Adsorptive Stripping Voltammetric Quercetin Determination in Pharmaceuticals and Urine Samples Using a Long Service-Life Array of Carbon Composite Microelectrodes

This article presents for the first time a new working electrode with a long service life- the bismuth-plated array of carbon composite microelectrodes for the simple, fast and sensitive determination of quercetin by adsorptive stripping voltammetry. The main experimental conditions were selected. The calibration graph was linear from 1 × 10<sup>-9</sup> to 2 × 10<sup>-8</sup> mol L<sup>-1</sup> with an accumulation time of 60 s. The detection limit was equal to 4.8 × 10<sup>-10</sup> mol L<sup>-1</sup>. The relative standard deviation for 2 × 10<sup>-8</sup> mol L<sup>-1</sup> of quercetin was 4.4% (n = 7). Possible interference effects resulting from the presence of other organic and surface active compounds and interfering ions were studied. The developed procedure was successfully applied to determine quercetin in pharmaceutical preparations and the spiked urine samples.

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Publication Details

Journal
Molecules
Published
2024-09-20
DOI
https://doi.org/10.3390/molecules29184464
Citations
1
Primary Topic
Electrochemical sensors and biosensors
Type
article
Field-Weighted Citation Impact
0.21
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article

Adsorptive Stripping Voltammetric Quercetin Determination in Pharmaceuticals and Urine Samples Using a Long Service-Life Array of Carbon Composite Microelectrodes

Iwona Gęca, Mieczysław Korolczuk
1 citations
Molecules
Electrochemical sensors and biosensors
0.21
article

Adsorptive Stripping Voltammetric Quercetin Determination in Pharmaceuticals and Urine Samples Using a Long Service-Life Array of Carbon Composite Microelectrodes

Iwona Gęca, Mieczysław Korolczuk
article en
1 citations

Abstract

This article presents for the first time a new working electrode with a long service life- the bismuth-plated array of carbon composite microelectrodes for the simple, fast and sensitive determination of quercetin by adsorptive stripping voltammetry. The main experimental conditions were selected. The calibration graph was linear from 1 × 10<sup>-9</sup> to 2 × 10<sup>-8</sup> mol L<sup>-1</sup> with an accumulation time of 60 s. The detection limit was equal to 4.8 × 10<sup>-10</sup> mol L<sup>-1</sup>. The relative standard deviation for 2 × 10<sup>-8</sup> mol L<sup>-1</sup> of quercetin was 4.4% (n = 7). Possible interference effects resulting from the presence of other organic and surface active compounds and interfering ions were studied. The developed procedure was successfully applied to determine quercetin in pharmaceutical preparations and the spiked urine samples.

MoleculesVol. 29(18)
Maria Curie-Skłodowska University (PL)
Responsible consumption and production
Openalex Percentile: Top 48%
Electrochemical sensors and biosensors
0.21
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