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Highly sensitive determination of chlorpromazine by electrochemically treated pencil graphite fiber as both solid-phase microextraction fiber and working electrode for use in voltammetry method

机译:电化学处理的铅笔状石墨纤维作为固相微萃取纤维和伏安法中的工作电极高灵敏度测定氯丙嗪

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This paper describes the electrochemical modification of a pencil graphite fiber used as both a solid phase microextraction fiber and a working electrode in differential pulse voltammetry (DPV). The combination of solid phase microextraction and DPV was applied as a highly selective and sensitive method for the determination of chlorpromazine. The pencil graphite fibers were electrochemically treated in phosphoric acid and sodium hydroxide solutions. Experimental parameters influencing the extraction efficiency of SPME, such as NaOH concentration, ionic strength of the sample, stirring rate, and extraction time were studied and optimized. Under the optimum conditions, analytical parameters such as linearity, precision and limit of detection were evaluated. The linear dynamic range was from 0.35 to 35 μg L~(-1) and the limit of detection was 0.2 μg L~(-1). Intra- and inter-day precision of the method was satisfactory with a relative standard deviation of 2.2 and 4.8%, respectively. The method was successfully applied for the determination, of chlorpromazine in human plasma and urine.
机译:本文介绍了在差分脉冲伏安法(DPV)中用作固相微萃取纤维和工作电极的铅笔状石墨纤维的电化学改性方法。固相微萃取和DPV的组合作为测定氯丙嗪的高度选择性和灵敏方法。铅笔状石墨纤维在磷酸和氢氧化钠溶液中进行了电化学处理。研究并优化了影响SPME萃取效率的实验参数,例如NaOH浓度,样品的离子强度,搅拌速率和萃取时间。在最佳条件下,评估了线性,精密度和检出限等分析参数。线性动态范围为0.35至35μgL〜(-1),检出限为0.2μgL〜(-1)。该方法的日内和日间精度令人满意,相对标准偏差分别为2.2和4.8%。该方法已成功用于人体血浆和尿液中氯丙嗪的测定。

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