Khalichi P, Cvitkovitch D G, Santerre J P
Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ont., Canada M5S 3G9.
Biomaterials. 2004 Nov;25(24):5467-72. doi: 10.1016/j.biomaterials.2003.12.056.
Hydrolytic degradation by-products associated with the constitutive monomers 2,2-bis [4-(2-hydroxy-3-methacryloxypropoxy) phenyl] propane (bis-GMA), bisphenol A polyethylene glycol diether dimethacrylate (bis-EMA), and triethylene glycol dimethacrylate (TEDGMA) used in dental restorative composites include bis-hydroxy-propoxyphenyl propane (bis-HPPP), ethoxylated bisphenol A (E-bisPA), methacrylic acid (MA), and triethylene glycol (TEG). These products are generated from the interaction of human salivary esterases with the composites. Recent findings have indicated that TEGDMA has the ability to modulate oral bacteria but it is unclear which components of TEGDMA are related to the observed effects. The objective of the current study was to investigate the influence of TEGDMA derived degradation products MA and TEG on the growth of three strains of oral bacteria: S. mutans strains NG8 and JH1005, and S. salivarius AT2. Bacterial growth rates were measured at 37 degrees C, and pH values of 5.5 (representative of cariogenic state) or 7.0 at concentrations of 0-50mmol/l for MA (Sigma, US) and 0-100mmol/l for TEG (Sigma, US). It was found that at pH 5.5 TEG significantly stimulated the growth of both S. mutans strains ( p<0.05 ) in the concentration range of 0.5-10.0mmol/l and stimulated the growth of S. salivarius AT2 for the entire concentration range tested (p<0.05). TEG (above 50mmol/1) did not significantly affect the doubling times of S. salivarius at pH of 7.0 and it inhibited the growth of both S. mutans strains above 50mmol/l at the same pH value. At pH 5.5 MA inhibited the growth of all three strains with increasing concentration. At neutral pH, the growth of S. mutans NG8 strain was significantly reduced by MA ( p<0.05 ) above 10mmol/l. In summary, these results indicate that TEG and MA modulate the growth rate of important oral bacteria in a concentration and pH dependent manner.
牙科修复复合材料中使用的组成单体2,2-双[4-(2-羟基-3-甲基丙烯酰氧基丙氧基)苯基]丙烷(双酚A甘油醚甲基丙烯酸酯,bis-GMA)、双酚A聚乙二醇二醚二甲基丙烯酸酯(双酚A乙氧基化二甲基丙烯酸酯,bis-EMA)和三乙二醇二甲基丙烯酸酯(TEDGMA)的水解降解副产物包括双羟基丙氧基苯基丙烷(bis-HPPP)、乙氧基化双酚A(E-bisPA)、甲基丙烯酸(MA)和三乙二醇(TEG)。这些产物是人体唾液酯酶与复合材料相互作用产生的。最近的研究结果表明,TEGDMA有调节口腔细菌的能力,但尚不清楚TEGDMA的哪些成分与观察到的效果有关。本研究的目的是研究TEGDMA衍生的降解产物MA和TEG对三种口腔细菌菌株生长的影响:变形链球菌菌株NG8和JH1005,以及唾液链球菌AT2。在37℃下测量细菌生长速率,MA(美国Sigma公司)浓度为0-50mmol/L、TEG(美国Sigma公司)浓度为0-100mmol/L时,pH值为5.5(代表致龋状态)或7.0。结果发现,在pH 5.5时,TEG在0.5-10.0mmol/L浓度范围内显著刺激两种变形链球菌菌株的生长(p<0.05),并在整个测试浓度范围内刺激唾液链球菌AT2的生长(p<0.05)。在pH 7.0时,TEG(高于50mmol/L)对唾液链球菌的倍增时间没有显著影响,在相同pH值下,高于50mmol/L时,它抑制两种变形链球菌菌株的生长。在pH 5.5时,MA随着浓度增加抑制所有三种菌株的生长。在中性pH值下,MA在高于10mmol/L时显著降低变形链球菌NG8菌株的生长(p<0.05)。总之,这些结果表明,TEG和MA以浓度和pH值依赖的方式调节重要口腔细菌菌株的生长速率。