Asian Journal of Research in Chemistry

  • Year: 2011
  • Volume: 4
  • Issue: 1

Development and Validation of High Performance Liquid Chromatographic Method for Estimation of Deflazacort in Pharmaceutical Formulation

  • Author:
  • D.D. Chougule, N.S. Naikwade
  • Total Page Count: 3
  • DOI:
  • Page Number: 140 to 142

Appasaheb Birnale College of Pharmacy, Sangli. South-Shivaji Nagar, Sangli-416416 (MS)

Abstract

A simple, selective, rapid and precise reverse phase HPLC method has been developed for the estimation of Deflazacort in pharmaceutical dosage form. A Hypersil BDS C18 (250 mm X 4.6mm) column was used for separation. The mobile phase was ammonium acetate buffer solution: acetonitrile (50:50 v/v). Flow rate 1.0ml/min with detection at 254 nm. The retention time of Deflazacort was 6.03min. Linearity obtained in the concentration range of 20–100μg/ml with correlation coefficient of 0.998. The result of the analysis were validated statistically and recovery studies confirmed by the accuracy of the proposed method. The proposed RP-HPLC method for the estimation of Deflazacort in dosage form is accurate, precise, linear, robust, simple, rapid and selective.

Keywords

RP-HPLC, Deflazacort