SIMPLE AND RAPID LIQUID CHROMATOGRAPHIC METHOD FOR REAL-TIME QUANTIFICATION OF NAPROXEN / ESOMEPRAZOLE MAGNESIUM COMBINATION TABLETS
Venkateswara Rao, S Sandya, P Vasavi, Sunitha G N, Panikumar Durga Anumolu
Abstract
Venkateswara Rao, S Sandya, P Vasavi, Sunitha G N, Panikumar Durga Anumolu
Abstract
Purpose: In this present investigation a simple, rapid and accurate reverse phase- liquid chromatographic method for the real- time quantification of naproxen and esomeprazole magnesium in tablet dosage form has been developed and validated. Materials and Methods: Isocratic elution mode with a mixture of phosphate buffer, pH 4.0 and acetonitrile in the ratio of 55:45 v/v was selected as the mobile phase with a universal C18 column (250x4.6mm, 5μm) by using waters alliance 2695 HPLC system with UV-detector. The retention time of naproxen and esomeprazole magnesium were found to be 2.229 min and 3.379 min, respectively at flow rate of 1.0ml/min with UV detector to evaluate at 306 nm. Results: A linear relation ship was found between peak area response and concentration in the range of 18.75 μg/mL- 112.5 μg/mL and 1μg/mL- 6 μg/mL for naproxen and esomeprazole magnesium. The % RSD values were found to be less than 2 for accuracy and precision studies. Conclusion: The method can be applied to quality control of pharmaceutical formulations containing naproxen and esomeprazole magnesium.
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Purpose: In this present investigation a simple, rapid and accurate reverse phase- liquid chromatographic method for the real- time quantification of naproxen and esomeprazole magnesium in tablet dosage form has been developed and validated. Materials and Methods: Isocratic elution mode with a mixture of phosphate buffer, pH 4.0 and acetonitrile in the ratio of 55:45 v/v was selected as the mobile phase with a universal C18 column (250x4.6mm, 5μm) by using waters alliance 2695 HPLC system with UV-detector. The retention time of naproxen and esomeprazole magnesium were found to be 2.229 min and 3.379 min, respectively at flow rate of 1.0ml/min with UV detector to evaluate at 306 nm. Results: A linear relation ship was found between peak area response and concentration in the range of 18.75 μg/mL- 112.5 μg/mL and 1μg/mL- 6 μg/mL for naproxen and esomeprazole magnesium. The % RSD values were found to be less than 2 for accuracy and precision studies. Conclusion: The method can be applied to quality control of pharmaceutical formulations containing naproxen and esomeprazole magnesium.
Key concepts: Esomeprazole, Chromatography, Naproxen, Phosphate buffered saline, Chemistry, Magnesium, High-performance liquid chromatography, Dosage form