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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >High-speed separation and characterization of major constituents in Radix Paeoniae Rubra by fast high-performance liquid chromatography coupled with diode-array detection and time-of-flight mass spectrometry
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High-speed separation and characterization of major constituents in Radix Paeoniae Rubra by fast high-performance liquid chromatography coupled with diode-array detection and time-of-flight mass spectrometry

机译:快速高效液相色谱结合二极管阵列检测和飞行时间质谱技术对Pa药中的主要成分进行高速分离和表征

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摘要

A fast high-performance liquid chromatography (HPLC) method coupled with diode-array detection (DAD) and electrospray ionization time-of-flight mass spectrometry (ESI-TOFMS) has been developed for rapid separation and sensitive identification of major constituents in Radix Paeoniae Rubra (RPR). The total analysis time on a short column packed with 1.8-mu m porous particles was about 20 min without a loss in resolution, six times faster than the performance of a conventional column analysis (115 min). The MS fragmentation behavior and structural characterization of major compounds in RPR were investigated here for the first time. The targets were rapidly screened from RPR matrix using a narrow mass window of 0.01 Da to restructure extracted ion chromatograms. Accurate mass measurements (less than 5 ppm error) for both the deprotonated molecule and characteristic fragment ions represent reliable identification criteria for these compounds in complex matrices with similar if not even better performance compared with tandem mass spectrometry. A total of 26 components were screened and identified in RPR including 11 monoterpene glycosides, 11 galloyl glucoses and 4 other phenolic compounds. From the point of time savings, resolving power, accurate mass measurement capability and full spectral sensitivity, the established fast HPLC/DAD/TOFMS method turns out to be a highly useful technique to identify constituents in complex herbal medicines. Copyright (C) 2008 John Wiley & Sons, Ltd.
机译:快速高效液相色谱(HPLC)方法与二极管阵列检测(DAD)和电喷雾电离飞行时间质谱(ESI-TOFMS)结合使用,已开发出来,可快速分离和敏感地鉴定Pa药中的主要成分卢布拉(RPR)。在装有1.8微米多孔颗粒的短柱上,总分析时间约为20分钟,而没有分离度损失,比常规柱分析(115分钟)快六倍。本文首次研究了RPR中主要化合物的MS断裂行为和结构特征。使用0.01 Da的窄质量窗从RPR基质中快速筛选目标,以重组提取的离子色谱图。去质子化的分子和特征性碎片离子的准确质量测量值(小于5 ppm误差)代表了这些化合物在复杂基质中的可靠鉴定标准,其性能与串联质谱法相似甚至更好。在RPR中筛选和鉴定了总共26种成分,包括11种单萜糖苷,11种没食子酰基葡萄糖和4种其他酚类化合物。从节省时间,分辨能力,准确的质量测量能力和全光谱灵敏度的角度出发,已建立的快速HPLC / DAD / TOFMS方法被证明是鉴定复杂草药中成分的非常有用的技术。版权所有(C)2008 John Wiley&Sons,Ltd.

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