LC–MS/MS assay for quantitation of enalapril and enalaprilat in plasma for bioequivalence study in Indian subjects
Author(s) -
Dhiman Halder,
Shubhasis Dan,
Murari Mohun Pal,
Easha Biswas,
Nilendra Chatterjee,
Pradipta Sarkar,
Umesh Chandra Halder,
Tapan Kumar Pal
Publication year - 2017
Publication title -
future science oa
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 23
ISSN - 2056-5623
DOI - 10.4155/fsoa-2016-0071
Subject(s) - enalaprilat , bioequivalence , enalapril , metabolite , bioavailability , pharmacology , protein precipitation , active metabolite , chemistry , bioanalysis , pharmacokinetics , chromatography , medicine , angiotensin converting enzyme , biochemistry , blood pressure
Background: Enalapril (EPL) is an angiotensin-converting enzyme inhibitor for the treatment of hypertension and chronic heart failure. Enalaprilat (EPLT) is an active metabolite that contributes to the overall activity of EPL. Aim: To quantitate EPL along with its metabolite EPLT using LC–MS/MS, a bioanalytical method was developed and validated with tolbutamide in human plasma using a protein precipitation technique. Results: The sensitive and selective method has an LLOQ of 1 ng/ml with a linearity range of 1–500 ng/ml for both EPL and EPLT using 300 µl of plasma without any matrix effect. Conclusion: Linearity, specificity, accuracy, precision and stability, as well as its application to the analysis of plasma samples after oral administration of 20 mg of EPL maleate in healthy volunteers demonstrate applicability to bioavailability/bioequivalence studies.
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