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Spectrophotometric methods for the determination of gemifloxacin in pharmaceutical formulations

机译:分光光度法测定药物制剂中的吉非沙星

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This paper describes two simple spectrophotometric methods for the determination of the antibiotic gemifloxacin mesylate (GFX) in pharmaceutical formulations. The first (A) is an indirect method in which oxidation of the drug with a known excess of cerium (IV) sulphate is followed by determination of the residual oxidant by adding excess methyl orange and measuring residual dye at 507nm. The second (B) is a derivatisation method involving reaction of GFX with 1,2-naphthoquinone-4-sulphonate (NQS) in alkaline medium (pH 11) to form an orange-coloured product exhibiting maximum absorption (@l"m"a"x) at 411nm. The methods were linear in the concentration ranges 2-9 and 5-30@mg/mL for methods A and B, respectively, with intra-day precision (as RSD) <1.5% for both. When applied to the determination of GFX in pharmaceutical tablets, the results were in good agreement with those obtained by capillary electrophoresis. The two methods are useful for routine analysis of GFX in quality control laboratories.
机译:本文介绍了两种简单的分光光度法,用于测定药物制剂中的甲磺酸吉非沙星(GFX)。第一种(A)是一种间接方法,其中用已知过量的硫酸铈(IV)氧化药物,然后通过添加过量的甲基橙并在507nm处测量残留染料来确定残留氧化剂。第二种(B)是衍生化方法,包括在碱性介质(pH 11)中,GFX与1,2-萘醌-4-磺酸盐(NQS)反应,形成具有最大吸收(@l” m” a)的橙色产品“ x”在411nm处。方法A和B的浓度范围分别为2-9和5-30 @ mg / mL,呈线性,两种方法的日内精密度(如RSD)均<1.5%。药物片剂中GFX的测定结果与毛细管电泳法的测定结果吻合良好,这两种方法可用于质量控制实验室中GFX的常规分析。

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