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Casein Phosphopeptide-Amorphous Calcium Phosphate Reduces Streptococcus mutans Biofilm Development on Glass Ionomer Cement and Disrupts Established Biofilms

机译:酪蛋白磷酸肽-无定形磷酸钙减少玻璃链离聚物水泥上变形链球菌生物膜的发展并破坏已建立的生物膜。

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摘要

Glass ionomer cements (GIC) are dental restorative materials that are suitable for modification to help prevent dental plaque (biofilm) formation. The aim of this study was to determine the effects of incorporating casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) into a GIC on the colonisation and establishment of Streptococcus mutans biofilms and the effects of aqueous CPP-ACP on established S mutans biofilms. S. mutans biofilms were either established in flow cells before a single ten min exposure to 1% w/v CPP-ACP treatment or cultured in static wells or flow cells with either GIC or GIC containing 3% w/w CPP-ACP as the substratum. The biofilms were then visualised using confocal laser scanning microscopy after BacLight LIVE/DEAD staining. A significant decrease in biovolume and average thickness of S. mutans biofilms was observed in both static and flow cell assays when 3% CPP-ACP was incorporated into the GIC substratum. A single ten min treatment with aqueous 1% CPP-ACP resulted in a 58% decrease in biofilm biomass and thickness of established S. mutans biofilms grown in a flow cell. The treatment also significantly altered the structure of these biofilms compared with controls. The incorporation of 3% CPP-ACP into GIC significantly reduced S. mutans biofilm development indicating another potential anticariogenic mechanism of this material. Additionally aqueous CPP-ACP disrupted established S. mutans biofilms. The use of CPP-ACP containing GIC combined with regular CPP-ACP treatment may lower S. mutans challenge.
机译:玻璃离聚物粘固剂(GIC)是牙齿修复材料,适用于改性以防止形成牙菌斑(生物膜)。这项研究的目的是确定将酪蛋白磷酸肽无定形磷酸钙(CPP-ACP)掺入GIC对变形链球菌生物膜的定殖和建立的影响以及水性CPP-ACP对已建立的变形链球菌生物膜的影响。变形链球菌生物膜要么在流通池中暴露于1%w / v CPP-ACP处理前十分钟,要么在静态孔或流通池中培养,其中GIC或含有3%w / w CPP-ACP的GIC作为流动膜。底层。 BacLight LIVE / DEAD染色后,使用共聚焦激光扫描显微镜观察生物膜。当将3%CPP-ACP掺入GIC基质中时,在静态和流通池分析中均观察到变形链球菌生物膜的生物体积和平均厚度显着降低。用1%CPP-ACP水溶液处理10分钟,导致生物膜生物量和在流通池中生长的变形链球菌生物膜厚度减少58%。与对照相比,该处理还显着改变了这些生物膜的结构。将3%CPP-ACP掺入GIC中可显着降低变形链球菌生物膜的发育,这表明该材料还有另一种潜在的抗龋齿机理。另外,水性CPP-ACP破坏了已建立的变形链球菌生物膜。结合使用GIC的CPP-ACP和常规CPP-ACP治疗可以降低变形链球菌的攻击。

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