Method development and validation of Alfuzosin HCl and Dutasteride in pharmaceutical dosage form by RP-HPLC

Abstract

A simple, economic, rapid, precise and accurate reverse phase high pressure liquid chromatographic method was developed and validated for the simultaneous determination of Alfuzosin and Dutasteride in Pharmaceutical dosage form. The RP-HPLC separation was Performed on XterraC18 column (250mmL×4.6mmI.D×5μ) using mobile phase acetonitrile: phosphate buffer (pH-6.5): water (75:15:10v/v/v) at a flow rate of 0.8 ml/min at an ambient temperature. Quantitation by HPLC was achieved with UV detection at 245nm based on peak area with linear calibration curves at concentration ranges 5-25μg/ml for ALFU and 10-50 μg/ml for DUTA, respectively. The limit of detections (LOD) was 0.0045 μg/ml for ALFU and 0.03 μg/ml for DUTA. The developed method was validated in terms of accuracy, precision, linearity, robustness and results will be validated statistically according to ICH guidelines.

Authors and Affiliations

P. Madhusudhan , M. Radhakrishna Reddy , N. Devanna

Keywords

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  • EP ID EP159716
  • DOI -
  • Views 75
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How To Cite

P. Madhusudhan, M. Radhakrishna Reddy, N. Devanna (2015). Method development and validation of Alfuzosin HCl and Dutasteride in pharmaceutical dosage form by RP-HPLC. International Journal of Novel Trends in Pharmaceutical Sciences, 5(3), 95-101. https://europub.co.uk/articles/-A-159716