Quantitative determination of carfilzomib in mouse plasma by liquid chromatography-tandem mass spectrometry and its application to a pharmacokinetic study
Autor: | Doyun Kim, Yu Fen Zheng, Soo Kyung Bae, Wooin Lee, Ji Eun Park, Jiseon Kim, Jee Sun Min, Jung Ho Kim |
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Rok vydání: | 2017 |
Předmět: |
Chlorpropamide
Electrospray ionization Clinical Biochemistry Analytical chemistry Pharmaceutical Science Tandem mass spectrometry 030226 pharmacology & pharmacy Analytical Chemistry 03 medical and health sciences Mice Plasma 0302 clinical medicine Liquid chromatography–mass spectrometry Limit of Detection Tandem Mass Spectrometry Drug Discovery Protein precipitation Animals Spectroscopy Detection limit Chromatography Chemistry Selected reaction monitoring Reproducibility of Results Triple quadrupole mass spectrometer 030220 oncology & carcinogenesis Oligopeptides Blood sampling Chromatography Liquid |
Zdroj: | Journal of pharmaceutical and biomedical analysis. 146 |
ISSN: | 1873-264X |
Popis: | A highly sensitive and rapid LC-MS/MS method was developed and validated to determine the levels of carfilzomib in mice plasma by using chlorpropamide as an internal standard. Carfilzomib and chlorpropamide were extracted from 5 μL of plasma after protein precipitation with acetonitrile. Chromatographic separation was performed on Phenomenex Luna C18 column (50×2.0mm id, 3μm). The mobile phase consisted of 0.1% formic acid in acetonitrile -0.1% formic acid in water (1:1v/v) and the flow rate was 0.3mL/min. The total chromatographic run time was 2.5min. Detection was performed on a triple quadrupole mass spectrometer equipped with positive-ion electrospray ionization by selected reaction monitoring of the transitions at m/z 720.20>100.15 (for carfilzomib) and m/z 277.05>111.05 (for the internal standard). The lower limit of quantification was 0.075ng/mL and the linear range was 0.075-1250ng/mL (r≥0.9974). All validation data, including selectivity, precision, accuracy, matrix effect, recovery, dilution integrity, stability, and incurred sample reanalysis, were well within acceptance limits. This newly developed bioanalytical method was simple, highly sensitive, required only a small volume of plasma, and was suitable for application in pharmacokinetic studies in mice that used serial blood sampling. |
Databáze: | OpenAIRE |
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