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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Development and validation method for determination of Paroxetine and its metabolites by nonaqueous capillary electrophoresis in human urine. Experimental design for evaluating the ruggedness of the method
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Development and validation method for determination of Paroxetine and its metabolites by nonaqueous capillary electrophoresis in human urine. Experimental design for evaluating the ruggedness of the method

机译:非尿液毛细管电泳法测定人尿中帕罗西汀及其代谢物的开发与验证方法。用于评估方法坚固性的实验设计

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摘要

A simple, rapid, and sensitive procedure using nonaqueous capillary electrophoresis (NACE) to measure Paroxetine (one of the mostly used antidepressants for mental diseases treatment) and three metabolites has been developed and validated. Optimum separation of paroxetine and metabolites was obtained on a 57 cm x 75 mum capillary using a nonaqueous buffer system of 9:1 methanol-acetonitrile containing 25 mm ammonium acetate and 1% acetic acid, with temperature and voltage of 25degreesC and 15 W, respectively, and hydrodynamic injection. Fluoxetine was used as an internal standard. Good results were obtained for different aspects including stability of the solutions, linearity, accuracy, and precision. Detection limits between 9.3 and 23.1 mug (,) L-1 were obtained for paroxetine and its metabolites. A ruggedness test of the method was carried out using the Plackett-Burman fractional factorial model with a matrix of 15 experiments. This method has been used to determine paroxetine and its main metabolite B at clinically relevant levels in human urine. Prior to NACE determination, the samples were purified and enriched by means of an extraction-preconcentration step with a preconditioned C-18 cartridge and eluting the compounds with methanol. [References: 28]
机译:已经开发并验证了使用非水毛细管电泳(NACE)来测量帕罗西汀(一种用于精神疾病治疗的最常用抗抑郁药之一)和三种代谢物的简单,快速,灵敏的方法。使用含有25 mm乙酸铵和1%乙酸的9:1甲醇-乙腈非水缓冲液,在57 cm x 75 m的毛细管上获得帕罗西汀​​和代谢物的最佳分离,温度和电压分别为25°C和15 W以及流体动力注射。氟西汀用作内标。在各个方面都获得了良好的结果,包括解决方案的稳定性,线性,准确性和精度。帕罗西汀及其代谢物的检出限在9.3和23.1马克杯(,)L-1之间。使用Plackett-Burman分数阶乘模型并采用15个实验矩阵对方法进行了耐用性测试。该方法已用于测定人尿中临床相关水平的帕罗西汀及其主要代谢物B。在确定NACE之前,通过使用预调节的C-18柱的萃取-浓缩步骤纯化并富集样品,并用甲醇洗脱化​​合物。 [参考:28]

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