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dc.contributor.authorChiloeches, Alberto
dc.contributor.authorZágora, Jakub
dc.contributor.authorPlachá, Daniela
dc.contributor.authorTorres, Marcelo D. T.
dc.contributor.authorDe la Fuente-Núñez, Cesar
dc.contributor.authorLópez Fabal, Fátima
dc.contributor.authorGil-Romero, Yolanda
dc.contributor.authorFernández-García, Raquel
dc.contributor.authorFernández-García, Marta
dc.contributor.authorEcheverría, Coro
dc.contributor.authorMuñoz-Bonilla, Alexandra
dc.date.accessioned2024-02-15T11:28:04Z
dc.date.available2024-02-15T11:28:04Z
dc.date.issued2023
dc.identifier.issn2576-6422spa
dc.identifier.urihttps://hdl.handle.net/10641/4013
dc.description.abstractCombining different antimicrobial agents has emerged as a promising strategy to enhance efficacy and address resistance evolution. In this study, we investigated the synergistic antimicrobial effect of a cationic biobased polymer and the antimicrobial peptide (AMP) temporin L, with the goal of developing multifunctional electrospun fibers for potential biomedical applications, particularly in wound dressing. A clickable polymer with pendent alkyne groups was synthesized by using a biobased itaconic acid building block. Subsequently, the polymer was functionalized through click chemistry with thiazolium groups derived from vitamin B1 (PTTIQ), as well as a combination of thiazolium and AMP temporin L, resulting in a conjugate polymer−peptide (PTTIQ-AMP). The individual and combined effects of the cationic PTTIQ, Temporin L, and PTTIQ-AMP were evaluated against Gram-positive and Gram-negative bacteria as well as Candida species. The results demonstrated that most combinations exhibited an indifferent effect, whereas the covalently conjugated PTTIQ-AMP displayed an antagonistic effect, potentially attributed to the aggregation process. Both antimicrobial compounds, PTTIQ and temporin L, were incorporated into poly(lactic acid) electrospun fibers using the supercritical solvent impregnation method. This approach yielded fibers with improved antibacterial performance, as a result of the potent activity exerted by the AMP and the nonleaching nature of the cationic polymer, thereby enhancing long-term effectiveness.spa
dc.language.isoengspa
dc.publisherACS Applied BioMaterialsspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCationic polymersspa
dc.subjectAntimicrobial peptidespa
dc.subjectSupercritical impregnationspa
dc.subjectAntimicrobialspa
dc.titleSynergistic Combination of Antimicrobial Peptides and Cationic Polyitaconates in Multifunctional PLA Fibers.spa
dc.typejournal articlespa
dc.type.hasVersionAMspa
dc.rights.accessRightsopen accessspa
dc.description.extent4532 KBspa
dc.identifier.doi10.1021/acsabm.3c00576spa
dc.relation.publisherversionhttps://pubs.acs.org/doi/full/10.1021/acsabm.3c00576spa


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