Comparative pharmacokinetics of swertiamarin in rats after oral administration of swertiamarin alone,Qing Ye Dan tablets and co-administration of swertiamarin and oleanolic acid |
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Authors: | Gui-li Xu Hong-liang Li Jian-chang He En-fu Feng Pan-pan Shi Yue-qiong Liu Chang-xiao Liu |
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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 |
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Abstract: | Ethnopharmacological relevanceQing 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 methodsAn 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.ResultsThe 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.ConclusionsThe data indicate that oleanolic acid and the other ingredients present in QYDT could affect the pharmacokinetic behaviour of swertiamarin in rats. |
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Keywords: | Swertiamarin Qing Ye Dan tablet Oleanolic acid Pharmacokinetics Interactions |
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