Polyphenolic and Methylxanthine Bioaccessibility of Cocoa Bean Shell Functional Biscuits: Metabolomics Approach and Intestinal Permeability through Caco-2 Cell Models

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Analítica, Nutrición e Bromatoloxíagl
dc.contributor.authorRojo Poveda, Olga
dc.contributor.authorBarbosa Pereira, Letricia
dc.contributor.authorEl Khattabi, Charaf
dc.contributor.authorYoul, Estelle N.H.
dc.contributor.authorBertolino, Marta
dc.contributor.authorDelporte, Cédric
dc.contributor.authorPochet, Stéphanie
dc.contributor.authorStévigny, Caroline
dc.date.accessioned2020-12-16T12:42:11Z
dc.date.available2020-12-16T12:42:11Z
dc.date.issued2020
dc.description.abstractCocoa bean shell (CBS), a by-product with considerable concentrations of bioactive compounds and proven biofunctional potential, has been demonstrated to be a suitable ingredient for high-fiber functional biscuits adapted to diabetic consumers. In this work, the in vitro bioaccessibility and intestinal absorption of polyphenols and methylxanthines contained in these biscuits were evaluated, and the effect of the food matrix was studied. Biscuits containing CBS and the CBS alone underwent in vitro digestion followed by an intestinal permeability study. The results confirmed that compounds were less bioavailable in the presence of a food matrix, although the digestion contributed to their release from this matrix, increasing the concentrations available at the intestinal level and making them capable of promoting antioxidant and antidiabetic activities. After digestion, CBS biscuits were shown to possess α-glucosidase inhibition capacity comparable to that of acarbose. Moreover, the presence of the food matrix improved the stability of polyphenols throughout the digestion process. Intestinal absorption of flavan-3-ols seemed to be limited to a maximum threshold and was therefore independent of the sample, while procyanidin was not absorbed. Methylxanthine absorption was high and was boosted by the presence of the food matrix. The results confirmed the biofunctional potential of CBS-based biscuitsgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThe present work was supported by COVALFOOD “Valorisation of high added-value compounds from cocoa industry by-products as food ingredients and additives”. This project received funding from the European Union’s Seventh Framework Programme for research and innovation under the Marie Skłodowska-Curie grant agreement no. 609402—2020 researchers: Train to Move (T2M)gl
dc.identifier.citationRojo-Poveda, O.; Barbosa-Pereira, L.; El Khattabi, C.; Youl, E.N.; Bertolino, M.; Delporte, C.; Pochet, S.; Stévigny, C. Polyphenolic and Methylxanthine Bioaccessibility of Cocoa Bean Shell Functional Biscuits: Metabolomics Approach and Intestinal Permeability through Caco-2 Cell Models. Antioxidants 2020, 9, 1164gl
dc.identifier.doi10.3390/antiox9111164
dc.identifier.essn2076-3921
dc.identifier.urihttp://hdl.handle.net/10347/24023
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/609402
dc.relation.publisherversionhttps://doi.org/10.3390/antiox9111164gl
dc.rights© 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/)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCocoa bean shellgl
dc.subjectBiscuitsgl
dc.subjectFunctional foodsgl
dc.subjectPolyphenolsgl
dc.subjectMethylxanthinesgl
dc.subjectIn vitro digestiongl
dc.subjectα-glucosidase inhibitiongl
dc.subjectBioaccessibilitygl
dc.subjectMetabolomicsgl
dc.subjectCaco-2 absorptiongl
dc.titlePolyphenolic and Methylxanthine Bioaccessibility of Cocoa Bean Shell Functional Biscuits: Metabolomics Approach and Intestinal Permeability through Caco-2 Cell Modelsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication8ec5c206-7aba-4869-8abc-feea997a22f7
relation.isAuthorOfPublication.latestForDiscovery8ec5c206-7aba-4869-8abc-feea997a22f7

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