Fabrication and characterisation of spin coated oxidised PMMA to provide a robust surface for on-chip assays

材料科学 生物分子 纳米技术 基质(水族馆) 旋涂 化学工程 涂层 图层(电子) 表面等离子共振 单层 共价键 氧气 紫外线 表面改性 光化学 光电子学 有机化学 化学 纳米颗粒 海洋学 地质学 工程类
作者
M. Rowinska,Susan M. Kelleher,Felipe Soberon,Antonio J. Ricco,Stephen Daniels
出处
期刊:Journal of Materials Chemistry B [The Royal Society of Chemistry]
卷期号:3 (1): 135-143 被引量:17
标识
DOI:10.1039/c4tb01748j
摘要

A method to prepare a highly stable carboxylic acid functional surface on various substrates for use in bioassays is reported. A thin layer of a poly(methylmethacrylate) (PMMA) is achieved by spin coating dissolved PMMA onto a variety of underlying substrates at various thicknesses in a range of c. 5-27 nm. Varying the PMMA concentration, time and spinning speed controls the thickness of the spin coated layer. The root-mean-squared roughness values of the spin coated PMMA are less than 1.5 nm, resulting in smooth and uniform layer. Substrate functionalisation is carried out by either ultraviolet/ozone (UV/O3) or oxygen plasma oxidation. Both techniques result in initially stable, highly functional films as demonstrated by the covalent attachment of amino-modified oligonucleotides, however longevity studies comparing the stability of films attached following oxidative activation show better stability for UV/O3 activated substrates when compared to oxygen plasma activated substrates. PMMA films activated by UV/O3 yield highly stable (for up to 24 days) functional surfaces that retain immobilised biomolecules after several extended wash steps. In contrast, films attached to surfaces pre-treated with oxygen plasma discharge lose their functionality within 5 days of oxidation. Direct DNA and sandwich antibody assays were successfully demonstrated on the UV/O3 functionalised surfaces, showing a low level of non-specific binding. Furthermore, the quenching of fluorescently labelled biomolecules bound to PMMA-coated gold-coated slides is shown to be dependent on the PMMA thickness, indicating potential usage in surface-plasmon resonance-based assays.
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