Author/Authors :
Chu، نويسنده , , Yang and Zhang، نويسنده , , Hong-chao and Li، نويسنده , , Shuming and Wang، نويسنده , , Jun-mei and Wang، نويسنده , , Xiang-yang and Li، نويسنده , , Wei and Zhang، نويسنده , , Lan-lan and Ma، نويسنده , , Xiao-hui and Zhou، نويسنده , , Shui-ping and Zhu، نويسنده , , Yonghong and Liu، نويسنده , , Chang-xiao، نويسنده ,
Abstract :
Ginsenoside Rc (GRc) is a potential pharmacologically active ingredient isolated from ginseng (Panax ginseng C.A. Meyer, Araliaceae). A simple, rapid and sensitive method for determination of GRc in rat plasma was developed based on liquid chromatography–tandem mass spectrometry (LC–MS/MS). The analyte and internal standard (IS), ginsenoside Rb1 (GRb1), were extracted from plasma with n-butanol and chromatographied on a C18 column eluted with a mobile phase of methanol and water containing 0.1% formic acid. The detection was performed by positive ion electrospray ionization in selective reaction monitoring mode (SRM), monitoring the transitions m/z 1101.6 → 789.3 and m/z 1131.7 → 364.7 for GRc and IS, respectively. The assay was linear over the concentration range of 5–5000 ng/mL with a limit of quantitation (LOQ) of 5 ng/mL. The accuracy was between 86.7% and 114.9%, and the precision was less than 9.7%. This method was successfully applied to investigate the pharmacokinetic study of GRc in rats after intravenous (2 mg/kg) and oral (20 mg/kg) administration, and the result showed that the ginsenoside was poorly absorbed with an absolute bioavailability being approximately 0.17%.
Keywords :
Ginsenoside Rc , Pharmacokinetics , Bioavailability , LC–MS/MS