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Voltammetric Determination of Sulfadoxine and Its Application in Pharmaceuticals and Urine Samples

机译:伏安定的伏安法测定及其在药品和尿液样品中的应用

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The voltammetric behaviour of Sulfadoxine (SDN) was studied at a glassy carbon electrode in 0.2 M phosphate buffer solutions using cyclic, differential-pulse (DPV) and square wave voltammetry (SWV). The dependence of the current on pH, concentration, and scan rate was investigated to optimize the experimental conditions for the determination of SDN. The oxidation process was shown to be diffusion controlled, irreversible over the pH range from 3.0-9.2. An analytical method was developed for the determination of SDN in phosphate buffer solution at pH 3.0 as a supporting electrolyte. A DPV method showed a good linear response as compared to SWV. The anodic peak current varied linearly with SDN concentration in the range 0.310-4.34 μg ml-1 of SDN with a limit of detection (LOD) of 0.01 μg ml-1. The recovery was determined in the range from 95.6-100.1%. The proposed method was successfully applied to the quantitative determination of SDN in pharmaceutical formulations and an urine as real samples.
机译:使用循环微分脉冲(DPV)和方波伏安法(SWV)在0.2 M磷酸盐缓冲液中的玻璃碳电极上研究了磺胺多辛(SDN)的伏安行为。研究了电流对pH,浓度和扫描速率的依赖性,以优化用于确定SDN的实验条件。氧化过程显示受扩散控制,在3.0-9.2的pH范围内不可逆。建立了一种分析方法,用于测定pH 3.0的磷酸盐缓冲溶液中作为支持电解质的SDN。与SWV相比,DPV方法显示出良好的线性响应。阳极峰值电流在SDN浓度为0.310-4.34μgml-1的SDN中线性变化,检测限(LOD)为0.01μgml-1。确定的回收率为95.6-100.1%。所提出的方法已成功应用于药物制剂和尿液中SDN的定量测定。

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