UPLC/MS/MS法同时测定人血浆中人参皂苷Re和Rg1含量及对参附冻干粉针剂的药代动力学评价
2009
Objective To develop a rapid and sensitive method for the pharmacokinetic study of ginsenoside Re and Rg1 in SHEN-FU injective powder in human plasma by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC/ESI/MS/MS). Methods A Waters C18 column (1.7 μm, 2.1×100 mm) was used in this study. The detection of Re and Rg1 was performed on a triple-quadruple mass spectrometer with multiple-reaction monitoring (MRM) mode using the following transitions:m/z 969.6→789.3 for Re; m/z 823.5→643.2 for Rg1 and m/z 803.5→387.1 for digoxin. A total of 324 plasma samples from 18 healthy volunteers were tested. Results A total run could be accomplished in 4 minutes. Only 50 μL plasma sample was needed to detect Re and Rg1.The lowest detectable concentration for both Re and Rg1 was 0.025 ng/mL. Good linearity appeared from 0.1 to 200 ng/mL (r^2>0.999). The decline of Re and Rg1 in plasma could be described by a triple-compartment model. Conclusion The proposed method provides a rapid and sensitive method for the quantification of Re and Rg1 in human plasma, which has been successfully applied to the pharmacokinetic study on intravenous infusion of SHEN-FU powder.
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