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抗蛋白硅氮化表面:UV 诱导形成聚氧化乙烯单层。

Protein-repellent silicon nitride surfaces: UV-induced formation of oligoethylene oxide monolayers.

机构信息

Laboratory of Organic Chemistry, Wageningen University, Dreijenplein 8, 6703 HB Wageningen, The Netherlands.

出版信息

ACS Appl Mater Interfaces. 2011 Mar;3(3):697-704. doi: 10.1021/am100985c. Epub 2011 Feb 10.

Abstract

The grafting of polymers and oligomers of ethylene oxide onto surfaces is widely used to prevent nonspecific adsorption of biological material on sensors and membrane surfaces. In this report, we show for the first time the robust covalent attachment of short oligoethylene oxide-terminated alkenes (CH(3)O(CH(2)CH(2)O)(3)(CH(2))(11)-(CH═CH(2)) [EO(3)] and CH(3)O(CH(2)CH(2)O)(6)(CH(2))(11)-(CH═CH(2)) [EO(6)]) from the reaction of alkenes onto silicon-rich silicon nitride surfaces at room temperature using UV light. Reflectometry is used to monitor in situ the nonspecific adsorption of bovine serum albumin (BSA) and fibrinogen (FIB) onto oligoethylene oxide coated silicon-rich silicon nitride surfaces (EO(n)-Si(x)N(4), x > 3) in comparison with plasma-oxidized silicon-rich silicon nitride surfaces (SiO(y)-Si(x)N(4)) and hexadecane-coated Si(x)N(4) surfaces (C(16)-Si(x)N(4)). A significant reduction in protein adsorption on EO(n)-Si(x)N(4) surfaces was achieved, adsorption onto EO(3)-Si(x)N(4) and EO(6)-Si(x)N(4) were 0.22 mg m(-2) and 0.08 mg m(-2), respectively. The performance of the obtained EO(3) and EO(6) layers is comparable to those of similar, highly protein-repellent monolayers formed on gold and silver surfaces. EO(6)-Si(x)N(4) surfaces prevented significantly the adsorption of BSA (0.08 mg m(-2)). Atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), X-ray reflectivity and static water contact angle measurements were employed to characterize the modified surfaces. In addition, the stability of EO(6)-Si(x)N(4) surfaces in phosphate-buffered saline solution (PBS) and alkaline condition (pH 10) was studied. Prolonged exposure of the surfaces to PBS solution for 1 week or alkaline condition for 2 h resulted in only minor degradation of the ethylene oxide moieties and no oxidation of the Si(x)N(4) substrates was observed. Highly stable antifouling coatings on Si(x)N(4) surfaces significantly broaden the application potential of silicon nitride-coated microdevices, and in particular of microfabricated filtration membranes.

摘要

聚合物和氧化乙烯低聚物接枝到表面上被广泛用于防止传感器和膜表面上的生物材料的非特异性吸附。在本报告中,我们首次展示了短的乙氧基封端烯烃(CH(3)O(CH(2)CH(2)O)(3)(CH(2))(11)-(CH═CH(2)) [EO(3)]和 CH(3)O(CH(2)CH(2)O)(6)(CH(2))(11)-(CH═CH(2)) [EO(6)])在室温下通过烯烃与富硅氮化硅表面的反应牢固地共价附着到富硅氮化硅表面上,该反应使用了紫外光。反射测量法用于原位监测牛血清白蛋白(BSA)和纤维蛋白原(FIB)在聚氧化乙烯涂层富硅氮化硅表面(EO(n)-Si(x)N(4),x > 3)上的非特异性吸附,与等离子体氧化富硅氮化硅表面(SiO(y)-Si(x)N(4))和十六烷涂层 Si(x)N(4)表面(C(16)-Si(x)N(4))进行比较。在 EO(n)-Si(x)N(4)表面上实现了蛋白质吸附的显著减少,在 EO(3)-Si(x)N(4)和 EO(6)-Si(x)N(4)上的吸附分别为 0.22 mg m(-2)和 0.08 mg m(-2)。所获得的 EO(3)和 EO(6)层的性能与在金和银表面上形成的类似的、高度蛋白质排斥的单层相当。EO(6)-Si(x)N(4)表面显著阻止了 BSA 的吸附(0.08 mg m(-2))。原子力显微镜(AFM)、X 射线光电子能谱(XPS)、X 射线反射率和静态水接触角测量用于对修饰表面进行表征。此外,研究了 EO(6)-Si(x)N(4)表面在磷酸盐缓冲盐水(PBS)和碱性条件(pH 10)中的稳定性。将表面长时间暴露于 PBS 溶液中 1 周或碱性条件 2 h 仅导致氧化乙烯部分的轻微降解,并且没有观察到 Si(x)N(4)基底的氧化。Si(x)N(4)表面上的高度稳定的抗污涂层显著拓宽了氮化硅涂层微器件的应用潜力,特别是微制造过滤膜的应用潜力。

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