Simultaneous Estimation of Diphenhydramine Hydrochloride and Naproxen Sodium in Raw and Tablet Formulation by Reverse Phase - High-Performance Liquid Chromatographic Method
Mohammed Al Bratty, Gunasekar Manoharan
Abstract
Open-access reader
Mohammed Al Bratty, Gunasekar Manoharan
Abstract
Open-access reader
Aims: A simple, reproducible method was developed for the simultaneous determination of Diphenhydramine and Naproxen in tablet formulation using reverse phase HPLC method.Methodology: HPLC separation was carried over on Thermo hypersil -keystone C18 (250 x 4.6 mm, 0.5 ) isocratic mode column using a mobile phase comprising a 30:70 (% v/v) of methanol and 0.5 mM phosphate buffer.The detection was proceeded out by UV detector at 270 nm.The linearity range taken for Diphenhydramine and Naproxen were 15 -35 mcg/ml and 100-500 mcg/ml respectively.Results: The percentage recovery was found to be 99.74% and 101.11% for Diphenhydramine and Naproxen respectively.The amount of Diphenhydramine and Naproxen found in tablet was Original Research Article 25.006 mg and 219.07 mg respectively. of Diphenhydramine and Naproxen Diphenhydramine and 4.9 minutes for Naproxen Conclusion: The proposed method shows very less time consuming analysis.The proposed method of analysis shows good separation at less retention time and less cost.The developed method can be successfully applied for the de bulk powder and combined tablet dosage form.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aims: A simple, reproducible method was developed for the simultaneous determination of Diphenhydramine and Naproxen in tablet formulation using reverse phase HPLC method.Methodology: HPLC separation was carried over on Thermo hypersil -keystone C18 (250 x 4.6 mm, 0.5 ) isocratic mode column using a mobile phase comprising a 30:70 (% v/v) of methanol and 0.5 mM phosphate buffer.The detection was proceeded out by UV detector at 270 nm.The linearity range taken for Diphenhydramine and Naproxen were 15 -35 mcg/ml and 100-500 mcg/ml respectively.Results: The percentage recovery was found to be 99.74% and 101.11% for Diphenhydramine and Naproxen respectively.The amount of Diphenhydramine and Naproxen found in tablet was Original Research Article 25.006 mg and 219.07 mg respectively. of Diphenhydramine and Naproxen Diphenhydramine and 4.9 minutes for Naproxen Conclusion: The proposed method shows very less time consuming analysis.The proposed method of analysis shows good separation at less retention time and less cost.The developed method can be successfully applied for the de bulk powder and combined tablet dosage form.
Key concepts: Chemistry, Chromatography, Naproxen, Diphenhydramine hydrochloride, High-performance liquid chromatography, Diphenhydramine, Phase (matter), Naproxen Sodium