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Synthesis, characterization and functional properties of galactosylated derivatives of chitosan through amide formation

dc.contributor.authorMatute, Ana I. Ruiz
dc.contributor.authorCardelle-Cobas, Alejandra
dc.contributor.authorGarcía-Bermejo, Ana B.
dc.contributor.authorMontilla, Antonia
dc.contributor.authorOlano, Agustin
dc.contributor.authorCorzo, Nieves
dc.date.accessioned2021-06-27T17:07:41Z
dc.date.available2021-06-27T17:07:41Z
dc.date.issued2013-12
dc.description.abstractLow molecular weight chitosan (LMWC) and chitooligosaccharide (COS) derivatives were obtained by the introduction of lactobionic acid (LA) through amide formation, obtaining different complexes COS-LA and LMWC-LA (1-5), with a degree of substitution (DS) between 3 and 16%. The synthesis of these derivatives was monitored by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), High-Performance Liquid Chromatography-Size Exclusion Chromatography (HPLC-SEC) and proton Nuclear Magnetic Resonance (1H NMR) analyses. Different functional properties, solubility, water binding capacity (WBC) and fat binding capacity (FBC), as well as the antioxidant activity (DPPH radical scavenging activity) of these derivatives were evaluated. Solubility, WBC and FBC increased in all of the chitosan derivatives respect to those of the native LMWC or COS. The most substituted derivative (LMWC-LA1, DS 15%) presented the highest value of solubility (14.4mg/mL) while the highest levels of WBC and FBC were obtained for the derivative with a DS of 3% (LMWC-LA5; 4730% and 7100%, respectively). COS and COS-LA presented the best DPPH scavenging abilities, as shown by their low values of EC50 (1.29 and 3.45mg/mL, respectively). An inverse relationship between the DS of chitosan derivatives and antioxidant activity was observed. LMWC-LA5 (3% DS) was the derivative with the highest DPPH activity, being higher than LMWC in all the concentrations assayed (10.2-14.3% and 6.9-13.7%, respectively). Due to their enhanced functional properties, these chitosan derivatives could be considered as very promising for their future use as additives in the food industry (i.e. to bind fat and cholesterol or avoid hardening of foods).pt_PT
dc.description.versioninfo:eu-repo/semantics/acceptedVersionpt_PT
dc.identifier.doi10.1016/j.foodhyd.2013.03.016pt_PT
dc.identifier.eid84877067473
dc.identifier.issn0268-005X
dc.identifier.urihttp://hdl.handle.net/10400.14/34013
dc.identifier.wos000320614500010
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectChitooligosaccharidespt_PT
dc.subjectChitosanpt_PT
dc.subjectFunctional propertiespt_PT
dc.subjectGlycosylationpt_PT
dc.subjectLactobionic acidpt_PT
dc.titleSynthesis, characterization and functional properties of galactosylated derivatives of chitosan through amide formationpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage255pt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage245pt_PT
oaire.citation.titleFood Hydrocolloidspt_PT
oaire.citation.volume33pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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