首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >The simultaneous determination of coumarins in Angelica gigas root by high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry.
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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.

机译:高效液相色谱-二极管阵列检测器与电喷雾电离/质谱联用同时测定当归中的香豆素。

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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 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.
机译:已开发出一种基于高效液相色谱-二极管阵列检测器的电喷雾电离/质谱(HPLC-DAD / MS)方法,用于同时测定9种香豆素化合物,诺达肯宁(1),波丹酮(2),果胶(3) ),地松酚(4),7-羟基-6-(2R-羟基-3-甲基丁-3-烯基)香豆素(5),去甲基枯死皮脂(6),去cursin(7),去甲酚薄荷酸酯(8)和​​异欧前胡素(9) )在韩国药材Cham-Dang-Gui中,当归的干燥根。使用反相C18柱(5微米,4.5毫米x 250毫米),使用乙腈-水梯度溶剂系统,以1.0毫升/分钟的流速通过HPLC分析甲醇提取物。用DAD对六种香豆素(1、3、4和6-8)的分析是在330 nm处进行的,并且所有样品在0.2-250 microg / ml的范围内均显示出极好的线性(r(2)= 0.998-0.999)。化合物。平均回收率(n = 3)在96.5%和110.8%之间。还使用电喷雾电离多级串联质谱(ESI-MS(n))讨论了每个峰的鉴定。这些香豆素化合物的量在A. gigas样品中评估。同时,DAD无法定量3个香豆素(2、5和9),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在选定的离子监测/选定的反应监测模式下成功完成。

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