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Original Research Article | OPEN ACCESS

Development and Validation of a Stability-Indicating RP-HPLC Method for Simultaneous Determination of Paracetamol, Tramadol HCl and Domperidone in a Combined Dosage Form

K Karunakaran1 , G Navaneethan1, K P Elango2

1Department of Sciences, Sona College of Technology (Anna University), Salem 636 005; 2Department of Chemistry, Gandhigram Rural Institute (Deemed University), Gandhigram 624 302, India.

For correspondence:-  K Karunakaran   Email: drkk@sonatech.ac.in   Tel:+914274099998

Received: 4 March 2011        Accepted: 7 December 2011        Published: 21 February 2012

Citation: Karunakaran K, Navaneethan G, Elango KP. Development and Validation of a Stability-Indicating RP-HPLC Method for Simultaneous Determination of Paracetamol, Tramadol HCl and Domperidone in a Combined Dosage Form. Trop J Pharm Res 2012; 11(1):99-106 doi: 10.4314/tjpr.v11i1.13

© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop a stability indicating RP-HPLC method for a combination drug product containing a high dose of paracetamol (PR) and low doses of domperidone (DM) and tramadol HCL (TR).
Methods: The analytes are well separated by a reverse phase column and an isocratic mobile phase consisting of 0.1 %v/v trifluoroacetic acid: acetonitrile: methanol in the ratio 70:25:5 (v/v) with a flow rate of 1.0 mL/min. The effluent was monitored at 272 nm. The drug products were subjected to stress conditions of acid, base, peroxide, thermal and photolytic degradation and peak homogeneity of PR, TR and DM were obtained using photo diode array detector.
Results: The degradation products were well resolved from PR, TR and DM peaks, thus indicating the stability-indicating nature of the method. The assay was linear from 165 – 495 µg/mL for PR, 18.75 – 56.25 µg/mL for TR, and 5 – 15 µg/mL for DM. Although the tablet contained high and low doses of the drugs, the intra- and inter-day variations were < 2.0 %.
Conclusion: The proposed method was validated according to the ICH guidelines and proved suitable for stability and homogeneity testing, as well as for quality control of the combined drugs in pharmaceutical preparations.

Keywords: HPLC, Isocratic, Peak purity, Simultaneous determination, Paracetamol, Tramadol, Domperidone

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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