Literature DB >> 12580081

[Pharmacokinetic studies of 20(R)-ginsenoside RG3 in human volunteers].

H Pang1, H L Wang, L Fu, C Y Su.   

Abstract

AIM: To study the pharmacokinetics of 20 (R)-ginsenoside Rg3 (GRg3) in human.
METHODS: High-performance liquid chromatography-ultraviolet detection method was used in this study.
RESULTS: The pharmacokinetics of GRg3 in 14 healthy volunteers were investigated. After a single oral dose of 3.2 mg.kg-1 in 8 male volunteers, the plasma concentration-time course fitted well to a two-compartment open model, with the following pharmacokinetic parameters: Tmax(0.66 +/- 0.10) h, Cmax(16 +/- 6) ng.mL-1, T1/2 alpha(0.46 +/- 0.12) h, T1/2 beta(4.9 +/- 1.1) h, T1/2(Ka)(0.28 +/- 0.04) h, AUC0-infinity(77 +/- 26) ng.mL-1.h. No kinetic analysis was made after an oral dose of 0.8 mg.kg-1 GRg3 in 6 other volunteers because of the low concentration, but a good correlation between Cmax and dosage of the two groups was found.
CONCLUSION: The absorption of GRg3 was rapid in man, and its elimination was rapid after oral administration of ginsenoside Rg3. The pharmacokinetic results shows that it exhibited first order kinetic characteristics.

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Year:  2001        PMID: 12580081

Source DB:  PubMed          Journal:  Yao Xue Xue Bao        ISSN: 0513-4870


  10 in total

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