Selected article for: "chinese medicine and high performance"

Author: Li, Tao; Wang, Yiwei; Wang, Yanli; Liang, Rixin; Zhang, Dong; Zhang, Huihui; Chen, Li; Yang, Weipeng
Title: Development of an SPE–HPLC–MS method for simultaneous determination and pharmacokinetic study of bioactive constituents of Yu Ping Feng San in rat plasma after oral administration
  • Cord-id: hli34i91
  • Document date: 2013_2_13
  • ID: hli34i91
    Snippet: ETHNOPHARMACOLOGICAL RELEVANCE: Yu Ping Feng San (YPFS, in Chinese: Jade Windscreen Powder), a well-known traditional Chinese medicine, is commonly used to cure the diseases of respiratory systems and immune systems. AIM OF THE STUDY: A selective and sensitive high-performance liquid chromatography coupled with mass spectrometry method (HPLC–MS) was developed and validated for simultaneous quantification of cycloastragenol, formononetin, calycosin, 4′-O-β-glucopyranosyl-5-O-methylvisamminol
    Document: ETHNOPHARMACOLOGICAL RELEVANCE: Yu Ping Feng San (YPFS, in Chinese: Jade Windscreen Powder), a well-known traditional Chinese medicine, is commonly used to cure the diseases of respiratory systems and immune systems. AIM OF THE STUDY: A selective and sensitive high-performance liquid chromatography coupled with mass spectrometry method (HPLC–MS) was developed and validated for simultaneous quantification of cycloastragenol, formononetin, calycosin, 4′-O-β-glucopyranosyl-5-O-methylvisamminol (GMV) and cimifugin in rat plasma after oral administration of Yu Ping Feng San decoction. MATERIALS AND METHODS: Plasma samples were extracted via solid-phase extraction (SPE), separated on a Zorbax SB-C18 column, detected by single quadruple mass spectrometry with an electrospray ionization interface, and quantified using selected ion monitoring mode. The current SPE–HPLC–MS assay was validated for linearity, intra-day and inter-day precisions, accuracy, extraction recovery and stability. The method was applied to a comparative pharmacokinetic study after administration of Yu Ping Feng San to rats at different doses (10, 20 and 40 g/kg). RESULTS: The calibration curves were linear over the ranges 0.50–50 ng/mL and 17.36–1736 ng/mL. Intra- and inter-day precisions (relative standard deviations) were from 0.45% to 10.95%, and accuracy (relative recovery) from 95% to 115%. The extraction recoveries were greater than 88.42% for all analytes. Dose-dependence was shown for some constituents in the drug concentration–time profiles. Among all the active ingredients detected, cimifugin had the highest blood concentration (881–1510 ng/mL), and cycloastragenol had the longest retention time in the rat body (15.06–20.44 h). CONCLUSION: This analytical method is a selective, sensitive, precise, accurate, and reliable assay for simultaneous determination of cycloastragenol, calycosin, formononetin, GMV, and cimifugin in rat plasma.

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