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Indirect spectrophotometric method for determination of captopril using Cr(Vi) and diphenylcarbazide

机译:Cr(Vi)和二苯卡巴肼间接分光光度法测定卡托普利

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摘要

A spectrophotometric method for the indirect determination of captopril (CP) in pharmaceutical formulations is proposed. The proposed procedure is based on the oxidation of captopril by potassium dichromate and the determination excess oxidant on the basis of its reaction with diphenylcarbazide (DPC). Under the optimum conditions, a good linear relationship (r = 0.9997) was obtained in the range of 0.08-3.5 μg mL-1. The assay limits of detection and quantitation were 0.024 and 0.08 μg mL-1, respectively. The results obtained for captopril determination in pharmaceuticals using the proposed method and those obtained with the US Pharmacopoeia method were in good agreement at the 95% confidence level.
机译:提出了一种间接测定药物制剂中卡托普利(CP)的分光光度法。拟议的程序基于重铬酸钾对卡托普利的氧化作用,并根据其与二苯卡巴肼(DPC)的反应确定了过量的氧化剂。在最佳条件下,在0.08-3.5μgmL-1的范围内获得了良好的线性关系(r = 0.9997)。检测和定量的分析极限分别为0.024和0.08μgmL-1。使用拟议方法测定卡托普利的结果与采用美国药典方法测定的结果在95%的置信水平上吻合良好。

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