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Nanostructured layers of adsorbed collagen: conditions, mechanisms and applications

机译:纳米结构层吸附胶原:病症,机制和应用

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The nanometer-scale organization of collagen (type I) adsorbed on polystyrene (PS) and plasma-oxidized PS (PSox) was investigated using atomic force microscopy (AFM) as well as radioassays and X-ray photoelectron spectroscopy. The surface properties induced by plasma treatment of PS were examined: PSox was more hydrophilic than PS, owing to oxygen incorporation, and was covered by a layer of polyelectrolyte which could be swollen by water. Collagen adsorbed on PS formed elongated structures, the density and the height of which increased with the adsorption duration. On PSox, a smooth and homogeneous collagen layer was formed after up to 2 h of adsorption, but elongated structures appeared after 24 h. A similar contrast was found between CH_3- and OH-terminated self-assembled monolayers, indicating the role of surface hydrophilicity. The adsorption duration affected the nanostructure of adsorbed collagen layers, not only through the adsorbed amount but also owing to reorganizations of the adsorbed phase. Compared with collagen adsorbed on PSox, collagen adsorbed on PS was more easily picked up for attachment to the AFM probe and more easily displaced along the surface plane by scanning with the atomic force microscope or by drying. This suggests that collagen molecules adsorbed on PS leave segments protruding into the solution, while they form a felt of lying molecules on PSox. The observed elongated structures may be due to association of collagen segments, and/or to particular interactions with the atomic force microscope probe. The respective importance of these two mechanisms may depend on the chemical nature of the substratum. Nanostructured collagen layers offer attractive perspectives to control mammalian cell response or as a template to create nanostructured polymer surfaces.
机译:使用原子力显微镜(AFM)以及放射性和X射线光电子能量,研究吸附在聚苯乙烯(PS)和血浆氧化PS(PSOx)上吸附的胶原型(Ⅰ型)组织。通过氧气掺入,研究了PS的等离子体处理诱导的PS对PS的处理诱导的表面特性,并且由于氧气掺入,PSOx比PS更亲水,并且由水晶硅电解质层覆盖,该电极可以被水溶胀。吸附在PS形成的细长结构的胶原,其密度和高度随吸附持续时间而增加。在PSOx上,在吸附高达2小时后形成光滑和均匀的胶原层,但是在24小时后出现细长的结构。在CH_3-和OH封端的自组装单层之间发现了类似的对比,表明表面亲水性的作用。吸附持续时间影响吸附的胶原层的纳米结构,不仅通过吸附量而且由于吸附相的重组。与吸附在PSOx上的胶原蛋白相比,更容易地拾取到PS上的胶原蛋白,以通过用原子力显微镜或通过干燥扫描沿着表面平面沿着表面平面容易地置换。这表明吸附在PS离开段突出到溶液中的胶原蛋白分子,同时它们形成PSOx上的含有躺着的含量。观察到的细长结构可能是由于胶原段的关联,和/或与原子力显微镜探针的特定相互作用。这两个机制的各自重要性可能取决于下基的化学性质。纳米结构胶原层提供有吸引力的观点来控制哺乳动物细胞反应或作为模板以产生纳米结构化聚合物表面。

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