Cargando…

In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes

BACKGROUND: In Guided Tissue Regeneration (GTR), barrier membranes are used to allow selective cell populations to multiply and to promote periodontal regeneration. A frequent complication is membrane exposure to the oral cavity followed by bacterial colonization. The purpose of this in-vitro-study...

Descripción completa

Detalles Bibliográficos
Autores principales: Rudolf, Jan-Luca, Moser, Corina, Sculean, Anton, Eick, Sigrun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933891/
https://www.ncbi.nlm.nih.gov/pubmed/31878907
http://dx.doi.org/10.1186/s12903-019-0979-y
_version_ 1783483297463009280
author Rudolf, Jan-Luca
Moser, Corina
Sculean, Anton
Eick, Sigrun
author_facet Rudolf, Jan-Luca
Moser, Corina
Sculean, Anton
Eick, Sigrun
author_sort Rudolf, Jan-Luca
collection PubMed
description BACKGROUND: In Guided Tissue Regeneration (GTR), barrier membranes are used to allow selective cell populations to multiply and to promote periodontal regeneration. A frequent complication is membrane exposure to the oral cavity followed by bacterial colonization. The purpose of this in-vitro-study was to elucidate, if rinsing with a chlorhexidine digluconate solution (CHX) prevents bacterial adhesion, and whether it interferes with attachment of periodontal ligament (PDL) fibroblasts and epithelial cells to membrane surfaces. METHODS: Firstly, two bioresorbable membranes (polylactide-based and collagen-based) were dipped into 0.06% CHX and 0.12% CHX, before biofilms (2-species representing periodontal health, 6-species representing a periodontitis) were formed for 2 h and 8 h. Subsequently, colony forming units (cfu) were counted. Secondly, the membranes were treated with CHX and inoculated in bacteria suspension two-time per day for 3 d before cfu were determined. In additional series, the influence of CHX and bacterial lysates on attachment of epithelial cells and PDL fibroblasts was determined. Parameter-free tests were applied for statistical analysis. RESULTS: Cfu in “healthy” biofilms did not differ between the two membranes, more cfu were counted in “periodontitis” biofilm on collagen than on polylactide membranes. One-time dipping of membranes into CHX solutions did not markedly influence the cfu counts of both biofilms on polylactide membrane; those on collagen-based membrane were significantly reduced with being 0.12% CHX more active than 0.06% CHX. More-fold CHX dipping of membranes reduced concentration-dependent the cfu counts of both biofilms on both membranes. In general, the number of attached gingival epithelial cells and PDL fibroblasts was higher on collagen than on polylactide membrane. Lysates of the periodontopathogenic bacteria inhibited attachment of PDL fibroblasts to membranes. CHX decreased in a concentration-dependend manner the number of attached gingival epithelial cells and PDL fibroblasts. CONCLUSIONS: The present in-vitro results appear to indicate that membranes in GTR should only be used when bacteria being associated with periodontal disease have been eliminated. An exposure of the membrane should be avoided. Rinsing with CHX may prevent or at least retard bacterial colonization on membrane exposed to the oral activity. However, a certain negative effect on wound healing cannot be excluded.
format Online
Article
Text
id pubmed-6933891
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69338912019-12-30 In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes Rudolf, Jan-Luca Moser, Corina Sculean, Anton Eick, Sigrun BMC Oral Health Research Article BACKGROUND: In Guided Tissue Regeneration (GTR), barrier membranes are used to allow selective cell populations to multiply and to promote periodontal regeneration. A frequent complication is membrane exposure to the oral cavity followed by bacterial colonization. The purpose of this in-vitro-study was to elucidate, if rinsing with a chlorhexidine digluconate solution (CHX) prevents bacterial adhesion, and whether it interferes with attachment of periodontal ligament (PDL) fibroblasts and epithelial cells to membrane surfaces. METHODS: Firstly, two bioresorbable membranes (polylactide-based and collagen-based) were dipped into 0.06% CHX and 0.12% CHX, before biofilms (2-species representing periodontal health, 6-species representing a periodontitis) were formed for 2 h and 8 h. Subsequently, colony forming units (cfu) were counted. Secondly, the membranes were treated with CHX and inoculated in bacteria suspension two-time per day for 3 d before cfu were determined. In additional series, the influence of CHX and bacterial lysates on attachment of epithelial cells and PDL fibroblasts was determined. Parameter-free tests were applied for statistical analysis. RESULTS: Cfu in “healthy” biofilms did not differ between the two membranes, more cfu were counted in “periodontitis” biofilm on collagen than on polylactide membranes. One-time dipping of membranes into CHX solutions did not markedly influence the cfu counts of both biofilms on polylactide membrane; those on collagen-based membrane were significantly reduced with being 0.12% CHX more active than 0.06% CHX. More-fold CHX dipping of membranes reduced concentration-dependent the cfu counts of both biofilms on both membranes. In general, the number of attached gingival epithelial cells and PDL fibroblasts was higher on collagen than on polylactide membrane. Lysates of the periodontopathogenic bacteria inhibited attachment of PDL fibroblasts to membranes. CHX decreased in a concentration-dependend manner the number of attached gingival epithelial cells and PDL fibroblasts. CONCLUSIONS: The present in-vitro results appear to indicate that membranes in GTR should only be used when bacteria being associated with periodontal disease have been eliminated. An exposure of the membrane should be avoided. Rinsing with CHX may prevent or at least retard bacterial colonization on membrane exposed to the oral activity. However, a certain negative effect on wound healing cannot be excluded. BioMed Central 2019-12-26 /pmc/articles/PMC6933891/ /pubmed/31878907 http://dx.doi.org/10.1186/s12903-019-0979-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Rudolf, Jan-Luca
Moser, Corina
Sculean, Anton
Eick, Sigrun
In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title_full In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title_fullStr In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title_full_unstemmed In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title_short In-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
title_sort in-vitro antibiofilm activity of chlorhexidine digluconate on polylactide-based and collagen-based membranes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933891/
https://www.ncbi.nlm.nih.gov/pubmed/31878907
http://dx.doi.org/10.1186/s12903-019-0979-y
work_keys_str_mv AT rudolfjanluca invitroantibiofilmactivityofchlorhexidinedigluconateonpolylactidebasedandcollagenbasedmembranes
AT mosercorina invitroantibiofilmactivityofchlorhexidinedigluconateonpolylactidebasedandcollagenbasedmembranes
AT sculeananton invitroantibiofilmactivityofchlorhexidinedigluconateonpolylactidebasedandcollagenbasedmembranes
AT eicksigrun invitroantibiofilmactivityofchlorhexidinedigluconateonpolylactidebasedandcollagenbasedmembranes