Voltammetric Determination of LSD with a Schiff Base – Chemically Modified Electrode in Aqueous Solution

M. F. Ribeiro, Érica Naomi Oiye, Juliana Midori Toia Katayama, J. W. C. Júnior, E. R. Dockal, M. F. D. Oliveira
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引用次数: 3

Abstract

In recent years, practical, inexpensive, and highly specific electroanalytical methods based on modified electrodes have been increasingly developed for forensic science. Simple modification of the carbon paste electrode with Schiff base complexes has become a promising strategy to detect and quantify narcotics. In this context, we aimed to develop voltammetric methods to quantify lysergic acid diethylamide (LSD) by using a carbon paste electrode modified with the complex [UO2(Ac-ophen)]·H2O. The use of an aqueous solution of KCl as supporting electrolyte makes the methodology less polluting, which contrasts with methods that still employ toxic solvents. The developed method for Differential Pulse Voltammetry provides a linear response at various concentrations of LSD and affords analytical curves with standard deviation, detection, and quantification limits around 2.45, 0.625, and 2.08 μmol L, respectively. The recovery values of 103 and 108% prove that the developed method is suitable for application in forensic science.
希夫碱修饰电极伏安法测定水溶液中LSD的含量
近年来,基于修饰电极的实用、廉价、高特异性的电分析方法在法医科学中得到了越来越多的发展。利用希夫碱配合物对碳糊电极进行简单修饰已成为一种很有前途的毒品检测和定量方法。在此背景下,我们的目的是建立伏安法,通过使用配合物[UO2(Ac-ophen)]·H2O修饰的碳糊电极来定量麦角酸二乙基酰胺(LSD)。与仍然使用有毒溶剂的方法相比,使用氯化钾水溶液作为支撑电解质使该方法污染更少。所建立的差分脉冲伏安法在不同浓度的LSD下具有良好的线性响应,分析曲线的标准偏差、检测限和定量限分别在2.45、0.625和2.08 μmol L左右。回收率分别为103和108%,证明该方法适用于法医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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