Cargando…

Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo

Biofilms are prevalent in non‐healing chronic wounds and implicated in delayed healing. Tolerance to antimicrobial treatments and the host's immune system leave clinicians with limited interventions against biofilm populations. It is therefore essential that effective treatments be rigorously t...

Descripción completa

Detalles Bibliográficos
Autores principales: Roche, Eric D., Woodmansey, Emma J., Yang, Qingping, Gibson, Daniel J., Zhang, Hongen, Schultz, Gregory S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850490/
https://www.ncbi.nlm.nih.gov/pubmed/30868761
http://dx.doi.org/10.1111/iwj.13080
_version_ 1783469436914630656
author Roche, Eric D.
Woodmansey, Emma J.
Yang, Qingping
Gibson, Daniel J.
Zhang, Hongen
Schultz, Gregory S.
author_facet Roche, Eric D.
Woodmansey, Emma J.
Yang, Qingping
Gibson, Daniel J.
Zhang, Hongen
Schultz, Gregory S.
author_sort Roche, Eric D.
collection PubMed
description Biofilms are prevalent in non‐healing chronic wounds and implicated in delayed healing. Tolerance to antimicrobial treatments and the host's immune system leave clinicians with limited interventions against biofilm populations. It is therefore essential that effective treatments be rigorously tested and demonstrate an impact on biofilm across multiple experimental models to guide clinical investigations and protocols. Cadexomer iodine has previously been shown to be effective against biofilm in various in vitro models, against methicillin‐resistant Staphylococcus aureus biofilm in mouse wounds, and clinically in diabetic foot ulcers complicated by biofilm. Similarities between porcine and human skin make the pig a favoured model for cutaneous wound studies. Two antiseptic dressings and a gauze control were assessed against mature biofilm grown on ex vivo pig skin and in a pig wound model. Significant reductions in biofilm were observed following treatment with cadexomer iodine across both biofilm models. In contrast, silver carboxymethylcellulose dressings had minimal impact on biofilm in the models, with similar results to the control in the ex vivo model. Microscopy and histopathology indicate that the depth of organisms in wound tissue may impact treatment effectiveness. Further work on the promising biofilm efficacy of cadexomer iodine is needed to determine optimal treatment durations against biofilm.
format Online
Article
Text
id pubmed-6850490
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-68504902019-11-18 Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo Roche, Eric D. Woodmansey, Emma J. Yang, Qingping Gibson, Daniel J. Zhang, Hongen Schultz, Gregory S. Int Wound J Original Articles Biofilms are prevalent in non‐healing chronic wounds and implicated in delayed healing. Tolerance to antimicrobial treatments and the host's immune system leave clinicians with limited interventions against biofilm populations. It is therefore essential that effective treatments be rigorously tested and demonstrate an impact on biofilm across multiple experimental models to guide clinical investigations and protocols. Cadexomer iodine has previously been shown to be effective against biofilm in various in vitro models, against methicillin‐resistant Staphylococcus aureus biofilm in mouse wounds, and clinically in diabetic foot ulcers complicated by biofilm. Similarities between porcine and human skin make the pig a favoured model for cutaneous wound studies. Two antiseptic dressings and a gauze control were assessed against mature biofilm grown on ex vivo pig skin and in a pig wound model. Significant reductions in biofilm were observed following treatment with cadexomer iodine across both biofilm models. In contrast, silver carboxymethylcellulose dressings had minimal impact on biofilm in the models, with similar results to the control in the ex vivo model. Microscopy and histopathology indicate that the depth of organisms in wound tissue may impact treatment effectiveness. Further work on the promising biofilm efficacy of cadexomer iodine is needed to determine optimal treatment durations against biofilm. Blackwell Publishing Ltd 2019-03-13 /pmc/articles/PMC6850490/ /pubmed/30868761 http://dx.doi.org/10.1111/iwj.13080 Text en © 2019 The Authors. International Wound Journal published by Medicalhelplines.com Inc and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Roche, Eric D.
Woodmansey, Emma J.
Yang, Qingping
Gibson, Daniel J.
Zhang, Hongen
Schultz, Gregory S.
Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title_full Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title_fullStr Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title_full_unstemmed Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title_short Cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
title_sort cadexomer iodine effectively reduces bacterial biofilm in porcine wounds ex vivo and in vivo
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850490/
https://www.ncbi.nlm.nih.gov/pubmed/30868761
http://dx.doi.org/10.1111/iwj.13080
work_keys_str_mv AT rocheericd cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo
AT woodmanseyemmaj cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo
AT yangqingping cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo
AT gibsondanielj cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo
AT zhanghongen cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo
AT schultzgregorys cadexomeriodineeffectivelyreducesbacterialbiofilminporcinewoundsexvivoandinvivo