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In vitro efficacy of cold atmospheric pressure plasma on S. sanguinis biofilms in comparison of two test models

机译:比较两个测试模型的冷大气压血浆对血红球菌生物膜的体外功效

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摘要

Dental plaque critically affects the etiology of caries, periodontitis and periimplantitis. The mechanical removal of plaque can only be performed partially due to limited accessibility. Therefore, plaque still represents one of the major therapeutic challenges. Even though antiseptic mouth rinses reduce the extent of biofilm temporarily, plaque removal remains incomplete and continuous usage can even result in side effects. Here we tested argon plasma produced by kinpen09 as one option to inactivate microorganisms and to eliminate plaque. S. sanguinis biofilms cultivated in either the European Biofilm Reactor (EUREBI) or in 24 well plates were treated with argon plasma. In both test systems a homogeneous, good analyzable and stable biofilm was produced on the surface of titan plates within 72 h (>6,9 log10 CFU/ml). Despite the significantly more powerful biofilm production in EUREBI, the difference of 0.4 log10 CFU/ml between EUREBI and the 24 well plates was practically not relevant. For that reason both test models were equally qualified for the analysis of efficacy of cold atmospheric pressure plasma. We demonstrate a significant reduction of the biofilm compared to the control in both test models. After plasma application of 180 s the biofilm produced in EUREBI or in 24 well plates was decreased by 0.6 log10 CFU/ml or 0.5 log10 CFU/ml, respectively. In comparison to recently published studies analyzing the efficacy of kinpen09, S. sanguinis produces a hardly removable biofilm. Future investigations using reduced distances between plasma source and biofilm, various compositions of plasma and alternative plasma sources will contribute to further optimization of the efficacy against S. sanguinis biofilms.
机译:牙菌斑严重影响龋齿,牙周炎和种植体周炎的病因。由于可及性有限,只能部分地机械去除牙菌斑。因此,斑块仍然代表着主要的治疗挑战之一。即使抗菌漱口液暂时减少了生物膜的覆盖范围,但菌斑清除仍不完全,连续使用甚至可能导致副作用。在这里,我们测试了kinpen09产生的氩等离子体,作为灭活微生物和消除斑块的一种选择。在欧洲生物膜反应器(EUREBI)或24孔板中培养的S. sanguinis生物膜用氩等离子体处理。在这两个测试系统中,在72小时内(> 6,9 log10 CFU / ml),在钛板表面上均质,可分析且稳定的生物膜形成。尽管在EUREBI中生物膜的生产能力大大增强,但EUREBI与24孔板之间的差异仅为0.4 log10 CFU / ml。因此,两个测试模型均具有分析冷大气压等离子体功效的资格。在两个测试模型中,我们都证明了与对照相比生物膜的显着减少。血浆施加180 s后,EUREBI或24孔板中产生的生物膜分别降低了0.6 log10 CFU / ml或0.5 log10 CFU / ml。与最近发表的分析kinpen09功效的研究相比,血红链球菌产生难以去除的生物膜。使用减少的血浆源和生物膜之间的距离,血浆的各种组成以及替代血浆源的未来研究将有助于进一步优化针对血红链球菌生物膜的功效。

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