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Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine

Resveratrol (3,5,4′-trihydroxystilbene) is a natural compound that can be found in high concentrations in red wine and in many typical foods found in human diet. Over the past decades, resveratrol has been widely investigated for its potential beneficial effects on human health. At the same time, nu...

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Autores principales: Di Fabio, Elisa, Incocciati, Alessio, Palombarini, Federica, Boffi, Alberto, Bonamore, Alessandra, Macone, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587181/
https://www.ncbi.nlm.nih.gov/pubmed/33050326
http://dx.doi.org/10.3390/molecules25204603
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author Di Fabio, Elisa
Incocciati, Alessio
Palombarini, Federica
Boffi, Alberto
Bonamore, Alessandra
Macone, Alberto
author_facet Di Fabio, Elisa
Incocciati, Alessio
Palombarini, Federica
Boffi, Alberto
Bonamore, Alessandra
Macone, Alberto
author_sort Di Fabio, Elisa
collection PubMed
description Resveratrol (3,5,4′-trihydroxystilbene) is a natural compound that can be found in high concentrations in red wine and in many typical foods found in human diet. Over the past decades, resveratrol has been widely investigated for its potential beneficial effects on human health. At the same time, numerous analytical methods have been developed for the quantitative determination of resveratrol isomers in oenological and food matrices. In the present work, we developed a very fast and sensitive GC–MS method for the determination of resveratrol in red wine based on ethylchloroformate derivatization. Since this reaction occurs directly in the water phase during the extraction process itself, it has the advantage of significantly reducing the overall processing time for the sample. This method presents low limits of quantification (LOQ) (25 ng/mL and 50 ng/mL for cis- and trans-resveratrol, respectively) and excellent accuracy and precision. Ethylchloroformate derivatization was successfully applied to the analysis of resveratrol isomers in a selection of 15 commercial Italian red wines, providing concentration values comparable to those reported in other studies. As this method can be easily extended to other classes of molecules present in red wine, it allows further development of new GC–MS methods for the molecular profiling of oenological matrices.
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spelling pubmed-75871812020-10-29 Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine Di Fabio, Elisa Incocciati, Alessio Palombarini, Federica Boffi, Alberto Bonamore, Alessandra Macone, Alberto Molecules Article Resveratrol (3,5,4′-trihydroxystilbene) is a natural compound that can be found in high concentrations in red wine and in many typical foods found in human diet. Over the past decades, resveratrol has been widely investigated for its potential beneficial effects on human health. At the same time, numerous analytical methods have been developed for the quantitative determination of resveratrol isomers in oenological and food matrices. In the present work, we developed a very fast and sensitive GC–MS method for the determination of resveratrol in red wine based on ethylchloroformate derivatization. Since this reaction occurs directly in the water phase during the extraction process itself, it has the advantage of significantly reducing the overall processing time for the sample. This method presents low limits of quantification (LOQ) (25 ng/mL and 50 ng/mL for cis- and trans-resveratrol, respectively) and excellent accuracy and precision. Ethylchloroformate derivatization was successfully applied to the analysis of resveratrol isomers in a selection of 15 commercial Italian red wines, providing concentration values comparable to those reported in other studies. As this method can be easily extended to other classes of molecules present in red wine, it allows further development of new GC–MS methods for the molecular profiling of oenological matrices. MDPI 2020-10-09 /pmc/articles/PMC7587181/ /pubmed/33050326 http://dx.doi.org/10.3390/molecules25204603 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Di Fabio, Elisa
Incocciati, Alessio
Palombarini, Federica
Boffi, Alberto
Bonamore, Alessandra
Macone, Alberto
Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title_full Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title_fullStr Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title_full_unstemmed Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title_short Ethylchloroformate Derivatization for GC–MS Analysis of Resveratrol Isomers in Red Wine
title_sort ethylchloroformate derivatization for gc–ms analysis of resveratrol isomers in red wine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587181/
https://www.ncbi.nlm.nih.gov/pubmed/33050326
http://dx.doi.org/10.3390/molecules25204603
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