Department of Oral Microbiology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan.
J Dent Res. 2011 Jul;90(7):900-5. doi: 10.1177/0022034511402996. Epub 2011 Mar 29.
Oral biofilms such as dental plaque cause dental caries and periodontitis, as well as aspiration pneumonia and infectious endocarditis by translocation. Hence, the suppression of oral biofilm formation is an issue of considerable importance. Mechanical removal, disinfectants, inhibition of polysaccharide formation, and artificial sugar have been used for the reduction of oral biofilm. From the viewpoint of the inhibition of bacterial adherence, we investigated whether aqueous biocompatible 2-methacryloyloxyethyl phosphorylcholine (MPC)-polymer can reduce streptococcal colonization and biofilm formation. We examined the effects of MPC-polymer on streptococcal adherence to saliva-coated hydroxyapatite and oral epithelial cells, and the adherence of Fusobacterium nucleatum to streptococcal biofilm. MPC-polymer application markedly inhibited both the adherence and biofilm formation of Streptococcus mutans on saliva-coated hydroxyapatite and streptococcal adherence to oral epithelial cells, and reduced the adherence of F. nucleatum to streptococcal biofilms. A small-scale clinical trial revealed that mouthrinsing with MPC-polymer inhibited the increase of oral bacterial numbers, especially of S. mutans. These findings suggest that MPC-polymer is a potent inhibitor of bacterial adherence and biofilm development, and may be useful to prevent dental-plaque-related diseases. (UMIN Clinical Trial Registry UMIN000003471).
口腔生物膜(如牙菌斑)可导致龋齿和牙周炎,也可通过易位导致吸入性肺炎和感染性心内膜炎。因此,抑制口腔生物膜的形成是一个非常重要的问题。机械清除、消毒剂、抑制多糖形成和人工糖已被用于减少口腔生物膜。从抑制细菌黏附的角度出发,我们研究了水溶性生物相容的 2-甲基丙烯酰氧乙基磷酸胆碱(MPC)-聚合物是否可以减少链球菌的定植和生物膜形成。我们研究了 MPC 聚合物对链球菌黏附于唾液包被羟基磷灰石和口腔上皮细胞以及黏附于链球菌生物膜的产黑色素普雷沃菌的影响。MPC 聚合物的应用显著抑制了唾液包被羟基磷灰石上的变异链球菌黏附和生物膜形成,以及链球菌黏附于口腔上皮细胞,并减少了产黑色素普雷沃菌对链球菌生物膜的黏附。一项小规模临床试验表明,用 MPC 聚合物漱口可抑制口腔细菌数量的增加,特别是变形链球菌。这些发现表明,MPC 聚合物是一种有效的细菌黏附抑制剂和生物膜形成抑制剂,可能有助于预防与牙菌斑相关的疾病。(UMIN 临床研究注册 UMIN000003471)。