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首页> 外文期刊>Journal of biomedical materials research, Part A >Bactericidal effect of photocatalytically‐active nanostructured TiO 2 2 surfaces on biofilms of the early oral colonizer, Streptococcus oralis Streptococcus oralis
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Bactericidal effect of photocatalytically‐active nanostructured TiO 2 2 surfaces on biofilms of the early oral colonizer, Streptococcus oralis Streptococcus oralis

机译:光催化 - 活性纳米结构TiO 2 2表面对早期口腔殖民症生物膜,链球菌的杀菌作用

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Abstract This study evaluated the photocatalytic bactericidal effect of nanostructured anatase‐rich titanium dioxide (TiO 2 ) on microbial biofilms. Commercially pure titanium discs were spin‐coated with photocatalytic TiO 2 nanoparticles (P25). Uncoated discs were used as control (CTRL). Half of the CTRL and half of the P25‐coated surfaces were coated with purified saliva (SAL) to give four different groups (CTRL, CTRL?+?SAL, P25 and P25?+?SAL). Streptococcus oralis were allowed to form biofilms on the discs for 18 h and non‐adherent cells were rinsed off. Bacterial viability was assessed at time 0 with Live/Dead BacLight staining and epifluorescence microscopy. The remaining discs were divided into a non‐UV group and UVA‐irradiated (+UV) group (irradiation time, 6 or 24 h). Thereafter, viability was assessed as above. Viability at time 0 was high and no dead cells were seen on any of the surfaces, even after 24 h, in the absence of UVA. However, after 24 h of exposure, the proportion of viable cells was reduced by 40% on the P25 discs compared to 0 and 6 h, and this effect was enhanced with a salivary pellicle. Members of mixed species biofilms differ in their susceptibility to the bactericidal effect of the surfaces tested and further investigations are needed to optimize the conditions. ? 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2321–2328, 2017.
机译:摘要本研究评估了纳米结构富含锐钛钛二氧化钛(TiO 2)对微生物生物膜的光催化杀伤作用。使用光催化TiO 2纳米颗粒(P25)旋涂商业纯钛盘。未涂覆的光盘用作对照(CTRL)。将CTRL的一半和P25涂覆的表面的一半涂覆有纯化的唾液(SAL),得到四个不同的基团(CTRL,CTRL?+α+α,P25和P25?+?SAL)。将链球菌在圆盘上形成生物膜,在圆盘上形成18小时,并将非粘附细胞冲洗。用活/死Bachlow染色和离荧光显微镜进行测定的细菌活力。将剩余的盘分为非UV组和UVA辐照(+ UV)组(照射时间,6或24小时)。此后,如上所述评估活力。在时间0的活力高,并且在没有UVA的情况下,即使在24小时后,任何表面都没有看到死细胞。然而,在暴露24小时后,与0和6小时相比,P24的活细胞比例降低了40%,并用唾液薄膜增强这种效果。混合物种生物膜的成员在其对所测试的表面的杀菌作用的易感性方面不同,并且需要进一步研究以优化条件。还2017年Wiley期刊,Inc。J生物密制A部分:105A:2321-2328,2017。

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