EGERFOOD Regional Research Centre, College of Károly Eszterházy, Leányka u. 6, Eger, 3300, Hungary.
Bioprocess Biosyst Eng. 2010 Oct;33(8):947-52. doi: 10.1007/s00449-010-0418-6. Epub 2010 Mar 12.
An amperometric detector and an enzymatic reaction were combined for the measurement of L-ascorbic acid. The enzyme cell (containing immobilized ascorbate oxidase) was connected to a flow injection analyzer (FIA) system with a glassy carbon electrode as an amperometric detector. During optimization and measurements two sample injectors were used, one before and one after the enzyme cell, thus eliminating the background interferences. Subtraction of the signal area given in the presence of enzyme from the one given in the absence of enzyme was applied for measuring analyte concentrations and calibration at 400 mV. Analysis capacity of system is 25 samples/hour. The relative standard deviation (RSD) was below 5% (5 times repeated, 400 μmol/L conc.), linearity up to 400 μmol/L, limit of detection (LOD) 5 μmol/L, fitting of calibration curve in 25-400 μmol/L range was R (2) = 0.99.
安培检测器与酶反应相结合,用于测量 L-抗坏血酸。酶池(含有固定化抗坏血酸氧化酶)与带有玻碳电极的流动注射分析仪(FIA)系统相连,作为安培检测器。在优化和测量过程中使用了两个样品注射器,一个在酶池之前,一个在酶池之后,从而消除了背景干扰。通过从有酶存在时的信号面积中减去无酶存在时的信号面积,用于测量分析物浓度和在 400 mV 下进行校准。系统的分析能力为每小时 25 个样品。相对标准偏差(RSD)低于 5%(重复 5 次,浓度为 400 μmol/L),线性度高达 400 μmol/L,检测限(LOD)为 5 μmol/L,在 25-400 μmol/L 范围内校准曲线的拟合度为 R(2)= 0.99。