Department of Operative Dentistry and Periodontology, Albert-Ludwigs-University, Hugstetter Strasse 55, Freiburg, Germany.
Arch Oral Biol. 2013 Sep;58(9):1139-47. doi: 10.1016/j.archoralbio.2013.04.011. Epub 2013 May 18.
Biofilm formation on implant materials plays a major role in the aetiology of periimplantitis. The aim of this study was to examine in vivo the initial bacterial adhesion on six different implant materials.
The implant materials Ti-m, TiUnite®, ZiUnite®, ATZ-m, ATZ-s, TZP-A-m were tested using bovine enamel slabs as controls. All materials, fixed on splint systems, were examined after 30 min and 120 min of oral exposure. DAPI staining was used for quantitative analysis of the initially adherent microorganisms. Initial adherent microorganisms were visualised by fluorescence In situ-hybridisation (FISH) and quantified by confocal laser scanning microscopy (CLSM). The targets of the oligonucleotide probes were Eubacteria, Veillonella spp., Fusobacterium nucleatum, Actinomyces naeslundii and Streptococcus spp.
DAPI analysis showed that increasing the time of oral exposure resulted in an increasing amount of initial adherent bacteria. The highest level of colonisation was on ZiUnite®, with the lowest occurring on the bovine enamel, followed by Ti-m. This early colonisation correlated significantly with the surface roughnesses of the materials. FISH and CLSM showed no significant differences relating to total bacterial composition. However, Streptococcus spp. was shown to be the main colonisers on each of the investigated materials.
it could be shown that within an oral exposure time of 30 min and 120 min, despite the salivary acquired pellicle initial biofilm formation is mainly influenced directly or indirect by the material surface topography. Highly polished surfaces should minimise the risk of biofilm formation, plaque accumulation and possibly periimplantitis.
种植体材料表面生物膜的形成是引发种植体周围炎的主要原因。本研究旨在体内检测六种不同种植体材料表面初始细菌黏附情况。
采用牛牙釉质片作为对照,检测 Ti-m、TiUnite®、ZiUnite®、ATZ-m、ATZ-s、TZP-A-m 种植体材料。所有材料均通过夹板系统固定,在口腔暴露 30min 和 120min 后进行检测。使用 DAPI 染色对初始黏附微生物进行定量分析。通过荧光原位杂交(FISH)对初始黏附微生物进行可视化观察,并通过共聚焦激光扫描显微镜(CLSM)进行定量。寡核苷酸探针的靶标为真细菌、韦荣球菌属、核梭杆菌、奈瑟氏放线菌和链球菌属。
DAPI 分析表明,口腔暴露时间的延长导致初始黏附细菌数量的增加。ZiUnite®的定植水平最高,牛牙釉质最低,其次是 Ti-m。这种早期定植与材料表面粗糙度显著相关。FISH 和 CLSM 显示,细菌总组成无显著差异。然而,链球菌属是每种被研究材料的主要定植菌。
在口腔暴露 30min 和 120min 内,尽管唾液获得了获得性薄膜,初始生物膜的形成主要直接或间接受到材料表面形貌的影响。高度抛光的表面应最大限度地降低生物膜形成、菌斑堆积和种植体周围炎的风险。