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 liquid chromatography tandem mass spectrometry methods for the determination of gentamicin, lincomycin, and spectinomycin in the presence of their impurities in pharmaceutical formulations.
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Development and validation of liquid chromatography tandem mass spectrometry methods for the determination of gentamicin, lincomycin, and spectinomycin in the presence of their impurities in pharmaceutical formulations.

机译:在药物制剂中存在杂质的情况下,测定庆大霉素,林可霉素和大观霉素的液相色谱串联质谱法的开发和验证。

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Liquid chromatography with tandem mass spectrometry (LC/MS/MS) methods for the determination of gentamicin, lincomycin and spectinomycin in the presence of their impurities were developed and tested. Chromatographic separations were achieved using gradient elution on a C18 column. All components were ionized by positive-ion electrospray and detected by multi reaction monitoring (MRM) with an LC-tandem mass spectrometer. Calibration curves were linear with correlation coefficients better than 0.99. The developed method for the determination of gentamicin provides complete base line separation of components C1, C1a, C2, C2a and C2b mentioned in the European and British Pharmacopoeias. The second developed method makes possible a simultaneous analysis of the active compounds of both lincomycin and spectinomycin. Additionally, all impurities defined in the pharmacopoeias for all three active components were determined and their identities confirmed. The methods were tested in routine quality control analysis.
机译:开发并测试了串联色谱法(LC / MS / MS)在庆大霉素,林可霉素和大观霉素存在下的测定方法。色谱分离是通过在C18色谱柱上使用梯度洗脱实现的。所有成分均通过正离子电喷雾离子化,并通过LC串联质谱仪进行多反应监测(MRM)进行检测。校准曲线呈线性,相关系数优于0.99。测定庆大霉素的已开发方法提供了欧洲和英国药典中提到的组分C1,C1a,C2,C2a和C2b的完全基线分离。第二种开发的方法可以同时分析林可霉素和壮观霉素的活性化合物。另外,确定在药典中定义的所有三种活性成分的所有杂质,并确认其身份。在常规质量控制分析中对这些方法进行了测试。

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