Simultaneous quantification of the new HIV protease inhibitors atazanavir and tipranavir in human plasma by high-performance liquid chromatography coupled with electrospray ionization tandem mass spec
- 作者：Crommentuyn ; K.M.L. ; Rosing ; H. ; Hillebrand ; M.J.X. ; Huitema ; A.D.R. ; Beijnen ; J.H.
- 关键词：Atazanavir ; Tipranavir
- 刊名：Journal of Chromatography B ; Analytical Technologies in the Biomedical and Life Sciences
- 出版年：2004
- 期刊代码：124_15700232
- 类别：ch
- 出版时间：May 25, 2004
- 卷：804
- 期：2
- 页码：359-367
- 文件大小：164 K
摘要
We have developed and validated an assay, using liquid chromatography coupled with electrospray tandem mass spectrometry (LC–MS/MS), for the quantification of the novel protease inhibitors (PIs) atazanavir and tipranavir. The sample pre-treatment consisted of protein precipitation with a mixture of methanol and acetronitrile using 100μl plasma for atazanavir and 50μl for tipranavir. Chromatographic separation was achieved on an Inertsil ODS3 column (50mm×2.0mm i.d., particle size 5μm), with a quick stepwise gradient using an acetate buffer (pH 5) and methanol, at a flow rate of 0.5ml/min. The analytical run time was 5.5min. The triple quadrupole mass spectrometer operated in the positive ion-mode and multiple reaction monitoring (MRM) was used for drug quantification. The assay was linear over a concentration range of 0.05–10μg/ml for atazanavir and 0.1–75μg/ml for tipranavir. Saquinavir-d5 was used as internal standard. The intra- and inter-day coefficients of variation were less than 3.8%for atazanavir and less than 10.4%for tipranavir. Accuracies were within ±7.3 and ±7.2%for atazanavir and tipranavir, respectively. Both drugs were stable under various relevant storage conditions. The validated concentration ranges proved to be adequate to measure concentrations of human immunodeficiency virus type-1 (HIV-1)-infected individuals. The developed method could easily be combined with a previously developed LC–MS/MS assay for the quantification of protease inhibitors.