Department of Endodontics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.
College of Stomatology, Shanghai Jiao Tong University, Shanghai 200011, China.
Scanning. 2021 Dec 20;2021:6400605. doi: 10.1155/2021/6400605. eCollection 2021.
To compare the effects of bleaching associated with Er:YAG and Nd:YAG laser on enamel structure and mixed biofilm formation on teeth surfaces.
Sixty-eight enamel samples were randomly divided into four groups ( = 17), control, Opalescence Boost only, Opalescence Boost plus Er: YAG laser, and Opalescence Boost plus Nd:YAG laser. The structure was observed using SEM after bleaching. Subsequently, the treated enamel samples were also cultured in suspensions of , , , and () for 24 and 48 h. Biofilm formation was quantified by crystal violet staining, and the structure was visualized by confocal laser scanning microscopy. The data were analyzed using the Kruskal-Wallis method.
The enamel structure significantly changed after bleaching. There was no obvious difference in the biofilm formation after 24 h; however, after 48 hours, the amount of biofilm increased significantly. Remarkably, the amount was significantly higher on enamel bleached only, however, there was no significant difference between samples bleached with Er:YAG or Nd:YAG laser compared to the control.
Bleaching only appeared to markedly promote biofilm formation after 48 h, and the biofilms on samples bleached with Er:YAG or Nd:YAG laser did not change significantly, showing that bleaching with Er:YAG or Nd:YAG laser can be safely applied in clinical practice.
比较 Er:YAG 和 Nd:YAG 激光联合漂白对牙釉质结构和混合生物膜在牙齿表面形成的影响。
将 68 个牙釉质样本随机分为 4 组(每组 17 个):对照组、仅使用 Opalescence Boost 漂白剂组、使用 Opalescence Boost 联合 Er:YAG 激光漂白组、使用 Opalescence Boost 联合 Nd:YAG 激光漂白组。漂白后用 SEM 观察结构。然后,将处理过的牙釉质样本也在浓度为 、 、 、和 ( )的悬浮液中培养 24 和 48 小时。用结晶紫染色定量生物膜形成,并用共聚焦激光扫描显微镜观察结构。使用 Kruskal-Wallis 方法分析数据。
漂白后牙釉质结构明显改变。24 小时后生物膜形成无明显差异;然而,48 小时后生物膜量显著增加。值得注意的是,仅漂白的牙釉质上的生物膜量明显更高,然而,与对照组相比,用 Er:YAG 或 Nd:YAG 激光漂白的样本之间没有显著差异。
仅漂白似乎在 48 小时后明显促进生物膜形成,而用 Er:YAG 或 Nd:YAG 激光漂白的样本中的生物膜没有明显变化,表明用 Er:YAG 或 Nd:YAG 激光漂白可以安全地应用于临床实践。