首页> 美国卫生研究院文献>Regenerative Biomaterials >Biomolecular functionalization for enhanced cell–material interactions of poly(methyl methacrylate) surfaces
【2h】

Biomolecular functionalization for enhanced cell–material interactions of poly(methyl methacrylate) surfaces

机译:生物分子功能化增强聚(甲基丙烯酸甲酯)表面的细胞-材料相互作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The integration of implants or medical devices into the body tissues requires of good cell–material interactions. However, most polymeric materials used for these applications lack on biological cues, which enhanced mid- and long-term implant failure due to weak integration with the surrounding tissue. Commonly used strategies for tissue–material integration focus on functionalization of the material surface by means of natural proteins or short peptides. However, the use of these biomolecules involves major drawbacks such as immunogenic problems and oversimplification of the constructs. Here, designed elastin-like recombinamers (ELRs) are used to enhance poly(methyl methacrylate) surface properties and compared against the use of short peptides. In this study, cell response has been analysed for different functionalization conditions in the presence and absence of a competing protein, which interferes on surface–cell interaction by unspecific adsorption on the interface. The study has shown that ELRs can induce higher rates of cell attachment and stronger cell anchorages than short peptides, being a better choice for surface functionalization.
机译:将植入物或医疗设备集成到人体组织中需要良好的细胞-材料相互作用。然而,用于这些应用的大多数聚合物材料缺乏生物学线索,由于与周围组织的整合较弱,生物线索增加了中长期植入失败。组织-材料整合的常用策略集中于通过天然蛋白质或短肽对材料表面进行功能化。然而,这些生物分子的使用涉及主要缺点,例如免疫原性问题和构建体的过度简化。在这里,设计的弹性蛋白样重组子(ELR)用于增强聚(甲基丙烯酸甲酯)表面性能,并与使用短肽进行比较。在这项研究中,已经分析了在存在和不存在竞争性蛋白质的情况下针对不同功能化条件的细胞反应,该蛋白质通过界面上的非特异性吸附来干扰表面-细胞相互作用。研究表明,与短肽相比,ELRs可以诱导更高的细胞附着率和更强的细胞锚定性,是表面功能化的更好选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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