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Determination of grepafloxacin and clinafloxacin by capillar zone electrophoresis

机译:毛细管区带电泳法测定格列帕沙星和克林沙星

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A simple and rapid capillary zone electrophoresis determination method with UV detection of grepafloxacin and clinafloxacin has been developed. The separation was performed in 35 mM borate-35 mM phosphate buffer solution (pH 8.6), containing 6% (v/v) of acetonitrile. Analyses were realised using fused-silica capillaries (57 cm length * 75 μm I.D.) and the operating conditions were: 15 kV applied voltage, 30 ℃ and detection at 279 nm. Piromidic acid was used as an internal standard. The linear concentration range of application was 1.0-120.0 μg ml~(-1) for both compounds, with a detection limit of 0.2 μg ml~(-1) for grepafloxacin and 0.3 μg ml~(-1) for clinafloxacin. The analysis yielded good reproducibility (RSD between 3.37 and 1.74%). It was applied to the determination of grepafloxacin and clinafloxacin in human and rat urine samples. The method was validated using HPLC as a reference method. Recovery levels were between 94.5 and 103%.
机译:建立了一种简便,快速的毛细管区带电泳测定方法,该方法通过紫外检测格列沙星和克林沙星。分离是在35 mM硼酸盐-35 mM磷酸盐缓冲溶液(pH 8.6)中进行的,该溶液中含有6%(v / v)的乙腈。使用熔融石英毛细管(57厘米长* 75μmI.D.)进行分析,操作条件为:施加电压15 kV,30℃,在279 nm处检测。吡mid酸用作内标。两种化合物的线性应用浓度范围是1.0-120.0μgml〜(-1),格列沙星的检出限为0.2μgml〜(-1),克林沙星的检出限为0.3μgml〜(-1)。分析产生了良好的重现性(RSD在3.37和1.74%之间)。它用于测定人和大鼠尿液样品中的格列氟沙星和克林沙星。使用HPLC作为参考方法验证了该方法。回收率在94.5%至103%之间。

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