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Original Research Article | OPEN ACCESS

Development and Validation of Analytical Method for Losartan-Copper Complex Using UV-Vis Spectrophotometry

Syed S ul Hassan1, Syeda FA Zaidi1, Imran Tariq1 , Muhammad T Ansari2

1University College of Pharmacy, University of the Punjab, Lahore-54000; 2Department of Pharmacy, Bahaudin Zakariya University, Multan, Pakistan.

For correspondence:-  Imran Tariq   Email: imran1982@hotmail.com   Tel:00923224218583

Received: 3 August 2012        Accepted: 26 April 2013        Published: 12 June 2013

Citation: Hassan SS, Zaidi SF, Tariq I, Ansari MT. Development and Validation of Analytical Method for Losartan-Copper Complex Using UV-Vis Spectrophotometry. Trop J Pharm Res 2013; 12(3):407-411 doi: 10.4314/tjpr.v12i3.20

© 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 new spectrophotometric method for the analysis of losartan potassium in pharmaceutical formulations by making its complex with copper.
Method: A coloured complex based on UV/Vis spectroscopic method was developed for the determination of losartan potassium concentration in pharmaceutical formulations in the visible region. The colored complex of losartan was formed with cupric acetate (5:4). Analysis was carried out by the two methods - absorption ratio and calibration curve methods. The proposed method was validated in terms of linearity, accuracy and precision.
Results: The λ maximum of the complex was recorded at 530 nm.  Beer`s law was obeyed in the range of 10 - 50 µg/ml with a correlation coefficient (r2) of 0.9989. Mean analytical results from the calibration curve and absorption ratio methods were 99.42 and 99.16 % with relative standard deviation (RSD) of 0.97 and 0.82 %, respectively. Mean recovery was between 98.61 and 101.35 % and precision expressed as relative standard deviation (RSD) was 0.91 %.
Conclusion: The proposed method is simple, easy to apply, low-cost, and requires relatively inexpensive instruments. Thus, it is a suitable alternative to currently used spectrophotometric methods for the determination of losartan in bulk and solid dosage forms. 

Keywords: Losartan, Copper complex, Spectrophotometry, Validation

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Thompson Reuters (ISI): 0.523 (2021)
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