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Amperometric PMMA-microchip with integrated gold working electrode for enzyme assays

机译:带有集成金工作电极的安培PMMA微芯片,用于酶分析

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The use of a gold film in-channel detector combined with a poly( methyl methacrylate) ( PMMA) CE microchip has been tested for alkaline phosphatase (AP) enzymatic assays. Tris-borate or Tris-Gly (pH 9.0, 50 mmol L-1) buffer solutions were appropriate as running buffer. Signals for three common AP products: alpha- naphthol, p-nitrophenol, and ascorbic acid, were obtained. They were reproducible (RSD 4.4% for six successive electropherograms corresponding to 5 mmol L-1 a- naphthol solution) and the response was dependent on concentration ( linear relationship for ascorbic acid solutions between 5 and 20 mmol L-1 concentration). Use of an end- channel gold. lm electrode was also investigated. If one of the reagents (substrate or enzyme) is included in the running buffer, two different types of enzymatic assay are feasible in less than 3 min.
机译:金膜通道内检测器与聚甲基丙烯酸甲酯(PMMA)CE微芯片结合使用已通过碱性磷酸酶(AP)酶法检测。 Tris-borate或Tris-Gly(pH 9.0,50 mmol L-1)缓冲溶液适合作为运行缓冲液。获得了三种常见AP产品的信号:α-萘酚,对硝基苯酚和抗坏血酸。它们是可重现的(对应于5 mmol L-1萘酚溶液的六个连续电泳图,RSD为4.4%),响应取决于浓度(5-20​​ mmol L-1浓度的抗坏血酸溶液的线性关系)。使用终端通道黄金。还对lm电极进行了研究。如果运行缓冲液中包含一种试剂(底物或酶),则可以在不到3分钟的时间内进行两种不同类型的酶促测定。

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