Department of Chemistry, Faculty of Sciences, University of Burgos, Plaza Misael Bañuelos s/n, 09001 Burgos, Spain.
Talanta. 2012 May 15;93:301-6. doi: 10.1016/j.talanta.2012.02.037. Epub 2012 Feb 22.
An enzymatic amperometric procedure for the direct measurement of As(V) in the presence of As(III) was developed. The method is based on the inhibitive action of this species on acid phosphatase enzyme (AcP) activity. Screen-printed carbon electrodes (SPCEs) were used as support for the cross-linking immobilization of the enzyme AcP. 2-Phospho-l-ascorbic acid was used as a novel substrate, in arsenic determination, which amperometric response decreased by the presence of As(V) ions. The optimum working conditions were found using experimental design methodology. Under these conditions, repeatability and reproducibility of the constructed biosensors were determined, reaching values below 8% in terms of residual standard deviation. The capability of detection obtained for As(V) was 0.11 μM for AcP/SPCE biosensors. Analysis of the possible effect of the presence of foreign ions in the solution was performed. The method was successfully applied to the determination of the As(V) content in a ground water sample.
开发了一种在存在 As(III) 的情况下直接测量 As(V)的酶安培法。该方法基于该物种对酸性磷酸酶(AcP)活性的抑制作用。丝网印刷碳电极(SPCE)被用作酶 AcP 交联固定化的支撑。2-磷酸-L-抗坏血酸被用作砷测定的新型底物,其电流响应因存在 As(V)离子而降低。通过实验设计方法确定了最佳工作条件。在这些条件下,确定了构建的生物传感器的重复性和重现性,其残留标准偏差低于 8%。获得的 AcP/SPCE 生物传感器对 As(V)的检测能力为 0.11 μM。对溶液中存在的外来离子的可能影响进行了分析。该方法成功地应用于测定地下水样品中的 As(V)含量。