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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Liquid chromatography/electrospray ionization mass spectrometry for the characterization of twenty-three flavonoids in the extract of Dalbergia odorifera
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Liquid chromatography/electrospray ionization mass spectrometry for the characterization of twenty-three flavonoids in the extract of Dalbergia odorifera

机译:液相色谱/电喷雾电离质谱法表征黄檀提取物中的23种黄酮类化合物

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摘要

A method incorporating high-performance liquid chromatography (HPLC) with electrospray ionization and tandem mass spectrometry, with parallel analysis by HPLC with UV detection using a diode-array detector, was developed for the qualitative characterization of flavonoids in D. odorifera. Twenty-three flavonoids, including six isoflavones, six neoflavones, four isoflavanones, three flavanones, two chalcones, one isoflavanonol and one pterocarpan, were unambiguously identified by comparing their retention times, UV and NIS spectra with those of authentic compounds. Furthermore, the collision-induced dissociations of the [M-H](-) ions were studied to clarify the MS behavior of the different types of flavonoids. In negative ion ESI-MS all the flavonoids yielded prominent [M-H](-) ions in the first order mass spectra. Fragments involving losses of CH3, H2O, CO, C2H2O, and CO2 were observed in the MS/MS spectra. Each of the seven types of flavonoid showed characteristic MS/MS fragmentation patterns. The isoflavanones, flavanones and chalcones were observed to undergo retro-Diels-Alder fragmentations. The spectra of almost all the neoflavonoids unexpectedly exhibited only [M-H-CH3](-) radical anions as base peaks without any further fragmentation. Substitution positions also remarkably influenced the fragmentation behavior, which could assist in distinction among the flavonoid isomers. The fragmentation rules deduced here could aid in the characterization of other flavonoids of these types. Copyright © 2005 John Wiley & Sons, Ltd.
机译:开发了一种将高效液相色谱(HPLC)与电喷雾电离和串联质谱相结合的方法,并通过HPLC与使用二极管阵列检测器的UV检测进行并行分析,以定性表征香茅中的类黄酮。通过将它们的保留时间,UV和NIS光谱与真实化合物的保留时间,UV和NIS光谱进行比较,可以明确鉴定出23种黄酮类化合物,包括6种异黄酮,6种新黄酮,4种异黄酮,3种黄烷酮,2种查耳酮,1种异黄酮醇和1种罗丹烷。此外,研究了[M-H](-)离子的碰撞诱导解离,以阐明不同类型类黄酮的MS行为。在负离子ESI-MS中,所有黄酮在一级质谱中均产生显着的[M-H](-)离子。在MS / MS光谱中观察到了涉及CH3,H2O,CO,C2H2O和CO2损失的碎片。七种类黄酮均显示出特征性的MS / MS碎片图谱。观察到异黄酮,黄烷酮和查耳酮经历了Diels-Alder逆向裂解。几乎所有新黄酮类的光谱出乎意料地仅显示[M-H-CH3](-)自由基阴离子作为基峰,而没有任何进一步的断裂。取代位置也显着影响片段化行为,这可能有助于区分类黄酮异构体。此处推导的碎裂规则可能有助于表征这些类型的其他类黄酮。版权与复制; 2005年John Wiley&Sons,Ltd.

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