A quick and Sensitive Liquid Chromatography–tandem Mass Spectrometry (LC-MS) Method for the Determination of Enalapril and Enalaprilat in Human Plasma: Application to a Bioequivalence Study

Document Type : Research Paper

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school of pharmacy zanjan university

Abstract

A rapid and sensitive liquid chromatography–tandem mass spectrometry (LC-MS) method for the estimation of enalapril and enalaprilat in human plasma. Detection of analytes was achieved by tandem mass spectrometry with electrospray ionization (ESI) interface in positive ion mode was operated under the multiple-reaction monitoring mode. Sample pretreatment involved in a one-step protein precipitation (PPT) with percholoric acid (HClO4) of 0.15ml plasma. The reconstituted samples were chromatographed on C18 column by pumping methanol: water: acid formic74:24:2 (v/v)at a flow rate of 0.2 mL/min.Each plasma samplewaschromatographedwithin1.25min.The standard curves were found to be linear in the range of 0.1–20ng/mL for enalapril and enalaprilat with mean correlation coefficient of ≥0.999 for each analyte. The intra-day and inter-day precision and accuracy results were well within the acceptable limits.The limit of quantification(LOQ) was 0.1ng/ml for enalapril andenalaprilat. The mean (SD) Cmax, Tmax, AUC0–tand AUC0–∞ values of enalaprilversusenalaprilatafter administration of the 10 mg enalapril, respectively, were in this manner: 141.33(3.51) versus73.33 (5.03) ng/mL, 1.15(1.45) versus 4.12 (1.74) hours, 142.57 (34.34) versus 425.94(13.09) ng/mL/h, and 150.74 (16.69) versus 455.80 (65.11) ng/mL/h. The mean (SD) t1/2 was 2.72 (2.01) hours for the enalapril and 6.34 (2.13) hours for the enalaprilat. The developed assay method was successfully applied to a pharmacokinetic study in human male volunteers.

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Iranian Journal of Pharmaceutical Sciences
Volume 12, Issue 1
January 2016
Pages 21-34

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