Determination of pinostrobin in rat plasma by LC-MS/MS: application to pharmacokinetics

J Pharm Biomed Anal. 2011 Dec 5;56(4):841-5. doi: 10.1016/j.jpba.2011.07.038. Epub 2011 Jul 30.

Abstract

A rapid and sensitive method for the determination of pinostrobin in rat plasma was developed using liquid chromatography tandem mass spectrometry (LC-MS/MS) for the first time. Isoliquiritigenin was used as an internal standard in rat plasma. Chromatographic separation was performed on an HiQ Sil C(18) column with isocratic elution at a flow rate of 1mL/min. The mobile phase consisted of water and methanol (9:91, v/v) containing 0.1% formic acid. The quantification limit was 10ng/mL within a linear range of 10-1000ng/mL (R=0.9984). The intra- and inter-day assay precision ranged from 3.8-5.3% to 3.2-5.2%, respectively, and the intra- and inter-day assay accuracy was between 93.2-95.1% and 95.5-104.3%, respectively. Our results indicated that the LC-MS/MS method is effective for pharmacokinetic study of pinostrobin in rat plasma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calibration
  • Chromatography, Liquid / methods
  • Female
  • Flavanones / blood*
  • Flavanones / chemistry
  • Flavanones / pharmacokinetics
  • Flavanones / standards
  • Parasympatholytics / blood*
  • Parasympatholytics / chemistry
  • Parasympatholytics / pharmacokinetics
  • Parasympatholytics / standards
  • Rats
  • Reference Standards
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tandem Mass Spectrometry / methods*

Substances

  • Flavanones
  • Parasympatholytics
  • pinostrobin