<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-14T09:50:11Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/6124" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/6124</identifier><datestamp>2022-11-15T13:25:37Z</datestamp><setSpec>com_10259_3844</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_3845</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">Olmo Alonso, Fabiola</subfield>
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<subfield code="a">Garoz Ruiz, Jesús</subfield>
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<subfield code="a">Colina Santamaría, Álvaro</subfield>
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<subfield code="a">Heras Vidaurre, Aránzazu</subfield>
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<subfield code="c">2020-09</subfield>
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<subfield code="a">In this work, UV/Vis spectroelectrochemistry (SEC), in a thin-layer regime and parallel configuration, is selected to solve a&#xd;
complex mixture that contains dopamine (DA), ascorbic acid (AA) and uric acid (UA). These molecules, like many other&#xd;
biological compounds, are assuming a highly important place in analytical and biomedical fields due to the fundamental role&#xd;
that they play in human metabolism. In addition, low or high levels of these compounds are associated with diseases such as&#xd;
Parkinson’s disease. For this reason, the quantification of these biomolecules is becoming increasingly critical. However, some&#xd;
drawbacks must be overcome, because the three molecules coexist in the human body, and the species are subject to mutual&#xd;
interference. In fact, they are all oxidized at similar potentials, and their UV/Vis absorption bands overlap, greatly complicating&#xd;
their quantification. For this reason, derivative SEC together with suitable chemometric tools such as PARAFAC are proposed to&#xd;
solve this complex matrix. This technique allows us to separate the contribution of each of these molecules present in a sample&#xd;
and to quantify all of them, achieving high resolution and reproducibility. Besides, detection limits at the micromolar level are&#xd;
achieved for DA, AA and UA in mixture solutions. This work thus demonstrates the great potential for derivative potentiodynamic&#xd;
SEC combined with the appropriate chemometric tools in solving complex mixtures, a field where SEC is still taking the&#xd;
first steps.</subfield>
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<subfield code="a">1618-2642</subfield>
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<subfield code="a">http://hdl.handle.net/10259/6124</subfield>
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<subfield code="a">10.1007/s00216-020-02564-1</subfield>
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<subfield code="a">1618-2650</subfield>
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<subfield code="a">Spectroelectrochemistry</subfield>
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<subfield code="a">PARAFAC</subfield>
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<subfield code="a">Quantitative analysis</subfield>
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<subfield code="a">Derivative of absorbance with respect towavelength</subfield>
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<subfield code="a">Derivative UV/Vis spectroelectrochemistry in a thin-layer regime: deconvolution and simultaneous quantification of ascorbic acid, dopamine and uric acid</subfield>
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