Yaghmoor Rayan B, Abdel-Hadi Mohammad, Petridis Haralampos, Allan Elaine, Young Anne M
Department of Restorative Dentistry, College of Dental Medicine, Umm Al-Qura University, Makkah 24381, Saudi Arabia.
Unit of Prosthodontics, Department of Restorative Dentistry, UCL Eastman Dental Institute, Rockefeller Building, London WC1E 6HX, UK.
J Funct Biomater. 2023 Dec 29;15(1):13. doi: 10.3390/jfb15010013.
With the phase-out of amalgam and the increase in minimally invasive dentistry, there is a growing need for high-strength composite materials that can kill residual bacteria and promote tooth remineralization. This study quantifies how antibacterial polylysine (PLS) and re-mineralizing monocalcium phosphate monohydrate (MCPM) affect biofilms and the strength of dental composites. For antibacterial studies, the MCPM-PLS filler percentages were 0-0, 8-4, 12-6, and 16-8 wt% of the composite filler phase. Composite discs were immersed in 0.1% sucrose-supplemented broth containing (UA159) and incubated in an anaerobic chamber for 48 h. Surface biomass was determined by crystal violet (CV) staining. Growth medium pH was measured at 24 and 48 h. Biofilm bacterial viability (CFU), exo-polysaccharide (water-soluble glucan (WSG) and water-insoluble glucan (WIG)), and extracellular DNA (eDNA) were quantified. This was by serial dilution plate counting, phenol-sulfuric acid microassay, and fluorometry, respectively. The biaxial flexural strengths were determined after water immersion for 1 week, 1 month, and 1 year. The MCPM-PLS wt% were 8-4, 8-8, 16-4 and 16-8. The normalized biomass, WSG, and WIG showed a linear decline of 66%, 64%, and 55%, respectively, as the PLS level increased up to 8%. The surrounding media pH (4.6) was all similar. A decrease in bacterial numbers with the 12-6 formula and a significant reduction with 16-8 compared to the 0-0 formulation was observed. The eDNA concentrations in biofilms formed on 12-6 and 16-8 formulations were significantly less than the 0-0 control and 8-4 formulations. Doubling MCPM and PLS caused a 14 and 19% reduction in strength in 1 week, respectively. Average results were lower at 1 month and 1 year but affected less upon doubling MCPM and PLS levels. Moreover, a 4% PLS may help to reduce total biomass and glucan levels in biofilms on the above composites. Higher levels are required to reduce eDNA and provide bactericidal action, but these can decrease early strength.
随着汞合金的逐步淘汰以及微创牙科的兴起,对能够杀灭残留细菌并促进牙齿再矿化的高强度复合材料的需求日益增长。本研究量化了抗菌聚赖氨酸(PLS)和再矿化一水磷酸二氢钙(MCPM)如何影响生物膜以及牙科复合材料的强度。在抗菌研究中,MCPM - PLS填料百分比为复合材料填料相的0 - 0、8 - 4、12 - 6和16 - 8 wt%。将复合圆盘浸入含有(UA159)的0.1%蔗糖补充肉汤中,并在厌氧箱中孵育48小时。通过结晶紫(CV)染色测定表面生物量。在24小时和48小时测量生长培养基的pH值。对生物膜细菌活力(CFU)、胞外多糖(水溶性葡聚糖(WSG)和水不溶性葡聚糖(WIG))以及细胞外DNA(eDNA)进行定量。分别通过系列稀释平板计数、苯酚 - 硫酸微量测定法和荧光测定法进行。在水浸1周、1个月和1年后测定双轴弯曲强度。MCPM - PLS wt%为8 - 4、8 - 8、16 - 4和16 - 8。随着PLS水平增加至8%,归一化生物量、WSG和WIG分别呈线性下降,降幅为66%、64%和55%。周围培养基pH值(4.6)均相似。观察到12 - 6配方的细菌数量减少,与0 - 0配方相比,16 - 8配方的细菌数量显著减少。在12 - 6和16 - 8配方上形成的生物膜中的eDNA浓度显著低于0 - 0对照和8 - 4配方。将MCPM和PLS加倍分别导致1周时强度降低14%和19%。1个月和1年时的平均结果较低,但MCPM和PLS水平加倍时影响较小。此外,4%的PLS可能有助于降低上述复合材料上生物膜中的总生物量和葡聚糖水平。需要更高水平来降低eDNA并提供杀菌作用,但这些会降低早期强度。