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Analysis of ofloxacin and flavoxate HCl either individually or in combination via a green chromatographic approach with a pharmacokinetic study of ofloxacin in biological samples

机译:氧氟沙星和盐酸氟伏沙星的单独分析或通过绿色色谱方法结合生物样品中氧氟沙星的药代动力学研究进行分析

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A new sensitive and rapid micellar liquid chromatographic method was developed for the determination of ofloxacin (OFL) and flavoxate hydrochloride (FLV) in different pharmaceutical formulations. The analyses were carried out on a BDS Hypersil phenyl column (4.6 mm ?— 250 mm, 5 ??m particle size) using a micellar mobile phase consisting of 0.15 M sodium dodecyl sulfate, 15% n-propanol, 0.3% triethylamine, and 0.02 M orthophosphoric acid (pH 2.5) with UV detection at 325 nm. The proposed method exhibited good linearity over the concentration range of 2.0a€“40.0 ??g mLa?’1 for the two drugs with lower detection limits of 0.16 ??g mLa?’1 for OFL and 0.32 ??g mLa?’1 for FLV. The proposed method was applied to the determination of OFL and FLV in their co-formulated and single ingredient dosage forms with good percentage recoveries (99.86a€“99.98%) and small standard deviation values (?±0.18 to ?±1.26). The results of the proposed method were statistically compared with those obtained by the comparison methods revealing no significant differences in the performance of the two methods regarding accuracy and precision. To achieve high sensitivity that allows the pharmacokinetic study of OFL, fluorescence detection at 290/485 nm was employed. A linear relationship was achieved for OFL in plasma and urine over the concentration ranges of 0.01a€“0.10 and 0.01a€“0.20 ??g mLa?’1 with mean percentage recoveries of 100.8 ?± 2.85% and 101.1 ?± 2.78%, respectively. A pharmacokinetic study of OFL in human plasma and urine was conducted.
机译:建立了一种灵敏,快速的胶束液相色谱新方法,用于测定不同药物制剂中的氧氟沙星(OFL)和盐酸黄酮酸(FLV)。使用由0.15 M十二烷基硫酸钠,15%正丙醇,0.3%三乙胺和0.15 M组成的胶束流动相,在BDS Hypersil苯基色谱柱(4.6 mmφ-250 mm,粒径5φm)上进行分析。 0.02 M正磷酸(pH 2.5),在325 nm处有UV检测。所提出的方法在两种药物的浓度范围为2.0a?40.0?g mLa?1时表现出良好的线性,OFL和0.32?gmLa?1的检测限较低,为0.16?gmLa?'1。 FLV为1。所提出的方法用于共同配制和单一成分剂型中OFL和FLV的测定,回收率好(99.86a-99.98%),标准偏差小(±0.18至±1.26)。将该方法的结果与通过比较方法获得的结果进行统计比较,发现这两种方法在准确性和精确度方面的性能没有显着差异。为了获得允许OFL药代动力学研究的高灵敏度,采用了290/485 nm的荧光检测。血浆和尿液中OFL在0.01a±0.10和0.01a±0.20 g·g mLa?1的浓度范围内达到线性关系,平均回收率分别为100.8±2.85%和101.1±2.78% , 分别。进行了人血浆和尿液中OFL的药代动力学研究。

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