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Comparative pharmacokinetics of swertiamarin in rats after oral administration of swertiamarin alone,Qing Ye Dan tablets and co-administration of swertiamarin and oleanolic acid
Authors:Gui-li Xu  Hong-liang Li  Jian-chang He  En-fu Feng  Pan-pan Shi  Yue-qiong Liu  Chang-xiao Liu
Affiliation:1. School of Chemical Engineering and Technology of Tianjin University, 92 Wei-Jin Road, Tianjin 300072, PR China;2. Department of Pharmacy, Kunming General Hospital of Chengdu Military Region, 212 Da-Guan Road, Kunming 650032, PR China;3. School of Pharmaceutical Science, Sun Yat-sen University, Guangzhou 510006, PR China
Abstract:

Ethnopharmacological relevance

Qing Ye Dan is a well-known herbal drug that is widely used to treat viral hepatitis in the Yi and Hani minority regions in the Yunnan province of China.

Materials and methods

An LC–MS/MS method was developed to determine the levels of swertiamarin in rat plasma. Swertiamarin and naringin (internal standard, IS) were extracted from rat plasma using solid-phase extraction (SPE) to purify the samples. The pharmacokinetics of the following different administration methods of swertiamarin in rats were studied: oral administration of swertiamarin alone, a Qing Ye Dan tablet (QYDT) and co-administration of swertiamarin and oleanolic acid, with each method delivering approximately 20 mg/kg of swertiamarin. Non-compartmental pharmacokinetic profiles were constructed by using the software DAS (version 2.1.1), and the pharmacokinetic parameters were compared using an unpaired Student's t-test.

Results

The results showed that the pharmacokinetic parameters Cmax, AUC0–∞, Vz/F and CLz/F were significantly different (P<0.05) among the three types of swertiamarin administration.

Conclusions

The data indicate that oleanolic acid and the other ingredients present in QYDT could affect the pharmacokinetic behaviour of swertiamarin in rats.
Keywords:Swertiamarin   Qing Ye Dan tablet   Oleanolic acid   Pharmacokinetics   Interactions
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