Antimicrobial coatings prepared from Dhvar-5-click-grafted chitosan powders.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
15 01 2019
Historique:
received: 28 03 2018
revised: 22 11 2018
accepted: 04 12 2018
pubmed: 12 12 2018
medline: 23 2 2020
entrez: 12 12 2018
Statut: ppublish

Résumé

Antimicrobial peptides (AMP) are powerful components of the innate immune system, as they display wide activity spectrum and low tendency to induce pathogen resistance. Hence, the development of AMP-based coatings is a very promising strategy to prevent biomaterials-associated infections. This work aims to investigate if Dhvar-5-chitosan conjugates, previously synthesized by us via azide-alkyne "click" reaction, can be applied as antimicrobial coatings. Ultrathin coatings were prepared by spin coater after dissolving Dhvar-5-chitosan conjugate powder in aqueous acetic acid. Peptide orientation and exposure from the surface was confirmed by ellipsometry and contact angle measurements. Bactericidal activity was evaluated against Staphylococcus epidermidis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, the most prevalent pathogens in implant-associated infections. Results showed that Dhvar-5-chitosan coatings displayed bactericidal effect. Moreover, since Dhvar-5 has head-to-tail amphipathicity, it was clear that the bactericidal potency was dependent on which domain of the peptide (cationic or hydrophobic) was exposed. In this context, Dhvar-5 immobilized through its C-terminus (exposing its hydrophobic end) presented higher antimicrobial activity against Gram-positive bacteria and reduced adhesion of Gram-negative bacteria. This orientation-dependent antimicrobial activity was further corroborated by the anti-biofilm assay, as covalent immobilization of Dhvar-5 through its C-terminus provided anti-biofilm properties to the chitosan thin film. Immobilization of Dhvar-5 showed no cytotoxic effect against HFF-1 cells, as both metabolic activity and cell morphology were similar to control. In conclusion, Dhvar-5-chitosan coatings are promising antimicrobial surfaces without cytotoxic effects against human cells. STATEMENT OF SIGNIFICANCE: AMP-tethering onto ground biomaterial is still a poorly explored strategy in research. In this work, AMP-tethered ground chitosan is used to produce highly antibacterial ultrathin films. Powdered AMP-tethered chitosan appears as an alternative solution for antimicrobial devices production, as it is suitable for large scale production, being easier to handle for fabrication of different coatings and materials with antimicrobial properties and without inducing toxicity.

Identifiants

pubmed: 30528610
pii: S1742-7061(18)30726-8
doi: 10.1016/j.actbio.2018.12.001
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Coated Materials, Biocompatible 0
Dhvar-5 0
Histatins 0
Powders 0
Chitosan 9012-76-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

242-256

Informations de copyright

Copyright © 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Mariana Barbosa (M)

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, University of Porto, Rua do Campo Alegre, s/n, Porto 4169-007, Portugal; i3S, Instituto de Investigação e Inovação em Saúde, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; INEB, Instituto de Engenharia Biomédica, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; Faculdade de Engenharia, University of Porto, Rua Dr. Roberto Frias, s/n, Porto 4200-391, Portugal.

Fabíola Costa (F)

i3S, Instituto de Investigação e Inovação em Saúde, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; INEB, Instituto de Engenharia Biomédica, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal.

Cláudia Monteiro (C)

i3S, Instituto de Investigação e Inovação em Saúde, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; INEB, Instituto de Engenharia Biomédica, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal.

Filipa Duarte (F)

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, University of Porto, Rua do Campo Alegre, s/n, Porto 4169-007, Portugal.

M Cristina L Martins (MCL)

i3S, Instituto de Investigação e Inovação em Saúde, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; INEB, Instituto de Engenharia Biomédica, University of Porto, Rua Alfredo Allen, 208, Porto 4200-135, Portugal; Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Rua de Jorge Viterbo Ferreira, 228, Porto 4050-013, Portugal. Electronic address: CMartins@ineb.up.pt.

Paula Gomes (P)

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, University of Porto, Rua do Campo Alegre, s/n, Porto 4169-007, Portugal. Electronic address: pgomes@fc.up.pt.

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Classifications MeSH