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Research Article


 

Simultaneous Quantification of Paracetamol and Meloxicam in Tablets by High Performance Liquid Chromatography

 

Madhusudhanareddy Induri*, Bhagavan R Mantripragada2, Rajendra P Yejella3, Pavankumar R Kunda2, Meechel Arugula4 and Rajkumar Boddu1

*1Department of Pharmaceutical Chemistry, Malla Reddy College of Pharmacy, Maisammaguda, Dhulapally, Secunderabad, Andhra Pradesh 500014, 2Department of Pharmaceutical Chemistry, C.M. College of Pharmacy, Maisammaguda, Dhulapally, Secunderabad, Andhra Pradesh 500014, 3Department of Pharmaceutical Chemistry, College of Pharmaceutical Sciences, Andhra University, Visakhapatnam, Andhra Pradesh 530003, 4Department of Pharmaceutical Analysis, St. Ann’s College of Pharmacy, Cantonment, Vizianagaram, Andhra Pradesh 530003, India

 

For correspondence: E-mail:  msreddyinduri@yahoo.com; Tel: +91-8125863579

Received: 5 December 2010                                                         Revised accepted: 26 June 2011

Tropical Journal of Pharmaceutical Research, Aug 2011; 10(4): 475-481 http://dx.doi.org/10.4314/tjpr.v10i4.13

Abstract

 

Purpose: To develop and validate a simple, rapid and inexpensive RP-HPLC method for the simultaneous estimation of paracetamol and meloxicam in tablets.

Methods: For the analysis of the drugs, chromatographic analysis was performed on XTerra symmetry C18 column (100 × 4.6 mm, 5 µ particle size) with mobile phase consisting of methanol and phosphate buffer (pH 9.2) in the ratio of 50:50 v/v, at a flow rate of 0.8 mL/min and eluents monitored at 244 nm. The method was validated for linearity, accuracy, precision, robustness and application for assay as per International Conference on Harmonization (ICH) guidelines.

Results: The retention times of paracetamol and meloxicam were 2.467 and 4.971 min, respectively. The calibration curves of peak area versus concentration, which was linear from 5 - 60 µg/mL for paracetamol and 1 - 12 µg/mL for meloxicam, had regression coefficient (r2) greater than 0.999. The method had the requisite accuracy, precision, and robustness for simultaneous determination of paracetamol and meloxicam in tablets.

Conclusion: The proposed method is simple, low-cost, accurate, precise and can be successfully employed in routine quality control for the simultaneous analysis of paracetamol and meloxicam in tablets.

 

Keywords: Paracetamol, Meloxicam, RP-HPLC, Simultaneous analysis, Tablets.

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