Main Article Content


A Rapid and Precise Reverse Phase High Performance Liquid Chromatographic method has been developed for the validated of Reserpine and Dihydralazine, in its pure form as well as in tablet dosage form. Chromatography was carried out on X-Terra C18 (4.6 x 150mm, 5µm) column using a mixture of Methanol: TEA Buffer pH 4.5: Acetonitrile (65:15:20) as the mobile phase at a flow rate of 1.0ml/min, the detection was carried out at 212 nm. The retention time of the Reserpine and Dihydralazine was 2.090, 5.289 ±0.02min respectively. The method produce linear responses in the concentration range of 5-25mg/ml of Reserpine and 45-225mg/ml of Dihydralazine. The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.   


Reserpine Dihydralazine RP-HPLC validation

Article Details