A validated assay by liquid chromatography–tandem mass spectrometry for the simultaneous quantification of elvitegravir and rilpivirine in HIV positive patients. (3rd May 2013)

• Record Type: Journal Article
• Authors: Aouri, Manel; Calmy, Alexandra; Hirschel, Bernard; Telenti, Amalio; Buclin, Thierry; Cavassini, Matthias; Rauch, Andri; Decosterd, Laurent A.
• Is Part Of: Journal of mass spectrometry. Volume 48:Number 5(2013:May)
• Page Start: 616
• Page End: 625
• Publication Date: 2013-05-03
• Subjects: elvitegravir -- rilpivirine -- tandem mass spectrometry -- analytical methods validation -- therapeutic drug monitoring -- stable‐labeled isotopes -- anti‐HIV therapy; Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/jms.3200
• Languages: English
• ISSNs: 1076-5174

Abstract

Abstract : Because of the large variability in the pharmacokinetics of anti‐HIV drugs, therapeutic drug monitoring in patients may contribute to optimize the overall efficacy and safety of antiretroviral therapy. An LC–MS/MS method for the simultaneous assay in plasma of the novel antiretroviral agents rilpivirine (RPV) and elvitegravir (EVG) has been developed to that endeavor. Plasma samples (100 μL) extraction is performed by protein precipitation with acetonitrile, and the supernatant is subsequently diluted 1:1 with 20‐mM ammonium acetate/MeOH 50:50. After reverse‐phase chromatography, quantification of RPV and EVG, using matrix‐matched calibration samples, is performed by electrospray ionization–triple quadrupole mass spectrometry by selected reaction monitoring detection using the positive mode. The stable isotopic‐labeled compounds RPV‐ 13 C6 and EVG‐D6 were used as internal standards. The method was validated according to FDA recommendations, including assessment of extraction yield, matrix effects variability (<6.4%), as well as EVG and RPV short and long‐term stability in plasma. Calibration curves were validated over the clinically relevant concentrations ranging from 5 to 2500 ng/ml for RPV and from 50 to 5000 ng/ml for EVG. The method is precise (inter‐day CV%: 3–6.3%) and accurate (3.8–7.2%). Plasma samples were found to be stable (<15%) in all considered conditions (RT/48 h, +4°C/48 h, −20°C/3 months and 60°C/1 h). Selected metabolite profiles analysis in patients' samples revealed the presence of EVG glucuronide, that was well separated from parent EVG, allowing to exclude potential interferences through the in‐source dissociation of glucuronide to parent drug. This new, rapid and robust LCMS/MS assay for the simultaneous quantification of plasma concentrations of these two major new anti‐HIV drugs EVG and RPV offers an efficient analytical tool for clinical pharmacokinetics studies and routine therapeutic drug monitoring service. Copyright © 2013 John Wiley & Sons, Ltd.