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A novel method for the determination of tiopronin by using potassium ferricyanide as spectroscopic probe reagent in pharmaceutical and urine samples

机译:铁氰化钾作为光谱探针试剂测定药物和尿液中硫普罗宁的新方法

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In this paper, a novel method has been established to determine tiopronin using potassium ferri- cyanide as spectroscopic probe reagent. It has been demonstrated that Fe(III) is reduced to Fe(II) by tiopro- nin, and the in situ formed Fe(II) reacts with potassium ferricyanide to form soluble Prussian blue. Beer's law is obeyed in the range of tiopronin concentration of 0.040-9.00 μg/mL at the maximal absorption wavelength of 735 nm. The linear regression equation is A = 0.0153 + 0.1605c (μg/mL) with a correlation coefficient of 0.9997 and the apparent molar absorption coefficient of 2.6 × 104 L/mol cm. The detection limit is 0.030 μg/mL and RSD is 1.3%. The parameters with regard to determination have been optimized and the reaction mechanism has been discussed. This method has been successfully applied to determine tiopronin in phar- maceutical and urine samples with satisfactory results.
机译:本文建立了一种以亚铁氰化钾为光谱探针试剂测定硫普罗宁的新方法。业已证明,硫代普罗宁将Fe(III)还原为Fe(II),并且原位形成的Fe(II)与铁氰化钾反应形成可溶性普鲁士蓝。在735 nm的最大吸收波长下,在tiopronin浓度为0.040-9.00μg/ mL的范围内遵守比尔定律。线性回归方程为A = 0.0153 + 0.1605c(μg/ mL),相关系数为0.9997,表观摩尔吸收系数为2.6×104 L / mol cm。检出限为0.030μg/ mL,RSD为1.3%。关于测定的参数已经优化,并且已经讨论了反应机理。该方法已成功应用于药物和尿液样品中硫普罗宁的测定,结果令人满意。

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