Back to Search Start Over

Determination of stilbene derivatives in Burgundy red wines by ultra-high-pressure liquid chromatography.

Authors :
Boutegrabet, Lemia
Fekete, Agnes
Hertkorn, Norbert
Papastamoulis, Yorgos
Waffo-Téguo, Pierre
Mérillon, Jean
Jeandet, Philippe
Gougeon, Régis
Schmitt-Kopplin, Philippe
Source :
Analytical & Bioanalytical Chemistry; Dec2011, Vol. 401 Issue 5, p1517-1525, 9p
Publication Year :
2011

Abstract

The polyphenols, for example stilbenes and flavonoids, are an important family of compounds present in grapes and wines. Several studies have shown that stilbenes are antioxidants and cancer-preventing agents. For the first time, eight natural stilbenes (trans-resveratrol, trans-piceid, cis-piceid, trans-astringin, trans-piceatannol, (+)- trans-ε-viniferin, pallidol, and hopeaphenol), isolated and purified from Vitis vinifera, were simultaneously analysed by ultra-high-pressure liquid chromatography coupled with photodiode-array detection. Separation of the stilbenes by UHPLC was optimized with the assistance of 'Quality-by-Design' commercial software. Four different reversed-phase columns packed with 1.5-1.7-μm particles were tested and compared for their retention behaviour and separation efficiency. On the basis of the performance characteristics determined, the VisionHT C18 HL column was selected for the stilbenes studied, because resolution of the critical pair was 1.5 with a peak width of 2-4 s. The optimized method resulted in highly repeatable retention times (RSD 0.03-0.07%), peak areas (RSD 3-6%), and linear ranges were between 0.005 and 50 mg L for most of the compounds. All stilbenes, except trans-astringin, trans-piceatannol, and pallidol were identified and quantified in Burgundy red wines at different concentrations after direct injection of the wines. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16182642
Volume :
401
Issue :
5
Database :
Complementary Index
Journal :
Analytical & Bioanalytical Chemistry
Publication Type :
Academic Journal
Accession number :
64384863
Full Text :
https://doi.org/10.1007/s00216-011-4879-5