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Development of a liquid chromatographic method for the control of related substances in chlorprothixene hydrochloride
G M Duignan1, J H Miller, G G Skellern
1Department of Pharmaceutical Sciences, University of Strathclyde, Glasgow, UK.
Journal of Pharmaceutical and Biomedical Analysis
|February 1, 1996
Abstract:
The development of a reversed-phase liquid chromatographic method, using a mobile phase containing a mixture of anion and cation ion-pairing agents and a base-deactivated octyldecylsilyl column as stationary phase, is described for the control of all known impurities in (Z)-chlorprothixene hydrochloride (bulk drug). Validation of the method showed it to be reproducible, selective for both (Z) chlorprothixene hydrochloride and its E-isomer, accurate and linear over the concentration range of analysis with a limit of detection of 0.3 microgram ml-1.