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高效液相色谱法测定生物流体中的美西律

Determination of mexiletine in biological fluids by high-performance liquid chromatography.

作者信息

Breithaupt H, Wilfling M

出版信息

J Chromatogr. 1982 Jun 11;230(1):97-105. doi: 10.1016/s0378-4347(00)81434-6.

Abstract

A high-performance liquid chromatographic method for the determination of the anti-arrhythmic drug mexiletine in human plasma, urine, and cerebrospinal fluid is described. Following extraction with diethyl ether, mexiletine and the internal standard 4-methylmexiletine were derivatized with 2,4-dinitrofluorobenzene. Analyses were performed using an alternating on-column enrichment technique on small Perisorb RP-2 30-40 micrometers pre-columns with pre-column backflushing for direct injection onto the analytical column of Spherisorb ODS 5 micrometers. Complete separation from endogenous constituents of plasma, urine or cerebrospinal fluid was achieved by isocratic reversed-phase ion-pair chromatography with 1-heptanesulfonic acid (0.005 M; PIC B7)-acetonitrile-tetrahydrofuran (42:48:10, v/v) as eluent. Interferences from other drugs were not observed. The limit of detection was 10 ng/ml (C.V. 6.5%). Day-to-day coefficients of variation were below 9%. The applicability of this rapid method for pharmacokinetic studies and clinical routine is demonstrated.

摘要

描述了一种用于测定人血浆、尿液和脑脊液中抗心律失常药物美西律的高效液相色谱法。用乙醚萃取后,美西律和内标4-甲基美西律用2,4-二硝基氟苯衍生化。分析采用交替柱上富集技术,在30-40微米的小Perisorb RP-2预柱上进行,通过预柱反冲直接进样到5微米的Spherisorb ODS分析柱上。采用等度反相离子对色谱法,以1-庚烷磺酸(0.005 M;PIC B7)-乙腈-四氢呋喃(42:48:10,v/v)为洗脱剂,实现了与血浆、尿液或脑脊液中内源性成分的完全分离。未观察到其他药物的干扰。检测限为10 ng/ml(变异系数6.5%)。日间变异系数低于9%。证明了该快速方法在药代动力学研究和临床常规中的适用性。

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