Division of Operative Dentistry, Department of Ecological Dentistry, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8575, Japan.
Division of Molecular Biology and Oral Biochemistry, Department of Oral Science, Graduate School of Dentistry, Kanagawa Dental University, 82 Inaoka-cho, Yokosuka, Kanagawa, 238-8580, Japan.
Sci Rep. 2022 Mar 22;12(1):4897. doi: 10.1038/s41598-022-08963-x.
We investigated the biofilm removal effects of laser activated irrigation (LAI) using a pig model, focusing on the impact of the fiber tip position, and used a high-speed camera to observe the occurrence and positioning of the cavitation associated with laser irradiation. A total of 16 roots of deciduous mandibular second premolars from 4 pigs were used. After a pulpectomy, the canals were left open for 2 weeks and sealed for 4 weeks to induce intraradicular biofilm. Root canal irrigation was then performed with Er:YAG laser activation. The fiber tip was inserted at two different positions, i.e., into the root canal in the intracanal LAI group and into the pulp chamber in the coronal LAI group. Intracanal needle irrigation with saline or 5% NaOCl was utilized in the positive control and conventional needle irrigation (CNI) groups. SEM and qPCR were carried out to evaluate treatment efficacy. Statistical analysis was performed using ANOVA and a Tukey-Kramer post-hoc test for qPCR and with a Steel-Dwass test to compare the SEM scores, with α = 0.05. A high-speed camera was used to observe the generation of cavitation bubbles and the movement of the induced bubbles after laser irradiation. The intracanal and coronal LAI groups showed significantly lower amounts of bacteria than either the positive control or CNI groups. There was no significant difference found between the intracanal and coronal LAI groups. SEM images revealed opened dentinal tubules with the destruction of biofilm in both LAI groups. High-speed camera images demonstrated cavitation bubble production inside the root canal after a single pulse irradiation pulse. The generated bubbles moved throughout the entire internal multi-rooted tooth space. Coronal LAI can generate cavitation in the root canal with a simply placed fiber inside the pulp chamber, leading to effective biofilm removal. This method could thus contribute to the future development of endodontic treatments for refractory apical periodontitis caused by intraradicular biofilm.
我们使用猪模型研究了激光激活冲洗(LAI)的生物膜去除效果,重点研究了光纤尖端位置的影响,并使用高速摄像机观察与激光照射相关的空化的发生和定位。总共使用了 4 只猪的 16 颗下颌第二前磨牙的恒牙。在牙髓切除术之后,将根管开放 2 周并用封闭剂封闭 4 周以诱导根管内生物膜。然后用 Er:YAG 激光激活进行根管冲洗。光纤尖端插入两个不同的位置,即根管内的 LAI 组和牙髓室内的 LAI 组。在阳性对照组和常规针冲洗(CNI)组中,使用腔内针冲洗生理盐水或 5% NaOCl。用 SEM 和 qPCR 评价治疗效果。qPCR 采用 ANOVA 和 Tukey-Kramer 事后检验进行统计分析,SEM 评分采用 Steel-Dwass 检验进行比较,α=0.05。使用高速摄像机观察激光照射后空化气泡的产生和诱导气泡的运动。LAI 组的细菌数量明显低于阳性对照组或 CNI 组。LAI 组之间没有发现显著差异。SEM 图像显示 LAI 组的牙本质小管张开,生物膜被破坏。高速摄像机图像显示单次脉冲照射后根管内产生空化气泡。生成的气泡在整个内部多根牙间隙内移动。LAI 可在牙髓室内简单放置光纤的情况下在根管内产生空化,从而有效去除生物膜。因此,这种方法可能有助于未来开发针对根管内生物膜引起的难治性根尖周炎的根管治疗方法。