Greenway G M, Ongomo P
School of Chemistry, University of Hull, UK.
Analyst. 1990 Oct;115(10):1297-9. doi: 10.1039/an9901501297.
Ascorbate oxidase was immobilised on cyanogen bromide activated-Sepharose 4B and incorporated in a flow-injection system with amperometric detection at a glassy carbon electrode at +0.6 V. On passage through the immobilised ascorbate oxidase a fraction of the L-ascorbic acid was converted into dehydroascorbic acid and the decrease in signal was measured. This could be directly related to the amount of L-ascorbic acid present. The calibration graph was linear over the range 0-400 ng ml(-1) with a correlation coefficient of 0.9994. The detection limit (2 sigma) in phosphate buffer (0.08 M, pH 5.5) was 4.0 ng ml(-1). The relative standard deviation for a 200 ng ml(-1) standard was 1.0% (n = 10) and the sampling throughput was 30 samples h(-1). The method was used for the simple and rapid determination of L-ascorbic acid in fruit and vegetable juice.
抗坏血酸氧化酶固定在溴化氰活化的琼脂糖凝胶4B上,并与流动注射系统相结合,在+0.6 V的玻碳电极上进行安培检测。当L-抗坏血酸通过固定化的抗坏血酸氧化酶时,一部分被转化为脱氢抗坏血酸,并测量信号的降低。这可以直接与存在的L-抗坏血酸的量相关。校准曲线在0-400 ng ml⁻¹范围内呈线性,相关系数为0.9994。在磷酸盐缓冲液(0.08 M,pH 5.5)中的检测限(2σ)为4.0 ng ml⁻¹。200 ng ml⁻¹标准品的相对标准偏差为1.0%(n = 10),进样通量为30个样品 h⁻¹。该方法用于水果和蔬菜汁中L-抗坏血酸的简单快速测定。