Bioanalytical Department, Cadila Pharmaceuticals Limited, 1389-Trasad road, Dholka, Gujarat, India.
Drug Test Anal. 2012 Feb;4(2):94-103. doi: 10.1002/dta.241. Epub 2011 Feb 21.
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.
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。