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Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry
ABSTRACT: In this paper, the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the veterinary drug closantel using a renewable silver amalgam film electrode (Hg(Ag)FE) is presented. As observed in SWAdSV, closantel provided one well-shaped reduction peak suitable for analytical...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Vienna
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346127/ https://www.ncbi.nlm.nih.gov/pubmed/28344363 http://dx.doi.org/10.1007/s00706-016-1862-z |
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author | Brycht, Mariola Nosal-Wiercińska, Agnieszka Sipa, Karolina Rudnicki, Konrad Skrzypek, Sławomira |
author_facet | Brycht, Mariola Nosal-Wiercińska, Agnieszka Sipa, Karolina Rudnicki, Konrad Skrzypek, Sławomira |
author_sort | Brycht, Mariola |
collection | PubMed |
description | ABSTRACT: In this paper, the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the veterinary drug closantel using a renewable silver amalgam film electrode (Hg(Ag)FE) is presented. As observed in SWAdSV, closantel provided one well-shaped reduction peak suitable for analytical purposes at potential ca. −1.4 V in the Britton–Robinson (B-R) buffer at pH 7.0. At optimal conditions, the SWAdSV response of Hg(Ag)FE for determining closantel was linear over two concentration ranges of 5.0 × 10(−8) to 2.0 × 10(−7) mol dm(−3) and 2.0 × 10(−7) to 1.2 × 10(−6) mol dm(−3) with a detection limit of 1.1 × 10(−8) mol dm(−3). In addition, a relevance of the developed SWAdSV method was successfully verified by the quantitative analysis of closantel in the commercial formulation Closamectin Pour-On with satisfactory results (RSD = 5.8%, recovery = 101.8%). The results showed that the developed procedure can be adequate for screening purposes. Also, the electrochemical behavior of closantel was characterized by cyclic voltammetry, and it was found that closantel exhibited a quasi-reversible behavior with cathodic peak on the forward scan at ca. −1.4 V and anodic peak on the reverse scan at ca. −1.35 V vs. Ag/AgCl in B–R buffer, pH 7.0. As the obtained results showed that the electrode mechanism of closantel is controlled by the adsorption, the effect of adsorption was studied using the electrochemical impedance spectroscopy technique. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-5346127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-53461272017-03-22 Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry Brycht, Mariola Nosal-Wiercińska, Agnieszka Sipa, Karolina Rudnicki, Konrad Skrzypek, Sławomira Monatsh Chem Original Paper ABSTRACT: In this paper, the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the veterinary drug closantel using a renewable silver amalgam film electrode (Hg(Ag)FE) is presented. As observed in SWAdSV, closantel provided one well-shaped reduction peak suitable for analytical purposes at potential ca. −1.4 V in the Britton–Robinson (B-R) buffer at pH 7.0. At optimal conditions, the SWAdSV response of Hg(Ag)FE for determining closantel was linear over two concentration ranges of 5.0 × 10(−8) to 2.0 × 10(−7) mol dm(−3) and 2.0 × 10(−7) to 1.2 × 10(−6) mol dm(−3) with a detection limit of 1.1 × 10(−8) mol dm(−3). In addition, a relevance of the developed SWAdSV method was successfully verified by the quantitative analysis of closantel in the commercial formulation Closamectin Pour-On with satisfactory results (RSD = 5.8%, recovery = 101.8%). The results showed that the developed procedure can be adequate for screening purposes. Also, the electrochemical behavior of closantel was characterized by cyclic voltammetry, and it was found that closantel exhibited a quasi-reversible behavior with cathodic peak on the forward scan at ca. −1.4 V and anodic peak on the reverse scan at ca. −1.35 V vs. Ag/AgCl in B–R buffer, pH 7.0. As the obtained results showed that the electrode mechanism of closantel is controlled by the adsorption, the effect of adsorption was studied using the electrochemical impedance spectroscopy technique. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2016-10-28 2017 /pmc/articles/PMC5346127/ /pubmed/28344363 http://dx.doi.org/10.1007/s00706-016-1862-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Brycht, Mariola Nosal-Wiercińska, Agnieszka Sipa, Karolina Rudnicki, Konrad Skrzypek, Sławomira Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title | Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title_full | Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title_fullStr | Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title_full_unstemmed | Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title_short | Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
title_sort | electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346127/ https://www.ncbi.nlm.nih.gov/pubmed/28344363 http://dx.doi.org/10.1007/s00706-016-1862-z |
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