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RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR ESTIMATION OF CHOLINE FENOFIBRATE IN TABLET DOSAGE FORM.
Satishkumar Shetty A, Dhananjay*, Manzoor Ahmed, Kuppast I.J, Anilkumar S.M, Ravi M.C
ABSTRACT The objective of the current study was to develop a simple, accurate, precise and rapid RP-HPLC method And subsequently validate as per ICH guidelines for the determination of Choline fenofibrate using mobile phase [mixture of Phosphate buffer pH-3.6 and acetonitrile in the ratio of 35:65] as the solvent. The proposed method involves the measurement of Retention time at selected analytical wavelength. 300.0 nm was selected as the analytical wavelength. The retention time of Choline fenofibrate was found to be 5.121. The linearity of the proposed method was investigated in the range of 20-100 μg/ml (r 2= 0.999). The method was statistically validated for its linearity, accuracy and precision. Both inter-day and intra-day variation was found to be showing less % RSD (Relative Standard Deviation) value indicating high grade of precision of the method. Keywords: Choline fenofibrate, HPLC, Method validation, acetonitrile and buffer. [Download Article] [Download Certifiate] |