World Journal of Pharmaceutical
and Medical Research

( An ISO 9001:2015 Certified International Journal )

An International Peer Reviewed Journal for Pharmaceutical and Medical Research and Technology
An Official Publication of Society for Advance Healthcare Research (Reg. No. : 01/01/01/31674/16)
ISSN 2455-3301
IMPACT FACTOR: 6.842

ICV : 78.6

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Abstract

ASSAY METHOD DEVELOPMENT AND VALIDATION FOR S IMULTANEOUS ESTIMATION OF PAROXETINE AND CLONAZEPAM BY RP- HPLC

N. Naidu*, M. Yellappa, Lingam Praveenkumar, Malapati Indira Pothakamuri Koteswararao

ABSTRACT

A simple, precise, rapid, specific and accurate reverse phase high performance liquid chromatography method was developed for simultaneous estimation of Paroxetine and Clonazepam in pharmaceutical dosage form. Chromatographic separation was performed on INERTSIL ODS 3V column,C18(250x4.6 ID) column, with mobile phase comprising of mixture of buffer (pH7, adjusted with ammonium acetate),methanol , acetonitrile in the ratio of 3:2:5, at the flow rate 1.0 ml/min. The detection was carried out at 224 nm. The retention times of paroxetine and clonazepam were found to be 2.367 and 4.867 mins respectively with a run time of 6 mins, theoretical levels for paroxetine and clonazepam were 2320 and 3211 respectively, with a resolution of 8.249. As per ICH guidelines the method was validated for linearity, accuracy, precision, limit of detection and limit of quantitation, robustness and ruggedness. Linearity of paroxetine was found in the range of 60-140?g/mL and that for clonazepam was found to be 2.4-5.6 ?g/mL.

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