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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 >Development and validation of a liquid chromatographic method for the analysis of squaric acid dibutyl ester and its impurities
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Development and validation of a liquid chromatographic method for the analysis of squaric acid dibutyl ester and its impurities

机译:液相色谱法分析基础酸二丁基酯及其杂质的发展与验证

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摘要

A simple, fast and selective stability indicating liquid chromatographic method has been described for the simultaneous determination of squaric acid dibutyl ester and its impurities. The chromatographic separation was achieved on a C2 column (250 mm x 4.6 mm i.d., 5 mu m) using a mobile phase consisting of 0.15% phosphoric acid - acetonitrile - methanol (30:60:10, v/v/v). Isocratic elution was performed at a flow rate of 1.0 mL min(-1). The analytes were detected by UV at 252 nm. The method was validated according to the ICH guidelines and satisfactory results were obtained. The specificity of the developed method was tested using forced degradation solutions of the drug substance.
机译:已经描述了一种简单,快速和选择性的稳定性,表明液相色谱法同时测定种族酸二丁基酯及其杂质。 使用由0.15%磷酸 - 乙腈 - 甲醇(30:60:10,v / v / v)组成的流动相,在C2柱(250mm×4.6mm I.D.,5μm)上实现色谱分离。 以1.0mL min(-1)的流速进行等级洗脱。 通过UV在252nm处检测分析物。 该方法根据ICH指南验证,并获得了令人满意的结果。 使用药物的强制降解溶液测试所开发方法的特异性。

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