Hypochlorous-Acid-Generating Electrochemical Scaffold for Treatment of Wound Biofilms.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
25 02 2019
Historique:
received: 13 04 2018
accepted: 07 01 2019
entrez: 27 2 2019
pubmed: 26 2 2019
medline: 15 9 2020
Statut: epublish

Résumé

Biofilm formation causes prolonged wound infections due to the dense biofilm structure, differential gene regulation to combat stress, and production of extracellular polymeric substances. Acinetobacter baumannii, Staphylococcus aureus, and Pseudomonas aeruginosa are three difficult-to-treat biofilm-forming bacteria frequently found in wound infections. This work describes a novel wound dressing in the form of an electrochemical scaffold (e-scaffold) that generates controlled, low concentrations of hypochlorous acid (HOCl) suitable for killing biofilm communities without substantially damaging host tissue. Production of HOCl near the e-scaffold surface was verified by measuring its concentration using needle-type microelectrodes. E-scaffolds producing 17, 10 and 7 mM HOCl completely eradicated S. aureus, A. baumannii, and P. aeruginosa biofilms after 3 hours, 2 hours, and 1 hour, respectively. Cytotoxicity and histopathological assessment showed no discernible harm to host tissues when e-scaffolds were applied to explant biofilms. The described strategy may provide a novel antibiotic-free strategy for treating persistent biofilm-associated infections, such as wound infections.

Identifiants

pubmed: 30804362
doi: 10.1038/s41598-019-38968-y
pii: 10.1038/s41598-019-38968-y
pmc: PMC6389966
doi:

Substances chimiques

Anti-Bacterial Agents 0
Hypochlorous Acid 712K4CDC10

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

2683

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI091594
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008336
Pays : United States

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Auteurs

Mia Mae Kiamco (MM)

The Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA, USA.

Hannah M Zmuda (HM)

The Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA, USA.

Abdelrhman Mohamed (A)

The Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA, USA.

Douglas R Call (DR)

The Paul G. Allen School for Global Animal Health, Washington State University, Pullman, WA, USA.

Yash S Raval (YS)

Divisions of Clinical Microbiology, Rochester, MN, USA.

Robin Patel (R)

Divisions of Clinical Microbiology, Rochester, MN, USA.
Divisions of Infectious Diseases, Mayo Clinic, Rochester, MN, USA.

Haluk Beyenal (H)

The Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA, USA. beyenal@wsu.edu.

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