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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Quality by Design approach in the development of hydrophilic interaction liquid chromatographic method for the analysis of iohexol and its impurities
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Quality by Design approach in the development of hydrophilic interaction liquid chromatographic method for the analysis of iohexol and its impurities

机译:亲水相互作用色谱法开发用于碘海醇及其杂质分析的设计质量法

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This study presents the development of hydrophilic interaction liquid chromatographic method for the analysis of iohexol, its endo-isomer and three impurities following Quality by Design (QbD) approach. The main objective of the method was to identify the conditions where adequate separation quality in minimal analysis duration could be achieved within a robust region that guarantees the stability of method performance. The relationship between critical process parameters (acetonitrile content in the mobile phase, pH of the water phase and ammonium acetate concentration in the water phase) and critical quality attributes is created applying design of experiments methodology. The defined mathematical models and Monte Carlo simulation are used to evaluate the risk of uncertainty in models prediction and incertitude in adjusting the process parameters and to identify the design space. The borders of the design space are experimentally verified and confirmed that the quality of the method is preserved in this region. Moreover, Plackett-Burman design is applied for experimental robustness testing and method is fully validated to verify the adequacy of selected optimal conditions: the analytical column ZIC HILIC (100 mm x 4.6 mm, 5 mu m particle size); mobile phase consisted of acetonitrile-water phase (72 mM ammonium acetate, pH adjusted to 6.5 with glacial acetic acid) (86.7:13.3) v/v; column temperature 25 degrees C, mobile phase flow rate 1 mL min(-1), wavelength of detection 254 nm. (C) 2015 Elsevier B.V. All rights reserved.
机译:这项研究介绍了亲水相互作用色谱法的发展,该方法用于按照碘量法(QbD)分析碘海醇,其内异构体和三种杂质。该方法的主要目的是确定可以在保证方法性能稳定性的稳健区域内以最小分析持续时间获得足够分离质量的条件。关键工艺参数(流动相中的乙腈含量,水相的pH和水相中的乙酸铵浓度)与关键的质量属性之间的关系是通过实验方法设计而建立的。定义的数学模型和蒙特卡洛模拟用于评估模型预测中不确定性的风险和调整过程参数的不确定性,并确定设计空间。通过实验验证了设计空间的边界,并确认了该方法的质量在该区域得以保留。此外,采用Plackett-Burman设计进行实验鲁棒性测试,并充分验证了方法的有效性,以验证所选最佳条件的适当性:分析柱ZIC HILIC(100 mm x 4.6 mm,粒径5μm);流动相由乙腈-水相(72 mM醋酸铵,用冰醋酸将pH调节至6.5)(86.7:13.3)v / v组成;柱温25摄氏度,流动相流速1 mL min(-1),检测波长254 nm。 (C)2015 Elsevier B.V.保留所有权利。

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