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首页> 外文期刊>Transactions of the Japan Society for Computational Engineering and Science >Modification of Poly(dimethylsiloxane) by Mesostructured Siliceous Films for Constructing Protein-Interactive Surfaces
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Modification of Poly(dimethylsiloxane) by Mesostructured Siliceous Films for Constructing Protein-Interactive Surfaces

机译:介孔硅质膜对聚二甲基硅氧烷的改性作用以构建蛋白质相互作用表面

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摘要

We investigated the coating process of mesostructured triblock copolymer-tetraethoxysilane (P123-TEOS) and mesoporous silica (MPS) films on a bioinert poly(dimethylsiloxane) (PDMS) with the different cross-linker concentrations through an oxygen-plasma treatment to evaluate the mesostructure formation and adsorption ability of proteins (albumin, fibrinogen, γ-globulin, fetal bovine serum). In the PDMS preparation, the cross-linker concentration affected the polymer network formation and the siliceous layer was formed on the most-surfaces by the plasma treatment. The transparent siliceous films of P123-TEOS and MPS were successfully covered on the cross-linked PDMS without voiding and the coating film thicknesses were ca. 100 nm. The FT-IR spectra indicated that the change from P123-TEOS to MPS occurred with preserving the PDMS chemical bonds by the calcination. Especially, the XRD patterns and nitrogen adsorption and desorption isotherms of the MPS on PDMS indicated the mesostructured film formation with preserving the ordered nanopore structures (BJH pore sizes: 1.6-4.2 nm, BET surface areas: 394-602 m~(2)/g). The hydrophobic PDMS surfaces became more wettable by the coating. The adsorption amounts of acidic proteins (albumin, fibrinogen) were changed by the coating. For the fibrinogen, the P123-TEOS on PDMS exhibited the most adsorption sites. Therefore, the bio-interactive properties of the PDMS surfaces were demonstrated based on the coating processes.
机译:我们通过氧等离子体处理研究了具有不同交联剂浓度的生物惰性聚(二甲基硅氧烷)(PDMS)上介孔结构的三嵌段共聚物-四乙氧基硅烷(P123-TEOS)和介孔二氧化硅(MPS)膜的涂层工艺,以评价介孔结构蛋白质(白蛋白,纤维蛋白原,γ-球蛋白,胎牛血清)的形成和吸附能力。在PDMS制备中,交联剂浓度影响聚合物网络的形成,并且通过等离子体处理在最表面上形成硅质层。 P123-TEOS和MPS的透明硅质薄膜已成功地覆盖在交联的PDMS上,没有空隙,并且涂膜的厚度约为。 100纳米FT-IR光谱表明,从P123-TEOS到MPS的变化是通过煅烧保留了PDMS化学键而发生的。尤其是,PDS上MPS的XRD图谱和氮吸附等温线表明中型结构膜的形成,保留了有序的纳米孔结构(BJH孔径:1.6-4.2 nm,BET表面积:394-602 m〜(2)/ G)。疏水性PDMS表面变得更易被涂层润湿。酸性蛋白质(白蛋白,纤维蛋白原)的吸附量被涂层改变。对于纤维蛋白原,PDMS上的P123-TEOS表现出最多的吸附位。因此,基于涂覆过程证明了PDMS表面的生物相互作用特性。

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