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Molecular Engineering of Supramolecular Scaffold Coatings that Can Reduce Static Platelet Adhesion

机译:可以减少静态血小板粘附的超分子支架涂层的分子工程

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Novel supramolecular coatings that make use of low-molecular weight ditopic monomers with guanine end groups are studied using fluid tapping AFM. These molecules assemble on highly oriented pyrolytic graphite (HOPG) from aqueous solutions to form nanosized banding structures whose sizes can be systematically tuned at the nanoscale by tailoring the molecular structure of the monomers. The nature of the self-assembly in these systems has been studied through a combination of the self-assembly of structural derivatives and molecular modeling. Furthermore, we introduce the concept of using these molecular assemblies as scaffolds to organize functional groups on the surface. As a first demonstration of this concept, scaffold monomers that contain a monomethyl triethyleneglycol branch were used to organize these "functional" units on a HOPG surface. These supramolecular grafted assemblies have been shown to be stable at biologically relevant temperatures and even have the ability to significantly reduce static platelet adhesion.
机译:使用流体攻丝AFM研究了利用具有鸟嘌呤端基的低分子量二位单体的新型超分子涂层。这些分子从水溶液在高度定向的热解石墨(HOPG)上组装,形成纳米级的带状结构,通过调整单体的分子结构,可以在纳米级系统地调节其大小。通过结合结构导数的自组装和分子建模,研究了这些系统中自组装的性质。此外,我们介绍了使用这些分子组件作为支架来组织表面官能团的概念。作为该概念的第一个证明,包含单甲基三乙二醇支链的支架单体被用于在HOPG表面上组织这些“功能”单元。这些超分子接枝组件已显示在生物学相关温度下稳定,甚至具有显着降低静态血小板粘附的能力。

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