Abstract

A simple and cost effective spectrophotometric method is described for the determination of torsemide in pure form and in pharmaceutical formulations. The method is based on the formation of blue colored chromogen when the drug reacts with Folin-Ciocalteu (F-C) reagent in alkaline medium. The colored species has an absorption maximum at 760 nm and obeys beer's law in the concentration range 30 – 150 ug mL−1. The absorbance was found to increase linearly with increasing concentration of TSM, which is corroborated by the calculated correlation coefficient value of 0.9999 (n=8). The apparent molar absorptivity and sandell sensitivity were 1.896×103L mol−1cm−1and 0.183 μg cm−2, respectively. The slope and intercept of the equation of the regression line are 5.4x10−3and 1.00×10−4respectively. The limit of detection was 0.94.The optimum experimental parameters for the reaction have been studied. The validity of the described procedure was assessed. Statistical analysis of the results has been carried out revealing high accuracy and good precision. The proposed method was successfully applied to the determination of TSM in pharmaceutical formulations.

Highlights

  • To the best of our knowledge, there is no work in the literature reported about the visible spectrophotometric method for the analysis of TSM in either biological fluids or pharmaceutical formulations

  • The method uses the well known reduction reaction involving Folin-Ciocalteu (F-C) reagent and TSM resulting in the formation of a blue chromogen that could be measured at 760 nm

  • The F-C reagent is used in the determination of many phenolic compounds[7] and a large number of substances of pharmaceutical interest[8,9,10,11,12,13,14,15]

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Summary

Introduction

The author has made an attempt to develop simple and sensitive spectrophotometric method for the estimation of TSM in pure drug and in pharmaceutical formulations. The purpose of this investigation was to develop a simple and sensitive visible spectrophotometric method for the quantization of TSM in pure drug and in pharmaceutical formulations.

Results
Conclusion
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