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高效液相色谱-二极管阵列检测器联用电喷雾电离/质谱法同时测定当归根中的香豆素类成分。

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

作者信息

Ahn Mi-Jeong, Lee Mi Kyeong, Kim Young Choong, Sung Sang Hyun

机构信息

Department of Crops Biotechnology, College of Life Sciences and Natural Resources, Jinju National University, Jinju, Gyeongnam 660-758, Republic of Korea.

出版信息

J Pharm Biomed Anal. 2008 Jan 22;46(2):258-66. doi: 10.1016/j.jpba.2007.09.020. Epub 2007 Sep 26.

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 microm, 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 microg/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-MS(n)). 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.

摘要

已开发出一种基于高效液相色谱 - 二极管阵列检测器与电喷雾电离/质谱联用(HPLC - DAD/MS)的方法,用于同时测定韩国草药当归(伞形科植物当归的干燥根)中的九种香豆素化合物,即紫花前胡苷(1)、紫花前胡酮(2)、异补骨脂素(3)、紫花前胡醇(4)、7 - 羟基 - 6 - (2R - 羟基 - 3 - 甲基丁 - 3 - 烯基)香豆素(5)、去甲基紫花前胡素(6)、紫花前胡素(7)、紫花前胡醇当归酸酯(8)和异欧前胡素(9)。甲醇提取物通过HPLC进行分析,使用反相C18柱(5微米,4.5毫米×250毫米),采用梯度乙腈 - 水溶剂系统,流速为1.0毫升/分钟。使用DAD对六种香豆素(1、3、4和6 - 8)在330纳米处进行分析,所有化合物在0.2 - 250微克/毫升范围内显示出良好的线性(r² = 0.998 - 0.999)。平均回收率(n = 3)在96.5%至110.8%之间。还通过电喷雾电离多级串联质谱(ESI - MSⁿ)对每个峰进行了鉴定讨论。对当归样品中这些香豆素化合物的含量进行了评估。同时,三种香豆素(2、5和9)无法通过DAD进行定量,因为这些峰与其他峰重叠。这些化合物的测定可以通过HPLC - ESI/MS在选择离子监测/选择反应监测模式下成功完成。

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