LC determination and pharmacokinetic study of vitexin-4″-O-glucoside in rat plasma after oral administration

Nat Prod Res. 2012;26(10):962-7. doi: 10.1080/14786419.2010.535165. Epub 2011 Aug 11.

Abstract

A simple and specific high-performance liquid chromatography (HPLC) method was developed for the pharmacokinetic study of vitexin-4″-O-glucoside (VOG) in rats after oral administration. The plasma samples were deproteinised with methanol after the addition of an internal standard, hesperidin. HPLC analysis was performed on a Diamonsil C(18) analytical column, using methanol -0.5% aqueous phosphoric acid (45:55, v/v) as the mobile phase with ultraviolet detection at 330 nm. The calibration curve was linear over the range of 5-450 µg mL(-1) in rat plasma. The average extraction recovery of VOG was 98.74% ± 0.44%, and the relative standard deviations of the intra- and inter-day precisions were not greater than 4.1% and 2.0%, respectively. The validated method was successfully applied during a pharmacokinetic study in rats after oral administration of VOG at different doses, and all the results indicated that the pharmacokinetics of VOG in rats obeyed nonlinear processes.

Publication types

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

MeSH terms

  • Administration, Oral
  • Animals
  • Chromatography, High Pressure Liquid / methods*
  • Glucosides / blood
  • Glucosides / pharmacokinetics*
  • Isoflavones / blood
  • Isoflavones / pharmacokinetics*
  • Rats
  • Reference Standards
  • Reproducibility of Results
  • Spectrophotometry, Ultraviolet

Substances

  • Glucosides
  • Isoflavones
  • isovitexin-4'-O-glucoside