Streptococcus mutans is the major cause of dental plaque and is often associated with biofilm formation. The aim of this study is to evaluate the activity of a hydrosoluble derivative of chitosan against S. mutans biofilms in vitro and in vivo. Strains of S. mutans were isolated from the dental plaque of 84 patients enrolled in the study. The antibacterial activity of chitosan was determined by broth microdilutions. The effect of chitosan at different concentrations and exposure times on S. mutans biofilms at different phases of development was assessed by a clinical study using the classical "4-day plaque regrowth" experiment in adult volunteers. The MIC values of chitosan were between 0.5 and 2 g/L. Compared to distilled water, the chitosan solution significantly decreased the vitality of plaque microflora (p <= 0.05). Chlorhexidine, used as a positive control, reduced vitality even further. The results showed that S. mutans in the adhesion phase (4 h) was completely inhibited by chitosan at any concentration (0.1, 0.2, 0.5XMIC) or exposure time investigated (1, 15, 30, 60 min), while S. mutans at successive stages of accumulation (12-24 h) was inhibited only by higher concentrations and longer exposure times. These data confirm the effective action of chitosan against S. mutans biofilms.

Pasquantonio, G., Greco, C., Prenna, M., Ripa, C., Vitali, L., Petrelli, D., et al. (2008). Antibacterial activity and anti-biofilm effect of chitosan against strains of Streptococcus mutans isolated in dental plaque. INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 21(4), 993-997.

Antibacterial activity and anti-biofilm effect of chitosan against strains of Streptococcus mutans isolated in dental plaque

PASQUANTONIO, GUIDO;
2008-01-01

Abstract

Streptococcus mutans is the major cause of dental plaque and is often associated with biofilm formation. The aim of this study is to evaluate the activity of a hydrosoluble derivative of chitosan against S. mutans biofilms in vitro and in vivo. Strains of S. mutans were isolated from the dental plaque of 84 patients enrolled in the study. The antibacterial activity of chitosan was determined by broth microdilutions. The effect of chitosan at different concentrations and exposure times on S. mutans biofilms at different phases of development was assessed by a clinical study using the classical "4-day plaque regrowth" experiment in adult volunteers. The MIC values of chitosan were between 0.5 and 2 g/L. Compared to distilled water, the chitosan solution significantly decreased the vitality of plaque microflora (p <= 0.05). Chlorhexidine, used as a positive control, reduced vitality even further. The results showed that S. mutans in the adhesion phase (4 h) was completely inhibited by chitosan at any concentration (0.1, 0.2, 0.5XMIC) or exposure time investigated (1, 15, 30, 60 min), while S. mutans at successive stages of accumulation (12-24 h) was inhibited only by higher concentrations and longer exposure times. These data confirm the effective action of chitosan against S. mutans biofilms.
2008
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/28 - MALATTIE ODONTOSTOMATOLOGICHE
English
Con Impact Factor ISI
Biofilm; Chitosan; Streptococcus mutans
chitosan; adult; antibacterial activity; article; bacterial strain; bacterium isolation; biofilm; broth dilution; concentration response; controlled study; female; human; human experiment; male; minimum inhibitory concentration; mouth flora; phase transition; priority journal; solvent effect; Streptococcus mutans; tooth plaque; Adult; Anti-Bacterial Agents; Biofilms; Chitosan; Dental Plaque; Female; Humans; Male; Microbial Sensitivity Tests; Middle Aged; Streptococcus mutans
Pasquantonio, G., Greco, C., Prenna, M., Ripa, C., Vitali, L., Petrelli, D., et al. (2008). Antibacterial activity and anti-biofilm effect of chitosan against strains of Streptococcus mutans isolated in dental plaque. INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 21(4), 993-997.
Pasquantonio, G; Greco, C; Prenna, M; Ripa, C; Vitali, L; Petrelli, D; Di Luca, M; Ripa, S
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/59124
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