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Voltammetric determination of dipyrone using a N,N′- ethylenebis(salicylideneaminato)oxovanadium(IV) modified carbon-paste electrode

机译:用N,N'-乙撑双(水杨酰亚胺)氧钒(IV)修饰的碳糊电极伏安测定伏滴酮

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摘要

The preparation and electrochemical characterization of a carbon paste electrode modified with N.N′-ethylenebis(salicylideneiminato) oxovanadium(IV) complex ([VO(Salen)]) as well as its behavior as electrocatalyst toward the oxidation of dipyrone were investigated. The electrochemical behavior of the modified electrode and the electrooxidation of dipyrone were explored using cyclic voltammetry. The voltammetric response of the modified electrode is based on two reactions. One electrochemical related to the oxidation of the metallic center of the [VO(Salen)] and the other involving the chemical redox process involving the oxidized form of the complex and the reduced form of dipyrone. The best voltammetric response was observed for a paste composition of 25% (m/m) [VO(Salen)], KCl solution pH from 5.5 to 8.0 as the electrolyte and potential scan rate of 10 mV s-1 in the presence of dipyrone. A linear voltammetric response for dipyrone was obtained in the concentration range from 9.9 × 106 to 2.8 × 10 -3 mol L-1, with a detection limit of 7.2 × 10 -6 mol L-1. Among of several compounds tested as potential interference, only ascorbic acid presented some interference. The proposed electrode is useful for the quality control and routine analysis of dipyrone in pharmaceutical formulations.
机译:研究了用N.N'-乙撑双(水杨酰亚胺亚胺基)氧钒(IV)配合物([VO(Salen)])修饰的碳糊电极的制备,电化学性能以及其作为对双嘧啶氧化的电催化剂的行为。用循环伏安法研究了修饰电极的电化学行为和双嘧啶的电氧化作用。修饰电极的伏安响应基于两个反应。一种电化学涉及[VO(Salen)]金属中心的氧化,另一种涉及化学氧化还原过程,该过程涉及配合物的氧化形式和双嘧啶的还原形式。对于糊状成分为25%(m / m)[VO(Salen)],KCl溶液的pH为5.5至8.0的电解质,在双嘧啶存在下,电位扫描速率为10 mV s-1,观察到最佳伏安响应。在9.9×106至2.8×10 -3 mol L-1的浓度范围内获得了对双嘧啶的线性伏安响应,检出限为7.2×10 -6 mol L-1。在测试为潜在干扰的几种化合物中,只有抗坏血酸表现出一些干扰。所提出的电极可用于药物制剂中双嘧啶的质量控制和常规分析。

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