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Inhibiting Bacterial Adhesion by Mechanically Modulated Microgel Coatings

机译:通过机械调制的微凝胶涂层抑制细菌粘附

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摘要

Bacterial infection is a severe problem especially when associated with biomedical applications. This study effectively demonstrates that poly-N-isopropylmethacrylamide based microgel coatings prevent bacterial adhesion. The coating preparation via a spraying approach proved to be simple and both cost and time efficient creating a homogeneous dense microgel monolayer. In particular, the influence of cross-linking density, microgel size, and coating thickness was investigated on the initial bacterial adhesion. Adhesion of Staphylococcus aureus ATCC 12600 was imaged using a parallel plate flow chamber setup, which gave insights in the number of the total bacteria adhering per unit area onto the surface and the initial bacterial deposition rates. All microgel coatings successfully yielded more than 98% bacterial adhesion. Bacterial adhesion depends both on the cross-linking density/stiffness of the microgels and on the thickness of the microgel coating. Bacterial adhesion decreased when a lower cross-linking density was used at equal coating thickness and at equal cross-linking density with a thicker microgel coating. The highest reduction in the number of bacterial adhesion was achieved with the microgel that produced the thickest coating (h = 602 nm) and had the lowest cross-linking density. The results provided in this paper indicate that microgel coatings serve as an interesting and easy applicable approach and that it can be fine-tuned by manipulating the microgel layer thickness and stiffness.
机译:细菌感染是一个严重的问题,尤其是与生物医学应用相关时。该研究有效地证明了聚-N-异丙基甲基丙烯酰胺基微凝胶涂层防止细菌粘附。通过喷涂方法的涂层制备证明是简单的,成本和时间效率,产生均匀的致密微凝胶单层。特别地,对初始细菌粘附研究了交联密度,微凝胶尺寸和涂层厚度的影响。使用平行板流量室设置成像金黄色葡萄球菌ATCC 12600的粘附,这使得每单位面积粘附在表面和初始细菌沉积速率上的总细菌的数量的洞察力。所有微凝胶涂层成功地产生了98%以上的细菌粘附。细菌粘附取决于微凝胶的交联密度/刚度和微凝胶涂层的厚度。当以相等的涂层厚度使用较低的交联密度和具有较厚的微凝胶涂层时的交联密度等于交联密度时,细菌粘附降低。通过产生厚涂层(H = 602nm)的微凝胶实现了细菌粘附数量的最高减少,并且具有最低的交联密度。本文提供的结果表明,微凝胶涂层用作有趣且易于适用的方法,并且可以通过操纵微凝胶层厚度和刚度来进行微调。

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  • 来源
    《Biomacromolecules》 |2019年第1期|共11页
  • 作者单位

    Univ Groningen Univ Med Ctr Groningen Dept Biomed Engn FB40 WJ Kolff Inst Biomed Engn &

    Mat Sci FB41 Antonius Deusinglaan 1 NL-9713 AV Groningen Netherlands;

    Univ Groningen Univ Med Ctr Groningen Dept Biomed Engn FB40 WJ Kolff Inst Biomed Engn &

    Mat Sci FB41 Antonius Deusinglaan 1 NL-9713 AV Groningen Netherlands;

    Univ Groningen Univ Med Ctr Groningen Dept Biomed Engn FB40 WJ Kolff Inst Biomed Engn &

    Mat Sci FB41 Antonius Deusinglaan 1 NL-9713 AV Groningen Netherlands;

    Univ Groningen Univ Med Ctr Groningen Dept Biomed Engn FB40 WJ Kolff Inst Biomed Engn &

    Mat Sci FB41 Antonius Deusinglaan 1 NL-9713 AV Groningen Netherlands;

    Univ Groningen Univ Med Ctr Groningen Dept Biomed Engn FB40 WJ Kolff Inst Biomed Engn &

    Mat Sci FB41 Antonius Deusinglaan 1 NL-9713 AV Groningen Netherlands;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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