Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136340
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dc.creatorDurão, J
dc.creatorVale, N
dc.creatorGomes, MS
dc.creatorGomes, P
dc.creatorBarrias, CC
dc.creatorGales, L
dc.date.accessioned2021-09-20T10:53:16Z-
dc.date.available2021-09-20T10:53:16Z-
dc.date.issued2019
dc.identifier.issn2218-273X
dc.identifier.urihttps://hdl.handle.net/10216/136340-
dc.description.abstractNitric oxide (NO) is an endogenously produced molecule that has been implicated in several wound healing mechanisms. Its topical delivery may improve healing in acute or chronic wounds. In this study an antimicrobial peptide was synthesized which self-assembled upon a pH shift, forming a hydrogel. The peptide was chemically functionalized to incorporate a NO-donor moiety on lysine residues. The extent of the reaction was measured by ninhydrin assay and the NO release rate was quantified via the Griess reaction method. The resulting compound was evaluated for its antimicrobial activity against Escherichia coli, and its effect on collagen production by fibroblasts was assessed. Time-kill curves point to an initial increase in bactericidal activity of the functionalized peptide, and collagen production by human dermal fibroblasts when incubated with the NO-functionalized peptide showed a dose-dependent increase in the presence of the NO donor within a range of 0–20 µM.
dc.description.sponsorshipThis work was financed by FEDER (Fundo Europeu de Desenvolvimento Regional) funds via COMPETE 2020 (Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020), and by Portuguese funds through FCT (Fundação para a Ciência e a Tecnologia/ Ministério da Ciência, Tecnologia e Ensino Superior) in the framework of the projects “Institute for Research and Innovation in Health Sciences” (POCI-01-0145-FEDER-007274) and PTDC/QUI-QFI/29914/2017, as well through the grant SFRH/BD/84914/2012. Thanks to FCT also for supporting Research Unit LAQV-REQUIMTE through the project UID/QUI/5006/2013.
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F84914%2F2012/PT
dc.relation.ispartofBiomolecules, vol.9(1):4
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectAntimicrobial activity
dc.subjectCollagen
dc.subjectFmoc-Pexiganan
dc.subjectNO release
dc.subject.meshAntimicrobial Cationic Peptides / chemical synthesis
dc.subject.meshAntimicrobial Cationic Peptides / chemistry
dc.subject.meshAntimicrobial Cationic Peptides / pharmacology
dc.subject.meshCell Line
dc.subject.meshCollagen / metabolismo
dc.subject.meshEscherichia coli / drug effects
dc.subject.meshFibroblasts / cytology
dc.subject.meshFibroblasts / drug effects
dc.subject.meshFibroblasts / metabolismo
dc.subject.meshHumans
dc.subject.meshHydrogels / chemistry
dc.subject.meshHydrogen-Ion Concentration
dc.subject.meshKinetics
dc.subject.meshNitric Oxide / metabolismo
dc.subject.meshWound Healing / drug effects
dc.titleNitric oxide release from antimicrobial peptide hydrogels for wound healing
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/biom9010004
dc.relation.publisherversionhttps://www.mdpi.com/2218-273X/9/1/4
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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