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采用固相萃取(SPE)和高效液相色谱-串联质谱法(HPLC-MS/MS)对咖啡中的异黄酮进行定量分析。

Quantification of isoflavones in coffee by using solid phase extraction (SPE) and high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).

作者信息

Caprioli Giovanni, Navarini Luciano, Cortese Manuela, Ricciutelli Massimo, Torregiani Elisabetta, Vittori Sauro, Sagratini Gianni

机构信息

School of Pharmacy, University of Camerino, Via Sant'Agostino 1, 62032, Camerino, Italy.

Illycaffè SpA, R & D, via Flavia 110, Trieste, I-34147, Italy.

出版信息

J Mass Spectrom. 2016 Sep;51(9):698-703. doi: 10.1002/jms.3802.

Abstract

A new method for extracting isoflavones from espresso coffee (EC) was coupled with high-performance liquid chromatography-tandem mass spectrometry (MS/MS) for the first time to analyse five isoflavones, which included both a glycosilated form, genistin and the aglycons daidzein, genistein, formononetin and biochanin A. Isoflavones were extracted from coffee samples using methanol, stored in a freezer overnight to precipitate proteic or lipidic residues and purified on SPE C18 cartridges before high-performance liquid chromatography-MS/MS analysis. The recovery percentages obtained by spiking the matrix at concentrations of 10 and 100 µg l(-1) with a standard mixture of isoflavones were in the range of 70 to 104%. The limits of detection and limits of quantification were in the range of 0.015-0.3 µg l(-1) and 0.05-1 µg l(-1) , respectively. Once validated, the method was used to analyze the concentrations of isoflavones in six ECs and ten ground coffee samples. Only formononetin and biochanin A were found, and their respective concentrations ranged from 0.36 to 0.41 µg l(-1) and from 0.58 to 3.26 µg l(-1) in ECs and from 0.36 to 4.27 µg kg(-1) and from 0.71 to 3.95 µg kg(-1) in ground coffees. This method confirms the high specificity and selectivity of MS/MS systems for detecting bioactives in complex matrices such as coffee.Copyright © 2016 John Wiley & Sons, Ltd.

摘要

一种从浓缩咖啡(EC)中提取异黄酮的新方法首次与高效液相色谱 - 串联质谱法(MS/MS)联用,以分析五种异黄酮,其中包括糖基化形式的染料木苷以及苷元大豆苷元、染料木素、芒柄花黄素和鹰嘴豆芽素A。使用甲醇从咖啡样品中提取异黄酮,将其在冰箱中储存过夜以沉淀蛋白质或脂质残留物,并在进行高效液相色谱 - MS/MS分析之前在SPE C18柱上进行纯化。通过向基质中添加浓度为10和100μg l⁻¹的异黄酮标准混合物获得的回收率在70%至104%之间。检测限和定量限分别在0.015 - 0.3μg l⁻¹和0.05 - 1μg l⁻¹范围内。该方法经验证后,用于分析六种浓缩咖啡和十种研磨咖啡样品中的异黄酮浓度。仅检测到芒柄花黄素和鹰嘴豆芽素A,它们在浓缩咖啡中的各自浓度范围为0.36至0.41μg l⁻¹和0.58至3.26μg l⁻¹,在研磨咖啡中的浓度范围为0.36至4.27μg kg⁻¹和0.71至3.95μg kg⁻¹。该方法证实了MS/MS系统在检测咖啡等复杂基质中的生物活性物质方面具有高特异性和选择性。版权所有© 2016 John Wiley & Sons, Ltd.

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