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Evaluation of dental adhesive systems incorporating an antibacterial monomer eugenyl methacrylate (EgMA) for endodontic restorations

机译:结合抗菌单体甲基丙烯酸烯丙酯(EgMA)进行牙髓修复的牙科胶粘剂系统评估

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摘要

Objective The purpose of this study was to incorporate EgMA, an antibacterial monomer into two commercial dental adhesive systems for their application in endodontic restoration with the aim to disinfect the root canal space before curing and to inhibit bacterial growth on their surfaces after being cured. Methods EgMA monomer was added at 20% wt. into the formulation of the single-component self-etch, Clearfil Universal Bond™ (CUB) and into the catalyst and the adhesive components of the total-etch Adper Scotchbond-multipurpose™ (SBMP) adhesive systems. The degree of conversion (DC) was calculated from FTIR spectra, glass transition temperature (Tg) determined by DSC, water sorption and solubility were measured gravimetrically, and surface free energy (SFE) via contact angle measurements. The bonding performance to coronal and middle root canal dentin was assessed through push-out bond strength after filling the canals with a composite core material and the surface integrity was observed using SEM and confocal laser scanning microscopy (CLSM). The standard agar diffusion test (ADT) was used to identify the sensitivity of three endodontically pathogenic bacteria, Enterococcus faecalis, Streptococcus mutans and Propionibacterium acnes to uncured EgMA modified adhesives. Multispecies biofilm model from these strains was grown on the disc surface of cured adhesives and investigated using quantitative microbial culture and CLSM with live/dead staining. MTT assay was also used to determine the cytotoxicity of these adhesives. Results The incorporation of EgMA lowered polymerization exotherm and enhanced the hydrophobic character of these adhesives, without changing the DC and Tg in comparison to the controls (without EgMA). The total push-out bond strengths of the EgMA-containing adhesives were not significantly different from those of the controls (p > 0.05). The modification of self-etch adhesive system enhanced the bond strength in the middle region of the roots canal. SEM of debonded specimens and CLSM examination showed the integrity of the resin-dentin interfaces. For all three bacteria tested, the sizes of the inhibition zones produced by uncured EgMA modified adhesives were significantly greater (p < 0.05) than those of the controls. The results of biofilm inhibition tests showed less CFU for total bacteria on bonding agents with EgMA compared to the control materials (p < 0.05). The modification at 20% monomer concentration had no adverse effects on cytocompatibility of both adhesives tested. Significance The inclusion of EgMA endows dental adhesives with effective antibacterial effects without influencing their curing properties, bonding ability to root canal dentin, and cytotoxicity against human gingival fibroblasts, indicating the usefulness of their application in endodontic restorations.
机译:目的这项研究的目的是将一种抗菌单体EgMA掺入两个商业牙科胶粘剂体系中,以用于牙髓修复,目的是在固化前对根管间隙进行消毒并在固化后抑制其表面的细菌生长。方法以20重量%添加EgMA单体。包括单组分自蚀刻Clearfil Universal Bond™(CUB)的配方,以及总蚀刻Adper Scotchbond-multipurpose™(SBMP)粘合剂系统的催化剂和粘合剂组分。由FTIR光谱计算转化度(DC),通过DSC测定玻璃化转变温度(Tg),通过重量分析法测量吸水率和溶解度,并通过接触角测量来测量表面自由能(SFE)。用复合芯材料填充管后,通过推出粘合强度评估与冠状和中根管牙本质的粘合性能,并使用SEM和共聚焦激光扫描显微镜(CLSM)观察表面完整性。使用标准琼脂扩散测试(ADT)来确定三种牙髓病原性细菌,粪肠球菌,变形链球菌和痤疮丙酸杆菌对未固化的EgMA改性粘合剂的敏感性。将来自这些菌株的多物种生物膜模型生长在固化粘合剂的圆盘表面上,并使用定量微生物培养和带活/死染色的CLSM进行研究。 MTT测定法还用于确定这些胶粘剂的细胞毒性。结果与对照(无EgMA)相比,EgMA的加入降低了聚合放热并增强了这些粘合剂的疏水特性,而没有改变DC和Tg。含EgMA的胶粘剂的总推出强度与对照组无显着差异(p> 0.05)。自蚀刻胶粘剂体系的改进增强了根管中间区域的粘结强度。脱粘试样的SEM和CLSM检查表明树脂-牙本质界面的完整性。对于所有测试的三种细菌,未固化的EgMA改性胶粘剂产生的抑制区的大小均明显大于对照组(p <0.05)。生物膜抑制测试的结果表明,与对照材料相比,使用EgMA的粘合剂对总细菌的CFU更少(p <0.05)。在单体浓度为20%时的改性对两种测试的粘合剂的细胞相容性均无不利影响。意义包含EgMA使牙科用粘合剂具有有效的抗菌效果,而不会影响其固化性能,与根管牙本质的粘合能力以及对人牙龈成纤维细胞的细胞毒性,表明它们在牙髓修复体中的用途。

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