贵金属
貴金屬
귀금속
PRECIOUS METALS
2014年
1期
63-69
,共7页
叶丽清%闫莉莉%向明武%高云涛%贝玉祥
葉麗清%閆莉莉%嚮明武%高雲濤%貝玉祥
협려청%염리리%향명무%고운도%패옥상
分析化学%甲啶铂%多壁碳纳米管%离子液体%玻碳电极%电化学行为%伏安法
分析化學%甲啶鉑%多壁碳納米管%離子液體%玻碳電極%電化學行為%伏安法
분석화학%갑정박%다벽탄납미관%리자액체%파탄전겁%전화학행위%복안법
analytical chemistry%picoplatin%multi-walled carbon nanotubes%ionic liquids%glassy carbon electrode%electrochemical behavior%voltammetry
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。
採用循環伏安法(CV)和差分脈遲伏安法(DPV),研究瞭甲啶鉑在多壁碳納米管-離子液體怱飾玻碳電極(MWNTs-[ODMIM]PF6/GCE)上的電化學行為,建立瞭甲啶鉑的測定方法;以紫外-可見光譜法和電化學方法相結閤,研究瞭甲啶鉑與 DNA 的嵌插結閤作用。結果錶明:甲啶鉑在MWNTs-[ODMIM]PF6/GCE上有一對氧化還原峰,氧化峰電位Epa與還原峰電位Epc分彆為-0.07 V、-0.36 V,峰電位之差為?E=0.29 V,Ipa/Ipc=1.11。在優化條件下,甲啶鉑的氧化峰電流與其濃度在2.66~532μmol/L範圍內成良好的線性關繫(r=0.9994),檢齣限為1.33μmol/L。方法操作簡便,準確可靠、靈敏度高,可用于甲啶鉑含量的直接測定。
채용순배복안법(CV)화차분맥충복안법(DPV),연구료갑정박재다벽탄납미관-리자액체총식파탄전겁(MWNTs-[ODMIM]PF6/GCE)상적전화학행위,건립료갑정박적측정방법;이자외-가견광보법화전화학방법상결합,연구료갑정박여 DNA 적감삽결합작용。결과표명:갑정박재MWNTs-[ODMIM]PF6/GCE상유일대양화환원봉,양화봉전위Epa여환원봉전위Epc분별위-0.07 V、-0.36 V,봉전위지차위?E=0.29 V,Ipa/Ipc=1.11。재우화조건하,갑정박적양화봉전류여기농도재2.66~532μmol/L범위내성량호적선성관계(r=0.9994),검출한위1.33μmol/L。방법조작간편,준학가고、령민도고,가용우갑정박함량적직접측정。
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.