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首页> 外文期刊>Analytical chemistry letters >Development and Validation of Spectrophotometric Methods for the Determination of Amoxicillin trihydrate and Dicloxacillin sodium in Their Binary Mixture
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Development and Validation of Spectrophotometric Methods for the Determination of Amoxicillin trihydrate and Dicloxacillin sodium in Their Binary Mixture

机译:开发和验证光谱光度测量的方法测定阿莫西林三水合和双氯西林钠二元混合物

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摘要

Three sensitive and cost-effective spectrophotometric methods are introduced for the determination of amoxicillin and dicloxacillin in their binary mixtures with minimum sample pretreatment, with or without the presence of their common impurity; 6-aminopenicillanic acid (6-APA). In this work, dicloxacillin is determined by dual wavelength, derivative ratio and isoabsorptive spectrophotometric methods. However, amoxicillin is determined by direct UV spectrophotometry at 273.6 nm and by the first derivative ratio spectrophotometric method (DD method). For method (A); the dual wavelength method, the wavelengths selected for the determination of dicloxacillin were 223.6 and 237 nm. Method (B); the isoabsorptive spectrophotometric method, comprises measuring the total content of the mixture at their isoabsorptive point (230.4nm), and then the content of dicloxacillin can be calculated by subtraction. Method (C) is the first derivative of ratio spectra for the determination of amoxicillin (using 8 μg/mL of dicloxacillin as a divisor at 231 nm) and dicloxacillin (using 20 μg/mL of 6-APA as a divisor at 234.6 nm) in presence of their common impurity; 6-APA. Statistical comparison of the results obtained from the suggested methods with those of the reported HPLC method showed no significant difference with respect to accuracy and precision. The developed methods can be used for quality control analysis of the studied drugs in laboratories lacking HPLC qualifications.
机译:三个敏感和具有成本效益的介绍了光谱光度测量的方法阿莫西林和双氯西林的决心他们的二元混合物最小样本预处理,有或没有的存在他们共同的杂质;(6-APA)。由双波长导数比率和isoabsorptive光谱光度测量的方法。然而,阿莫西林是由直接的紫外线分光光度法在273.6 nm和第一导数分光光度法测定比(DD方法)。方法,波长的选择测定双氯西林223.6和237人nm。分光光度法测定,包括测量总含量的混合物isoabsorptive点(230.4海里),然后双氯西林的含量可以通过计算减法。比值光谱的测定阿莫西林(使用8双氯西林的μg / mL因子在231 nm)和双氯西林(使用20μg / mL 6-APA作为除数为234.6海里)他们共同的杂质的存在;统计结果的比较的建议与方法报告显示没有明显的高效液相色谱方法对准确性和差异精度。研究药物的质量控制分析实验室缺乏高效液相色谱条件。

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