首页> 外文期刊>Journal of Applied Oral Science >Analysis by confocal laser scanning microscopy of the MDPB bactericidal effect on S. mutans biofilm CLSM analysis of MDPB bactericidal effect on biofilm
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Analysis by confocal laser scanning microscopy of the MDPB bactericidal effect on S. mutans biofilm CLSM analysis of MDPB bactericidal effect on biofilm

机译:通过共聚焦激光扫描显微镜分析对变形链球菌生物膜的MDPB杀菌作用CLSM分析对生物膜的MDPB杀菌作用

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Since bacteria remain in the dentin following caries removal, restorative materials with antibacterial properties are desirable to help maintaining the residual microorganisms inactive. The adhesive system Clearfil Protect Bond (PB) contains the antibacterial monomer 12-methacryloyloxydodecylpyridinium bromide (MDPB) in its primer, which has shown antimicrobial activity. However, its bactericidal effect against biofilm on the dentin has been little investigated. Objective: The aim of this study was to analyze by confocal laser scanning microscopy (CLSM) and viable bacteria counting (CFU) the MDPB bactericidal effect against S. mutans biofilm on the dentin surface. Material and methods: Bovine dentin surfaces were obtained and subjected to S. mutans biofilm formation in BHI broth supplemented with 1% (w/v) sucrose for 18 h. Samples were divided into three groups, according to the primer application (n=3): Clearfil Protect Bond (PB), Clearfil SE Bond, which does not contain MDPB, (SE) and saline (control group). After the biofilm formation, Live/ Dead stain was applied directly to the surface of each sample. Next, 10 μL of each primer were applied on the samples during 590 s for the real-time CLSM analysis. The experiment was conducted in triplicate. The primers and saline were also applied on the other dentin samples during 20, 90, 300 and 590 s (n=9 for each group and period evaluated) and the CFU were assessed by colonies counting. Results: The results of the CLSM showed that with the Se application, although non-viable bacteria were detected at 20 s, there was no increase in their count during 590 s. In contrast, after the PB application there was a gradual increase of non-viable bacteria over 590 s. Conclusions: The quantitative analysis demonstrated a significant decrease of S. mutans CFU at 90 s PB exposure and only after 300 s of Se application. Protect Bond showed an earlier antibacterial effect than Se Bond.
机译:由于去除龋齿后细菌保留在牙本质中,因此需要具有抗菌特性的修复材料来帮助保持残留的微生物失活。粘合剂体系Clearfil Protect Bond(PB)的底漆中包含抗菌单体12-甲基丙烯酰氧基十二烷基吡啶鎓溴化吡啶(MDPB),具有抗菌活性。然而,很少研究其对牙本质上的生物膜的杀菌作用。目的:本研究的目的是通过共聚焦激光扫描显微镜(CLSM)和活菌计数(CFU)分析针对牙本质表面变形链球菌生物膜的MDPB杀菌作用。材料和方法:获得牛牙本质表面,并在补充1%(w / v)蔗糖的BHI肉汤中进行变形链球菌生物膜形成18小时。根据引物应用(n = 3)将样品分为三组:Clearfil保护键(PB),Clearfil SE键(不含MDPB),(SE)和盐水(对照组)。生物膜形成后,将活/死染色剂直接施加到每个样品的表面。接下来,在590 s的时间内将10μL的每种引物应用于样品,以进行实时CLSM分析。实验一式三份进行。在20、90、300和590 s(每个组和评估的时期,n = 9)期间,还将引物和盐水涂在其他牙本质样品上,并通过菌落计数评估CFU。结果:CLSM的结果表明,使用Se后,尽管在20 s时发现了不活细菌,但在590 s内其计数没有增加。相反,PB施用后,超过590 s的非活细菌逐渐增加。结论:定量分析表明,在暴露90 s PB时以及仅在施用硒300 s后,变形链球菌CFU显着降低。 Protect Bond具有比Se Bond更早的抗菌作用。

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