Separation and structural elucidation of cefsulodin and its impurities in both positive and negative ion mode in cefsulodin sodium bulk material using liquid chromatography/tandem mass spectrometry

• Published in: Rapid communications in mass spectrometry 2021-08, Vol.35 (15), p.e9125-n/a
• Main Authors: Ren, Xiaojuan, Liu, Guijun, Tang, Kaixian, Zhou, Ping, Wang, Jian
• Format: Article
• Language: English
• Subjects: Acetonitrile; Ammonium sulfate; Analytical chemistry; Aqueous solutions; Cephalosporins; Chromatography; Impurities; Ions; Liquid chromatography; Mass spectrometry; Negative ions; Quality control; Scientific imaging; Separation; Sodium; Spectroscopy
• ISSN: 0951-4198; 1097-0231
• DOI: 10.1002/rcm.9125

Rationale The structural identification of impurities in cephalosporins has been reported. However, to the best of our knowledge, there was no report on the impurities of cefsulodin sodium, which is necessary for the quality control. Thus, the aim of this study was to separate and characterize the impurities in cefsulodin sodium raw material using liquid chromatography/tandem mass spectrometry (LC/MS/MS). Methods The analytes were separated on a Kromasil 100‐5C18 column (4.6 mm × 250 mm, 5 μm) using a gradient elution with a mobile phase consisting of 1% ammonium sulphate aqueous solution and acetonitrile in the first dimension. The separation in the second dimension was carried on a Shimadzu Shim‐pack GISS C18 column (50 mm × 2.1 mm, 1.9 μm) with a mobile phase consisting of 10 mM ammonium formate solution and methanol. Results The fragmentation behaviors of cefsulodin and its impurities were studied and the structures of the impurities were deduced based on the MSn data. The structures of ten unknown impurities were proposed based on the work carried out in this study. The degradation behaviors of cefsulodin sodium were also studied. This revealed that cefsulodin sodium should be stored in a dry, cool and dark closed container. Conclusions Based on the characterization of impurities, this study not only revealed the mechanism by which impurities were produced, thus providing guidance to pharmaceutical companies for manufacturing process improvement and impurity control, but also provided a scientific basis for further improvement of official monographs in pharmacopoeias.