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Enantioseparation of Nadifloxacin by High performance liquid Chromatography

机译:高效液相色谱法拆分纳地沙星

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A rapid isocratic chiral HPLC method has been developed for the separation of R-Nadifloxacin from S-Nadifloxacin. Good resolution viz. Rs> 4.0 between R- and S- forms of Nadifloxacin was achieved by RP-HPLC using endcappedC18 stationary phase and chiral mobile phase. Chirality to the mobile phase was imparted with addition of β-CD in phosphate buffer with EDTA.Column temperature was 45°C and flow rate was kept 1.5 mL min-1.The elution was monitored by UV-vis detector at λ-290 nm. The calibration curve showed excellent linearity over concentration range 0.040-20 μg mL-1.This method was further used to determine the amount of R-Nadifloxacin in pure and active pharmaceutical ingredient of S-Nadifloxacin and is capable to quantitate and detect R-Nadifloxacin to the levels of 0.040μg mL-1and 0.020μg mL-1 respectively. The average recovery of R-Nadifloxacin was 99.09 %. The method is better than the already reported one for the enantioseparation of the Nadifloxacin.
机译:已经开发了一种快速等度手性HPLC方法,用于从S-纳迪沙星中分离R-纳迪沙星。良好的分辨率,即。使用封端的C18固定相和手性流动相,通过RP-HPLC测定纳迪沙星的R型和S型之间的Rs> 4.0。在EDTA磷酸盐缓冲液中加入β-CD可提高流动相的手性。柱温为45 ° C,流速保持在1.5 mL min -1 。通过UV-vis检测器在λ-290nm下监测洗脱。校准曲线在0.040-20μgmL -1 浓度范围内显示出极好的线性。该方法可用于测定S-纳地沙星纯净和活性药物成分中R-纳地沙星的含量,并且能够分别定量和检测R-纳地沙星的含量为0.040μgmL -1 和0.020μgmL -1 。 R-纳地沙星的平均回收率为99.09%。该方法优于已报道的纳地沙星对映体分离方法。

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