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J Pharm Biomed Anal ; 149: 57-65, 2018 Feb 05.
Article in English | MEDLINE | ID: mdl-29101816

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).


Subject(s)
Chromatography, High Pressure Liquid/methods , Drug Contamination/prevention & control , Quality Control , Spiramycin/standards , Tandem Mass Spectrometry/methods , Acetonitriles/chemistry , Chemistry, Pharmaceutical/instrumentation , Chemistry, Pharmaceutical/methods , Chemistry, Pharmaceutical/standards , Chromatography, High Pressure Liquid/instrumentation , Porosity , Reference Standards , Spiramycin/chemistry , Tandem Mass Spectrometry/instrumentation , Time Factors
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