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Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities

机译：氟尿利嗪及其主要生产杂质快速色谱分析方法的开发和验证

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O’Connor Niamh; Geary Michael; Wharton Mary; Sweetman Paul;
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年度 2013
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1. Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities [J] . Niamh O’Connor, Michael Geary, Mary Wharton, Journal of Pharmaceutical Analysis . 2013,第3期

机译：氟尿利嗪及其主要生产杂质快速色谱分析方法的开发和验证
2. Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities [J] . Niamh OConnor, Michael Geary, Mary Wharton, 药物分析学报（英文） . 2013,第003期

机译：氟尿利嗪及其主要生产杂质快速色谱分析方法的开发和验证
3. Development and Validation of a Stability-Indicating Liquid Chromatographic Method with Mass-Spectrometric Detection for the Analysis of Apixaban and Determination of Production Related Impurities [J] . Arous Basima, Al-Mardini Mohammad Amer Pharmaceutical Chemistry Journal . 2018,第6期

机译：一种稳定性指示液相色谱法的稳定性光谱检测的开发和验证，用于分析Apixaban和生产相关杂质的测定
4. Development and validation of a high performance sephadex gel chromatographic method for analysis of high polymer in cefotiam hydrochloride for injection [C] . Ming Chang, Ran Zhou, Fei Wang, International Conference on Medical Engineering and Bioinformatics . 2015

机译：高性能Sephadex凝胶色谱法分析盐酸小鸡盐酸高分子分析的开发与验证
5. Development and Validation of a Reversed-Phase Liquid Chromatographic Method to Quantify Pantoprazole Sodium Raw Material and the Corresponding Degradation Products [D] . Yaghi, Rose 2018

机译：反相液相色谱法量化Pan托拉唑钠原料及相应降解产物的开发与验证
6. Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities [O] . Niamh O’Connor, Michael Geary, Mary Wharton, 2013

机译：氟尿利嗪及其主要生产杂质快速色谱分析方法的开发和验证
7. Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities [O] . Niamh OâConnor, Michael Geary, Mary Wharton, 2013

机译：开发和验证用于分析氟桂利嗪及其主要生产杂质的快速色谱方法

Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities

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