4.1 Article

Evaluation of an antibacterial orthodontic adhesive incorporated with niobium-based bioglass: an in situ study

Journal

BRAZILIAN ORAL RESEARCH
Volume 33, Issue -, Pages -

Publisher

SOCIEDADE BRASILEIRA DE PESQUISA ODONTOLOGICA
DOI: 10.1590/1807-3107bor-2019.vol33.0010

Keywords

Tooth Remineralization; Anti-Infective Agents; Dental Enamel; Orthodontics

Funding

  1. CAPES

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This in situ study aimed to evaluate the antibacterial and anti-demineralization effects of an experimental orthodontic adhesive containing triazine and niobium phosphate bioglass (TAT) around brackets bonded to enamel surfaces. Sixteen volunteers were selected to use intra-oral devices with six metallic brackets bonded to enamel blocks. The experimental orthodontic adhesives were composed by 75% BisGMA and 25% TEGDMA containing 0% TAT and 20% TAT. Transbond XT adhesive (TXT) was used as a control group. Ten volunteers, mean age of 29 years, were included in the study. The six blocks of each volunteer were detached from the appliance after 7 and 14 days to evaluate mineral loss and bacterial growth including total bacteria, total Streptococci, Streptococci mutans, and Lactobacilli. Statistical analysis was performed using GLM model - univariate analysis of variance for microhardness and 2-way ANOVA for bacterial growth (p<0.05). The 20% TAT adhesive caused no difference between distances from bracket and the sound zone at 10-mu m deep after 7 and 14 days. After 14 days, higher mineral loss was shown around brackets at 10- to 30-mu m deep for TXT and 0% TAT adhesives compared to 20% TAT. S. mutans growth was inhibited by 20% TAT adhesive at 14 days. Adhesive with 20% TAT showed lower S. mutans and total Streptococci growth than 0% TAT and TXT adhesives. The findings of this study show that the adhesive incorporated by triazine and niobium phosphate bioglass had an anti-demineralization effect while inhibiting S. mutans and total Streptococci growth. The use of this product may inhibit mineral loss of enamel, preventing the formation of white spot lesions.

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