Liquid chromatography-tandem mass spectrometry assay for the EGFR inhibitor pelitinib in plasma

Dino Luethi, Selvi Durmus, Alfred H. Schinkel, Jan H M Schellens, Jos H. Beijnen, Rolf W. Sparidans*

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    A bioanalytical liquid chromatography-tandem mass spectrometry assay for the tyrosine kinase inhibitor pelitinib was developed and validated in plasma. Acetonitrile containing the internal standard erlotinib was used to precipitate proteins. The extract was diluted with water and then directly injected onto the sub-2. μm particle, bridged ethylsilica hybrid trifunctional bonded C18 column. A gradient consisting of 0.02% (v/v) formic acid in a methanol-water mixture was used. The ionization mode of the electrospray interface was positive and the analyte was detected by a triple quadrupole mass spectrometer in the selected reaction monitoring mode. The calibration range of the assay was 1-200. ng/ml. The within day precision, the between day precision, and the accuracy were 3.5-7.4%, 4.5-8.6%, and 94.0-104.8%, respectively. The stability of the drug was sufficient under all relevant conditions. The validated assay was used to measure drug levels in wild-type FVB mice and pharmacokinetic parameters were assessed.

    Original languageEnglish
    Pages (from-to)22-25
    Number of pages4
    JournalJournal of chromatography. B
    Volume934
    DOIs
    Publication statusPublished - 1 Sept 2013

    Keywords

    • Bioanalytical assay
    • EGFR inhibitor
    • FVB mouse
    • LC-MS/MS
    • Pelitinib

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