分光光度法测定纯和药用口服液中对羟基苯甲酸甲酯的含量

S. Dhahir, H. Hussein
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引用次数: 10

摘要

本文介绍了一种简单、廉价、灵敏的分光光度法测定对羟基苯甲酸甲酯的纯度和剂型。该方法采用亚硝酸钠在酸性介质中5Co重氮化,然后与邻氨基苯甲酸偶联形成橙色,稳定后在442 nm下测定,浓度范围为1 ~ 9 μg∙ml-1,摩尔吸光度为1.6 × 106 L∙mol -1∙cm-1。Sandell的灵敏度为0.0095 μg∙cm-1,检测限为0.0065 μg∙ml-1,定量限为0.02 μg∙ml-1。考察了试剂浓度、反应时间、色稳期、摩尔比等因素对反应条件的影响。未观察到干扰,分析结果经统计学和回收率研究验证。本方法成功地测定了某些口服液中对羟基苯甲酸甲酯的含量。相对于高效液相色谱法和其他技术,该方法操作简便,准确度高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectrophotometric Determination of Methyl Paraben in Pure and Pharmaceutical Oral Solution
A simple, cheap and sensitive spectrophotometric method for the determination of methyl paraben in pure and dosage form has been described. The Method is based on the diazotization of the drug by sodium nitrite in acidic medium at 5Co followed by coupling with ortho-aminobenzoic acid to form orange color the product was stabilized and measured at 442 nm Beer’s law is obeyed in the concentration range of 1-9 μg∙ml-1 with molar absorptivity of 1.6x106 L∙mole-1∙cm-1., Sandell’s sensitivity were 0.0095 μg∙cm-1, The detection limit were 0.0065 μg∙ml-1, and The limit of Quantitation were 0.02 μg∙ml-1. All variables including the reagent concentration, reaction time, color stability period, and mole ratio were studied in order to optimize the reaction conditions. No interferences were observed Results of analysis were validated statistically and by recovery studies. These methods are successfully employed for the determination of methyl paraben in some oral solution. The developed method is easy to use and accurate for routine studies relative to HPLC and other techniques.
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