Universidad de Chile, Facultad de Odontología, Departamento de Odontología Restauradora, Santiago, Chile.
Universidade Estadual Paulista - UNESP, Faculdade de Odontologia, Departmento de Odontologia Restauradora, Araraquara, Brazil.
J Appl Oral Sci. 2017 Mar-Apr;25(2):177-185. doi: 10.1590/1678-77572016-0209.
To prepare nanocomposite cements based on the incorporation of bioactive glass nanoparticles (nBGs) into BiodentineTM (BD, Septodent, Saint-Maur-des-Fosses Cedex, France) and to assess their bioactive properties.
nBGs were synthesised by the sol-gel method. BD nanocomposites (nBG/BD) were prepared with 1 and 2% nBGs by weight; unmodified BD and GC Fuji IX (GIC, GC Corporation, Tokyo, Japan) were used as references. The in vitro ability of the materials to induce apatite formation was assessed in SBF by X-ray diffraction (XRD), attenuated total reflectance with Fourier transform infrared spectroscopy (ATR-FTIR), and scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis. BD and nBG/BD were also applied to dentine discs for seven days; the morphology and elemental composition of the dentine-cement interface were analysed using SEM-EDX.
One and two percent nBG/BD composites accelerated apatite formation on the disc surface after short-term immersion in SBF. Apatite was detected on the nBG/BD nanocomposites after three days, compared with seven days for unmodified BD. No apatite formation was detected on the GIC surface. nBG/BD formed a wider interfacial area with dentine than BD, showing blockage of dentine tubules and Si incorporation, suggesting intratubular precipitation.
The incorporation of nBGs into BD improves its in vitro bioactivity, accelerating the formation of a crystalline apatite layer on its surface after immersion in SBF. Compared with unmodified BD, nBG/BD showed a wider interfacial area with greater Si incorporation and intratubular precipitation of deposits when immersed in SBF.
将生物活性玻璃纳米颗粒(nBGs)掺入 BiodentineTM(BD,法国圣莫里斯德福斯塞克德)中制备纳米复合材料,并评估其生物活性。
采用溶胶-凝胶法合成 nBGs。通过重量比将 1%和 2%的 nBGs 掺入到 BD 中,制备 nBG/BD 纳米复合材料;未改性的 BD 和 GC Fuji IX(GC 公司,东京,日本)作为对照。通过 X 射线衍射(XRD)、衰减全反射傅里叶变换红外光谱(ATR-FTIR)和带有能量色散 X 射线(EDX)分析的扫描电子显微镜(SEM)评估材料在 SBF 中诱导磷灰石形成的体外能力。BD 和 nBG/BD 也应用于牙本质圆盘上 7 天;使用 SEM-EDX 分析牙本质-水泥界面的形态和元素组成。
在 SBF 短期浸泡后,1%和 2%nBG/BD 复合材料加速了圆盘表面的磷灰石形成。与未改性的 BD 相比,nBG/BD 纳米复合材料在 3 天后检测到磷灰石,而未改性的 BD 则在 7 天后检测到。GIC 表面未检测到磷灰石形成。nBG/BD 与牙本质形成的界面面积大于 BD,表明牙本质小管阻塞和 Si 掺入,提示管内沉淀。
将 nBGs 掺入 BD 可提高其体外生物活性,在 SBF 浸泡后加速其表面形成结晶磷灰石层。与未改性的 BD 相比,nBG/BD 在 SBF 浸泡时表现出更大的界面面积、更大的 Si 掺入和管内沉积物的沉淀。