipc=1.11。在优化条件下，甲啶铂的氧化峰电流与其浓度在2.66~532μmol/L范围内成良好的线性关系(r=0.9994)，检出限为1.33μmol/L。方法操作简便，准确可靠、灵敏度高，可用于甲啶铂含量的直接测定。
The electrochemical behavior of picoplatin at multi-walled carbon nanotubes ionic liquids modified glassy carbon electrode (MWNTs-[ODMIM]PF6/GCE) was investigated by cyclic voltammetry and differential pulse voltammetry, and the method of picoplatin determination was established. The mode of intercalation between picoplatin with DNA was studied by electrochemical methods combined with UV-visible spectroscopy. The results show that one pair of redox peaks of picoplatin was obtained at MWNTs-[ODMIM]PF6/GCE by cyclic voltammetry with-0.07 V ofEpaand-0.36 V ofEpc, ?E=0.29 V, andIpa/Ipc=1.11. Under optimal conditions, the oxidization peak current was linearly related to the concentration of picoplatin in the range of 2.66~532μmol/Lwith the detection limit of 1.33μmol/L. The method was convenient, accurate, credible and sensitive, it can be used in the direct determination of picoplatin.
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