牙胶粘剂对继发性龋齿厌氧菌生物膜形成的抑制作用

IF 0.5 Q4 ENGINEERING, BIOMEDICAL
Sroisiri Thaweboon, Takashi Saito, Boonyanit Thaweboon
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引用次数: 0

摘要

继发性龋齿是一种龋病,在充填物使用一段时间后,在现有修复体的边缘或旁边发现。它一般是由于修复后填充物中形成缺陷或裂缝引起的。这可以在材料和牙齿组织之间产生间隙,这将允许生物膜中的细菌进入界面。牙科粘合剂通常用于为复合水泥或填充材料提供固位。良好的粘接剂应能防止沿修复缘渗漏,并能抵抗咀嚼压力的机械负荷。近年来,将钙包合在胶黏剂单体中制成了Bio-Coat Ca,并对其对口腔细菌的抗菌性能进行了研究。没有发现关于厌氧菌的信息。本研究的目的是评估牙胶粘剂对继发性龋齿厌氧菌生物膜形成的抗菌潜力。将含有CMET(4-甲基丙烯氧基乙基三ellitic酸钙盐)和10-甲基丙烯氧基癸基二氢磷酸钙(MDCP) (Bio-Coat Ca, Sun Medical, Moriyama, Shiga, Japan)的粘合剂涂在唾液包被的96孔板的平底表面。然后在460 nm处用LED光聚合,紫外光消毒。制备牙龈卟啉单胞菌ATCC 33277、中间普雷沃氏菌ATCC 25611和核梭杆菌ATCC 25586为约1 × 10 8 CFU/mL的混悬液,加入孔中。在37°C的摇晃培养箱(120 r/min)中放置120分钟,以使细菌粘附。去除非贴壁细胞后,加入Schaedler肉液孵育48-72 h,使生物膜生长。每24 h更换一次培养基。在96孔板表面无黏合剂形成生物膜作为对照。使用WST微生物细胞计数试剂盒(Dojindo Molecular Technologies, USA)评估重要生物膜的数量。所有的测试都进行了三次,重复了三次。统计分析采用Mann-Whitney U检验。结果表明,牙胶粘剂对牙龈假单胞菌和核仁假单胞菌的抑菌率分别为56%和46%。另一方面,对中间芽孢杆菌无显著影响。这与我们之前关于原发性龋齿相关细菌的报道相似,Bio-Coat Ca粘合剂对变形链球菌的抗生物膜作用为65%,而对干酪乳杆菌和粘胶放线菌没有明显的抑制作用。提出了粘结剂的抑制作用是单体的酸性特性。这种新开发的胶粘剂是一种很有前途的预防继发性龋齿的材料。然而,本研究是在体外单种生物膜的形成上进行的,并且时间短。需要长期的临床研究来评估对患者的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of the Biofilm Formation of Anaerobic Bacteria Involved in Secondary Caries by Dental Adhesive
Secondary caries is a type of carious lesion found at the margins of or next to an existing restoration after the filling has been used for a period of time. It generally arises from the formation of defects or cracks in the filling material after restoration. This can create gaps between the material and the tooth tissue, which will allow bacteria in the biofilm to enter the interface. Dental adhesives are commonly used to provide retention for composite cement or filling materials. A good adhesive should be able to prevent leakage along the restoration margin as well as resist the mechanical load of chewing pressure. Recently, the inclusion of calcium in the adhesive monomer has been produced as Bio-Coat Ca, and its antimicrobial property against some oral bacteria has been studied. No information was found on anaerobes. The aim of this study was to evaluate the antimicrobial potential of dental adhesive on the biofilm formation of anaerobic bacteria involved in secondary caries. An adhesive containing CMET (calcium salt of 4-methacryloxyethyl trimellitic acid) and 10-methacryloyloxydecyl dihydrogen calcium phosphate (MDCP) (Bio-Coat Ca, Sun Medical, Moriyama, Shiga, Japan) was applied to the flat-bottom surface of the saliva-coated 96-well plate. Then it was polymerized with LED light at 460 nm and sterile with UV light. Porphyromonas gingivali s ATCC 33277, Prevotella intermedia ATCC 25611, and Fusobacterium nucleatum ATCC 25586 were prepared as a suspension of approximately 1 × 10 8 CFU/mL and added to the well. The plate was left for 120 min at 37°C in a shaking incubator (120 r/min) to allow bacterial adhesion. After removing non-adherent cells, Schaedler broth was added and further incubated for 48-72 h to grow the biofilm. The culture medium was changed every 24 h. A biofilm formed on a 96-well plate surface without the adhesive was set up as a control. The amount of vital biofilm was assessed by the WST Microbial Cell Counting Kit (Dojindo Molecular Technologies, USA). All tests were triplicated performed and repeated three times. As a statistical analysis, the Mann-Whitney U test was applied. The results showed that dental adhesive exhibited significant anti-biofilm formation of P. gingivalis and F. nucleatum at a percent inhibition of 56% and 46%, respectively. On the other hand, no significant effect was found on P. intermedia . This was similar to our previous report on bacteria associated with primary caries, which revealed that the anti-biofilm effect of Bio-Coat Ca adhesive on Streptococcus mutans was 65% while no significant suppressive action was observed Lactobacillus casei and Actinomyces viscosus . The inhibitory effect of the adhesive was proposed to be the acidic characteristic of the monomers. This newly developed adhesive could be a promising material for the prevention of secondary caries. However, this study was done on the single-species biofilm formation in vitro and conducted in a short time. Long-term clinical studies are needed to evaluate the effect on the patients.
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CiteScore
1.40
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14.30%
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