Soares Diana Gabriela, Ribeiro Ana Paula Dias, da Silveira Vargas Fernanda, Hebling Josimeri, de Souza Costa Carlos Alberto
Department of Dental Materials and Prosthodontics, Araraquara School of Dentistry, Univ. Estadual Paulista-UNESP, Rua Humaitá Street 1680, 14801-903, Araraquara, SP, Brazil.
Clin Oral Investig. 2013 Nov;17(8):1901-9. doi: 10.1007/s00784-012-0883-1. Epub 2012 Dec 6.
This study aimed to evaluate and correlate the efficacy and cytotoxicity of a 35 % hydrogen peroxide (HP) bleaching gel after different application times on dental enamel.
Enamel/dentin disks in artificial pulp chambers were placed in wells containing culture medium. The following groups were formed: G1, control (no bleaching); G2 and G3, three or one 15-min bleaching applications, respectively; and G4 and G5, three or one 5-min bleaching applications, respectively. Extracts (culture medium with bleaching gel components) were applied for 60 min on cultured odontoblast-like MDPC-23 cells. Cell metabolism (methyl tetrazolium assay) (Kruskal-Wallis/Mann-Whitney; α = 5 %) and cell morphology (scanning electron microscopy) were analyzed immediately after the bleaching procedures and the trans-enamel and trans-dentinal HP diffusion quantified (one-way analysis of variance/Tukey's test; α = 5 %). The alkaline phosphatase (ALP) activity was evaluated 24 h after the contact time of the extracts with the cells (Kruskal-Wallis/Mann-Whitney; α = 5 %). Tooth color was analyzed before and 24 h after bleaching using a spectrophotometer according to the Commission Internationale de l'Eclairage Lab* system (Kruskal-Wallis/Mann-Whitney; α = 0.05).
Significant difference (p < 0.05) in cell metabolism occurred only between G1 (control, 100 %) and G2 (60.6 %). A significant decrease (p < 0.05) in ALP activity was observed between G2, G3, and G4 in comparison with G1. Alterations on cell morphology were observed in all bleached groups. The highest values of HP diffusion and color alterations were observed for G2, with significant difference among all experimental groups (p < 0.05). G3 and G4 presented intermediate color change and HP diffusion values with no statistically significant differences between them (p > 0.05). The lowest amount of HP diffusion was observed in G5 (p < 0.05), which also exhibited no significant color alteration compared to the control group (p > 0.05).
HP diffusion through dental tissues and its cytotoxic effects were proportional to the contact time of the bleaching gel with enamel. However, shorter bleaching times reduced bleaching efficacy.
Shortening the in-office tooth bleaching time could be an alternative to minimize the cytotoxic effects of this clinical procedure to pulp tissue. However, the reduced time of bleaching agent application on enamel may not provide adequate esthetic outcome.
本研究旨在评估35%过氧化氢(HP)漂白凝胶在不同作用时间对牙釉质的疗效及细胞毒性,并进行相关性分析。
将人工牙髓腔中的釉质/牙本质盘置于含有培养基的孔中。分组如下:G1为对照组(未漂白);G2和G3分别为进行3次或1次15分钟的漂白处理;G4和G5分别为进行3次或1次5分钟的漂白处理。将提取物(含漂白凝胶成分的培养基)作用于培养的成牙本质细胞样MDPC - 23细胞60分钟。在漂白程序结束后立即分析细胞代谢(甲基四氮唑法)(Kruskal - Wallis/Mann - Whitney检验;α = 5%)和细胞形态(扫描电子显微镜),并对釉质和牙本质中HP的扩散进行定量分析(单因素方差分析/Tukey检验;α = 5%)。在提取物与细胞接触24小时后评估碱性磷酸酶(ALP)活性(Kruskal - Wallis/Mann - Whitney检验;α = 5%)。使用分光光度计根据国际照明委员会Lab*系统在漂白前和漂白24小时后分析牙齿颜色(Kruskal - Wallis/Mann - Whitney检验;α = 0.05)。
仅在G1(对照组,100%)和G2(60.6%)之间细胞代谢存在显著差异(p < 0.05)。与G1相比,G2、G3和G4的ALP活性显著降低(p < 0.05)。在所有漂白组中均观察到细胞形态改变。G2的HP扩散和颜色改变值最高,所有实验组之间存在显著差异(p < 0.05)。G3和G4呈现中等程度的颜色变化和HP扩散值,两者之间无统计学显著差异(p > 0.05)。G5中观察到的HP扩散量最低(p < 0.05),与对照组相比其颜色改变也无显著差异(p > 0.05)。
HP通过牙体组织的扩散及其细胞毒性作用与漂白凝胶与釉质的接触时间成正比。然而,较短的漂白时间会降低漂白效果。
缩短诊室牙齿漂白时间可能是将该临床操作对牙髓组织细胞毒性降至最低的一种替代方法。然而,漂白剂在釉质上作用时间的缩短可能无法提供足够的美学效果。