Eliades G, Kakaboura A, Palaghias G
Research Center for Biomaterials, Athens, Greece.
Dent Mater. 1998 Jan;14(1):57-63. doi: 10.1016/s0109-5641(98)00010-4.
The aim of the study was to evaluate the extent of the acid-base reaction and F- release in Compoglass (Vivadent) and Dyract (Dentsply/DeTrey) restoratives.
For evaluation of the extent of the acid-base reaction, two groups of three specimens (7 mm x 5 mm x 1 mm) were prepared for each material. The first group was immersed in distilled water, while the second was kept in dark and dry conditions. Micro-MIR FTIR spectroscopy was used to determine the extent of the acid-base reaction on directly irradiated material surfaces immediately after irradiation and following water storage for 30 min, 3 d, 1, 2, 4, 8 and 12 wks. The in-depth extent of the acid-base reaction of the specimens stored in water for 4 weeks was studied by sequential spectra acquisition after removal of the uppermost 20, 70, 100, 240 and 400 microns layer by controlled grinding and 1 wk re-immersion in water of the 400 microns reduced specimens. For the F- release measurements, five disk-shaped specimens (10 mm x 1.5 mm) were prepared from each material and stored in distilled water. The amount of F- released for the storage periods reported above was measured using an ionometer with an F- electrode. Statistical analysis was performed by ANOVA, Scheffé's test and regression analysis.
Storage in water promoted the development of an acid-base reaction on directly irradiated surfaces which reached a saturation point after 4 weeks. Depth profiling of the 4 wk immersed specimens revealed high salt concentration at the uppermost 100 microns layer. Re-immersion in water for 1 week of the 400 microns reduced specimens increased the salt concentration again at the uppermost region. Statistically significant differences were found in the acid-base rates and the in-depth salt yields between the materials (p < 0.05). The fluoride release after a 1 week initial "bursting" period was stabilized below 2 mg l-1 (p > 0.05) in both products. No positive correlation was found between acid-base reaction and fluoride release.
The development of a carboxylate-rich surface layer on polyacid-modified composite restoratives after water storage may explain their lower wear resistance compared with resin composites. The dynamic nature of these surfaces may provide several advantages regarding their interaction potential with hard dental tissues and their anticariogenic properties, but also some disadvantages concerning the quality of the surface texture obtained.
本研究旨在评估Compoglass(Vivadent)和Dyract(Dentsply/DeTrey)修复材料中的酸碱反应程度及氟释放情况。
为评估酸碱反应程度,每种材料制备两组,每组三个样本(7毫米×5毫米×1毫米)。第一组样本浸入蒸馏水中,第二组置于黑暗干燥环境。使用显微傅里叶变换红外光谱仪(Micro-MIR FTIR)在辐照后及储存于水中30分钟、3天、1周、2周、4周、8周和12周后,测定直接辐照材料表面的酸碱反应程度。对于在水中储存4周的样本,通过控制研磨去除最上层20、70、100、240和400微米的层,并将400微米减薄后的样本重新浸入水中1周后,通过连续光谱采集研究酸碱反应的深度情况。对于氟释放测量,每种材料制备五个圆盘形样本(10毫米×1.5毫米)并储存于蒸馏水中。使用带氟电极的离子计测量上述储存期内释放的氟量。采用方差分析、谢弗检验和回归分析进行统计分析。
储存在水中促进了直接辐照表面酸碱反应的发展,4周后达到饱和点。对浸泡4周的样本进行深度分析显示,最上层100微米层盐浓度较高。400微米减薄后的样本重新浸入水中1周后,最上层区域的盐浓度再次增加。两种材料在酸碱反应速率和深度盐产量方面存在统计学显著差异(p<0.05)。两种产品在最初1周的“爆发”期后,氟释放稳定在2毫克/升以下(p>0.05)。酸碱反应与氟释放之间未发现正相关。
储水后聚酸改性复合修复材料上富含羧酸盐表面层的形成,可能解释了其与树脂复合材料相比耐磨性较低的原因。这些表面的动态性质可能在其与硬牙组织的相互作用潜力及其防龋性能方面提供一些优势,但在获得的表面纹理质量方面也存在一些劣势。