López G P, Ratner B D, Tidwell C D, Haycox C L, Rapoza R J, Horbett T A
Department of Chemical Engineering, University of Washington, Seattle 98195.
J Biomed Mater Res. 1992 Apr;26(4):415-39. doi: 10.1002/jbm.820260402.
The glow discharge plasma deposition (GDPD) of tetraethylene glycol dimethyl ether is introduced as a novel method for obtaining surfaces that are resistant to protein adsorption and cellular attachment. Analysis of films by x-ray photoelectron spectroscopy and several biological assays indicate the formation of a fouling-resistant, PEO-like surface on several substrata (e.g., glass, polytetrafluoroethylene, polyethylene). Adsorption of 125I-radiolabelled proteins (fibrinogen, albumin and IgG) from buffer and plasma was very low (typically less than 20 ng/cm2) when compared to the untreated substrata, which exhibited much higher levels of protein adsorption. Not all coated substrata adsorbed equal amounts of protein (e.g., coated glass samples typically adsorbed more protein than coated polyethylene or coated polytetrafluoroethylene samples), suggesting that the substratum used may affect the amount of protein adsorbed. Measurement of dynamic platelet adhesion, using epifluorescent video microscopy, and endothelial cell attachment further demonstrates the short-term nonadhesiveness of these surfaces.
引入了乙二醇二甲醚的辉光放电等离子体沉积(GDPD)作为一种获得抗蛋白质吸附和细胞附着表面的新方法。通过X射线光电子能谱和几种生物学分析对薄膜进行分析,结果表明在几种基质(如玻璃、聚四氟乙烯、聚乙烯)上形成了抗污染的、类似聚环氧乙烷的表面。与未处理的基质相比,从缓冲液和血浆中吸附的125I放射性标记蛋白质(纤维蛋白原、白蛋白和IgG)非常低(通常小于20 ng/cm2),未处理的基质表现出更高水平的蛋白质吸附。并非所有涂覆的基质吸附等量的蛋白质(例如,涂覆的玻璃样品通常比涂覆的聚乙烯或涂覆的聚四氟乙烯样品吸附更多的蛋白质),这表明所使用的基质可能会影响吸附的蛋白质数量。使用落射荧光视频显微镜测量动态血小板粘附以及内皮细胞附着,进一步证明了这些表面的短期非粘附性。