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首页> 外文期刊>Orbital : the Electronic Journal of Chemistry >UV Spectrophotometry Method Validation for Quantification of Paracetamol in Tablet Formulations: A Proposal of Experimental Activity for Instrumental Analysis
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UV Spectrophotometry Method Validation for Quantification of Paracetamol in Tablet Formulations: A Proposal of Experimental Activity for Instrumental Analysis

机译:紫外分光光度法验证片剂中扑热息痛的定量:对仪器分析实验活性的建议

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In the present article it is described the validation of a simple, precise, accurate, rapid and low-cost UV spectrophotometric method for quantification of paracetamol in tablets. The method was linear in the range between 6.4 - 9.6 μg mL -1 , presenting a good correlation coefficient (r = 0.9984) and adequate limits of quantification (2.64 μg mL -1 ) and detection (0.87 μg mL -1 ). Precision and analysis showed low coefficient of variation ( 4.0 %) and a good average recovery percentual (99.22% - reference and 101.78% - generic) was obtained. The method was applied for paracetamol determination in two tablet formulations and these results are in good accordance with the declared values of manufacturer, at a 95% confidence level. The experimental activity is simple, showing it to be used in experimental activities on teaching laboratories improve student learning.
机译:在本文中,描述了一种简单,精确,准确,快速和低成本的紫外分光光度法定量片剂中扑热息痛的方法的验证。该方法在6.4-9.6μgmL -1范围内是线性的,具有良好的相关系数(r = 0.9984)和足够的定量限(2.64μgmL -1)和检测(0.87μgmL -1)。精密度和分析表明,变异系数低(<4.0%),并且平均回收率良好(基准为99.22%,通用为101.78%)。该方法用于两种片剂中对乙酰氨基酚的测定,这些结果与制造商的声明值非常一致,置信度为95%。实验活动很简单,表明可以在教学实验室的实验活动中使用它来提高学生的学习能力。

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