Method development and validation for the quantification of dasatinib, erlotinib, gefitinib, imatinib, lapatinib, nilotinib, sorafenib and sunitinib in human plasma by liquid chromatography coupled with tandem mass spectrometry

N. A.G. Lankheet*, M. J.X. Hillebrand, H. Rosing, J. H.M. Schellens, J. H. Beijnen, A. D.R. Huitema

*Corresponding author for this work

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