基于固体结合基质的改进安培生物传感器测定食品中的d -果糖

M. Streďanský, A. Pizzariello, S. Stredanska, S. Miertus
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引用次数: 34

摘要

基于固体结合基质(SBM)复合传感器的改进安培生物传感器被用于食品样品中d -果糖的测定。将d -果糖脱氢酶(EC 1.1.99.11)直接掺入含有2-十六烷酮作为SBM和化学修饰石墨的固体复合换能器中。采用六氰高铁酸盐(III)作为氧化还原介质,并通过电流法测量了d -果糖的存在所引起的电流变化。介绍了复合果糖生物传感器的电化学性能和特点。d -果糖浓度在50 × 10-6-10 × 10-3 mol l-1范围内呈线性关系,相关系数为0.999。对2 × 10-3 mol l - 1d -果糖在+0.20 V与SCE下的测量结果,稳态电流的相对标准偏差为2.11%。使用温和氧化步骤的化学改性石墨被证明可以提高生物传感器对阴离子干扰物(如l -抗坏血酸)的选择性。该生物传感器被证明在6个月内是稳定的,并且该电极对d -果糖的测定不受糖或食品样品中常见的其他干扰物的影响。将该生物传感器用于部分食品样品中d -果糖的测定,结果与市售d -果糖酶光度测定试剂盒一致。
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Determination of D-fructose in foodstuffs by an improved amperometric biosensor based on a solid binding matrix
An improved amperometric biosensor based on a solid binding matrix (SBM) composite transducer has been used for the determination of D-fructose in foodstuffs samples. The enzyme, D-fructose dehydrogenase (EC 1.1.99.11), was incorporated directly into a solid composite transducer containing both 2-hexadecanone as SBM and chemically modified graphite. Hexacyanoferrate(III) was used as a redox mediator and the current variation caused by the presence of D-fructose was measured amperometrically. The electrochemical properties and the characteristics of the composite fructose biosensors are described. The amperometric signals were fast, reproducible and linearly proportional to D-fructose concentrations in the range 50 × 10–6–10 × 10–3 mol l–1, with a correlation coefficient of 0.999. A set of measurements at +0.20 V versus SCE for 2 × 10–3 mol l–1D-fructose yielded a relative standard deviation for the steady-state current of 2.11%. The use of a chemically modified graphite by a mild oxidation step was shown to improve the biosensor selectivity against anionic interferents such as L-ascorbate. The biosensor proved to be stable for 6 months and the assay of D-fructose by this electrode was not influenced by the presence of sugars or other interferents commonly found in food samples. The biosensor was used for the determination of D-fructose in some food samples, and the results were consistent with those obtained with the commercially available D-fructose enzyme photometric kit.
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