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Development and validation of a rapid chromatographic method for the analysis of flunarizine and its main production impurities
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作者 Niamh O'Connor Michael Geary +1 位作者 Mary Wharton paul sweetman 《Journal of Pharmaceutical Analysis》 SCIE CAS 2013年第3期211-214,共4页
A rapid selective method for the analysis of flunarizine and its associated impurities was developed and validated according to ICH guidelines. The separation was carried out using a Thermo Scientific Hypersil Gold C1... A rapid selective method for the analysis of flunarizine and its associated impurities was developed and validated according to ICH guidelines. The separation was carried out using a Thermo Scientific Hypersil Gold C18 column (50 mm × 4.6 mm i.d., 1.9 μm particle size) with a gradient mobile phase of acetonitrile-ammonium acetate-tetrabutylammoniumhydrogen sulfate buffer, at a flow rate of 1,8 mL/min and UV detection at 230 nm. Naturally aged samples were also tested to determine sample stability. A profile of sample and impurity breakdown was also presented. 展开更多
关键词 FLUNARIZINE Sub 2 gm column Active pharmaceuticalingredient HPLC
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