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一种快速灵敏的液相色谱/串联质谱法同时测定人血浆中依那普利及其主要代谢物依那普利拉的方法:应用于生物等效性研究。

Rapid and sensitive liquid chromatography/tandem mass spectrometry method for simultaneous determination of enalapril and its major metabolite enalaprilat, in human plasma: application to a bioequivalence study.

机构信息

Bioanalytical Department, Cadila Pharmaceuticals Limited, 1389-Trasad road, Dholka, Gujarat, India.

出版信息

Drug Test Anal. 2012 Feb;4(2):94-103. doi: 10.1002/dta.241. Epub 2011 Feb 21.

DOI:10.1002/dta.241
PMID:21341376
Abstract

A rapid and most sensitive method for simultaneous determination of enalapril (ENP) and its metabolite, enalaprilat (ENPT), in human plasma using ESI-LC-MS/MS (electrospray ionization liquid chromatography tandem mass spectrometry) positive ion multiple reactions monitoring (MRM) mode, was developed and validated. The procedure involves a simple solid-phase extraction (SPE) followed by evaporation of the sample. Chromatographic separation was carried out on a Hypurity C(18) column (50 mm × 4.6 mm, 5 µm) with an isocratic mobile phase and a total run time of 2.0 min only. The MRM of ENP and ENPT is 377.10 → 234.20 and 349.20 → 206.10 respectively. The standard calibration curves showed excellent linearity within the range of 0.064 to 431.806 ng/mL for ENA and 0.064 to 431.720 ng/mL for ENPT (r ≥ 0.990). This is the only method which can quantitate upto 0.064 ng/mL for both ENP and ENPT in a single run with the shortest analysis time. In matrix effect experiment, this method shows a % CV (% coefficients of variation) of less than 5, which means that the proposed method is free from any kind of irregular ionization process. This method was successfully applied to a pharmacokinetic study after oral administration of enalapril maleate 20 mg tablet in Indian healthy male volunteers.

摘要

建立并验证了一种灵敏、快速的同时测定人血浆中依那普利(ENP)及其代谢物依那普利拉(ENPT)的 ESI-LC-MS/MS(电喷雾离子化液相色谱-串联质谱)正离子多反应监测(MRM)法。该方法采用固相萃取(SPE),操作简单,样品经蒸发干燥后即可进行色谱分析。采用 Hypurity C(18)柱(50mm×4.6mm,5μm),以等度洗脱方式,仅需 2.0min 即可完成色谱分离。ENP 和 ENPT 的 MRM 监测离子分别为 377.10→234.20 和 349.20→206.10。ENP 和 ENPT 的标准校正曲线在 0.064431.806ng/mL 和 0.064431.720ng/mL 范围内线性关系良好(r≥0.990)。这是唯一一种可以在单次运行中定量测定低至 0.064ng/mL 的 ENP 和 ENPT 的方法,且分析时间最短。在基质效应实验中,该方法的%CV(变异系数)小于 5,表明该方法不受任何不规则离子化过程的影响。该方法已成功应用于马来酸依那普利 20mg 片在印度健康男性志愿者体内的药代动力学研究。

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