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Antimicrobial activity of effervescent denture tablets on multispecies biofilms.
Coimbra, Flávia C T; Rocha, Millena M; Oliveira, Viviane C; Macedo, Ana Paula; Pagnano, Valéria O; Silva-Lovato, Cláudia H; Paranhos, Helena de F O.
Afiliación
  • Coimbra FCT; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Rocha MM; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Oliveira VC; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Macedo AP; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Pagnano VO; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Silva-Lovato CH; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
  • Paranhos HFO; Department of Dental Materials and Prosthodontics, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Gerodontology ; 38(1): 87-94, 2021 Mar.
Article en En | MEDLINE | ID: mdl-33000876
ABSTRACT

PURPOSE:

To investigate the impact of peroxide-based solutions in reducing viability and metabolic activity of multispecies biofilms on denture base acrylic resin surfaces and for removing them from these surfaces.

BACKGROUND:

Denture cleansers are effective in reducing monospecies biofilm; however, studies evaluating their action on multispecies biofilms are scarce. MATERIALS AND

METHODS:

Sixty-nine denture base acrylic resin specimens (Ø 15 × 3 mm) were sterilised then contaminated with Candida albicans, Staphylococcus aureus and Pseudomonas aeruginosa to form multispecies biofilms. Biofilms were grown for 24 hours; subsequently, specimens were immersed in three different cleansing solutions (n = 9) nitradine (NI), fixodent (FX) and phosphate-buffered saline (Control), according to the respective manufacturer's instructions. After applying the hygiene protocols, viability of microorganisms was evaluated by counting colony-forming units and assessing metabolic activity. Moreover, biofilm removal capacity was estimated based on extension of cell-covered areas visualised in fluorescent microscopy micrographics.

RESULTS:

Microbial counts were solution-dependent; NI was effective against all microorganisms (P < .05). FX exhibited moderate antimicrobial action, reducing P aeruginosa (P < .05) and S aureus (P < .05) viability by approximately 2 logs. Both peroxide-based solutions reduced metabolic activity (P < .001) and biofilm-covered areas on specimen surfaces (P < .001).

CONCLUSION:

Under the experimental conditions tested, these results demonstrated that peroxide-based solutions had favourable antimicrobial activity but promoted no broad elimination of aggregated multispecies biofilm. NI might be more suitable as complementary chemical agent for controlling multispecies denture biofilm.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Limpiadores de Dentadura / Antiinfecciosos Límite: Humans Idioma: En Revista: Gerodontology Año: 2021 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Limpiadores de Dentadura / Antiinfecciosos Límite: Humans Idioma: En Revista: Gerodontology Año: 2021 Tipo del documento: Article País de afiliación: Brasil