20(S)- and 20(R)-ginsenoside Rg(3) are a pair of epimers which could be deglycosylated to ginsenoside Rh-2 and protopanaxadiol (PPD) in vivo. To better understand the differences of pharmacokinetic parameters and metabolism behaviors of Rg(3) epimers in rat plasma, a sensitive and specific liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method was developed and fully validated. This chromatographic method separate 20(S)-/20(R)-Rg(3), 20(S)-/20(R)-Rh-2 and 20(S)-120(R)-PPD by gradient elution of 10 mM ammonium acetate solution (pH 5.0) and acetonitrile on a C18 column with a total run time of 15 min. 20(S)-protopanaxatriol (PPT) was used as internal standard, and multiple reaction monitoring (MRM) mode with negative electrospray ionization were performed. The lower limit of quantitations (LLOQs) were between 4.2 and 4.8 ng/ml, and the accuracies were between 91.7% and 112.2% with intra- and inter-day precisions less than 11.6%. This method was successfully applied to a pharmacokinetic study of intravenous and intra-gastric administration of 20(S)-Rg(3) and 20(R)-Rg(3) to rats. It has been found that both epimers can be deglycosylated to their corresponding chiral metabolites, i.e., Rh2 and PPD, with different extents. However, 20(R)-Rg(3) underwent single direction chiral inversion to 20(S)-Rg(3) in rats. Stereoselective pharmacokinetic parameters, metabolic degrees and chiral inversion extents of Rg(3) epimers in rats were also discussed for the first time. (C) 2016 Elsevier B.V. All rights reserved.
[1]Shanghai Univ Tradit Chinese Med, Sch Pharm, Shanghai 201203, Peoples R China.
[2]Shanghai Inst Food & Drug Control, Dept Chem, Shanghai 201203, Peoples R China.
[3]China Pharmaceut Univ, Coll Pharm, Nanjing 210009, Peoples R China.
[4]Shanghai Univ Tradit Chinese Med, Expt Ctr Teaching & Learning, Shanghai 201203, Peoples R China.
(8.0+极速模式)