Pharmacokinetic profile of 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside in mice after oral administration of Polygonum multiflorum extract

被引:17
作者
Lv, Guiyuan [2 ]
Gu, Hui [2 ]
Chen, Suhong [1 ]
Lou, Zhaohuan [2 ]
Shan, Letian [2 ]
机构
[1] Wenzhou Med Coll, Acad Tradit Chinese Med, Wenzhou 325035, Peoples R China
[2] Zhejiang Chinese Med Univ, Hangzhou, Zhejiang, Peoples R China
关键词
Pharmacokinetics; stilbene glycoside; traditional Chinese medicine; RP-HPLC; compartmental model; LIGHT-SCATTERING DETECTION; LIQUID-CHROMATOGRAPHY; ANTIOXIDANT ACTIVITIES; IN-VITRO; THUNB; STILBENE; CONSTITUENTS; COMPONENTS; ROOTS; VIVO;
D O I
10.3109/03639045.2011.597763
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Context: Stilbene glycoside (2,3,5,4'-tetrahydroxystilbene-2-O-beta-D-glucoside) is a main bioactive component of Polygonum multiflorum, a traditional Chinese medicine (TCM) commonly used in clinic for anti-aging treatment. Its medicinal activities, such as anti-oxidation, anti-inflammation and endothelial protection, have been extensively studied, but its pharmacokinetic property is still unclear. Objective: A pharmacokinetic study was undertaken to quantitatively determine P. multiflorum stilbene glycoside (PM-SG) in mouse plasma after oral administration of 100 mg/kg P. multiflorum extract. Materials and methods: A sensitive reversed-phase high-performance liquid chromatography (RP-HPLC) coupled with liquid-liquid phase extraction method was employed for this study. Pharmacokinetic parameters of PM-SG were determined in mice applying both compartmental and non-compartmental analyses. Results and discussion: The calibration curve for PM-SG in the plasma was linear (r(2) > 0.99) over the range of 0.66 to 56.40 mu g/ml, and the concentration-time curve was plotted with the maximum concentration (C-max) and time to reach maximum concentration (T-max) of 29.62 mu g/ml and 60 min, respectively. The intra-and inter-day variations were less than 3% for relative standard deviation (RSD) and relative error (RE), with a good recovery of more than 97% (RSD <3%). All pharmacokinetic parameters estimated by compartmental and non-compartmental models reached a same conclusion that PM-SG was rapidly absorbed and widely distributed throughout the body with a great efficiency of utility, followed by quick elimination and clearance. Conclusions: This was the first report on determination of the pharmacokinetic profile of PM-SG in mice after oral administration. The result may provide a meaningful basis for evaluating the clinical applications of such a bioactive compound from herbal medicines.
引用
收藏
页码:248 / 255
页数:8
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