| Literature DB >> 29101816 |
Qi Lin1, Getu Kahsay2, Tom de Waal1, Peixi Zhu1, Minh Tam1, Roel Teughels1, Wenhua Wang3, Ann Van Schepdael1, Erwin Adams4.
Abstract
This article describes the development and validation of a liquid chromatographic method for spiramycin using a column with superficially porous particles. Gradient elution was applied and the mobile phase consisted of phosphate buffer (0.2M; pH 8.3) - H2O - acetonitrile in a ratio 10:60:30 (v/v/v) for mobile phase A and 10:30:60 (v/v/v) for mobile phase B. UV detection was performed at 232nm. Compared to previous methods, the analysis time was about two times faster and impurities were better separated. Furthermore, impurities which were present above 0.25% were characterized using liquid chromatography coupled with mass spectrometry (LC/MS).Entities:
Keywords: Core-shell particle; Impurity characterization; Liquid chromatography; Spiramycin
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Year: 2017 PMID: 29101816 DOI: 10.1016/j.jpba.2017.10.041
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935