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dc.contributor.authorCachet, T.H
dc.contributor.authorKibwage, IO
dc.contributor.authorRoets, E
dc.contributor.authorHoogmartens, H.
dc.contributor.authorVanderhaeghe, H.
dc.date.accessioned2013-02-19T09:25:35Z
dc.date.issued1987
dc.identifier.citationJournal of Chromatography, 409 (1987) 91-100en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/10241
dc.description.abstractAn improved high-performance liquid chromatographic method for analysis of erythromycin is described. The separation can be performed under mild conditions of pH (6.5) and temperature (35T) on C, and CIS silica-based reversed-phase ma¬terials of different origins. The mobile phase, with a flow-rate of 1.5 ml/min, con¬tained various amounts of acetonitrile (25-40%, v/v), 5% (v/v) 0.2 M ammonium phosphate buffer pH 6.5, 20% (v/v) 0.2 M tetramethylammonium phosphate and water. UV detection at 215 nm allows quantitation of erythromycins A, Band C, N-demethylerythromycin A, erythromycin A enol ether and anhvdroerythromycin A. The column history plays a major role, older columns often giving better separations.en
dc.language.isoenen
dc.titleOptimization of the separation of erythromycin and related substances by high-performance liquid chromatographyen
dc.typeArticleen
local.embargo.terms6 monthsen


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