| dc.contributor.author | Hoogmartens, J | |
| dc.contributor.author | Roets, E | |
| dc.contributor.author | Debremaeker, D | |
| dc.contributor.author | Ngugi, JK | |
| dc.contributor.author | Chepkwony, HK | |
| dc.contributor.author | Kamau, Franco N. | |
| dc.date.accessioned | 2013-07-16T06:25:59Z | |
| dc.date.available | 2013-07-16T06:25:59Z | |
| dc.date.issued | 2002 | |
| dc.identifier.citation | J Chromatogr Sci. 2002 Oct;40(9):529-33. | en |
| dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/12433117 | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/47884 | |
| dc.description.abstract | An isocratic liquid chromatographic method with UV detection at 215 nm, which is suitable for the analysis of azithromycin (AZT) in bulk samples, is described. AZT is separated from its synthesis intermediates and a degradation product as well as from six unknown impurities on an XTerra RP18 column at 70 degrees C using a mobile phase consisting of acetonitrile-pH 6.5 0.2M K2HPO4-water (35:10:55, v/v/v) at 1.0 mL/min. The XTerra stationary phase contains methyl groups that are incorporated in the bulk structure of the material. This allows for special selectivities. Robustness is evaluated by a full factorial design experiment. The method shows good selectivity, repeatability, linearity, and sensitivity. | en |
| dc.language.iso | en | en |
| dc.title | Isocratic liquid chromatographic method for the analysis of azithromycin and its structurally related substances in bulk samples. | en |
| dc.type | Article | en |
| local.publisher | Department of Pharmaceutical Chemistry | en |
