University of São Paulo School of Dentistry, Department of Biomaterials and Oral Biology, São Paulo, Brazil.
Santa Catarina State University, Department of Chemistry, Santa Catarina, Brazil.
Dent Mater. 2018 May;34(5):746-755. doi: 10.1016/j.dental.2018.01.026.
This study describes the synthesis of brushite nanoparticles (CaHPO·2HO) functionalized with triethylene glycol dimethacrylate (TEGDMA) and their application in dental restorative composites with remineralizing capabilities.
Nanoparticles were synthesized, with TEGDMA being added to one of the precursor solutions at three different molar ratios (0:1, 0.5:1 and 1:1, in relation to the ammonium phosphate precursor). Then, they were added (10 vol%) to a photocurable dimethacrylate matrix containing 50 vol% of reinforcing glass particles. The resulting composites were tested for degree of conversion, biaxial flexural strength and elastic modulus (after 24h and 28days in water), and ion release (over a 28-day period). Commercial composites (one microhybrid and one microfilled) were tested as controls.
The final TEGDMA content in the functionalizing layer was modulated by the molar ratio added to the precursor solution. Functionalization reduced nanoparticle size, but did not reduce agglomeration. Improved mechanical properties were found for the composite containing nanoparticles with higher TEGDMA level in comparison to the composite containing non-functionalized nanoparticles or those with a low TEGDMA level. All brushite composites presented statistically significant reductions in strength after 28 days in water, but only the material with high-TEGDMA nanoparticles retained strength similar to the microhybrid commercial control. Overall, ion release was not affected by functionalization and presented steady levels for 28 days.
Though agglomeration was not reduced by functionalization, the improvement in the matrix-nanoparticle interface allowed for a stronger material, without compromising its remineralizing potential.
本研究描述了三甘醇二甲基丙烯酸酯(TEGDMA)功能化 brushite 纳米粒子(CaHPO·2HO)的合成及其在具有再矿化能力的牙科修复复合材料中的应用。
合成了纳米粒子,在其中一种前体溶液中加入 TEGDMA,摩尔比分别为 0:1、0.5:1 和 1:1(相对于磷酸铵前体)。然后,将其(体积比为 10%)加入到含有 50%体积比增强玻璃颗粒的光固化二甲基丙烯酸酯基质中。对所得复合材料的转化率、双轴弯曲强度和弹性模量(在水中 24 小时和 28 天后)以及离子释放(28 天期间)进行测试。商业复合材料(一种微混合和一种微填充)作为对照进行测试。
功能化层中的最终 TEGDMA 含量可通过添加到前体溶液中的摩尔比进行调节。功能化降低了纳米粒子的尺寸,但没有减少团聚。与含有未功能化纳米粒子或 TEGDMA 水平较低的纳米粒子的复合材料相比,含有高 TEGDMA 水平的纳米粒子的复合材料的机械性能得到了改善。所有 brushite 复合材料在水中 28 天后的强度均显著降低,但只有含有高 TEGDMA 纳米粒子的材料保留了与商业微混合对照材料相似的强度。总体而言,功能化对离子释放没有影响,28 天内释放水平稳定。
尽管功能化没有减少团聚,但改善了基质-纳米粒子界面,使材料更坚固,同时不影响其再矿化能力。