Liquid chromatography-tandem mass spectrometric assay for the PI3K/mTOR inhibitor GSK2126458 in mouse plasma and tumor homogenate

Publication date

2015-03-25

Authors

Dolman, EmmyISNI 0000000392581393
Westerhout, Ellen M.
Hamdi, Mohamed
Schellens, JohannesISNI 0000000042971906
Beijnen, JosISNI 0000000140305595
Sparidans, RolfISNI 0000000357085984

Editors

Advisors

Supervisors

Document Type

Article
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License

taverne

Abstract

A quantitative bioanalytical liquid chromatography-tandem mass spectrometric (LC-MS/MS) assay for GSK2126458, a dual PI3K/mTOR inhibitor, was developed and validated. Plasma and tumor homogenate samples were pre-treated using protein precipitation with acetonitrile containing dabrafenib as internal standard. After dilution with water, the extract was directly injected into the reversed-phase liquid chromatographic system. The eluate was transferred into the electrospray interface with positive ionization and compounds were detected in the selected reaction monitoring mode of a triple quadrupole mass spectrometer.The assay was completely validated for plasma in a 4-4000ng/ml calibration range with r2=0.9996±0.0003 using double logarithmic calibration (n=5). Within-run precisions (n=6) were 2.0-5.3% and between-run (3 runs; n=18) precisions 2.7-5.8%. Accuracies were between 101 and 105% for the whole calibration range. The drug was sufficiently stable under all relevant analytical conditions. Finally, the assay was successfully applied to determine plasma and tumor drug levels after oral administration of GSK2126458 to mice with AMC711T neuroblastoma xenografts.

Keywords

GSK2126458, LC-MS/MS, Mouse, Plasma, Tumor homogenate, Taverne, Analytical Chemistry, Drug Discovery, Pharmaceutical Science, Spectroscopy, Clinical Biochemistry

Citation

Dolman, M E M, Westerhout, E M, Hamdi, M, Schellens, J H M, Beijnen, J H & Sparidans, R W 2015, 'Liquid chromatography-tandem mass spectrometric assay for the PI3K/mTOR inhibitor GSK2126458 in mouse plasma and tumor homogenate', Journal of Pharmaceutical and Biomedical Analysis, vol. 107, pp. 403-408. https://doi.org/10.1016/j.jpba.2015.01.026