HPLC-DAD-ESIMS analysis of phenolic compounds in bayberries ( Myrica rubra Sieb. et Zucc.)
Qualitative analysis of the ethyl acetate extracts from three bayberry cultivars, Xiangshan, Biqi and Dongkui, was performed by means of a hyphenated technique of HPLC coupled to photodiode array detection and electrospray ionization mass spectrometry (HPLC-DAD-ESIMS). Three phenolic compounds were...
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Published in | Food chemistry Vol. 100; no. 2; pp. 845 - 852 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
2007
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Subjects | |
Online Access | Get full text |
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Summary: | Qualitative analysis of the ethyl acetate extracts from three bayberry cultivars,
Xiangshan,
Biqi and
Dongkui, was performed by means of a hyphenated technique of HPLC coupled to photodiode array detection and electrospray ionization mass spectrometry (HPLC-DAD-ESIMS). Three phenolic compounds were identified (gallic acid, protocatechuic acid, and quercetin 3-glucoside) and seven others (two myricetin hexoside and two myricetin deoxyhexoside derivatives; quercetin hexoside and quercetin deoxyhexoside derivatives; kaempferol hexoside derivative) partially identified. Quantification of phenolic compounds was performed by HPLC-DAD, which revealed that gallic acid (2.6–7.0
mg/kg FW) was the major phenolic acid in all analysed cultivars. Myricetin glycosides (71.1
mg/kg FW) were the major flavonol glycosides in cultivar
Xiangshan and quercetin glycosides (117.8
mg/kg FW) were the major ones in cultivar
Biqi. Cultivar
Dongkui had medium contents of quercetin glycosides (48.0
mg/kg FW) and myricetin glycosides (53.2
mg/kg FW). Kaempferol glyosides (3.1–4.6
mg/kg FW) were the lowest contents of flavonol glycosides in the assayed bayberries. These results are relevant not only from a nutritional point of view, but also in the control of color stability and haze formation during bayberry juice processing and storage. |
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Bibliography: | http://dx.doi.org/10.1016/j.foodchem.2005.09.024 |
ISSN: | 0308-8146 1873-7072 |
DOI: | 10.1016/j.foodchem.2005.09.024 |