A portable selective electrochemical sensor amplified with Fe3O4@Au-cysteamine-thymine acetic acid as conductive mediator for determination of mercuric ion

Mercury ion (Hg2+) is considered to be one of the most toxic heavy metal ions and can cause adverse effects on kidney function, the central nervous system, and the immune system. Therefore, it is important to develop a fast and simple method for sensitive and selective detection of Hg2+ in the envir...

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Veröffentlicht in:Talanta (Oxford) 2021-01, Vol.221, p.121669-121669, Article 121669
Hauptverfasser: Butmee, Preeyanut, Mala, Jittra, Damphathik, Chulalak, Kunpatee, Kanjana, Tumcharern, Gamolwan, Kerr, Margaret, Mehmeti, Eda, Raber, Georg, Kalcher, Kurt, Samphao, Anchalee
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container_title Talanta (Oxford)
container_volume 221
creator Butmee, Preeyanut
Mala, Jittra
Damphathik, Chulalak
Kunpatee, Kanjana
Tumcharern, Gamolwan
Kerr, Margaret
Mehmeti, Eda
Raber, Georg
Kalcher, Kurt
Samphao, Anchalee
description Mercury ion (Hg2+) is considered to be one of the most toxic heavy metal ions and can cause adverse effects on kidney function, the central nervous system, and the immune system. Therefore, it is important to develop a fast and simple method for sensitive and selective detection of Hg2+ in the environment. This research proposes a portable electrochemical sensor for rapid and selective detection of Hg2+. The sensor platform is designed based on thymine acetic acid anchored with cysteamine-conjugated core shell Fe3O4@Au nanoparticles (Fe3O4@Au/CA/T-COOH) immobilized on a sensing area of a screen-printed carbon electrode (SPCE) with the aid of an external magnetic field embedded in a homemade electrode holder for ease of handling. In the presence of Hg2+, the immobilized thymine combines specifically with Hg2+ and forms a thymine-Hg2+-thymine mismatch (T-Hg2+-T). The resulting amount of Hg2+ was determined by differential pulse anodic stripping voltammetry (DPASV). Under optimal conditions, the sensor exhibited two wide linearities in a range from 1 to 200 μg L−1 and 200–2200 μg L−1 with the reliability coefficient of determination of 0.997 and 0.999, respectively. The detection limit (LOD) and the quantification limit (LOQ) were also determined to be 0.5 μg L−1 and 1.0 μg L−1, respectively. The sensor was further applied for determination of Hg2+ in water samples, a certified reference material and fish samples. The results were compared with flow injection atomic spectroscopy-inductively coupled plasma-optical emission spectroscopy (FIAS-ICP-OES) systems as a reference method. Results obtained with the proposed sensor were relatively satisfactory, and they showed no significant differences at a 95% confidence level by t-test from the standard method. Therefore, considering its fast and simple advantages, this novel strategy provides a potential platform for construction of a Hg2+ electrochemical sensor. [Display omitted] •Fe3O4@Au-cysteamine-thymine acetic acid is exhibited for the determination of Hg2+.•Thymine-Hg2+ -Thymine structure on Fe3O4@Au-cysteamine-thymine acetic acid is efficiently performed for Hg2+ detection.•The analysis of Hg2+ can be performed in a few minutes compared to routine analysis.•The proposed sensor is high sensitivity and high selectivity for Hg2+ detection.
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Under optimal conditions, the sensor exhibited two wide linearities in a range from 1 to 200 μg L−1 and 200–2200 μg L−1 with the reliability coefficient of determination of 0.997 and 0.999, respectively. The detection limit (LOD) and the quantification limit (LOQ) were also determined to be 0.5 μg L−1 and 1.0 μg L−1, respectively. The sensor was further applied for determination of Hg2+ in water samples, a certified reference material and fish samples. The results were compared with flow injection atomic spectroscopy-inductively coupled plasma-optical emission spectroscopy (FIAS-ICP-OES) systems as a reference method. Results obtained with the proposed sensor were relatively satisfactory, and they showed no significant differences at a 95% confidence level by t-test from the standard method. Therefore, considering its fast and simple advantages, this novel strategy provides a potential platform for construction of a Hg2+ electrochemical sensor. 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Under optimal conditions, the sensor exhibited two wide linearities in a range from 1 to 200 μg L−1 and 200–2200 μg L−1 with the reliability coefficient of determination of 0.997 and 0.999, respectively. The detection limit (LOD) and the quantification limit (LOQ) were also determined to be 0.5 μg L−1 and 1.0 μg L−1, respectively. The sensor was further applied for determination of Hg2+ in water samples, a certified reference material and fish samples. The results were compared with flow injection atomic spectroscopy-inductively coupled plasma-optical emission spectroscopy (FIAS-ICP-OES) systems as a reference method. Results obtained with the proposed sensor were relatively satisfactory, and they showed no significant differences at a 95% confidence level by t-test from the standard method. Therefore, considering its fast and simple advantages, this novel strategy provides a potential platform for construction of a Hg2+ electrochemical sensor. 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Therefore, it is important to develop a fast and simple method for sensitive and selective detection of Hg2+ in the environment. This research proposes a portable electrochemical sensor for rapid and selective detection of Hg2+. The sensor platform is designed based on thymine acetic acid anchored with cysteamine-conjugated core shell Fe3O4@Au nanoparticles (Fe3O4@Au/CA/T-COOH) immobilized on a sensing area of a screen-printed carbon electrode (SPCE) with the aid of an external magnetic field embedded in a homemade electrode holder for ease of handling. In the presence of Hg2+, the immobilized thymine combines specifically with Hg2+ and forms a thymine-Hg2+-thymine mismatch (T-Hg2+-T). The resulting amount of Hg2+ was determined by differential pulse anodic stripping voltammetry (DPASV). Under optimal conditions, the sensor exhibited two wide linearities in a range from 1 to 200 μg L−1 and 200–2200 μg L−1 with the reliability coefficient of determination of 0.997 and 0.999, respectively. The detection limit (LOD) and the quantification limit (LOQ) were also determined to be 0.5 μg L−1 and 1.0 μg L−1, respectively. The sensor was further applied for determination of Hg2+ in water samples, a certified reference material and fish samples. The results were compared with flow injection atomic spectroscopy-inductively coupled plasma-optical emission spectroscopy (FIAS-ICP-OES) systems as a reference method. Results obtained with the proposed sensor were relatively satisfactory, and they showed no significant differences at a 95% confidence level by t-test from the standard method. Therefore, considering its fast and simple advantages, this novel strategy provides a potential platform for construction of a Hg2+ electrochemical sensor. [Display omitted] •Fe3O4@Au-cysteamine-thymine acetic acid is exhibited for the determination of Hg2+.•Thymine-Hg2+ -Thymine structure on Fe3O4@Au-cysteamine-thymine acetic acid is efficiently performed for Hg2+ detection.•The analysis of Hg2+ can be performed in a few minutes compared to routine analysis.•The proposed sensor is high sensitivity and high selectivity for Hg2+ detection.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.talanta.2020.121669</doi><tpages>1</tpages></addata></record>
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subjects Cysteamine
Electrochemical sensor
Fe3O4@Au nanoparticles
Mercuric ion
Thymine acetic acid
title A portable selective electrochemical sensor amplified with Fe3O4@Au-cysteamine-thymine acetic acid as conductive mediator for determination of mercuric ion
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