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三甲基硅烷等离子体涂层对表皮葡萄球菌生物膜的抑制作用。

Inhibition of Staphylococcus epidermidis biofilm by trimethylsilane plasma coating.

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, University of Missouri, Columbia, Missouri, USA.

出版信息

Antimicrob Agents Chemother. 2012 Nov;56(11):5923-37. doi: 10.1128/AAC.01739-12. Epub 2012 Sep 10.

Abstract

Biofilm formation on implantable medical devices is a major impediment to the treatment of nosocomial infections and promotes local progressive tissue destruction. Staphylococcus epidermidis infections are the leading cause of biofilm formation on indwelling devices. Bacteria in biofilms are highly resistant to antibiotic treatment, which in combination with the increasing prevalence of antibiotic resistance among human pathogens further complicates treatment of biofilm-related device infections. We have developed a novel plasma coating technology. Trimethylsilane (TMS) was used as a monomer to coat the surfaces of 316L stainless steel and grade 5 titanium alloy, which are widely used in implantable medical devices. The results of biofilm assays demonstrated that this TMS coating markedly decreased S. epidermidis biofilm formation by inhibiting the attachment of bacterial cells to the TMS-coated surfaces during the early phase of biofilm development. We also discovered that bacterial cells on the TMS-coated surfaces were more susceptible to antibiotic treatment than their counterparts in biofilms on uncoated surfaces. These findings suggested that TMS coating could result in a surface that is resistant to biofilm development and also in a bacterial community that is more sensitive to antibiotic therapy than typical biofilms.

摘要

生物膜在植入式医疗器械上的形成是治疗医院获得性感染的主要障碍,并促进局部进行性组织破坏。表皮葡萄球菌感染是留置装置生物膜形成的主要原因。生物膜中的细菌对抗生素治疗具有高度抗性,再加上人类病原体中抗生素耐药性的日益流行,进一步使生物膜相关器械感染的治疗复杂化。我们开发了一种新型的等离子体涂层技术。三甲基硅烷(TMS)被用作单体来涂覆广泛用于植入式医疗器械的 316L 不锈钢和 5 级钛合金的表面。生物膜测定的结果表明,这种 TMS 涂层通过抑制细菌细胞在生物膜早期发育阶段附着在 TMS 涂层表面上,显著降低了表皮葡萄球菌生物膜的形成。我们还发现,TMS 涂层表面上的细菌细胞比未涂层表面上生物膜中的细菌细胞对抗生素治疗更敏感。这些发现表明,TMS 涂层可以形成一种不易形成生物膜的表面,并且形成的细菌群落比典型的生物膜对抗生素治疗更敏感。

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