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Authordc.contributor.authorÁlvarez Vega, Rudy Carolina
Authordc.contributor.authorGiménez, Begoña
Authordc.contributor.authorMackie, Alan
Authordc.contributor.authorTorcello Gómez, Amelia
Authordc.contributor.authorQuintriqueo Cid, Alejandra Natalia
Authordc.contributor.authorOyarzún Ampuero, Felipe Andrés
Authordc.contributor.authorRobert Canales, Paz Soledad
Admission datedc.date.accessioned2022-12-05T21:13:21Z
Available datedc.date.available2022-12-05T21:13:21Z
Publication datedc.date.issued2022
Cita de ítemdc.identifier.citationFood Funct., 2022, 13, 1370–1379es_ES
Identifierdc.identifier.other10.1039/d1fo03688b
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/189614
Abstractdc.description.abstractAmong vegetable oils, chia oil has been gaining interest in recent years due to its high linolenic acid content (ALA, 18:3 omega 3). The aim of this work was to study the influence of the particle size of encapsulated purified chia oil (PCO) on the encapsulation efficiency and PCO release during in vitro digestion. PCO micro- and nano-sized particles with sodium alginate (SA) as an encapsulating agent (ME-PCO-SA and NE-PCO-SA) were designed by micro and nano spray-drying, respectively, applying a central composite plus star point experimental design. NE-PCO-SA showed a smaller particle size and higher encapsulation efficiency of PCO than ME-PCO-SA (0.16 mu m vs. 3.5 mu m; 98.1% vs. 92.0%). Emulsions (NE-PCO and ME-PCO) and particles (NE-PCO-SA and ME-PCO-SA) were subjected to in vitro static gastrointestinal digestion. ME-PCO and NE-PCO showed sustained oil release throughout the three phases of digestion (oral, gastric and intestinal phases), whereas the PCO release from ME-PCO-SA and NE-PCO-SA occurred mainly in the intestinal phase, showing the suitability of sodium alginate as an intestine-site release polymer. Nano-sized particles showed a significantly higher PCO release after in vitro digestion (NE-PCO-SA, 78.4%) than micro-sized particles (ME-PCO-SA, 69.8%), and also higher bioaccessibility of individual free fatty acids, such as C18:3 omega-3 (NE-PCO-SA, 23.6%; ME-PCO-SA, 7.9%), due to their greater surface area. However, when ME-PCO-SA and NE-PCO-SA were incorporated into yogurt, the PCO release from both particle systems after the digestion of the matrix was similar (NE-PCO-SA, 58.8%; ME-PCO-SA-Y, 61.8%), possibly because the calcium ions contained in the yogurt induced partial ionic gelation of SA, impairing the PCO release. Sodium alginate spray-dried micro and nanoparticles showed great potential for vehiculation of omega-3 rich oils in the design of functional foods.es_ES
Patrocinadordc.description.sponsorshipANID (Fondecyt Project) 1181329 21160009es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherThe Royal Society of Chemistry, Englandes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceFood & Functiones_ES
Keywordsdc.subjectWhey-protein concentratees_ES
Keywordsdc.subjectFatty-acidses_ES
Keywordsdc.subjectMicroencapsulationes_ES
Keywordsdc.subjectFoodes_ES
Keywordsdc.subjectStabilityes_ES
Keywordsdc.subjectOxidationes_ES
Keywordsdc.subjectAlginatees_ES
Keywordsdc.subjectKineticses_ES
Keywordsdc.subjectDeliveryes_ES
Títulodc.titleInfluence of the particle size of encapsulated chia oil on the oil release and bioaccessibility during in vitro gastrointestinal digestiones_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States