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Development and validation of a stability-indication LC-UV method for determination of daptomycin injectable form and kinetic study in alkaline medium

机译:碱性培养基测定稳定性指示LC-UV方法的发展与验证

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An isocratic liquid chromatography method (LC-UV) was developed and validated to determine daptomycin in injectable form. The method was carried out in a Waters XBridge C18 column (250 mm ?— 4.6 mm, 5 ??m). The mobile phase was composed of methanola€“acetonitrilea€“buffer (pH 2.2) (40:30:30 v/v/v) at a flow rate of 1.0 mLa?’1, using photodiode array (PDA) detection at 223 nm. The retention time obtained for daptomycin was 6.1 min and the method was linear in the range of 10 to 50 ??g mLa?’1 (r = 0.9999). Forced degradation studies were performed to verify the specificity and stability-indicating capability of the method. The degradation kinetics under alkaline conditions were also evaluated. The method showed suitable accuracy (99.17%) and precision (RSD 0.59%) A two level full factorial design was used to determine the method robustness. The proposed method was applied for the analysis of daptomycin injectable form, contributing to the improvement of the quality control of this pharmaceutical product.
机译:开发并验证了一种等级液相色谱法(LC-UV)以在可注射形式中测定达达霉素。该方法在水XBRIDGE C18柱中进行(250mm? - 4.6mm,5Ωm)。流动阶段由甲醇蛋白乙烯蛋白荷兰腈€“(pH 2.2)(40:30:30 v / v)以1.0mLaα1的流速组成,使用光电二极管阵列(PDA)检测在223 nm处。为达达霉素获得的保留时间为6.1分钟,该方法在10至50〜50Ω×1(r = 0.9999)的范围内。进行强制降解研究以验证该方法的特异性和稳定性指示性。还评估了碱性条件下的降解动力学。该方法显示出合适的精度(99.17%)和精度(RSD 0.59%),使用两级全部因子设计来确定方法鲁棒性。拟议的方法用于分析达托霉素可注射形式,有助于提高该药物产品的质量控制。

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