Hegde Rajesh N, Hosamani Ragunatharaddi R, Nandibewoor Sharanappa T
P.G. Department of Studies in Chemistry, Karnatak University, Dharwad-580 003, India.
Colloids Surf B Biointerfaces. 2009 Sep 1;72(2):259-65. doi: 10.1016/j.colsurfb.2009.04.013. Epub 2009 Apr 22.
The voltammetric oxidation of cinnarizine was investigated. In pH 2.5 Britton-Robinson buffer, cinnarizine shows an irreversible oxidation peak at about 1.20 V at a multi-walled carbon nanotube (MWCNT)-modified glassy carbon electrode. The cyclic voltammetric results indicate that MWCNT-modified glassy carbon electrode can remarkably enhance electrocatalytic activity towards the oxidation of cinnarizine. The electrocatalytic behavior was further exploited as a sensitive detection scheme for the cinnarizine determination by differential-pulse voltammetry. Under optimized conditions, the concentration range and detection limit are 9.0x10(-8) to 6.0x10(-6) M and 2.58x10(-9) M, respectively for cinnarizine. The proposed method was successfully applied to cinnarizine determination in pharmaceutical samples. The analytical performance of this sensor has been evaluated for the detection of analyte in urine as a real sample.
研究了桂利嗪的伏安氧化。在pH 2.5的 Britton-Robinson缓冲溶液中,桂利嗪在多壁碳纳米管(MWCNT)修饰的玻碳电极上于约1.20 V处显示出不可逆氧化峰。循环伏安法结果表明,MWCNT修饰的玻碳电极可显著增强对桂利嗪氧化的电催化活性。该电催化行为进一步被用作通过差分脉冲伏安法测定桂利嗪的灵敏检测方案。在优化条件下,桂利嗪的浓度范围和检测限分别为9.0×10⁻⁸至6.0×10⁻⁶ M和2.58×10⁻⁹ M。所提出的方法成功应用于药物样品中桂利嗪的测定。已评估该传感器对尿液中作为实际样品的分析物检测的分析性能。