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dc.contributor.authorFrancesko, Antonio
dc.contributor.authorSoares da Costa, Diana
dc.contributor.authorReis, Rui L.
dc.contributor.authorPashkuleva, Iva
dc.contributor.authorTzanov, Tzanko
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Enginyeria Química
dc.date.accessioned2013-01-07T09:09:56Z
dc.date.created2012-10-13
dc.date.issued2012-10-13
dc.identifier.citationFrancesko, A. [et al.]. Functional biopolymer-based matrices for modulation of chronic wound enzyme activities. "Acta biomaterialia", 13 Octubre 2012, vol. 9, núm. 2, p. 5216-5225.
dc.identifier.issn1742-7061
dc.identifier.urihttp://hdl.handle.net/2117/17193
dc.description.abstractCollagen, collagen/hyaluronic acid (HA) and collagen/HA/chitosan (CS) sponges loaded with epigallocatechin gallate (EGCG), catechin (CAT) and gallic acid (GA) were developed and evaluated as active chronic wound dressings. Their physico-mechanical properties, biostability, biocompatibility and ability to inhibit in vitro myeloperoxidase (MPO) and collagenase—major enzymes related with the persistent inflammation in chronic wounds—were investigated as a function of the biopolymer composition and the polyphenolic compound used. The results demonstrated that the molecular weight of HA influences significantly the bulk properties of the obtained materials: higher elastic modulus, swelling ability and biostability against collagenase were measured when HA with higher molecular weights (830 and 2000 kDa) were added to the collagen matrices. The addition of CS and the polyphenols increased further the biostability of the sponges. Preliminary in vitro tests with fibroblasts revealed that the cells were able to adhere to all sponges. Cell viability was not affected significantly by the addition of the polyphenols; however, the presence of CS or high molecular weight HA in the sponge composition was associated with lower cellular viability. Finally, all specimens containing polyphenols efficiently inhibited the MPO activity. The highest inhibition capacity was observed for EGCG (IC50 = 15 ± 1 μM) and it was coupled to the highest extent of binding to the biopolymers (>80%) and optimal release profile from the sponges that allowed for prolonged (up to 3–5 days) effects.
dc.format.extent10 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria química
dc.subject.lcshCollagen
dc.subject.lcshBiotechnology
dc.titleFunctional biopolymer-based matrices for modulation of chronic wound enzyme activities
dc.typeArticle
dc.subject.lemacBiotecnologia
dc.contributor.groupUniversitat Politècnica de Catalunya. GBMI - Grup de Biotecnologia Molecular i Industrial
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.actbio.2012.10.014
dc.rights.accessRestricted access - publisher's policy
drac.iddocument11160531
dc.description.versionPostprint (published version)
dc.relation.projectidinfo:eu-repo/grantAgreement/EC/FP7/229292/EU/Find and Bind: Mastering sweet cell-instructive biosystems by copycat nano-interaction of cells with natural surfaces for biotechnological applications/FIND AND BIND
dc.date.lift10000-01-01
upcommons.citation.authorFrancesko, A.; Soares da Costa, D.; Reis, R.; Pashkuleva, I.; Tzanov, T.
upcommons.citation.publishedtrue
upcommons.citation.publicationNameActa biomaterialia
upcommons.citation.volume9
upcommons.citation.number2
upcommons.citation.startingPage5216
upcommons.citation.endingPage5225


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