Soares Diana Gabriela, Sacono Nancy Tomoko, Ribeiro Ana Paula Dias, Basso Fernanda Gonçalves, Scheffel Débora Sales, Hebling Josimeri, Costa Carlos Alberto de Souza
J Adhes Dent. 2015 Apr;17(2):155-61. doi: 10.3290/j.jad.a33892.
To assess the cytotoxicity of 35% hydrogen peroxide (HP) bleaching gel applied for 15 min to sound or restored teeth with two-step self-etching adhesive systems and composite resin.
Sound and restored enamel/dentin disks were stored in water for 24 h or 6 months + thermocycling. The disks were adapted to artificial pulp chambers and placed in compartments containing culture medium. Immediately after bleaching, the culture medium in contact with dentin was applied for 1 h to previously cultured odontoblast-like MDPC-23 cells. Thereafter, cell viability (MTT assay) and morphology (SEM) were assessed. Data were analyzed by two-way ANOVA and Tukey's test (a = 5%).
In comparison to the negative control group (no treatment), no significant cell viability reduction occurred in those groups in which sound teeth were bleached. However, a significant decrease in cell viability was observed in the adhesive-restored bleached groups compared to negative control. No significant difference among bleached groups was observed with respect to the presence of restoration and storage time.
The application of 35% HP bleaching gel to sound teeth for 15 min does not cause toxic effects in pulp cells. When this bleaching protocol was performed in adhesive-restored teeth, a significant toxic effect occurred.
评估用两步自酸蚀粘结系统和复合树脂对健康牙或修复牙应用35%过氧化氢(HP)漂白凝胶15分钟后的细胞毒性。
将健康的和修复后的釉质/牙本质圆盘在水中储存24小时或6个月并进行热循环处理。将圆盘适配于人工牙髓腔,并置于含有培养基的隔室中。漂白后,立即将与牙本质接触的培养基应用于先前培养的成牙本质细胞样MDPC-23细胞1小时。此后,评估细胞活力(MTT法)和形态(扫描电子显微镜)。数据通过双向方差分析和Tukey检验进行分析(α = 5%)。
与阴性对照组(未处理)相比,健康牙齿漂白的组中未出现明显的细胞活力降低。然而,与阴性对照组相比,粘结修复漂白组的细胞活力显著降低。在漂白组之间,关于修复的存在和储存时间未观察到显著差异。
对健康牙齿应用35% HP漂白凝胶15分钟不会对牙髓细胞产生毒性作用。当在粘结修复的牙齿上进行这种漂白方案时,会出现显著的毒性作用。