Liquid chromatography-tandem mass spectrometric assay for the quantitative determination of the tyrosine kinase inhibitor quizartinib in mouse plasma using salting-out liquid-liquid extraction

Publication date

2017-09-01

Authors

Retmana, Irene A
Wang, Jing
Schinkel, Alfred H
Schellens, JohannesISNI 0000000042971906
Beijnen, JosISNI 0000000140305595
Sparidans, RolfISNI 0000000357085984

Editors

Advisors

Supervisors

Document Type

Article
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License

taverne

Abstract

A bioanalytical assay for quizartinib -a potent, and selective FLT3 tyrosine kinase inhibitor- in mouse plasma was developed and validated. Salting-out assisted liquid-liquid extraction (SALLE), using acetonitrile and magnesium sulfate, was selected as sample pretreatment with deuterated quizartinib as internal standard. Separation was performed with reversed-phase liquid chromatography followed by detection with positive electrospray-triple quadrupole mass spectrometry in the selected reaction monitoring mode. The assay was successfully validated for mouse plasma in a 2-2000ng/ml calibration range with r(2)=0.9958±0.0028 (n=7) for linear regression with the inverse square of the concentration as a weighting factor. The within-run precision (n=18), between-run precision and accuracy were 2.9-6.0%, 4.5-8.9% and 91.7-109.4% respectively. The drug was stable under all relevant conditions. Finally, the assay was successfully applied in a pharmacokinetic pilot study in plasma of FVB/NRj mice treated with quizartinb orally.

Keywords

Animals, Benzothiazoles, Chromatography, Liquid, Female, Linear Models, Mice, Phenylurea Compounds, Protein Kinase Inhibitors, Reproducibility of Results, Tandem Mass Spectrometry, Taverne

Citation

Retmana, I A, Wang, J, Schinkel, A H, Schellens, J H M, Beijnen, J H & Sparidans, R W 2017, 'Liquid chromatography-tandem mass spectrometric assay for the quantitative determination of the tyrosine kinase inhibitor quizartinib in mouse plasma using salting-out liquid-liquid extraction', Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, vol. 1061-1062, pp. 300-305. https://doi.org/10.1016/j.jchromb.2017.07.034