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J Pharm Biomed Anal ; 20(5): 745-52, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10701982

ABSTRACT

A reversed-phase liquid chromatography method has been developed for the separation of clindamycin from 7-epiclindamycin, clindamycin B, lincomycin, lincomycin B, 7-epilincomycin and other impurities of unknown identity. The method uses a Hypersil ODS, 5 microm, 250 x 4.6 mm i.d. column maintained at 45 degrees C. The mobile phase comprises acetonitrile phosphate buffer (1.35% v/v phosphoric acid, adjusted to pH 6.0 with ammonium hydroxide)-water (35:40:25, v/v) at a flow rate of 1.0 ml/min. UV detection is performed at 210 nm. The method was tested on several C-18 columns and showed good robustness. Robustness was further evaluated by performing a full-fraction factorial design experiment. The method showed good selectivity, linearity, and repeatability. It is also suitable for analysis of clindamycin formulations.


Subject(s)
Anti-Bacterial Agents/analysis , Clindamycin/analysis , Anti-Bacterial Agents/isolation & purification , Capsules/analysis , Chromatography, Liquid/methods , Chromatography, Liquid/standards , Clindamycin/isolation & purification , Hydrogen-Ion Concentration , Reproducibility of Results , Structure-Activity Relationship , Temperature
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