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

被引:102
作者
Ahn, Mi-Jeong [3 ]
Lee, Mi Kyeong [2 ]
Kim, Young Choong [1 ]
Sung, Sang Hyun [1 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Elcom Sci Co Ltd, Inst Life Sci, Seoul 152768, South Korea
[3] Jinju Natl Univ, Coll Life Sci & Nat Resources, Dept Crops Biotechnol, Jinju 660758, Gyeongnam, South Korea
关键词
Angelica gigas; coumarins; high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry; simultaneous determination; electrospray ionization multi-stage tandem mass spectroscopy;
D O I
10.1016/j.jpba.2007.09.020
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 C 18 column (5 mu m, 4.5 mm x 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 (r(2) = 0.998-0.999) in a range of 0.2-250 mu g/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. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 266
页数:9
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