Simultaneous determination of gefitinib and its major metabolites in mouse plasma by HPLC-MS/MS and its application to a pharmacokinetics study

被引:36
|
作者
Zheng, Nan [1 ,2 ]
Zhao, Can [1 ,3 ]
He, Xi-Ran [1 ,3 ]
Jiang, Shan-Tong [1 ,3 ]
Han, Shu-Yan [1 ,3 ]
Xu, Guo-Bing [1 ,2 ]
Li, Ping-Ping [1 ,3 ]
机构
[1] Minist Educ, Key Lab Carcinogenesis & Translat Res, Beijing 100142, Peoples R China
[2] Peking Univ, Canc Hosp & Inst, Natl Drug Clin Trial Ctr, Beijing 100142, Peoples R China
[3] Peking Univ, Canc Hosp & Inst, Dept Integrat Chinese & Western Med, Beijing 100142, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2016年 / 1011卷
基金
中国国家自然科学基金;
关键词
Gefitinib; Metabolites; LC-MS/MS; Mouse plasma; Pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; TYROSINE KINASE INHIBITOR; CELL LUNG-CANCER; ZD1839; QUANTIFICATION; VALIDATION; ERLOTINIB; IMATINIB; IRESSA; COLUMN;
D O I
10.1016/j.jchromb.2016.01.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gefitinib (Iressa) is the first oral EGFR tyrosine kinase inhibitor and it brings benefits to non-small cell lung cancer patients with EGFR mutation. In this study, a simple, rapid and credible high performance liquid chromatography-tandem mass spectrometry method was established and validated for the simultaneous quantification of gefitinib and its main metabolites M523595, M537194, M387783 and M608236 in NSCLC tumor-bearing mouse plasma. Sample extraction was done by protein precipitation using acetonitrile containing dasatinib as the internal standard. The chromatography run time was 6 min using an Agilent RRHD SB-C18 column with a gradient of acetonitrile and water (0.1% formic acid, v/v). The mass analysis was performed by a triple quadrupole mass spectrometry in positive multiple reaction monitoring mode. The calibration range was 0.5-100 ng/mL for M608236 and 1-200 ng/mL for other analytes with the correlation coefficients (r(2)) >= 0.99. For quality control samples, inter- and intra-assay precision was less than 15% and accuracies ranged from 92.6% to 107.58% for all analytes. The extraction recoveries were in the range of 86-105% and no significant matrix effect was observed. This simple and reproducible high throughput method was successfully applied to the pharmacokinetic study of gefitinib and its major metabolites in mouse. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 222
页数:8
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