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Disposable electrochemical sensor combined with molecularly imprinted solid-phase extraction for catabolites detection of flavan-3-ol in urine samples

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dc.contributor.authorMora-Granados, M.
dc.contributor.authorGonzález Crevillén, Agustín
dc.contributor.authorGonzález-Gómez D.
dc.contributor.authorGallego-Picó, A.
dc.contributor.orcidhttps://orcid.org/0000-0002-6167-6106
dc.contributor.orcidhttps://orcid.org/0000-0002-3321-9290
dc.date.accessioned2024-10-07T10:16:38Z
dc.date.available2024-10-07T10:16:38Z
dc.date.issued2021-07-26
dc.descriptionEste es el manuscrito aceptado del artículo. La versión registrada fue publicada por primera vez por Elsevier en Talanta, Volume 235, 2021, 122734, ISSN 0039-9140. Está disponible en línea en el sitio web del editor: https://doi.org/10.1016/j.talanta.2021.122734 This is the accepted manuscript of the article. The published version was first published by Elsevier in Talanta, Volume 235, 2021, 122734, ISSN 0039-9140; It is available online at the publisher's website: https://doi.org/10.1016/j.talanta.2021.122734
dc.description.abstractPolyphenols are bioactive substances of vegetal origin with a significant impact on human health. The assessment of polyphenol intake and excretion is therefore important. In this work, a new electrochemical approach based on molecularly imprinted polymer extraction and preconcentration, combined with a disposable carbon screen-printed sensor and adsorptive transfer differential pulse voltammetry detection has been proposed for quantifying of 4-hydroxyphenylacetic acid (4-HPA), which is a biomarker of flavan-3-ols intake, and other phenolic acids. The simple experimental performance has allowed the rapid data collection with relevant information about the profile of catabolites extracted. The method was validated over a concentration range of 10–200 mg L−1, R2 > 0.999. In the optimized conditions, the recovery value was 94% with RSD 8%. The limits of detection and quantification were 2.38 mg L−1 and 7.21 mg L−1, respectively. The method was validated by means of a chromatographic method, being the differences between the values of the 4-HPA concentrations obtained by both methods under 1%. The proposed method showed high recoveries, low detection limit, and good accuracy, providing a fast, reliable, and cheap procedure to quantify phenolic metabolites in urine, and representing therefore a good and interesting alternative method. Also, the procedure offers other advantages, including the miniaturization, the low use of organic solvents, the ability to analyse small volumes of samples, in situ analysis and simple instrumentation requirement.en
dc.description.versionversión original
dc.identifier.citationM. Mora-Granados, A.G. Crevillen, D. González-Gómez, A. Gallego-Picó, Disposable electrochemical sensor combined with molecularly imprinted solid-phase extraction for catabolites detection of flavan-3-ol in urine samples, Talanta, Volume 235, 2021, 122734, ISSN 0039-9140, https://doi.org/10.1016/j.talanta.2021.122734
dc.identifier.doihttps://doi.org/10.1016/j.talanta.2021.122734
dc.identifier.issn0039-9140
dc.identifier.urihttps://hdl.handle.net/20.500.14468/23935
dc.journal.titleTalanta
dc.journal.volume235
dc.language.isoen
dc.publisherElsevier
dc.relation.centerFacultades y escuelas::Facultad de Ciencias
dc.relation.departmentCiencias Analíticas
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subject23 Química
dc.subject.keywordsMolecularly imprinted polymer extractionen
dc.subject.keywordsPolyphenol metabolitesen
dc.subject.keywordsPhenolic acidsen
dc.subject.keywordsScreen-printed carbon electrodeen
dc.subject.keywordsHuman urineen
dc.subject.keywordsAdsorptive transfer differential pulse voltammetryen
dc.titleDisposable electrochemical sensor combined with molecularly imprinted solid-phase extraction for catabolites detection of flavan-3-ol in urine samplesen
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dc.typejournal articleen
dspace.entity.typePublication
relation.isAuthorOfPublication0f39284a-d95a-443a-bb2e-21297ec40b76
relation.isAuthorOfPublication.latestForDiscovery0f39284a-d95a-443a-bb2e-21297ec40b76
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