首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Stripping voltammetric and polarographic techniques for the determination of anti-fungal ketoconazole on the mercury electrode.
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Stripping voltammetric and polarographic techniques for the determination of anti-fungal ketoconazole on the mercury electrode.

机译:溶出伏安法和极谱法测定汞电极上的抗真菌酮康唑。

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摘要

The electroanalytical behaviour of ketoconazole in Britton-Robinson buffer is described. The reduction process on the hanging mercury drop electrode (HMDE) gives rise to one peak over -1.6 V (vs. Ag/AgCl/sat.KCl), within the pH range studied (4.7-9.6). The results showed that the reduction of ketoconazole is irreversible and the limiting current is adsorption controlled. The dependence of the peak current on the concentration was studied by means of different polarographic and voltammetric techniques. Using adsorptive stripping differential pulse voltammetry (AdS-DPV), the detection limit (DL) reached was 5.3 x 10(-11) mol l(-1). Two procedures, based on differential pulse polarography (DPP) and AdS-DPV in aqueous medium were developed for the determination of ketoconazole in a gel formulation and spiked urine samples, respectively.
机译:描述了酮康唑在Britton-Robinson缓冲液中的电分析行为。在所研究的pH范围(4.7-9.6)中,悬挂式汞滴电极(HMDE)的还原过程在-1.6 V(vs。Ag / AgCl / sat。KCl)上产生一个峰。结果表明,酮康唑的还原是不可逆的,极限电流是吸附控制的。通过不同的极谱法和伏安法研究了峰值电流对浓度的依赖性。使用吸附溶出差分脉冲伏安法(AdS-DPV),达到的检出限(DL)为5.3 x 10(-11)mol l(-1)。开发了两种方法,分别基于微分脉冲极谱法(DPP)和水性介质中的AdS-DPV,分别测定凝胶制剂和加标尿液样品中的酮康唑。

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