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Original Research Article | OPEN ACCESS

Determination of Venlafaxine and Modafinil in Individual Tablet Dosage Forms using Single RP-HPLC Method

Mohammad Younus1 , Fasiuddin Md Arif2, Paul M Richards3, Bharat D Kumar4

1Chandra Labs; 2Dr. Reddy’s Laboratories Ltd; 3Malla Reddy College of Pharmacy, Hyderabad Andhra Pradesh India; 4Vignan Institute of Pharmaceutical Sciences, Nalgonda Dist, Andhra Pradesh, India.

For correspondence:-  Mohammad Younus   Email: mdyounus1127@gmail.com   Tel:+918686062421

Received: 17 July 2012        Accepted: 10 April 2013        Published: 24 April 2013

Citation: Younus M, Arif FM, Richards PM, Kumar BD. Determination of Venlafaxine and Modafinil in Individual Tablet Dosage Forms using Single RP-HPLC Method. Trop J Pharm Res 2013; 12(2):239-245 doi: 10.4314/tjpr.v12i2.17

© 2013 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 simple and selective isocratic method for the determination of venlafaxine and modafinil in tablet dosage forms.
Methods: The compounds were analyzed on Waters symmetry C18 column (4.6 mm x 250 mm i.d, 5µm) using a mobile phase consisting of a mixture of ammonium acetate buffer (pH was adjusted to 4.0 with glacial acetic acid):10 % methanol in acetonitrile, in the ratio of 60:40. The flow rate was 1.0 ml/min and column effluents were monitored at 225 nm. The method was validated according to ICH guidelines.
Results: Venlafaxine and modafinil were eluted with retention times of 4.416 min and 6.443 min, respectively. The method was linear in the range of 1.0 - 50 µg/ml for both venlafaxine and modafinil. The relative standard deviation (%RSD) was < 1 for both drugs while mean recovery values at different concentration levels were within limits. The performance of the method was not changed when small variations in the method were made.
Conclusion: The proposed method is accurate, reproducible and low-cost, and can be used for the routine analysis of the individual drugs in formulations.

Keywords: Modified acidic fibroblast growth factor (MaFGF), Renal injury, Apoptotic death, Actinomycin D (Act D)

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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