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In vitro gastrointestinal digestion impact on the antioxidant activity of extracts produced from the macroalgae gracilaria gracilis and ulva rigida

dc.contributor.authorCunha, Sara A.
dc.contributor.authorNova, Paulo
dc.contributor.authorSalsinha, Ana S.
dc.contributor.authorGomes, Ana
dc.contributor.authorPintado, Manuela
dc.date.accessioned2022-05-12T14:28:15Z
dc.date.available2022-05-12T14:28:15Z
dc.date.issued2021-10-14
dc.description.abstractThe interest in edible algae has been growing over the years due to their richness in molecules with nutritional and bioactive potential, such as proteins, essential amino acids, vitamins and minerals. Furthermore, due to their interesting protein content, they have been described as a source of bioactive peptides, with scientifically documented antioxidant, anti-hypertensive and antimicrobial properties. In this work, water-soluble extracts were produced from the macroalgae Gracilaria gracilis and Ulva rigida, with focus on their antioxidant potential. Furthermore, the impact of in vitro gastrointestinal (GI) digestion on the antioxidant activity of both extracts was studied, with the goal of evaluating their potential as functional food ingredients. Extracts were produced by enzymatic hydrolysis, with a cellulase and a subtilisin protease, using a previously optimized method. Then, both were submitted to simulated GI conditions, similar to those found in the human digestive system. The antioxidant activity was determined by ORAC and ABTS assays in four stages of GI simulation (before digestion, and after mouth, stomach and intestine digestion). The antioxidant activity did not decrease throughout the different stages of digestion. Interestingly, the antioxidant capacity increased after some phases. For instance, both extracts presented higher ORAC values after all digestion phases, when compared to the non-digested extract, being statistically significant after stomach digestion, for G. gracilis extract (p < 0.05). On this study, both extracts maintained their antioxidant activity during in vitro GI digestion, with an increase after almost all digestion phases, when compared to the non-digested extract. The observed increase may be explained by the production of smaller and more bioactive peptides, by the action of the gastrointestinal enzymes, such as pepsin and pancreatin. In conclusion, since antioxidant activity is maintained throughout the GI tract, these results showed that G. gracilis and U. rigida extracts may be considered potential ingredients for the development of functional foods with antioxidant properties.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.3390/foods2021-11069pt_PT
dc.identifier.issn2673-9976
dc.identifier.urihttp://hdl.handle.net/10400.14/37520
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectBioactive hydrolysatespt_PT
dc.subjectFunctional foodpt_PT
dc.subjectActive ingredientspt_PT
dc.subjectMacroalgaept_PT
dc.subjectMarine speciespt_PT
dc.titleIn vitro gastrointestinal digestion impact on the antioxidant activity of extracts produced from the macroalgae gracilaria gracilis and ulva rigidapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.titleBiology and Life Sciences Forumpt_PT
oaire.citation.volume6pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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