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纳米结构钛表面表现出对表皮葡萄球菌生物膜形成的顽固性。

Nanostructured titanium surfaces exhibit recalcitrance towards Staphylococcus epidermidis biofilm formation.

机构信息

School of Engineering, Newcastle University, Newcastle Upon Tyne, NE1 7RU, UK.

School of Oral and Dental Sciences, University of Bristol, Bristol, BS1 2LY, UK.

出版信息

Sci Rep. 2018 Jan 18;8(1):1071. doi: 10.1038/s41598-018-19484-x.

Abstract

Titanium-based implants are ubiquitous in the healthcare industries and often suffer from bacterial attachment which results in infections. An innovative method of reducing bacterial growth is to employ nanostructures on implant materials that cause contact-dependent cell death by mechanical rupture of bacterial cell membranes. To achieve this, we synthesized nanostructures with different architectures on titanium surfaces using hydrothermal treatment processes and then examined the growth of Staphylococcus epidermidis on these surfaces. The structure obtained after a two-hour hydrothermal treatment (referred to as spear-type) showed the least bacterial attachment at short times but over a period of 6 days tended to support the formation of thick biofilms. By contrast, the structure obtained after a three-hour hydrothermal treatment (referred to as pocket-type) was found to delay biofilm formation up to 6 days and killed 47% of the initially attached bacteria by penetrating or compressing the bacteria in between the network of intertwined nano-spears. The results point to the efficacy of pocket-type nanostructure in increasing the killing rate of individual bacteria and potentially delaying longer-term biofilm formation.

摘要

钛基植入物在医疗保健行业中无处不在,但经常会受到细菌附着的影响,从而导致感染。一种减少细菌生长的创新方法是在植入材料上采用纳米结构,通过机械破坏细菌细胞膜来导致接触依赖性细胞死亡。为了实现这一目标,我们使用水热处理工艺在钛表面合成了具有不同结构的纳米结构,然后研究了表皮葡萄球菌在这些表面上的生长情况。在两小时水热处理后获得的结构(称为矛头型)在短时间内显示出最少的细菌附着,但在 6 天的时间内,它倾向于支持厚生物膜的形成。相比之下,在三小时水热处理后获得的结构(称为口袋型)被发现可以延迟生物膜形成长达 6 天,并通过穿透或压缩网络中交织的纳米矛头之间的细菌来杀死 47%的初始附着细菌。结果表明,口袋型纳米结构在提高单个细菌的杀伤率和潜在地延迟长期生物膜形成方面具有有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a650/5773551/bc9c5657a52f/41598_2018_19484_Fig1_HTML.jpg

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