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用于抑制性测定汞(II)的脲酶型安培生物传感器的研制。

Development of urease based amperometric biosensors for the inhibitive determination of Hg (II).

作者信息

Domínguez-Renedo O, Alonso-Lomillo M A, Ferreira-Gonçalves L, Arcos-Martínez M J

机构信息

Department of Chemistry, Factulty of Sciences, University of Burgos, Burgos, Spain.

出版信息

Talanta. 2009 Oct 15;79(5):1306-10. doi: 10.1016/j.talanta.2009.05.043. Epub 2009 Jun 6.

Abstract

Enzymatic amperometric procedures for measurement of Hg (II), based on the inhibitive action of this metal on urease enzyme activity, were developed. Screen-printed carbon electrodes (SPCEs) and gold nanoparticles modified screen-printed carbon electrodes (AuNPs/SPCEs) were used as supports for the cross-linking inmobilization of the enzyme urease. The amperometric response of urea was affected by the presence of Hg (II) ions which caused a decreasing in the current intensity. The optimum working conditions were found using experimental design methodology. Under these conditions, repeatability and reproducibility for both types of biosensors were determined, reaching values below 6% in terms of residual standard deviation. The detection limit obtained for Hg (II) was 4.2x10(-6)M for urease/SPCE biosensor and 5.6x10(-8)M for urease/AuNPs/SPCE biosensor. Analysis of the possible effect of the presence of foreign ions in the solution was performed. The method was applied to determine levels of Hg (II) in spiked human plasma samples.

摘要

基于汞(II)对脲酶活性的抑制作用,开发了用于测定汞(II)的酶促安培法。丝网印刷碳电极(SPCE)和金纳米颗粒修饰的丝网印刷碳电极(AuNPs/SPCE)用作脲酶交联固定化的载体。汞(II)离子的存在影响了尿素的安培响应,导致电流强度降低。使用实验设计方法找到了最佳工作条件。在此条件下,测定了两种类型生物传感器的重复性和再现性,残余标准偏差值低于6%。脲酶/SPCE生物传感器对汞(II)的检测限为4.2×10⁻⁶M,脲酶/AuNPs/SPCE生物传感器对汞(II)的检测限为5.6×10⁻⁸M。分析了溶液中存在外来离子可能产生的影响。该方法应用于加标人血浆样品中汞(II)含量的测定。

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