Article ID Journal Published Year Pages File Type
3963648 Journal of Reproduction and Contraception 2009 7 Pages PDF
Abstract

ObjectiveTo compare the content, uniformity of dosage units and dissolution rate of triphasic oral contraceptives from two pharmaceutical factories A and B.MethodsA High Performance Liquid Chromatography (HPLC) method for the simultaneous determination of levonorgestrel and ethinylestradiol was used. The content of levonorgestrel (LNG) was monitored by an UV detector at 247 nm, while ethinylestradiol (EE) was monitored by fluorescence detector with the excitation of 285 nm and emission wavelengths of 310 nm. The dissolution test was performed using the paddle method.ResultsThe content of levonorgestrel (LNG) and ethinylestradiol (EE) in product A was within 100.5%-122.4% while product B within 120.6%-140.9%. The uniformity value of dosage units of tablets from two factories was more than 15. The dissolution rate of tables from two factories was more than 60% within 60 min.ConclusionOnly the content of product A was in the ± 25% range of label claim. The uniformity of two products was not up to standard. The dissolution rate of the tablets from two products met the requirement of ChP2005.

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Health Sciences Medicine and Dentistry Obstetrics, Gynecology and Women's Health