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Static and hydrodynamic monitoring of citalopram based on its electro-oxidation behavior at a glassy-carbon surface

机译:基于西酞普兰在玻璃碳表面的电氧化行为,进行静态和流体动力学监测

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摘要

The electrooxidative behavior of citalopram (CTL) in aqueous media was studied by cyclic voltammetry (CV) and square-wave voltammetry (SWV) at a glassy-carbon electrode. The electrochemical behaviour of CTL involves two electrons and two protons in the irreversible and diffusion controlled oxidation of the tertiary amine group. The maximum analytical signal was obtained in a phosphate buffer (pH = 8.2). For analytical purposes, an SWV method and a flow-injection analysis (FI Lambda) system with amperometric detection were developed. The optimised SWV method showed a linear range between 1.10 x 10(-5) - 1.20 x 10(-4) mol L-1, with a limit of detection (LOD) of 9.5 x 10(-6) mol L-1. Using the FIA method, a linear range between 2.00 x 10(-6) - 9.00 x 10(-5) mol L-1 and an LOD of 1.9 x 10(-6) mol L-1 were obtained. The validation of both methods revealed good performance characteristics confirming applicability for the quantification of CTL in several pharmaceutical products.
机译:通过循环伏安法(CV)和方波伏安法(SWV)在玻碳电极上研究了西酞普兰(CTL)在水性介质中的电氧化行为。 CTL的电化学行为涉及叔胺基的不可逆和扩散控制的氧化中的两个电子和两个质子。在磷酸盐缓冲液(pH = 8.2)中获得最大分析信号。出于分析目的,开发了带有安培检测的SWV方法和流动注射分析(FI Lambda)系统。优化的SWV方法显示的线性范围为1.10 x 10(-5)-1.20 x 10(-4)mol L-1,检测极限(LOD)为9.5 x 10(-6)mol L-1。使用FIA方法获得的线性范围介于2.00 x 10(-6)-9.00 x 10(-5)mol L-1和LOD为1.9 x 10(-6)mol L-1。两种方法的验证均显示出良好的性能特征,从而证实了其在几种药物产品中定量CTL的适用性。

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