alexa Abstract | Development and validation of stability indicating RP-LC method for estimation of ranalozine in bulk and its pharmaceutical formulations

Journal of Chemical and Pharmaceutical Research
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An isocratic reverse phase liquid chromatography (RP-LC) method has been developed and subsequently validated for the determination of Ranalozine in Bulk and its pharmaceutical formulation. Separation was achieved with a Symmetry RP-18 ((Make: Waters Corporation; 150 mmx4.6 mm I.D; particle size 3 μm)) Column and Potassium dihydrogen phosphate monohydrate buffer (pH adjusted to 3.0 with diluted orthophosphoric acid): methanol: acetonitrile (400:400:200) v/v as eluent at a flow rate of 1.2 mL/min. UV detection was performed at 225nm. The method is simple, rapid, and selective. The described method of Ranalozine is linear over a range of 11.98 μg/mL to 37.92 μg/mL. The method precision for the determination of assay was below 1.0%RSD. The percentage recoveries of active pharmaceutical ingredient (API) from dosage forms ranged from 99.1 to 100.9%. The results showed that the proposed method is suitable for the precise, accurate and rapid determination of Ranalozine in bulk, its capsule dosage forms.

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Author(s): Brahma Reddy Gade Sita Ram Bandhakavi M V Satyanarayana and Pavani Peddi


Ranalozine, RP-LC, Validation, Dosage form, pharmaceutical formulations

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