蛇舌草
药代动力学
色谱法
化学
五加科
皂甙
甲酸
分析物
口服
串联质谱法
药理学
质谱法
植物
医学
生物
人参
替代医学
病理
作者
Miao Yu,Jiaxin Liu,Li Lin,Haiyan Xu,Xing Yao,Yunli Zhao,Zhiguo Yu
标识
DOI:10.1002/jssc.201600523
摘要
In Hedera helix hederacoside C, hederacoside D, and ɑ ‐hederin are three major bioactive saponins and play pivotal roles in the overall biological activity. In this study, a specific and sensitive ultra‐high performance liquid chromatography with tandem mass spectrometry method has been developed and validated for the quantification of three major bioactive saponins in rat plasma. Chromatographic separation was performed on a reversed‐phase Thermo Hypersil GOLD C 18 column (2.1 mm × 50 mm, 1.9 μm) using a gradient mobile phase system of acetonitrile‐water containing 0.1% formic acid. The assay was successfully applied to study the pharmacokinetic behavior of the three analytes in rats after oral and intravenous administration of a mixture of saponins (hederacoside C, hederacoside D, and ɑ ‐hederin). Further research was performed to compare the pharmacokinetic behavior of the three analytes after the oral administration of a mixture of saponins and an extract of saponins from Hedera helix , and results showed that double peaks were evident on concentration–time profile for each of the three saponins. The difference in the pharmacokinetic characteristics of three saponins between a mixture of saponins and an extract of saponins from Hedera helix was found in rat, which would be beneficial for the preclinical research and clinical use of Hedera helix .
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