Optimization of the separation of erythromycin and related substances by high-performance liquid chromatography
| dc.contributor.author | Cachet, T.H | |
| dc.contributor.author | Kibwage, IO | |
| dc.contributor.author | Roets, E | |
| dc.contributor.author | Hoogmartens, H. | |
| dc.contributor.author | Vanderhaeghe, H. | |
| dc.date.accessioned | 2013-02-19T09:25:35Z | |
| dc.date.issued | 1987 | |
| dc.identifier.citation | Journal of Chromatography, 409 (1987) 91-100 | en |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/10241 | |
| dc.description.abstract | An 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.iso | en | en |
| dc.title | Optimization of the separation of erythromycin and related substances by high-performance liquid chromatography | en |
| dc.type | Article | en |
| local.embargo.terms | 6 months | en |
Files in this item
This item appears in the following Collection(s)
-
Faculty of Health Sciences (FHS) [10418]

