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首页> 外文期刊>Electroanalysis >SECM visualization of spatial variability of enzyme-polymer spots. Part 2: Complex interference elimination by means of selection of higbest sensitivity sensor substructures and artificial neural networks
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SECM visualization of spatial variability of enzyme-polymer spots. Part 2: Complex interference elimination by means of selection of higbest sensitivity sensor substructures and artificial neural networks

机译:SECM可视化的酶聚合物斑点的空间变异性。第2部分:通过选择最大灵敏度传感器子结构和人工神经网络来消除复杂的干扰

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Polymer spots with entrapped glucose oxidase were fabricated on glass surfaces and the localized enzymatic response was subsequently visualized using scanning electrochemical microscopy (SECM) in the generator-collector mode. SECM images were obtained under simultaneous variation of the concentration of glucose (0 - 6 mM) and ascorbic acid (0 - 200 mu M), or, in a second set of experiments, of glucose (0 - 2 mM) and 2-deoxy-D(+)-glucose (0 - 4 mM). Aiming at the quantification of the mixture components discretization of the response surfaces of the overall enzyme/polymer spot into numerous spatially defined microsensor substructures was performed. Sensitivity of sensor substructures to measured analytes was calculated and patterns of variability in the data were analyzed before and after elimination of interferences using principal component analysis. Using artificial neural networks which were fed with the data provided by the sensor substructures showing highest sensitivity for glucose, glucose concentration could be calculated in solutions containing unknown amounts of ascorbic acid with a good accuracy (RMSE 0.17 mM). Using, as an input data set, measurements provided by sensing substructures showing highest sensitivity for ascorbic acid in combination with the response of the sensors showing highest dependence on the glucose concentration, the error of the ascorbic acid concentration calculation in solution containing the unknown amount of glucose was 10 mu M. Similarly, prediction of the glucose concentration in the presence of 2-deoxy-D(+)-glucose was possible with a RMSE of 0.1 mM while the error of the calculation of 2-deoxy-D(+)-glucose concentrations in the presence of unknown concentrations of glucose was 0.36 mM.
机译:在玻璃表面上制作了带有捕获的葡萄糖氧化酶的聚合物斑点,随后使用扫描电化学显微镜(SECM)以发生器-收集器模式显示了局部酶促反应。在同时改变葡萄糖(0-6 mM)和抗坏血酸(0-200μM)浓度的情况下获得SECM图像,或者在第二组实验中,同时改变葡萄糖(0-2 mM)和2-deoxy的浓度获得SECM图像。 -D(+)-葡萄糖(0-4 mM)。针对混合物成分的定量,将整个酶/聚合物斑点的响应表面离散化为许多空间定义的微传感器亚结构。计算了传感器子结构对被测分析物的敏感性,并在使用主成分分析消除干扰之前和之后分析了数据的变异性模式。使用人工神经网络,该人工神经网络将传感器子结构提供的数据显示为对葡萄糖具有最高的敏感性,可以在含有未知量抗坏血酸的溶液中以较高的准确度(RMSE 0.17 mM)计算葡萄糖浓度。使用感测显示抗坏血酸灵敏度最高的子结构以及传感器对葡萄糖浓度的依赖性最高的传感器的响应作为输入数据集,测量含未知量葡萄糖的溶液中抗坏血酸浓度的误差。葡萄糖为10μM。类似地,在存在2-deoxy-D(+)-葡萄糖的情况下,以0.1 mM的RMSE预测葡萄糖浓度是可能的,而2-deoxy-D(+)的计算误差在葡萄糖浓度未知的情况下,β-葡萄糖浓度为0.36mM。

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