| Literature DB >> 28445815 |
Nicolas Fabresse1, Fanta Fall2, Isabelle Etting1, Philippe Devillier3, Jean-Claude Alvarez1, Stanislas Grassin-Delyle4.
Abstract
Tranexamic acid is a widely used antifibrinolytic drug but its pharmacology and pharmacokinetics remains poorly understood. Owing to the recent knowledge on phospholipid-induced matrix effects during human plasma analysis, our aim was to develop a liquid chromatography-mass spectrometry method for the quantitation of tranexamic acid after efficient sample clean-up. Sample preparation consisted in phospholipid removal and protein precipitation. Hydrophilic interaction liquid chromatography was used and the detection was achieved with multiple reaction monitoring. The method was validated according to the European Medicine Agency guideline in the range 1.0-1000.0μg/mL. The performance of the method was excellent with a precision in the range 1.2-3.0%, an accuracy between 88.4 and 96.6% and a coefficient of variation of the internal standard-normalized matrix factor below 6.7%. This method is suitable for the quantification of tranexamic acid in the wide range of concentrations observed during clinical studies, with all the advantages related to phospholipid removal.Entities:
Keywords: EMA guideline; Human plasma; Liquid chromatography; Mass spectrometry; Phospholipid removal; Tranexamic acid
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Year: 2017 PMID: 28445815 DOI: 10.1016/j.jpba.2017.04.024
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935