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DOI: 10.1055/s-0029-1185577
© Georg Thieme Verlag KG Stuttgart · New York
Metabolome Analysis of Ephedra Plants with Different Contents of Ephedrine Alkaloids by Using UPLC‐Q‐TOF‐MS
Publication History
received October 15, 2008
revised February 24, 2009
accepted March 9, 2009
Publication Date:
20 April 2009 (online)
Abstract
Metabolome analysis of four varieties of Ephedra plants, which contain different amounts of ephedrine alkaloids, was demonstrated in this study. The metabolites were comprehensively analyzed by using ultra performance liquid chromatography (UPLC) coupled with quadrupole time-of-flight mass spectrometry (Q‐TOF‐MS) and the ephedrine alkaloids were also profiled. Subsequently, multivariate analyses of principal component analysis (PCA) and batch-learning self-organizing mapping (BL‐SOM) analysis were applied to the raw data of the total ion chromatogram (TIC). PCA was performed to visualize the fingerprints characteristic for each Ephedra variant and the independent metabolome clusters were formed. The metabolite fingerprints were also visualized by BL‐SOM analysis and were displayed as a lattice of colored individual cells which was characteristic for each Ephedra variant. BL‐SOM analysis was also used for identification of chemical marker peaks because the information assigned to a cell represented either increases or decreases in peak intensities. Using this analysis, ephedrine alkaloids were successfully selected from the TICs as chemical markers for each Ephedra variant and this result suggested that BL‐SOM analysis was an effective method for the selection of marker metabolites. We report our study here as a practical case of metabolomic study on medicinal resources.
Key words
Ephedra - Ephedraceae - metabolomics - UPLC‐Q‐TOF‐MS - multivariate analysis - ephedrine alkaloids
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Dr. Taketo Okada
Faculty of Pharmaceutical Sciences at Kagawa Campus,
Tokushima Bunri University
Shido 1314–1
Sanuki-city
Kagawa 769-2193
Japan
Phone: + 81 87 894 5111
Fax: + 81 87 894 0181
Email: okadat@kph.bunri-u.ac.jp
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