...
首页> 外文期刊>Advanced Functional Materials >Patterned Hydrogels for Controlled Platelet Adhesion from Whole Blood and Plasma
【24h】

Patterned Hydrogels for Controlled Platelet Adhesion from Whole Blood and Plasma

机译:用于控制全血和血浆中血小板粘附的图案化水凝胶

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

This work describes the preparation and properties of hydrogel surface chemistries enabling controlled and well-defined cell adhesion. The hydrogels may be prepared directly on plastic substrates, such as polystyrene slides or dishes, using a quick and experimentally simple photopolymerization process, compatible with photolithographic and microfluidic patterning methods. The intended application for these materials is as substrates for diagnostic cell adhesion assays, particularly for the analysis of human platelet function. The non-specific adsorption of fibrinogen, a platelet adhesion promoting protein, is shown to be completely inhibited by the hydrogel, provided that the film thickness is sufficient (>5 nm). This allows the hydrogel to be used as a matrix for presenting selected bioactive ligands without risking interference from non-specifically adsorbed platelet adhesion factors, even in undiluted whole blood and blood plasma. This concept is demonstrated by preparing patterns of proteins on hydrogel surfaces, resulting in highly controlled platelet adhesion. Further insights into the protein immobilization and platelet adhesion processes are provided by studies using imaging surface plasmon resonance. The hydrogel surfaces used in this work appear to provide an ideal platform for cell adhesion studies of platelets, and potentially also for other cell types.
机译:这项工作描述了水凝胶表面化学的制备和性质,可控制和明确定义细胞粘附。可以使用与光刻和微流体图案化方法兼容的快速和实验上简单的光致聚合工艺,直接在塑料基材(例如聚苯乙烯玻片或培养皿)上制备水凝胶。这些材料的预期用途是用作诊断性细胞粘附测定的底物,尤其是用于分析人体血小板功能的底物。如果膜厚足够(> 5 nm),则表明水凝胶可完全抑制纤维蛋白原(一种血小板粘附促进蛋白)的非特异性吸附。这使得水凝胶可用作呈现选定的生物活性配体的基质,即使在未稀释的全血和血浆中也不会受到非特异性吸附的血小板粘附因子的干扰。通过在水凝胶表面上制备蛋白质图案来证明这一概念,从而可以高度控制血小板的粘附。通过使用成像表面等离振子共振的研究,提供了对蛋白质固定和血小板粘附过程的进一步了解。在这项工作中使用的水凝胶表面似乎为血小板的细胞粘附研究提供了理想的平台,并且还可能为其他细胞类型提供了理想的平台。

著录项

  • 来源
    《Advanced Functional Materials》 |2010年第15期|P.2396-2403|共8页
  • 作者单位

    Division of Molecular Physics Department of Physics, Chemistry and Biology Linkoeping University, SE-581 83 Linkoeping (Sweden);

    rnDivision of Clinical Chemistry Department of Clinical and Experimental Medicine Linkoeping University, SE-581 85 Linkoeping (Sweden);

    rnDivision of Molecular Physics Department of Physics, Chemistry and Biology Linkoeping University, SE-581 83 Linkoeping (Sweden);

    rnDivision of Molecular Physics Department of Physics, Chemistry and Biology Linkoeping University, SE-581 83 Linkoeping (Sweden);

    rnDivision of Molecular Physics Department of Physics, Chemistry and Biology Linkoeping University, SE-581 83 Linkoeping (Sweden);

    rnDivision of Clinical Chemistry Department of Clinical and Experimental Medicine Linkoeping University, SE-581 85 Linkoeping (Sweden);

    rnDivision of Molecular Physics Department of Physics, Chemistry and Biology Linkoeping University, SE-581 83 Linkoeping (Sweden);

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号