Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode

A simple and rapid method was developed using cyclic and square wave voltammetric techniques for the determination of trace-level sulfur containing compound, 2-thiouracil, at a glassy carbon electrode. 2-thiouracil produced two anodic peaks at 0.334 V and 1.421 V and a cathodic peak at −0.534 V. The...

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Main Authors: Naveen M. Gokavi, Vijay P. Pattar, Atmanand M. Bagoji, Sharanappa T. Nandibewoor
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:International Journal of Electrochemistry
Online Access:http://dx.doi.org/10.1155/2013/627854
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spelling doaj-d07d7fae528043a5baccef5b6699b74e2020-11-24T20:44:03ZengHindawi LimitedInternational Journal of Electrochemistry2090-35292090-35372013-01-01201310.1155/2013/627854627854Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon ElectrodeNaveen M. Gokavi0Vijay P. Pattar1Atmanand M. Bagoji2Sharanappa T. Nandibewoor3P. G. Department of Studies in Chemistry, Karnatak University, Dharwad 580003, IndiaP. G. Department of Studies in Chemistry, Karnatak University, Dharwad 580003, IndiaP. G. Department of Studies in Chemistry, Karnatak University, Dharwad 580003, IndiaP. G. Department of Studies in Chemistry, Karnatak University, Dharwad 580003, IndiaA simple and rapid method was developed using cyclic and square wave voltammetric techniques for the determination of trace-level sulfur containing compound, 2-thiouracil, at a glassy carbon electrode. 2-thiouracil produced two anodic peaks at 0.334 V and 1.421 V and a cathodic peak at −0.534 V. The square wave voltammetry of 2-thiouracil gave a good linear response in the range of 1–20 μM with a detection limit of 0.16 μM and quantification limit of 0.53 μM (0.0679 μg/g), which is in good agreement as per IUPAC definition of trace component analysis (100 μg/g). The obtained recoveries range from 98.10% to 102.1%. The proposed method was used successfully for its quantitative determination in pharmaceutical formulations and urine as real samples.http://dx.doi.org/10.1155/2013/627854
collection DOAJ
language English
format Article
sources DOAJ
author Naveen M. Gokavi
Vijay P. Pattar
Atmanand M. Bagoji
Sharanappa T. Nandibewoor
spellingShingle Naveen M. Gokavi
Vijay P. Pattar
Atmanand M. Bagoji
Sharanappa T. Nandibewoor
Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
International Journal of Electrochemistry
author_facet Naveen M. Gokavi
Vijay P. Pattar
Atmanand M. Bagoji
Sharanappa T. Nandibewoor
author_sort Naveen M. Gokavi
title Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
title_short Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
title_full Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
title_fullStr Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
title_full_unstemmed Square Wave Voltammetric Determination of 2-Thiouracil in Pharmaceuticals and Real Samples Using Glassy Carbon Electrode
title_sort square wave voltammetric determination of 2-thiouracil in pharmaceuticals and real samples using glassy carbon electrode
publisher Hindawi Limited
series International Journal of Electrochemistry
issn 2090-3529
2090-3537
publishDate 2013-01-01
description A simple and rapid method was developed using cyclic and square wave voltammetric techniques for the determination of trace-level sulfur containing compound, 2-thiouracil, at a glassy carbon electrode. 2-thiouracil produced two anodic peaks at 0.334 V and 1.421 V and a cathodic peak at −0.534 V. The square wave voltammetry of 2-thiouracil gave a good linear response in the range of 1–20 μM with a detection limit of 0.16 μM and quantification limit of 0.53 μM (0.0679 μg/g), which is in good agreement as per IUPAC definition of trace component analysis (100 μg/g). The obtained recoveries range from 98.10% to 102.1%. The proposed method was used successfully for its quantitative determination in pharmaceutical formulations and urine as real samples.
url http://dx.doi.org/10.1155/2013/627854
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AT atmanandmbagoji squarewavevoltammetricdeterminationof2thiouracilinpharmaceuticalsandrealsamplesusingglassycarbonelectrode
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