Efficient identification of flavones, flavanones and their glycosides in routine analysis via off-line combination of sensitive NMR and HPLC experiments

被引:54
作者
Blunder, Martina [1 ,3 ]
Orthaber, Andreas [2 ,4 ]
Bauer, Rudolf [1 ]
Bucar, Franz [1 ]
Kunert, Olaf [2 ]
机构
[1] Graz Univ, Dept Pharmacognosy, Inst Pharmaceut Sci, Univ Pl 4, A-8010 Graz, Austria
[2] Graz Univ, Dept Pharmaceut Chem, Inst Pharmaceut Sci, Univ Pl 1, A-8010 Graz, Austria
[3] Uppsala Univ, Biomed Ctr, Dept Neurosci, Box 593, S-75124 Uppsala, Sweden
[4] Uppsala Univ, Dept Chem, Angstrom Labs, Box 523, S-75120 Uppsala, Sweden
基金
奥地利科学基金会;
关键词
NMR; Flavones; Flavanones; HPLC; MS; Data base; NUCLEAR-MAGNETIC-RESONANCE; NATURAL-PRODUCTS RESEARCH; C-13; NMR; MASS-SPECTROMETRY; SPE-NMR; PHENOLIC-COMPOUNDS; LIQUID-CHROMATOGRAPHY; HEART-DISEASE; ESI-MS/MS; SPECTROSCOPY;
D O I
10.1016/j.foodchem.2016.09.077
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We present a standardized, straightforward and efficient approach applicable in routine analysis of flavonoids combining sensitive NMR and HPLC experiments. The determination of the relative configuration of sugar moieties usually requires the acquisition of C-13 NMR shift values. We use a combination of HPLC and sensitive NMR experiments (1D-proton, 2D-HSQC) for the unique identification of known flavones, flavanones, flavonols and their glycosides. Owing to their broad range of polarity, we developed HPLC and UHPLC methods (H2O/MeOH/MeCN/HCOOH) which we applied and validated by analyzing 46 common flavones and flavanones and exemplified for four plant extracts. A searchable data base is provided with full data comprising complete proton and carbon resonance assignments, expansions of HSQC-spectra, HPLC parameters (retention time, relative retention factor), UV/Vis and mass spectral data of all compounds, which enables a rapid identification and routine analysis of flavones and flavanones from plant extracts and other products in nutrition and food chemistry. (C) 2016 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:600 / 609
页数:10
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