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In -situ immobilisation of glucose oxidase on a novel microporous silica support

机译:葡萄糖氧化酶在新型微孔二氧化硅载体上的原位固定

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Glucose oxidase has been covalently immobilised onto a highly porous, but robust microporous silica strudcture. The porosity of this microporous structure was adjusted by the inclusion of acetamide to improve the enzyme immobilisation procedure. The covalent enzyme attachment was achieved by an on-line immobilisation procedure in which the reagents were pumped through the support that had been placed in-situ in the reactor tube. Glucose oxidase was immobilised with glutaraldehyde cross-linking to the 3-aminopropyltriethoxysilane treated support. The narrow tube enzyme reactor produced was then incorporated into a flow injection system and it s activity tested using the determination of glucose with spectrophotometric detection at 436 nm. A linear calibration range was obtained for glucose between 5 X 10~(-4) and 5 X 10~(-3) mol l~(-1) with a limit of detection of 1.4 X 10~(-4) mol l~(-1). The %RSD was 4% at the 5 X 10~(-4) mol l~(-1) level.
机译:葡萄糖氧化酶已被共价固定在高度多孔但坚固的微孔二氧化硅结构上。通过加入乙酰胺来调节该微孔结构的孔隙率,以改善酶的固定程序。共价酶的连接是通过在线固定程序实现的,其中将试剂泵送通过原位放置在反应管中的载体。葡萄糖氧化酶通过戊二醛交联固定在3-氨丙基三乙氧基硅烷处理的载体上。然后将产生的窄管酶反应器并入流动注射系统,并通过在436 nm处使用分光光度法测定葡萄糖来测试其活性。葡萄糖的线性校正范围为5 X 10〜(-4)mol l〜(-1),检出限为1.4 X 10〜(-4)mol l〜。 (-1)。在5 X 10〜(-4)mol〜(-1)水平下,%RSD为4%。

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