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What is HPLC Method for Dosulepin Validation about?

A rapid and precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validated of Dosulepin in its pure form as well as in tablet dosage form. Chromatography was carried out on Xterra C18 (4.6×150mm, 5µ) column using a water (100% v/v) as the mobile phase at a flow rate of 1.0ml/min, the detection was carried out at 230nm. The retention time of the Dosulepin was 2.1 ±0.02min. The method produce linear responses in the concentration range of 5-25µg/ml of Dosulepin .

Author

Baru Chandrasekhar Rao

Language

EN