TY - JOUR AU - Bhupesh Sompura PY - 2012/05/14 Y2 - 2024/03/29 TI - SIMULTANEOUS ESTIMATION OF RAMIPRIL AND ITS ACTIVE METABOLITE RAMIPRILAT IN HUMAN PLASMA BY ESI-LC-MS/MS JF - Journal of Drug Delivery and Therapeutics JA - JDDT VL - 2 IS - 3 SE - Research DO - 10.22270/jddt.v2i3.138 UR - https://jddtonline.info/index.php/jddt/article/view/138 AB - A rapid and sensitive liquid chromatography tandem mass spectrometry method has been developed and validated for the simultaneous determination of ramipril and ramiprilat in human plasma. The solid-phase extraction technique was used for the extraction of ramipril and ramiprilat from human plasma. Enalapril was used as the internal standard (IS).Chromatography was performed on a Aquasil C18, 100mm×2.1mm, 5µ column, with the mobile phase consisting of acetonitrile-deionsed water (in a 65:35 ratio) and 1.0mLL-1 ammonium trifluoroacetate solution (1.0M), followed by detection using mass spectrometry. The method involves a simple reversed isocratic chromatography condition and mass spectrometry detection, which enables detection at sub-nanogram levels. The method was validated and the lower limit of quantification for ramipril and ramiprilat was found to be 0.1 ngmL−1and 0.1 ngmL−1, respectively. The mean recovery for ramipril and ramiprilat ranged from 63.5 to 74.3%. This method increased the sensitivity and selectivity; resulting in high-throughput analysis of ramipril and ramiprilat using single IS in a single experiment for bioequivalence studies, with a chromatographic run time of 3.0 min only. ER -