Title : Antimicrobial performance of commercial antiplaque/antigingivitis formulations
Abstract:
Introduced at least as early as 1995, plaque growth and regrowth methods (PGRM) are sometimes used to assess the potential efficacy of antimicrobial oral care formulations. In fact, PGRM models are recognized as an evaluation tool by the US FDA for products comprising cetylpyridinium chloride (CPC) and stannous fluoride (SnF2). These models, which may vary in design, typically assess plaque regrowth or glycolysis responses, or even plaque biofilm formation, when microbial species are exposed to the putative treatment. We recently introduced a glycolysis and automated plaque regrowth (GAPR) model that demonstrates sensitivity to a range of putative antimicrobial agents (Karlinsey & Karlinsey. Dent. J. 2024, 12(5), 146; https://doi.org/10.3390/dj12050146). In addition to bespoke recipes that assess microbial regrowth or glycolysis, the GAPR method utilizes harvested human plaque, which contrasts with the typical monospecies minimal inhibitory concentration (MIC) and kill-time (KT) evaluations. Despite the use of MIC and KT in ingredient/formulation screening, sometimes these evaluations conflict with other similar assays or do not mirror clinical outcomes. Using the GAPR method was a possible screening tool to help bridge the lab-clinic divide, in this presentation we provide background and methodology, as well as share some results when we applied our model to various commercial dentifrice and mouthwash products, including those with antiplaque benefits that lack formally recognized antimicrobial agents such as CPC or SnF2.
Audience Take Away Notes:
- To introduce the audience to PGRM models in the evaluation of antiplaque/antigingivitis agents.
- To describe the sensitivity of the microbial recipes to growth and glycolysis.
- To provide information about a novel PGRM screening tool in the evaluation of putative ingredients/formulations.
- To share results from commercially available dental products that may improve understanding of how the formulation may promote antiplaque/antigingivitis benefits.