Department of Restorative Dentistry, Dental Materials Division, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Department of Oral Diagnosis, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Sci Rep. 2021 Dec 10;11(1):23800. doi: 10.1038/s41598-021-03192-0.
The aim of this study was to evaluate the antimicrobial efficacy of non-thermal atmospheric plasma (NTAP) against Streptococcus mutans biofilms. Resin discs were fabricated, wet-polished, UV sterilized, and immersed in water for monomer extraction (37 °C, 24 h). Biofilms of bioluminescent S. mutans strain JM10 was grown on resin discs in anaerobic conditions for (37 °C, 24 h). Discs were divided into seven groups: control (CON), 2% chlorhexidine (CHX), only argon gas 150 s (ARG) and four NTAP treatments (30 s, 90 s, 120 s, 150 s). NTAP was applied using a plasma jet device. After treatment, biofilms were analyzed through the counting of viable colonies (CFU), bioluminescence assay (BL), scanning electron microscopy (SEM), and polymerase chain reaction (PCR). All NTAP-treated biofilm yielded a significant CFU reduction when compared to ARG and CON. BL values showed that NTAP treatment for 90 s, 120 s or 150 s resulted in statistically significantly lower metabolic activity when compared to the other groups. CHX displayed the lowest means of CFU and BL. SEM showed significant morphological changes in NTAP-treated biofilm. PCR indicated damage to the DNA structure after NTAP treatment. NTAP treatment was effective in lowering the viability and metabolism of S. mutans in a time-dependent manner, suggesting its use as an intraoral surface-decontamination strategy.
本研究旨在评估非热大气压等离子体(NTAP)对变形链球菌生物膜的抗菌效果。制备树脂圆盘,湿抛光,紫外线消毒,并将其浸入水中以提取单体(37°C,24 小时)。在厌氧条件下,生物发光变形链球菌 JM10 菌株的生物膜在树脂圆盘上生长(37°C,24 小时)。将圆盘分为七组:对照组(CON)、2%洗必泰(CHX)、仅氩气 150 秒(ARG)和四种 NTAP 处理(30 秒、90 秒、120 秒、150 秒)。使用等离子体射流装置进行 NTAP 处理。处理后,通过活菌计数(CFU)、生物发光测定(BL)、扫描电子显微镜(SEM)和聚合酶链反应(PCR)分析生物膜。与 ARG 和 CON 相比,所有 NTAP 处理的生物膜的 CFU 减少均具有统计学意义。BL 值表明,与其他组相比,NTAP 处理 90 秒、120 秒或 150 秒可导致代谢活性显著降低。CHX 显示出最低的 CFU 和 BL 平均值。SEM 显示 NTAP 处理后的生物膜发生了明显的形态变化。PCR 表明 NTAP 处理后 DNA 结构受损。NTAP 处理可有效降低变形链球菌的活力和代谢活性,呈时间依赖性,提示其可用作口腔内表面消毒策略。