1. Academic Validation
  2. Determination of a novel Aurora-A (AurA) kinase AKI603 by UPLC-MS/MS and its application to a bioavailability study in rat

Determination of a novel Aurora-A (AurA) kinase AKI603 by UPLC-MS/MS and its application to a bioavailability study in rat

  • J Pharm Biomed Anal. 2016 Jun 5;125:303-9. doi: 10.1016/j.jpba.2016.03.041.
Zhenzhen Zhao 1 Lingjie Huang 2 Xiaoli Gou 1 Zhangwei Li 1 Jiangying Chen 1 Dingsheng Wen 2 Fulin Jiang 1 Gui Lu 2 Huichang Bi 1 Min Huang 1 Guoping Zhong 3
Affiliations

Affiliations

  • 1 Laboratory of Drug Metabolism and Pharmacokinetics, School of Pharmaceutical Sciences, North Campus, Sun Yat-Sen University, No.74, 2nd Yat-Sen Road, Yuexiu District, Guangzhou City, Guangdong Province 510080, China.
  • 2 Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, 132 Waihuan Road East, Guangzhou City, Guangdong Province 510006, China.
  • 3 Laboratory of Drug Metabolism and Pharmacokinetics, School of Pharmaceutical Sciences, North Campus, Sun Yat-Sen University, No.74, 2nd Yat-Sen Road, Yuexiu District, Guangzhou City, Guangdong Province 510080, China. Electronic address: [email protected].
Abstract

A simple, sensitive and accurate ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of AKI603 in rat plasma has been firstly developed and validated. After a simple liquid-liquid extraction (LLE) with ethyl acetate, the analytes were separated on C18 column (2.1×100mm, 1.9μm, Thermo) by gradient elution with mobile phase of water (A) (containing 5mM ammonium acetate and 0.1% formic acid) and methanol (B) with a flow rate of 0.3mLmin(-1) and then analyzed by mass spectrometry in the positive multiple reactions monitoring (MRM) mode. The mass transitions monitored were m/z 410.0→352.9, m/z 457.1→367.9 for AKI603 and internal standard (Ly-7z), respectively. The developed method was validated for specificity, linearity and lower limit of quantification, intra- and inter-day precision and accuracy, extraction recovery, matrix effect and stability whose values satisfied the acceptable limits. The calibration curves for AKI603 was linear in concentration ranges of 0.025-5000ngmL(-1). The method has been successfully used to the bioavailability study of AKI603 administered to rats intravenously (2.5mg/kg) or orally (25mg/kg). The oral bioavailability of AKI603 in rats was calculated as 28.7±9.7%.

Keywords

AKI603; Method validation; Oral bioavailability study; Rat; UPLC-MS/MS.

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