Department of Chemistry, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia.
Anal Bioanal Chem. 2012 Aug;404(2):525-30. doi: 10.1007/s00216-012-6171-8. Epub 2012 Jun 15.
Glassy carbon electrode was modified by electropolymerization of 4-amino-3-hydroxynaphthalene sulfonic acid. Cyclic voltammetric study of quinine showed higher current response at the modified electrode compared to the bare and activated glassy carbon electrodes in pH 7.0 phosphate buffer solution. Under optimized conditions, a calibration curve was obtained by square wave voltammetry at the modified electrode. The linear relationship between the peak current and the concentration of quinine in the range of 1.0 × 10(-7) to 1.0 × 10(-5) M was I (pa) (in microamperes) = 6.26C (in micromolars) + 0.2997 (R (2) = 0.999). The detection limit calculated (S/N = 3) was 1.42 × 10(-8) M, which is much lower than similar reports. The method was successfully applied for the determination of quinine in spiked human urine, and pharmaceutical formulations and recovery values >90 % were obtained.
玻碳电极通过 4-氨基-3-羟基萘磺酸的电化学聚合进行修饰。在 pH 7.0 的磷酸盐缓冲溶液中,与裸玻碳电极和活化玻碳电极相比,奎宁在修饰电极上的电流响应更高。在优化条件下,通过修饰电极的方波伏安法得到校准曲线。在 1.0×10(-7) 至 1.0×10(-5) M 的范围内,峰电流与奎宁浓度之间存在线性关系,I(pa)(微安培)= 6.26C(微摩尔)+0.2997(R(2)=0.999)。计算得出的检测限(S/N=3)为 1.42×10(-8) M,远低于类似报道。该方法成功应用于人尿中奎宁的测定,以及药物制剂的测定,回收率>90%。