Division of Biomaterials and Tissue Engineering, UCL Eastman Dental Institute, University College London, London, UK.
Department of Conservative Dentistry, College of Dentistry, University of Baghdad, Baghdad, Iraq.
Int Endod J. 2018 Jun;51(6):649-662. doi: 10.1111/iej.12880. Epub 2017 Dec 16.
To investigate in situ Enterococcus faecalis biofilm removal from the lateral canal of a simulated root canal system using passive or active irrigation protocols.
Root canal models (n = 43) were manufactured from transparent resin materials using 3D printing. Each canal was created with an 18 mm length, apical size 30, a .06 taper and a lateral canal of 3 mm length, with 0.3 mm diameter. Biofilms were grown in the lateral canal and apical 3 mm of the main canal for 10 days. Three models from each group were examined for residual biofilm using SEM. The other forty models were divided into four groups (n = 10). The models were observed under a fluorescence microscope. Following 60 s of 9 mL of 2.5% NaOCl irrigation using syringe and needle, the irrigant was either left stagnant in the canal or activated using gutta-percha, sonic or ultrasonic methods for 30 s. Images were then captured every second using an external camera. The residual biofilm percentages were measured using image analysis software. The data were analysed using generalized linear mixed models. A significance level of 0.05 was used throughout.
The greatest level of biofilm removal was obtained with ultrasonic agitation (66.76%) followed by sonic (45.49%), manual agitation (43.97%) and passive irrigation groups (38.67%), respectively. The differences were significant between the residual biofilm in the passive irrigation and both sonic and ultrasonic groups (P = 0.001).
Agitation resulted in better penetration of 2.5% NaOCl into the lateral canal of an artificial root canal model. Ultrasonic agitation of NaOCl improved the removal of biofilm.
采用被动或主动冲洗方案,从模拟根管系统的侧支通道中清除原位粪肠球菌生物膜。
使用 3D 打印技术从透明树脂材料中制造根管模型(n=43)。每个通道的长度为 18mm,根尖大小为 30,锥度为 0.06,侧支通道长度为 3mm,直径为 0.3mm。在侧支通道和主通道的根尖 3mm 处培养生物膜 10 天。每组三个模型通过 SEM 检查残留生物膜。其余四十个模型分为四组(n=10)。使用荧光显微镜观察模型。用注射器和针头冲洗 9mL 2.5%次氯酸钠 60s 后,将冲洗液留在管内或使用牙胶、超声或超声方法激活 30s。然后使用外部摄像头每秒拍摄一张图像。使用图像分析软件测量残留生物膜的百分比。使用广义线性混合模型分析数据。整个过程的显著性水平为 0.05。
超声震荡(66.76%)后生物膜清除率最高,其次是超声震荡(45.49%)、手动震荡(43.97%)和被动冲洗组(38.67%)。被动冲洗组与超声和超声组的残留生物膜差异有统计学意义(P=0.001)。
震荡导致 2.5%次氯酸钠更好地渗透到人工根管模型的侧支通道中。次氯酸钠的超声震荡有助于清除生物膜。