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Spectrophotometric Determination of Methyl Paraben in Pure and Pharmaceutical Oral Solution

机译:分光光度法测定纯净和口服溶液中对羟基苯甲酸甲酯的含量

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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.
机译:已经描述了一种简单,廉价且灵敏的分光光度法测定纯净和剂型的对羟基苯甲酸甲酯。该方法基于亚硝酸钠在5Co的酸性介质中将亚硝酸钠对药物进行重氮化,然后与邻氨基苯甲酸偶合以形成橙色,产品被稳定并在442 nm处测量。在1的浓度范围内遵守比尔定律9μg?ml-1,摩尔吸光度为1.6x106 L?mol-1?cm-1。,Sandell的灵敏度为0.0095μg?cm-1,检出限为0.0065μg?ml-1,定量限为0.02微克/毫升-1。为了优化反应条件,研究了包括试剂浓度,反应时间,颜色稳定时间和摩尔比在内的所有变量。没有观察到干扰,分析结果通过统计学和回收率研究进行了验证。这些方法已成功用于某些口服溶液中对羟基苯甲酸甲酯的测定。相对于HPLC和其他技术,该开发的方法易于使用且准确用于常规研究。

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