Simultaneous quantitative determination of seven novel tyrosine kinase inhibitors in plasma by a validated UPLC-MS/MS method and its application to human microsomal metabolic stability study.

A rapid, sensitive and reproducible ultra-high performance liquid chromatography mass spectrometry method was developed and validated for simultaneous determination of seven tyrosine kinase inhibitors (dasatinib, foretinib, osimertinib, gefitinib, ibrutinib, linifanib and motesanib) in human plasma samples using quizartinib as internal standard (IS). The sample preparation was performed by liquid-liquid extraction method, using a mixture of ethyl acetate and tert butyl methyl ether (50:50, v/v) as extracting solvents. Chromatographic separation was achieved using acquity UPLC BEH C, 1.