Evaluation in a Dog Model of Three Antimicrobial Glassy Coatings: Prevention of Bone Loss around Implants and Microbial Assessments

PLoS One. 2015 Oct 21;10(10):e0140374. doi: 10.1371/journal.pone.0140374. eCollection 2015.

Abstract

Objectives: The aim of the present study is to evaluate, in a ligature-induced peri-implantitis model, the efficacy of three antimicrobial glassy coatings in the prevention of biofilm formation, intrasulcular bacterial growth and the resulting peri-implant bone loss.

Methods: Mandibular premolars were bilaterally extracted from five beagle dogs. Four dental implants were inserted on each hemiarch. Eight weeks after, one control zirconia abutment and three with different bactericidal coatings (G1n-Ag, ZnO35, G3) were connected. After a plaque control period, bacterial accumulation was allowed and biofilm formation on abutments was observed by Scanning Electron Microscopy (SEM). Peri-implantitis was induced by cotton ligatures. Microbial samples and peri-implant crestal bone levels of all implant sites were obtained before, during and after the breakdown period.

Results: During experimental induce peri-implantitis: colony forming units counts from intrasulcular microbial samples at implants with G1n-Ag coated abutment remained close to the basal inoculum; G3 and ZnO35 coatings showed similar low counts; and anaerobic bacterias counts at control abutments exhibited a logarithmic increase by more than 2. Bone loss during passive breakdown period was no statistically significant. Additional bone loss occurred during ligature-induce breakdown: 0.71 (SD 0.48) at G3 coating, 0.57 (SD 0.36) at ZnO35 coating, 0.74 (SD 0.47) at G1n-Ag coating, and 1.29 (SD 0.45) at control abutments; and statistically significant differences (p<0.001) were found. The lowest bone loss at the end of the experiment was exhibited by implants dressing G3 coated abutments (mean 2.1; SD 0.42).

Significance: Antimicrobial glassy coatings could be a useful tool to ward off, diminish or delay peri-implantitis progression.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alveolar Bone Loss / prevention & control*
  • Animals
  • Anti-Infective Agents / pharmacology*
  • Bacteria / growth & development
  • Bicuspid / surgery
  • Biofilms / drug effects
  • Biofilms / growth & development*
  • Calcium Compounds / pharmacology
  • Dental Abutments / microbiology
  • Dental Implantation, Endosseous / adverse effects
  • Dental Implantation, Endosseous / methods*
  • Dental Implants / adverse effects
  • Dental Plaque / microbiology
  • Dental Prosthesis Design
  • Dogs
  • Glass / chemistry
  • Microbial Sensitivity Tests
  • Microscopy, Electron, Scanning
  • Models, Animal
  • Osseointegration
  • Oxides / pharmacology
  • Peri-Implantitis / prevention & control*
  • Silver / pharmacology
  • Sodium Hydroxide / pharmacology
  • Surface Properties
  • Yeasts / growth & development
  • Zinc Oxide / analogs & derivatives
  • Zinc Oxide / pharmacology

Substances

  • Anti-Infective Agents
  • Calcium Compounds
  • Dental Implants
  • Oxides
  • Silver
  • soda lime
  • Sodium Hydroxide
  • Zinc Oxide

Grants and funding

This work was supported by the Spanish Ministry of Science and Innovation (MICINN) and The Spanish National Research Council (CSIC) under the projects MAT2012-38645 and 201360E012 respectively. B. Cabal acknowledges financial support from JAE-Doc program (CSIC, cofounded by FSE). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.