Action of chitosan‐based solutions against a model four‐species biofilm formed on cobalt‐chromium and acrylic resin surfaces

Author:

Raile Priscilla Neves1,Oliveira Viviane de Cássia12ORCID,Macedo Ana Paula1,Curylofo Patrícia Almeida1,Marcato Priscyla Daniely3,Watanabe Evandro24,Paranhos Helena de Freitas Oliveira1ORCID,Pagnano Valéria Oliveira1ORCID

Affiliation:

1. Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto University of São Paulo Ribeirão Preto São Paulo Brazil

2. Human Exposome and Infectious Diseases Network—HEID, School of Nursing of Ribeirão Preto University of São Paulo Ribeirão Preto São Paulo Brazil

3. Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo Ribeirão Preto São Paulo Brazil

4. Department of Restorative Dentistry, School of Dentistry of Ribeirão Preto University of São Paulo Ribeirão Preto São Paulo Brazil

Abstract

ObjectiveTo evaluate the anti‐biofilm action of chitosan, nanoparticulate chitosan, and denture cleanser Nitradine™ against biofilms comprising Candida albicans, Candida glabrata, Staphylococcus aureus, and Streptococcus mutans.BackgroundBiofilm removal from removable partial dentures (RPD) is important for success in prosthetic rehabilitation.Materials and MethodsThe anti‐biofilm action of the experimental chitosan‐based solutions and Nitradine™ was evaluated on acrylic resin and cobalt‐chromium alloy through assessing cell viability, cell metabolism, residual aggregated biofilm, and extracellular polymeric substance and biofilm morphology.ResultsOnly chitosan reduced the viability of C. albicans on cobalt‐chromium alloy surface, by 98% (a 1.7 log10 reduction in cfu). Chitosan‐based solutions neither promoted substantial alteration of the metabolic activity of the four‐species biofilm nor reduced the amount of the aggregated biofilm. After immersion in chitosan and nanoparticulate chitosan, viable microorganisms and extracellular polymeric substances distributed over the entire specimens' surfaces were observed. Nitradine™ reduced the viability and metabolic activity of biofilm grown on both surfaces, but it did not remove all aggregated biofilm and extracellular polymeric substances. After immersion in Nitradine™, approximately 35% of the specimens' surfaces remained covered by aggregated biofilm, mainly composed of dead cells.ConclusionAlthough chitosan and Nitradine™ promoted changes in the viability of microorganisms, neither solution completely removed the four‐species biofilm from the Co–Cr and acrylic resin surfaces. Thus, isolated use of hygiene solutions is not indicated for biofilm control on RPDs; this requires complementary mechanical removal.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

Geriatrics and Gerontology,General Dentistry

Reference50 articles.

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