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High-performance liquid chromatography method for analyzing citalopram and desmethylcitalopram from human serum.

机译:高效液相色谱法从人血清中分析西酞普兰和去甲基西酞普兰。

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This report describes a sensitive and specific method for analyzing a serotonin reuptake blocker, citalopram, and its active metabolite, desmethylcitalopram, in human serum. For high-performance liquid chromatography (HPLC) analysis, samples and standards are prepared with ASPEC automatic sample preparator using 100 mg Bond-Elut C-18 solid-phase extraction columns. The method is an isocratic HPLC method with a mobile phase of acetonitrile:methanol:50 mM dipotassium hydrogenphosphate, pH 4.7 (40:100). Detection is performed with diode array detector at 220 nm and the peak purity analyses at 210 to 365 nm. The intraassay coefficient of variation ranges from 3.7% to 7.3%, and the interassay coefficient of variation ranges from 6.9% to 9.9% at therapeutic drug concentrations. The detection limit is 15 nmol/l. The method is suitable for therapeutic drug monitoring in a clinical laboratory. A clear correlation, r = 0.72 (y = 0.36x + 17.94), between citalopram and its metabolite levels is observed in routine therapeutic drug monitoring service. A linear correlation between serum concentration and daily dose of citalopram in patient groups is also observed.
机译:该报告描述了一种敏感而具体的方法,用于分析人血清中的5-羟色胺再摄取阻滞剂西酞普兰及其活性代谢产物去甲基西酞普兰。对于高效液相色谱(HPLC)分析,使用100毫克Bond-Elut C-18固相萃取柱,使用ASPEC自动样品制备器制备样品和标准品。该方法是等度HPLC方法,其流动相为乙腈:甲醇:50 mM磷酸氢二钾,pH 4.7(40:100)。使用二极管阵列检测器在220 nm处进行检测,并在210至365 nm处进行峰纯度分析。在治疗药物浓度下,批内变异系数为3.7%至7.3%,批间变异系数为6.9%至9.9%。检出限为15 nmol / l。该方法适用于临床实验室中的治疗药物监测。在常规治疗药物监测服务中,西酞普兰与其代谢产物水平之间存在明显的相关性,r = 0.72(y = 0.36x + 17.94)。在患者组中,西酞普兰的血清浓度与每日剂量之间也存在线性关系。

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