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DEVELOPMENT AND VALIDATION OF UV SPECTROPHOTOMETRIC METHOD FOR THE ESTIMATION OF DEFERASIROX IN BULK AND PHARMACEUTICAL FORMULATION
Akshay Ravindra Kale*, Dr. Ganesh B. Gajeli, Raviraj N. Jalkote, Manmat B. Rumane, Neha R. Gate and Kaveri C. Dulange
ABSTRACT A simple, accurate, precise and sensitive UV spectrophotometric method was developed for the determination of Deferasirox in bulk and pharmaceutical dosage form. The solvent used ethanol and water (9:1) and the wavelength corresponding to maximum absorbance of the drug was found at 248nm. Beers law was observed in the concentration range of 2- 10μg/ml with correlation coefficent 0.9992. The linear regression equation obtained by least square regression method were y = 0.0762x + 0.1058, where y is the absorbance and x is the concentration of the pure drug solution. The method was validated for several parameters like accuracy, precision as per ICH guidelines. The values of relative standard deviation and % recovery were found to be satisfactory, indicating that the proposed method is precise and accurate and hence can be used for the routine analysis of Deferasirox in bulk and pharmaceutical formulation. Keywords: Deferasirox, UV Spectrophotometer, Method Validation. [Download Article] [Download Certifiate] |