&NA; Efavirenz is an antiretroviral drug used in the treatment of HIV‐positive patients. A simple, fast and sensitive high‐performance liquid chromatography (HPLC) method was developed in order to determine efavirenz… Click to show full abstract
&NA; Efavirenz is an antiretroviral drug used in the treatment of HIV‐positive patients. A simple, fast and sensitive high‐performance liquid chromatography (HPLC) method was developed in order to determine efavirenz in three types of samples provided from pharmacokinetic studies. The analysis took 5 min and was performed using a C18 analytical column (Discovery HS C18, 150 × 4.6 mm, particle size of 5 &mgr;m) in isocratic mode with a mobile phase containing acetonitrile and water (65:35, v/v), a flow rate of 1.6 mL min−1, a sample volume of 10 &mgr;L and UV detection at 245 nm. Three different sample matrices (Opti‐MEM medium, Krebs perfusion liquid and tissue lysate) and their treatment (dilution, SPE) were considered. The validated method was applied for the analysis of 805 real samples arising from in vitro transcellular transport assays and in vivo organ perfusion experiments in order to evaluate the interaction of efavirenz with ATP‐dependent drug efflux transporters. The lack of interaction of efavirenz with ABCB1, ABCG2 and ABCC2 transporters as well as technical aspects of this analysis, including the adhesion of efavirenz to the plastic materials and the stability of the drug during different tissue lysis approaches are discussed. Graphical abstract Figure. No caption available. HighlightsDetailed study of efavirenz interactions with cell membrane transporters.Development of HPLC determination of efavirenz in different sample matrices.Determination of efavirenz in transport study, perfusion of placenta and placenta tissue lysate.Pre‐treatment of low sample volumes for efavirenz determination in different matrices.Efavirenz stability for determination in placenta lysates − testing of different lysis agents.
               
Click one of the above tabs to view related content.