Quantitative analysis of tivantinib in rat plasma using ultra performance liquid chromatography with tandem mass spectrometry
- J Pharm Biomed Anal. 2016 Jul 15;126:98-102. doi: 10.1016/j.jpba.2016.05.003.
- 1. The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, 471003 Luoyang, PR China. Electronic address: [email protected].
- 2. School of Pharmacy, Chengdu University of Traditional Chinese Medicine, 611137 Chengdu, PR China.
- 3. Medical College of Henan University of Science and Technology, 471003 Luoyang, PR China.
In this work, a simple, sensitive and fast ultra performance liquid chromatography with tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the quantitative determination of tivantinib in rat plasma. Plasma samples were processed with a protein precipitation. The separation was achieved by an Acquity UPLC BEH C18 (2.1mm×50mm, 1.7μm) column with a gradient mobile phase consisting of 0.1% formic acid in water and acetonitrile. Detection was carried out using positive-ion electrospray tandem mass spectrometry via multiple reaction monitoring (MRM). The validated method had an excellent linearity in the range of 1.0-100ng/mL (r(2)>0.9967) with a lower limit of quantification (1.0ng/mL). The extraction recovery was in the range of 79.4-84.2% for tivantinib and 80.3% for carbamazepine (internal standard, IS). The intra- and inter-day precision was below 8.9% and accuracy was from -7.2% to 9.5%. No notable matrix effect and astaticism was observed for tivantinib. The method has been successfully applied to a pharmacokinetic study of tivantinib in rats for the first time, which provides the basis for the further development and application of tivantinib.
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Cat. No.Product NameDescriptionTargetResearch Area
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Research Areas: Cancer
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target: c-Met/HGFRResearch Areas: Cancer