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首页> 外文期刊>Journal of analytical chemistry >Titrimetric assay of ofloxacin in pharmaceuticals using cerium(IV) sulphate as an oxidimetric reagent
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Titrimetric assay of ofloxacin in pharmaceuticals using cerium(IV) sulphate as an oxidimetric reagent

机译:硫酸铈(IV)作为氧化剂的氧氟沙星滴定分析

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摘要

Two titrimetric methods which are simple, rapid, cost-effective and eco-riendly are described for the determination of ofloxacin (OFX) in bulk drug and in tablet formulations based on the oxidation of OFX by Ce(IV) sulphate. In direct titrimetry (method A), the acidified solution of OFX is titrated directly with Ce(IV) sulphate using ferroin as indicator, and indirect titrimetry (method B) involves the addition of known excess of Ce(IV) sulphate to an acidified solution of OFX followed by the determination of unreacted oxidant by back titration with ferrous ammonium sulphate (FAS) using the same ferroin indicator. In both the methods, the amount of Ce(IV) sulphate reacted corresponds to OFX concentration. Method A and method B permit the determination of OFX over the concentration range of 1.5-15 mg in both the methods and the quantitation is based on a 1: 5 reaction stoichiometry (OFX: Ce (IV) sulphate). The methods were statistically evaluated by calculating percent relative error (% RE) for accuracy and percent relative standard deviation (% RSD) for precision, and were applied successfully to the determination of OFX in tablets with mean recoveries in the range of 96.50-98.42%. No interference was observed from common additives found in pharmaceutical preparations. The accuracy and reliability of the methods were further ascertained by performing recovery tests s standard-addition technique.
机译:描述了两种简便,快速,经济高效且环保的滴定法,用于测定散剂和片剂中氧氟沙星(OFX)的含量,硫酸氧(Ox)被硫酸铈(IV)氧化。在直接滴定法(方法A)中,使用铁蛋白作为指示剂,用硫酸铈(IV)直接滴定OFX的酸化溶液,间接滴定法(方法B)涉及向酸化溶液中添加已知过量的硫酸铈(IV)使用相同的铁精指示剂,通过硫酸亚铁铵(FAS)的反滴定法测定OFX,然后测定未反应的氧化剂。在两种方法中,反应的硫酸铈(IV)的量均对应于OFX浓度。方法A和方法B允许在两种方法中都在1.5-15 mg的浓度范围内测定OFX,并且定量基于1:5反应化学计量(OFX:硫酸铈(IV))。通过计算准确性的相对误差百分比(%RE)和准确性的相对标准偏差百分比(%RSD),对方法进行统计学评估,并成功地用于测定平均回收率在96.50-98.42%范围内的片剂中的OFX 。没有观察到药物制剂中常见添加剂的干扰。通过执行恢复测试的标准添加技术进一步确定了该方法的准确性和可靠性。

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