A simple, sensitive and acute UV spectrophotometric method has been developed for the determination of alogliptin in bulk and pharmaceutical tablet dosage formulation. This method obeys Beerâ��s law in the concentration range of 3-18 �µg/ml with correlation coefficient of 0.9994 and absorption maximum at 272-282 nm in Distilled water. The percentage recovery of alogliptin ranged from 100.05 to 100.40 %. The developed method was validated for accuracy, precision, LOD, LOQ as per ICH guidelines. Statistical analysis proved that the developed method shows the % RSD within the acceptance limit. It was concluded that the developed method was simple, accurate, precise, reproducible, selective and it can be employed for the routine analysis of alogliptin in pure and tablet dosage form.
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