Development and Validation of RP-HPLC Method for the determination of Linezolid in pharmaceutical dosage form

Research Article
Nita P Nimbekar and Ambika S. Bhosle
DOI: 
http://dx.doi.org/10.24327/ijrsr.20251606.0067
Subject: 
Pharmacy
KeyWords: 
http://dx.doi.org/10.24327/ijrsr.20251606.0067
Abstract: 

A simple, precise, accurate sensitive and specific RP-HPLC method for the determination of Linezolid in pharmaceutical dosage form. Chromatogram was run through Sunfire C18 150 x 4.6 mm, 5m. Mobile phase containing 0.01N Potassium dihydrogen phosphate: Methanol taken in the ratio 65:35 was pumped through column at a flow rate of 1.2ml/min. Buffer used in this method was 0.01N Potassium dihydrogen phosphate (4.8ph) buffer. Temperature was maintained at 30°C. Optimized wavelength selected was 252.0nm. Retention time of Linezolid  was  found  to  be  2.469  min.  % RSD  of  the  Linezolid  were and    found to be 0.9 % RSD  of  Method  precision  of Linezolid was found to be 0.5. % Recovery was obtained as 100.29% for Linezolid. LOD, LOQ values obtained from regression equation of Linezolid were 0.10, 0.31. Regression equation of Linezolid is y = 39003x+14938. Retention times were decreased and that run time was decreased, so the method developed was simple and economical that can be adopted in regular Quality control test in Industries.