ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF OMEPRAZOLE AND ASPIRIN USING REVERSE PHASE HPLC METHOD IN BULK AND DOSAGE FORM

Abstract

A new simple, accurate, precise and reproducible RP-HPLC method has been developed for the simultaneous estimation of Aspirin and Omeprazole in bulk and pharmaceutical dosage form using C18 column (Agilent, 250 x 4.6 mm, 5 μm) in isocratic mode. The mobile phase consisted of Methanol and 0.1 M Dipotassium Phosphate buffer (pH 3) in the ratio of 60:40 v/v. The detection was carried out at 256 nm. The method was linear over the concentration range for Omeprazole 50-250 μg/ml and for Aspirin 10-50 μg/ml. The recoveries of Omeprazole and Aspirin were found to be 100.07 and 100.06% respectively. The validation of method was carried out utilizing ICH-guidelines. The described HPLC method was successfully employed for the analysis of pharmaceutical formulations containing combined dosage form.


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Peer Review History:


Received 22 August;   Revised 28 August; Accepted 5 September, Available online 15 September 2017


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Received file


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Average Peer review marks at initial stage: 5.0/10


Average Peer review marks at publication stage: 7.5/10


Reviewer(s) detail:


Name: Dr. Showkat Ahmad Bhawani


Affiliation: UNIMAS Sarawak,  Malaysia


E-mail: sabhawani@gmail.com


 


Name: Dr.  Maya Shaaban Eissa Hussein


Affiliation: Egyptian Russian University, Egypt


E-mail: maya-shaaban@hotmail.com


Comments of reviewer(s):


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Keywords: Omeprazole, Aspirin, reverse phase HPLC, validation
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How to Cite
R, V., and S. M. “ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF OMEPRAZOLE AND ASPIRIN USING REVERSE PHASE HPLC METHOD IN BULK AND DOSAGE FORM”. Universal Journal of Pharmaceutical Research, Vol. 2, no. 4, July 2017, doi:https://doi.org/10.22270/ujpr.v2i4.R6.
Section
Research Articles