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https://hdl.handle.net/10216/136340Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Durão, J | |
| dc.creator | Vale, N | |
| dc.creator | Gomes, MS | |
| dc.creator | Gomes, P | |
| dc.creator | Barrias, CC | |
| dc.creator | Gales, L | |
| dc.date.accessioned | 2021-09-20T10:53:16Z | - |
| dc.date.available | 2021-09-20T10:53:16Z | - |
| dc.date.issued | 2019 | |
| dc.identifier.issn | 2218-273X | |
| dc.identifier.uri | https://hdl.handle.net/10216/136340 | - |
| dc.description.abstract | Nitric 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.sponsorship | This 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.iso | eng | |
| dc.publisher | MDPI | |
| dc.relation | info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F84914%2F2012/PT | |
| dc.relation.ispartof | Biomolecules, vol.9(1):4 | |
| dc.rights | openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Antimicrobial activity | |
| dc.subject | Collagen | |
| dc.subject | Fmoc-Pexiganan | |
| dc.subject | NO release | |
| dc.subject.mesh | Antimicrobial Cationic Peptides / chemical synthesis | |
| dc.subject.mesh | Antimicrobial Cationic Peptides / chemistry | |
| dc.subject.mesh | Antimicrobial Cationic Peptides / pharmacology | |
| dc.subject.mesh | Cell Line | |
| dc.subject.mesh | Collagen / metabolismo | |
| dc.subject.mesh | Escherichia coli / drug effects | |
| dc.subject.mesh | Fibroblasts / cytology | |
| dc.subject.mesh | Fibroblasts / drug effects | |
| dc.subject.mesh | Fibroblasts / metabolismo | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Hydrogels / chemistry | |
| dc.subject.mesh | Hydrogen-Ion Concentration | |
| dc.subject.mesh | Kinetics | |
| dc.subject.mesh | Nitric Oxide / metabolismo | |
| dc.subject.mesh | Wound Healing / drug effects | |
| dc.title | Nitric oxide release from antimicrobial peptide hydrogels for wound healing | |
| dc.type | Artigo em Revista Científica Internacional | |
| dc.contributor.uporto | Instituto de Investigação e Inovação em Saúde | |
| dc.identifier.doi | 10.3390/biom9010004 | |
| dc.relation.publisherversion | https://www.mdpi.com/2218-273X/9/1/4 | |
| Appears in Collections: | I3S - Artigo em Revista Científica Internacional | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 10.3390-biom9010004.pdf | 1.12 MB | Adobe PDF | ![]() View/Open |
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