Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent

Q3 Physics and Astronomy
O. Fatibello‐Filho, H. Vieira
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引用次数: 8

Abstract

A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.
流动注射分光光度法以邻甲苯胺为试剂间接测定制剂中对乙酰氨基酚
建立了一种测定制剂中扑热息痛的分光光度流动注射法。本方法以次氯酸钠氧化扑热息痛为研究对象,以邻甲苯胺二氯化为显色剂,在430 nm处测定该氧化剂的过量。对乙酰氨基酚浓度在8.50 × 10-6 ~ 2.51 × 10-4 mol L-1范围内呈线性关系,检出限为5.0 × 10-6 mol L-1。1.20 × 10-4 mol L-1扑热息痛溶液(n = 10)的相对标准偏差小于1.2%。使用建议的流动注射方法和使用USP药典方法获得的药物制剂中对乙酰氨基酚的结果在95%的置信水平上是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ecletica Quimica
Ecletica Quimica Chemistry-Chemistry (all)
CiteScore
1.70
自引率
0.00%
发文量
32
审稿时长
28 weeks
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