Jiang Su Institute for Food and Drug Control, Nanjing 210008, China.
J Pharm Biomed Anal. 2013 Mar 5;75:94-104. doi: 10.1016/j.jpba.2012.11.029. Epub 2012 Nov 27.
The characterization of impurities present in micronomicin sulfate injection by liquid chromatography (LC) coupled with mass spectrometry (MS) is described. A reversed phase (RP)-LC method using a C₁₈ column resistant to an alkaline (pH 11) aqueous mobile phase was developed and coupled to MS with an electrospray ionization (ESI) source in the positive ion mode which provides MS(n) capability. A total of thirty six impurities were detected in commercial samples: five impurities were identified by comparison of their fragmentation patterns with those of available related substances, eleven of them were identified in accordance with relevant literature, while the other twenty impurities were newly identified using the MS/MS spectra of the available related reference substances as interpretative templates combined with knowledge of the nature of functional group fragmentation behaviors. This work was applied to evaluate the quality of micronomicin sulfate injection from different manufacturers.
本文描述了通过液相色谱(LC)与质谱(MS)联用技术对硫酸米卡星注射液中杂质的特性进行分析。建立了一种采用耐碱性(pH 11)水相流动相的反相(RP)-LC 方法,并与电喷雾电离(ESI)源在正离子模式下进行 MS 联用,从而提供 MS(n) 能力。在商业样品中检测到三十六个杂质:五个杂质通过与现有相关物质的碎片模式比较进行鉴定,十一个杂质根据相关文献进行鉴定,而其他二十个杂质则是使用可用相关参考物质的 MS/MS 光谱作为解释模板,并结合功能基团碎片行为的性质知识来新鉴定的。这项工作应用于评估来自不同制造商的硫酸米卡星注射液的质量。