Oxidative stability of DHA phenolic ester
International audience Docosahexaenoic acid vanillyl ester (DHA-VE) was synthesized from docosahexaenoic acid ethyl ester (DHA-EE) and vanillyl alcohol by a solvent-free alcoholysis process catalysed by Candida antarctica lipase B. Oxidative stability of pure DHA-VE and the crude reaction medium con...
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Online Access: | https://hal.univ-lorraine.fr/hal-01267385 https://doi.org/10.1016/j.foodchem.2014.07.124 |
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ftunivnantes:oai:HAL:hal-01267385v1 2023-05-15T14:02:59+02:00 Oxidative stability of DHA phenolic ester Roby, Mohamed H. H. de Castro, Vanessa C. Targino, Brenda N. Alves da Silva, Paulo H. Mangavel, Cecile Chrétien, Francoise Humeau, Catherine Desobry, Stéphane Laboratoire d'Ingénierie des Biomolécules (LIBio) Université de Lorraine (UL) Fayoum University Universidade Federal de Viçosa = Federal University of Viçosa (UFV) Structure et Réactivité des Systèmes Moléculaires Complexes (SRSMC) Institut de Chimie du CNRS (INC)-Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS) 2015-02 https://hal.univ-lorraine.fr/hal-01267385 https://doi.org/10.1016/j.foodchem.2014.07.124 en eng HAL CCSD Elsevier info:eu-repo/semantics/altIdentifier/doi/10.1016/j.foodchem.2014.07.124 hal-01267385 https://hal.univ-lorraine.fr/hal-01267385 doi:10.1016/j.foodchem.2014.07.124 ISSN: 0308-8146 EISSN: 1873-7072 Food Chemistry https://hal.univ-lorraine.fr/hal-01267385 Food Chemistry, Elsevier, 2015, 169, pp.41-48. ⟨10.1016/j.foodchem.2014.07.124⟩ [CHIM]Chemical Sciences info:eu-repo/semantics/article Journal articles 2015 ftunivnantes https://doi.org/10.1016/j.foodchem.2014.07.124 2022-09-28T00:18:30Z International audience Docosahexaenoic acid vanillyl ester (DHA-VE) was synthesized from docosahexaenoic acid ethyl ester (DHA-EE) and vanillyl alcohol by a solvent-free alcoholysis process catalysed by Candida antarctica lipase B. Oxidative stability of pure DHA-VE and the crude reaction medium consisting of 45% DHA-VE and 55% DHA-EE were compared with that of DHA-EE under various storage conditions. Oxidation progress was followed by determination of conjugated dienes and FTIR measurements. Analyses showed that DHA-EE was rapidly oxidised under all storage conditions in comparison with DHA-VE and crude reaction medium, whatever the temperature and the storage time. The grafting of vanillyl alcohol appeared as a powerful way to stabilize DHA against oxidation. Thanks to their stability, both DHA-VE and the crude reaction medium, allowing the production of the ester, offer huge potential as functional ingredients. Article in Journal/Newspaper Antarc* Antarctica Université de Nantes: HAL-UNIV-NANTES Food Chemistry 169 41 48 |
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Université de Nantes: HAL-UNIV-NANTES |
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language |
English |
topic |
[CHIM]Chemical Sciences |
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[CHIM]Chemical Sciences Roby, Mohamed H. H. de Castro, Vanessa C. Targino, Brenda N. Alves da Silva, Paulo H. Mangavel, Cecile Chrétien, Francoise Humeau, Catherine Desobry, Stéphane Oxidative stability of DHA phenolic ester |
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[CHIM]Chemical Sciences |
description |
International audience Docosahexaenoic acid vanillyl ester (DHA-VE) was synthesized from docosahexaenoic acid ethyl ester (DHA-EE) and vanillyl alcohol by a solvent-free alcoholysis process catalysed by Candida antarctica lipase B. Oxidative stability of pure DHA-VE and the crude reaction medium consisting of 45% DHA-VE and 55% DHA-EE were compared with that of DHA-EE under various storage conditions. Oxidation progress was followed by determination of conjugated dienes and FTIR measurements. Analyses showed that DHA-EE was rapidly oxidised under all storage conditions in comparison with DHA-VE and crude reaction medium, whatever the temperature and the storage time. The grafting of vanillyl alcohol appeared as a powerful way to stabilize DHA against oxidation. Thanks to their stability, both DHA-VE and the crude reaction medium, allowing the production of the ester, offer huge potential as functional ingredients. |
author2 |
Laboratoire d'Ingénierie des Biomolécules (LIBio) Université de Lorraine (UL) Fayoum University Universidade Federal de Viçosa = Federal University of Viçosa (UFV) Structure et Réactivité des Systèmes Moléculaires Complexes (SRSMC) Institut de Chimie du CNRS (INC)-Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS) |
format |
Article in Journal/Newspaper |
author |
Roby, Mohamed H. H. de Castro, Vanessa C. Targino, Brenda N. Alves da Silva, Paulo H. Mangavel, Cecile Chrétien, Francoise Humeau, Catherine Desobry, Stéphane |
author_facet |
Roby, Mohamed H. H. de Castro, Vanessa C. Targino, Brenda N. Alves da Silva, Paulo H. Mangavel, Cecile Chrétien, Francoise Humeau, Catherine Desobry, Stéphane |
author_sort |
Roby, Mohamed H. H. |
title |
Oxidative stability of DHA phenolic ester |
title_short |
Oxidative stability of DHA phenolic ester |
title_full |
Oxidative stability of DHA phenolic ester |
title_fullStr |
Oxidative stability of DHA phenolic ester |
title_full_unstemmed |
Oxidative stability of DHA phenolic ester |
title_sort |
oxidative stability of dha phenolic ester |
publisher |
HAL CCSD |
publishDate |
2015 |
url |
https://hal.univ-lorraine.fr/hal-01267385 https://doi.org/10.1016/j.foodchem.2014.07.124 |
genre |
Antarc* Antarctica |
genre_facet |
Antarc* Antarctica |
op_source |
ISSN: 0308-8146 EISSN: 1873-7072 Food Chemistry https://hal.univ-lorraine.fr/hal-01267385 Food Chemistry, Elsevier, 2015, 169, pp.41-48. ⟨10.1016/j.foodchem.2014.07.124⟩ |
op_relation |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.foodchem.2014.07.124 hal-01267385 https://hal.univ-lorraine.fr/hal-01267385 doi:10.1016/j.foodchem.2014.07.124 |
op_doi |
https://doi.org/10.1016/j.foodchem.2014.07.124 |
container_title |
Food Chemistry |
container_volume |
169 |
container_start_page |
41 |
op_container_end_page |
48 |
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1766273439939690496 |