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Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa

Procyanidin C1 is by far the main flavan-3-ol trimer in cocoa. Like other flavan-3-ols, however, it suffers a lot during heat treatments such as roasting. RP-HPLC-HRMS/MS(ESI(−))analysis applied to an aqueous model medium containing commercial procyanidin C1 proved that epimerization is the main rea...

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Autores principales: De Taeye, Cédric, Kankolongo Cibaka, Marie-Lucie, Collin, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368537/
https://www.ncbi.nlm.nih.gov/pubmed/28264525
http://dx.doi.org/10.3390/foods6030018
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author De Taeye, Cédric
Kankolongo Cibaka, Marie-Lucie
Collin, Sonia
author_facet De Taeye, Cédric
Kankolongo Cibaka, Marie-Lucie
Collin, Sonia
author_sort De Taeye, Cédric
collection PubMed
description Procyanidin C1 is by far the main flavan-3-ol trimer in cocoa. Like other flavan-3-ols, however, it suffers a lot during heat treatments such as roasting. RP-HPLC-HRMS/MS(ESI(−))analysis applied to an aqueous model medium containing commercial procyanidin C1 proved that epimerization is the main reaction involved in its degradation (accounting for 62% of degradation products). In addition to depolymerization, cocoa procyanidin C1 also proved sensitive to oxidation, yielding once- and twice-oxidized dimers. No chemical oligomer involving the native trimer was found in either model medium or cocoa, while two C1 isomers were retrieved. C1 degradation products exhibited antioxidant activity (monitored by RP-HPLC-Online TEAC) close to that of C1 (when expressed in µM TE/mg·kg(−1)).
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spelling pubmed-53685372017-04-05 Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa De Taeye, Cédric Kankolongo Cibaka, Marie-Lucie Collin, Sonia Foods Article Procyanidin C1 is by far the main flavan-3-ol trimer in cocoa. Like other flavan-3-ols, however, it suffers a lot during heat treatments such as roasting. RP-HPLC-HRMS/MS(ESI(−))analysis applied to an aqueous model medium containing commercial procyanidin C1 proved that epimerization is the main reaction involved in its degradation (accounting for 62% of degradation products). In addition to depolymerization, cocoa procyanidin C1 also proved sensitive to oxidation, yielding once- and twice-oxidized dimers. No chemical oligomer involving the native trimer was found in either model medium or cocoa, while two C1 isomers were retrieved. C1 degradation products exhibited antioxidant activity (monitored by RP-HPLC-Online TEAC) close to that of C1 (when expressed in µM TE/mg·kg(−1)). MDPI 2017-02-28 /pmc/articles/PMC5368537/ /pubmed/28264525 http://dx.doi.org/10.3390/foods6030018 Text en © 2017 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
De Taeye, Cédric
Kankolongo Cibaka, Marie-Lucie
Collin, Sonia
Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title_full Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title_fullStr Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title_full_unstemmed Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title_short Occurrence and Antioxidant Activity of C1 Degradation Products in Cocoa
title_sort occurrence and antioxidant activity of c1 degradation products in cocoa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368537/
https://www.ncbi.nlm.nih.gov/pubmed/28264525
http://dx.doi.org/10.3390/foods6030018
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