Stir bar sorptive extraction with gas chromatography-mass spectrometry for the determination of resveratrol, piceatannol and oxyresveratrol isomers in wines

被引:38
|
作者
Cacho, J. I. [1 ]
Campillo, N. [1 ]
Vinas, P. [1 ]
Hernandez-Cordoba, M. [1 ]
机构
[1] Univ Murcia, Fac Chem, Dept Analyt Chem, E-30100 Murcia, Spain
关键词
Stir bar sorptive extraction (SBSE); Gas chromatography-mass spectrometry (GC-MS); cis- and trans-resveratrol; cis- and trans-piceatannol; cis- and trans-oxyresveratrol; Wines; SOLID-PHASE MICROEXTRACTION; LIQUID-LIQUID MICROEXTRACTION; PHENOLIC-COMPOUNDS; TRANS-RESVERATROL; RAPID ANALYSIS; RED WINES; STILBENES; POLYPHENOLS; SAMPLES; AROMA;
D O I
10.1016/j.chroma.2013.09.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and highly sensitive procedure based on stir bar sorptive extraction coupled to gas chromatography-mass spectrometry by means of a thermal desorption unit (SBSE-TD-GC-MS) has been optimized for the determination of cis/trans isomers of resveratrol, piceatannol and oxyresveratrol in wine samples. Quantification of the cis-isomers was carried out by generating the standards from the corresponding trans-species once they had been preconcentrated on the SBSE extracting phase. The optimization of the acetylation derivatization, SBSE extraction and thermal desorption steps was investigated using Plackett-Burman designs, taking into account the high number of variables to be considered. The use of bisphenol F as internal standard allowed quantification of the samples against aqueous standards. Repeatability, expressed as relative standard deviation of 10 successive analyses was between 5% and 9%, confirming the high precision attained under the optimized conditions. Satisfactory recovery values of between 79% and 109% were obtained for spiked samples in the 0.2-1.0 mu g L-1 concentration range, depending on the compound. The main compound determined in the analyzed samples was trans-resveratrol, with concentrations in the range of 3-230 mu g L-1, depending on the type of wine. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 27
页数:7
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