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The simultaneous determination of coumarins in Angelica gigas root by high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry

Authors
Ahn, M.-J.Lee, M.K.Kim, Y.C.Sung, S.H.
Issue Date
2008
Keywords
Angelica gigas; Coumarins; Electrospray ionization multi-stage tandem mass spectroscopy; High performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry; Simultaneous determination
Citation
Journal of Pharmaceutical and Biomedical Analysis, v.46, no.2, pp 258 - 266
Pages
9
Indexed
SCOPUS
Journal Title
Journal of Pharmaceutical and Biomedical Analysis
Volume
46
Number
2
Start Page
258
End Page
266
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/28115
DOI
10.1016/j.jpba.2007.09.020
ISSN
0731-7085
1873-264X
Abstract
An high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry (HPLC-DAD/MS) based method has been developed for the simultaneous determination of nine coumarin compounds, nodakenin (1), peucedanone (2), marmesin (3), decursinol (4), 7-hydroxy-6-(2R-hydroxy-3-methylbut-3-enyl)coumarin (5), demethylsuberosin (6), decursin (7), decursinol angelate (8) and isoimperatorin (9) in the Korean medicinal herb, Cham-Dang-Gui, the dried root of Angelica gigas (Umbelliferae). The methanol extracts were analyzed by HPLC using a reversed-phase C18 column (5 μm, 4.5 mm × 250 mm) using a gradient acetonitrile-water solvent system at a flow rate of 1.0 ml/min. The analysis of six coumarins (1, 3, 4 and 6-8) with DAD was done at 330 nm and showed excellent linearity (r2 = 0.998-0.999) in a range of 0.2-250 μg/ml for all the compounds. The average recoveries (n = 3) were between 96.5% and 110.8%. Identification of each peak was also discussed with the electrospray ionization multi-stage tandem mass spectroscopy (ESI-MSn). The amount of these coumarin compounds was evaluated in A. gigas samples. Meanwhile, three coumarins (2, 5 and 9) could not been quantified by DAD because these peaks were overlapped with others. Determination of these compounds could be successfully accomplished with the HPLC-ESI/MS in selected ion monitoring/selected reaction monitoring mode. ? 2007 Elsevier B.V. All rights reserved.
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