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Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry
17α-Ethinyl estradiol (EE2), which is used worldwide in the treatment of some cancers and as a contraceptive, is often found in aquatic systems and is considered a pharmaceutically active compound (PhACs) in the environment. Current methods for the determination of this compound, such as chromatogra...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050357/ https://www.ncbi.nlm.nih.gov/pubmed/27738548 http://dx.doi.org/10.1155/2016/3217080 |
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author | Nunes, Chalder Nogueira Pauluk, Lucas Ely Felsner, Maria Lurdes Egéa dos Anjos, Vanessa Quináia, Sueli Pércio |
author_facet | Nunes, Chalder Nogueira Pauluk, Lucas Ely Felsner, Maria Lurdes Egéa dos Anjos, Vanessa Quináia, Sueli Pércio |
author_sort | Nunes, Chalder Nogueira |
collection | PubMed |
description | 17α-Ethinyl estradiol (EE2), which is used worldwide in the treatment of some cancers and as a contraceptive, is often found in aquatic systems and is considered a pharmaceutically active compound (PhACs) in the environment. Current methods for the determination of this compound, such as chromatography, are expensive and lengthy and require large amounts of toxic organic solvents. In this work, a voltammetric procedure is developed and validated as a screening tool for detecting EE2 in water samples without prior extraction, clean-up, or derivatization steps. Application of the method we elaborate here to EE2 analysis is unprecedented. EE2 detection was carried out using differential pulse adsorptive cathodic stripping voltammetry (DP AdCSV) with a hanging mercury drop electrode (HMDE) in pH 7.0 Britton-Robinson buffer. The electrochemical process of EE2 reduction was investigated by cyclic voltammetry at different scan rates. Electroreduction of the hormone on a mercury electrode exhibited a peak at −1.16 ± 0.02 V versus Ag/AgCl. The experimental parameters were as follows: −0.7 V accumulation potential, 150 s accumulation time, and 60 mV s(−1) scan rate. The limit of detection was 0.49 μg L(−1) for a preconcentration time of 150 s. Relative standard deviations were less than 13%. The method was applied to the detection of EE2 in water samples with recoveries ranging from 93.7 to 102.5%. |
format | Online Article Text |
id | pubmed-5050357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50503572016-10-13 Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry Nunes, Chalder Nogueira Pauluk, Lucas Ely Felsner, Maria Lurdes Egéa dos Anjos, Vanessa Quináia, Sueli Pércio J Anal Methods Chem Research Article 17α-Ethinyl estradiol (EE2), which is used worldwide in the treatment of some cancers and as a contraceptive, is often found in aquatic systems and is considered a pharmaceutically active compound (PhACs) in the environment. Current methods for the determination of this compound, such as chromatography, are expensive and lengthy and require large amounts of toxic organic solvents. In this work, a voltammetric procedure is developed and validated as a screening tool for detecting EE2 in water samples without prior extraction, clean-up, or derivatization steps. Application of the method we elaborate here to EE2 analysis is unprecedented. EE2 detection was carried out using differential pulse adsorptive cathodic stripping voltammetry (DP AdCSV) with a hanging mercury drop electrode (HMDE) in pH 7.0 Britton-Robinson buffer. The electrochemical process of EE2 reduction was investigated by cyclic voltammetry at different scan rates. Electroreduction of the hormone on a mercury electrode exhibited a peak at −1.16 ± 0.02 V versus Ag/AgCl. The experimental parameters were as follows: −0.7 V accumulation potential, 150 s accumulation time, and 60 mV s(−1) scan rate. The limit of detection was 0.49 μg L(−1) for a preconcentration time of 150 s. Relative standard deviations were less than 13%. The method was applied to the detection of EE2 in water samples with recoveries ranging from 93.7 to 102.5%. Hindawi Publishing Corporation 2016 2016-09-21 /pmc/articles/PMC5050357/ /pubmed/27738548 http://dx.doi.org/10.1155/2016/3217080 Text en Copyright © 2016 Chalder Nogueira Nunes et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nunes, Chalder Nogueira Pauluk, Lucas Ely Felsner, Maria Lurdes Egéa dos Anjos, Vanessa Quináia, Sueli Pércio Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title | Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title_full | Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title_fullStr | Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title_full_unstemmed | Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title_short | Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry |
title_sort | rapid screening method for detecting ethinyl estradiol in natural water employing voltammetry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050357/ https://www.ncbi.nlm.nih.gov/pubmed/27738548 http://dx.doi.org/10.1155/2016/3217080 |
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