首页> 外文期刊>Журнал аналитической химии >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)作为抗氧剂的滴定法测定氧氟沙星在药物中的含量

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摘要

Two titrirnetric methods which are simple, rapid, cost-effective and eco-riendly are described for the deter-mination 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) sul-phate 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 ltration 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 В 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 У calculating percent relative error (%RE) foraccuracy and percent relative standard deviation (% RSD) for precision, and were applied successfully to the detennination 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 via standard-addition technique.
机译:描述了两种简便易行,快速,经济高效且环保的滴定方法,用于确定散装药物和片剂中氧氟沙星(OFX)的含量,该方法基于硫酸铈(IV)对OFX的氧化作用。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)涉及将已知过量的硫酸铈(IV)加入酸化OFX溶液,然后使用相同的铁蛋白指示剂,通过硫酸亚铁铵(FAS)的反过滤,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В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))。对这些方法进行统计学评估⇨计算准确性的相对误差百分比(%RE)和相对标准偏差百分比(%RSD)以精确度计算,并成功地应用于片剂中OFX的测定,平均回收率在96.50-98.42%之间。没有观察到药物制剂中常见添加剂的干扰。通过标准添加技术进行恢复测试,进一步确定了方法的准确性和可靠性。

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