动力学光度法测定雷尼替丁对孔雀石绿被n -溴琥珀胺氧化速率的抑制作用

A. Taha, A. Abdel-Hady
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引用次数: 0

摘要

建立了一种简便、灵敏的动态分光光度法测定雷尼替丁的方法。该方法基于雷尼替丁对n -溴琥珀酰亚胺(NBS)氧化孔雀石绿(MG +)的抑制作用,采用分光光度法测定不同浓度雷尼替丁存在下,孔雀石绿在λ=617nm处的吸光度随时间的变化率。雷尼替丁的测定范围为0.08 ~ 2.40g ml -1,线性校准图,检出限为0.026g ml -1。该方法可用于雷尼替丁纯品和雷尼替丁片剂中雷尼替丁的含量测定。分析样品的回收率为97 ~ 100%,相对标准偏差为sr (%) =1.14 × 10 -4,表明该方法具有较高的准确度和精密度。研究了各种阳离子和阴离子对雷尼替丁含量测定的干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetics Spectrophotometric determination of Ranitidine based on its Inhibitory effect on the Oxidation Rate of Malachite green by N-bromosuccinide
A simple and sensitive kinetic spectrophotometric method is described for the determination of ranitidine. The method is based on the inhibiting effect of ranitidine on the rate of oxidation of malachite green (MG + ) with N-bromosuccinimide (NBS) The oxidation reaction was followed spectrophotometrically by measuring the rate of change of the absorbance of malachite green with time at λ=617nm in the presence of different concentrations of ranitidine using the recommended procedure. Ranitidine can be determined from 0.08 to 2.40 g ml -1 with a linear calibration graph and detection limit of 0.026 g ml -1 . The method was successfully applied for the determination of ranitidine in pure ranitidine samples and in ranitidine tablets. The recovery of the analyzed samples were 97-100% with relative standard deviation, sr (%) =1.14 x 10 -4 indicating high accuracy and precision of the suggested method. The interference of various cations and anions in the determination of ranitidine was studied.
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