Development and validation of a sensitive LC-MS/MS method for the quantitation of IMB-YH-4py5-2H, an antituberculosis candidate, and its application to the pharmacokinetic study

PLoS One. 2020 Feb 19;15(2):e0228797. doi: 10.1371/journal.pone.0228797. eCollection 2020.

Abstract

(E)-N,N-dimethyl-4-oxo-4-(4-(pyridin-4-yl)phenyl)but-2-enamide hydrochloride (IMB-YH-4py5-2H) is a novel Protein Kinase B (PknB) inhibitor with potent activity against Mycobacterium tuberculosis strains. In the present study, a sensitive and specific liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed and validated to determine IMB-YH-4py5-2H in rat plasma. Sample pretreatment was achieved by liquid-liquid extraction with ethyl acetate, and separation was performed on an XTerra MS C18 column (2.1×50 mm, 3.5 μm) with gradient elution (methanol and 0.1% formic acid) at a flow rate of 0.3 mL/min. Detection was performed in multiple reaction monitoring (MRM) mode. Linear calibration curves were obtained over a concentration range of 1-100 ng/mL. The intra-day and inter-day precisions were lower than 8.46%, and the accuracies ranged from -8.71% to 12.36% at all quality control levels. The extraction recoveries were approximately 70%, and the matrix effects were negligible. All quality control samples were stable under different storage conditions. The validated method was successfully applied to a preclinical pharmacokinetic study in Sprague-Dawley rats. IMB-YH-4py5-2H demonstrated improved pharmacokinetic properties (higher exposure level) compared with its leading compound. IMB-YH-4py5-2H was also distributed throughout the lung pronouncedly, especially inside alveolar macrophages, indicating its effectiveness against lower respiratory infections.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Animals
  • Antitubercular Agents / blood
  • Antitubercular Agents / isolation & purification
  • Antitubercular Agents / pharmacokinetics
  • Blood Chemical Analysis / methods*
  • Chromatography, Liquid / methods*
  • Limit of Detection*
  • Pyridines / blood*
  • Pyridines / isolation & purification
  • Pyridines / pharmacokinetics*
  • Rats
  • Rats, Sprague-Dawley
  • Tandem Mass Spectrometry / methods*

Substances

  • Antitubercular Agents
  • Pyridines

Grants and funding

This study was supported by the National Natural Science Foundation of China (http://www.nsfc.gov.cn/) (81603195) to JP; CAMS Initiative for Innovative Medicine (http://www.pumc.edu.cn/%E9%A6%96%E9%A1%B5/) (2016-I2M-3-014) to XFY, (2017-I2M-1-012) to JP, and (2016-I2M-2-002) to XW); and the National Mega-project for Innovative Drugs (2019ZX09721001) to XFY. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.