Abstract

Effective management of biofilm-related oral infectious diseases is a global challenge. Oral biofilm presents increased resistance to antimicrobial agents and elevated virulence compared with planktonic bacteria. Antimicrobial agents, such as chlorhexidine, have proven effective in the disruption/inhibition of oral biofilm. However, the challenge of precisely and continuously eliminating the specific pathogens without disturbing the microbial ecology still exists, which is a major factor in determining the virulence of a multispecies microbial consortium and the consequent development of oral infectious diseases. Therefore, several novel approaches are being developed to inhibit biofilm virulence without necessarily inducing microbial dysbiosis of the oral cavity. Nanoparticles, such as pH-responsive enzyme-mimic nanoparticles, have been developed to specifically target the acidic niches within the oral biofilm where tooth demineralization readily occurs, in effect controlling dental caries. Quaternary ammonium salts (QAS) such as dimethylaminododecyl methacrylate (DMADDM), when incorporated into dental adhesives or resin composite, have also shown excellent and durable antimicrobial activity and thus could effectively inhibit the occurrence of secondary caries. In addition, custom-designed small molecules, natural products and their derivatives, as well as basic amino acids such as arginine, have demonstrated ecological effects by modulating the virulence of the oral biofilm without universally killing the commensal bacteria, indicating a promising approach to the management of oral infectious diseases such as dental caries and periodontal diseases. This article aims to introduce these novel approaches that have shown potential in the control of oral biofilm. These methods may be utilized in the near future to effectively promote the clinical management of oral infectious diseases and thus benefit oral health.

Highlights

  • A structured community which consists of a wide range of microbes embedded with self-organized matrix of extracellular polysaccharides (EPS), is clearly recognized as a virulence factor to many oral infectious diseases including dental caries, gingivitis, periodontitis, periapical periodontitis and peri-implantitis [1,2,3,4,5]

  • This review will introduce some of the novel strategies for the disruption/inhibition of oral biofilm, including nanomaterials, quaternary ammonium salts, small molecules, arginine, and the natural products

  • Triethylaminododecyl acrylate (TEADDA), a new Quaternary ammonium salts (QAS) with a different functional group position of dimethylaminododecyl methacrylate (DMADDM), when combined with adhesive resin, shows enhanced mechanical properties but reduced antibacterial effects compared with DMADDM [80]

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Summary

Introduction

A structured community which consists of a wide range of microbes embedded with self-organized matrix of extracellular polysaccharides (EPS), is clearly recognized as a virulence factor to many oral infectious diseases including dental caries, gingivitis, periodontitis, periapical periodontitis and peri-implantitis [1,2,3,4,5]. Compared with bacteria in planktonic, mature biofilm tends to need higher concentrations of antimicrobial agents to be eradicated [1, 10, 11]. Recent studies have shown that the EPS matrix provides functions as scaffold for biofilm growth and maturation and provides emergent properties of biofilms including surface adhesion, spatial and chemical heterogeneities, synergistic/competitive interactions, and increased tolerance to antimicrobial agents. Little is understood about the most economic and effective ways of controlling oral biofilm due to the enhanced resistance to antibiotics and other antimicrobial agents [7, 16]. There have been increased attempts to develop ideal antimicrobial agents for the emergence of antibiotic-resistant bacteria [19]. This review will introduce some of the novel strategies for the disruption/inhibition of oral biofilm, including nanomaterials, quaternary ammonium salts, small molecules, arginine, and the natural products

Nanomaterials
Small Molecules
Arginine
Natural Products
Conclusion and Future Prospects
Full Text
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