首页> 外文期刊>Journal of Food Composition and Analysis >Cathodic adsorptive stripping voltammetric determination of rutin in soybean cultivars.
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Cathodic adsorptive stripping voltammetric determination of rutin in soybean cultivars.

机译:阴极吸附溶出伏安法测定大豆品种中的芦丁。

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摘要

A highly sensitive and selective cathodic adsorptive stripping voltammetric method for determination of rutin is presented. The method relies on the accumulation of a Cu(II)-rutin complex at a hanging mercury drop electrode (HMDE), followed by its reduction during a differential pulse voltammetric scan. The electrochemical behavior of the Cu(II)-rutin complex at HMDE was investigated by cyclic voltammetry. Results show that the electrode process is adsorption-controlled and gradually becomes less reversible at high scan rates where peak separation grows. Under the optimized conditions (phosphate buffer pH 6, --1.000 V accumulation potential, 180 s accumulation time, 70 mV pulse amplitude, 50 mV s--1 scan rate and 1.6 x 10--6 M Cu(II) concentration), the reduction peak current (Ipc) of the Cu(II)-rutin complex is linear (Ipc (nA) = 10.070 + 1.9 x 108 [Rutina]) to rutin concentration in the range from 2.0 x 10-- 7 to 1.4 x 10--6 M, with a correlation coefficient of 0.999. The detection and quantification limits obtained were 7.0 x 10--9 M and 2.2 x 10--8 M, respectively. The method was successfully applied to the determination of rutin in soybean cultivars, with recoveries of 94-105%
机译:提出了一种高度灵敏,选择性的阴极吸附溶出伏安法测定芦丁。该方法依赖于Cu(II)-芦丁络合物在悬挂式汞滴电极(HMDE)处的积累,然后在差分脉冲伏安扫描中将其还原。通过循环伏安法研究了Cu(II)-芦丁络合物在HMDE上的电化学行为。结果表明,电极过程是受吸附控制的,并且在高扫描速率下(逐渐增加峰分离)逐渐变得不可逆。在优化的条件下(磷酸盐缓冲液pH 6,--1.000 V累积电势,180 s累积时间,70 mV脉冲幅度,50 mV s -1 扫描速率和1.6 x 10 - -6 M Cu(II)浓度),Cu(II)-芦丁络合物的还原峰电流( I pc )是线性的( I pc (nA)= 10.070 + 1.9 x 10 8 [Rutina])至芦丁浓度范围为2.0 x 10 - 7 到1.4 x 10 -6 M,相关系数为0.999。检出限和定量限分别为7.0 x 10 -9 M和2.2 x 10 -8 M。该方法已成功用于大豆品种中芦丁的测定,回收率为94-105%。

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