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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7587181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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