Division of Orthodontics, Department of Developmental Sciences, College of Dentistry, University of Oklahoma Health Sciences Center, Oklahoma City, Okla.
Division of Dental Biomaterials, Department of Restorative Sciences, College of Dentistry, University of Oklahoma Health Sciences Center, Oklahoma City, Okla.
Am J Orthod Dentofacial Orthop. 2021 Jul;160(1):50-57. doi: 10.1016/j.ajodo.2020.03.026. Epub 2021 Jun 3.
The purpose of this study was to compare the metabolism of Streptococcus mutans biofilms after 1-7 days of growth on different orthodontic adhesives.
Specimens of 6 commercial orthodontic adhesives were fabricated in custom-made molds and polymerized using a light-emitting diode light-curing unit. Bioluminescent S mutans (UA159:JM10) biofilms were grown on ultraviolet-sterilized specimens for 1, 3, 5, and 7 days (n = 18 biofilms/d/product) in anaerobic conditions at 37°C. The metabolism of biofilms (relative luminescence unit [RLU]) was measured 0, 2, 4, and 6 minutes after exposure to D-luciferin solution using a microplate reader. A linear mixed-effects model was used to analyze the logarithm of RLU (log RLU). The model included fixed effects of products, days, and minutes. Tukey-Kramer post-hoc tests were then performed on the significant predictors of log RLU (α = 0.05).
Days (P <0.0001) and minutes (P <0.0001) were independent predictors of log RLU, but the products were not (P = 0.5869). After adjusting for minutes, the log RLU was analyzed with a post-hoc test, and all differences between days were significant with the exceptions of day 3 from day 5 (P = 0.0731) and day 5 from day 7 (P = 0.8802). After adjusting for day, log RLU was analyzed with a post-hoc test and all differences in minutes were significant.
No significant differences in the metabolism of S mutans biofilms were observed among the 6 orthodontic adhesives. Biofilms that were grown for 3 days demonstrated the highest levels of biofilm metabolism as evidenced by higher mean log RLU values relative to 1, 5, and 7-day growth durations.
本研究的目的是比较不同正畸粘接剂上 1-7 天生长的变形链球菌生物膜的代谢情况。
采用定制模具制作 6 种商业正畸粘接剂标本,采用发光二极管光固化仪聚合。在厌氧条件下,37°C 下,将变形链球菌(UA159:JM10)生物发光生物膜在经紫外线消毒的标本上生长 1、3、5 和 7 天(n=18 个生物膜/产品)。在暴露于 D-荧光素溶液 0、2、4 和 6 分钟后,使用微孔板读数器测量生物膜的代谢(相对发光单位 [RLU])。采用线性混合效应模型分析 RLU 的对数(log RLU)。该模型包括产品、天数和分钟的固定效应。然后对 log RLU 的显著预测因子(α=0.05)进行 Tukey-Kramer 事后检验。
天数(P<0.0001)和分钟(P<0.0001)是 log RLU 的独立预测因子,但产品不是(P=0.5869)。在调整分钟数后,对 log RLU 进行了事后检验,除第 3 天与第 5 天(P=0.0731)和第 5 天与第 7 天(P=0.8802)外,所有天数之间的差异均有统计学意义。在调整天数后,对 log RLU 进行了事后检验,所有分钟之间的差异均有统计学意义。
在 6 种正畸粘接剂中,变形链球菌生物膜的代谢没有明显差异。与 1、5 和 7 天的生长时间相比,生长 3 天的生物膜表现出最高的生物膜代谢水平,表现为更高的平均 log RLU 值。