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A sensitive LC-MS/MS method to determine the concentrations of erlotinib and its active metabolite OSI-420 in BALB/c nude mice plasma simultaneously and its application to a pharmacokinetic study

Meng-Yao Li, Qiong Wu, Han-Qing Li, Miao-Ran Ning, Ye Chen, Liang Li, Tian-Yan Zhou*, Wei Lu*   

  1. 1. State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Beijing 100191, China
    2. Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2012-04-13 Revised:2012-05-20 Online:2012-06-25 Published:2012-06-25
  • Contact: Tian-Yan Zhou*, Wei Lu*

Abstract:

A simple, rapid and sensitive LC-MS/MS method was developed to quantify erlotinib and its active metabolite, OSI-420, simultaneously in BALB/c nude mice plasma. Erlotinib, OSI-420 and propranolol (internal standard) were extracted from nude mice plasma samples by liquid-liquid extraction. Separation was achieved on a reversed phase C18 column with a mobile phase of acetonitrile-water (35:65, v/v) containing 5 mM ammonium formate (pH = 3.0). All compounds were monitored by mass spectrometry with electrospray positive ionization. The lower limit of quantification was 0.5 ng/mL for both erlotinib and OSI-420; accuracy was estimated by relative error, which was in the range from 0.07% to 8.00% for erlotinib and -2.83% to 6.67% for OSI-420; precision was validated by relative standard deviation, which was from 2.28% to 15.12% for erlotinib and from 1.96% to 11.50% for OSI-420. This method was applied to a pharmacokinetic study of BALB/c nude mice following oral administration of erlotinib at 12.5 mg/kg. A 2-compartment model was used to fit the pharmacokinetics of erlotinib and 1-compartment model for the pharmacokinetics of OSI-420. The ratio of the active metabolite to parent drug in mice was greater than previously reported in humans and probably reflects interspecies difference in the rate of conversion of erlotinib to OSI-420.

Key words: Erlotinib, OSI-420, LC-MS/MS, Pharmacokinetics, BALB/c nude mice

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