Ndolo Sedireng M, Sichilongo Kwenga, Massele Amos, Sepako Enoch, Vento Sandro
Department of Science, Molepolole College of Education, P/Bag 008 Molepolole, Gaborone 00267, Botswana.
Department of Chemistry, Faculty of Science, University of Botswana, PB UB00704, Gaborone 00267, Botswana
J Anal Toxicol. 2016 Jan-Feb;40(1):49-57. doi: 10.1093/jat/bkv119. Epub 2015 Oct 20.
Liquid chromatography (LC) and mass spectral behavior and analytical performance characteristics of efavirenz (EFV), emtricitabine (EMT) and tenofovir (TFV), i.e., individual components of Atripla(®), were probed. This was followed by estimation of their analytical performance characteristics employing LC and a parallel direct infusion sample introduction procedure. Performance characteristics using both types of sample introduction procedures were compared. Using liquid chromatography-mass spectrometry (LC-MS), linearities, i.e., correlation coefficients of the calibration curves of EFV, EMT and TFV, ranged between 0.9300 and 0.9990 in the full scan, selected ion monitoring and mass spectrometry/mass spectrometry (MS-MS) modes. The limits of detection (LODs) ranged between 0.5 and 11.6 µg/L. The lower limits of quantification (LLOQs) and the upper limits of quantification (ULOQs) were in the ranges of 0.9-23.2 and 1.6-38.7 µg/L, respectively. The LODs ranged between 0.8 and 114.7 µg/L. The LLOQs and the ULOQs were in the ranges of 1.6-29.4 and 2.7-49.0 µg/L, respectively. In the case of EMT, sodiated molecular ion at m/z 270 was used to adduce analytical performance characteristics from which lower detection limits were obtained compared with those in the literature where M+H at m/z 248 was used.