<?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>2026-06-26T21:18:30Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/73095" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/73095</identifier><datestamp>2025-03-18T15:14:53Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Pérez Ginés, Víctor</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Torrente Rodríguez, Rebeca Magnolia</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Pedrero Muñoz, María</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Martínez-Bosch, Neus</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>García de Frutos, Pablo</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Navarro, Pilar</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Pingarrón Carrazón, José Manuel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Campuzano Ruiz, Susana</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2023-06-22T12:43:21Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2023-06-22T12:43:21Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2023</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="issn">1572-6657</mods:identifier>
   <mods:identifier type="doi">10.1016/j.jelechem.2023.117312</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/73095</mods:identifier>
   <mods:identifier type="essn">1873-2569</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.1016/j.jelechem.2023.117312</mods:identifier>
   <mods:abstract>Pancreatic ductal adenocarcinoma (PDAC) is the solid tumor with the worst prognosis, representing today the third cause of cancer-related deaths in developed countries and expected to be the second in 2030. Today, CA19-9 remains the only clinically used marker for management of PDAC (FDA-approved as a disease moni- toring marker). This work reports a disposable amperometric immunoplatform for the determination of CA19-9. The immunoplatform skilfully combines the advantages of magnetic microsupports (MBs) for implementation of the immunoassay and amperometric transduction on screen-printed carbon electrodes (SPCEs). The method involves the preparation of sándwich immunocomplexes enzymatically labeled with the enzyme horseradish peroxidase (HRP) on the MBs and uses a detection antibody conjugated to HRP. Once the HRP- labeled sandwich immunocomplexes-bearing MBs were trapped on the SPCE surface, the variation of the catho- dic current was measured in the presence of H2O2 and hydroquinone (HQ), which was directly proportional to the concentration of CA19-9. Under the optimized experimental conditions, the immunoplatform allowed the amperometric determination of CA19-9 standards over the 5.0 to 500 U mL−1 concentration range, with a limit of detection (LOD) value of 1.5 U mL−1 in 1 h. The method exhibits good reproducibility and selectivity and the magnetic immunoconjugates shows a good storage stability. The immunoplatform was applied to the deter- mination of CA19-9 in serum samples of a medium-sized cohort (22 individuals) of healthy subjects and patients diagnosed with PDAC. The obtained results demonstrated the immunoplatform ability to discriminateboth types of individuals within 1 h after sample dilution. The developed immunoplatform represents an improvement in terms of cost, applicability and accessibility compared to the ELISA-based techniques currently used in the clinic.</mods:abstract>
   <mods:language>
      <mods:languageTerm>spa</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">https://creativecommons.org/licenses/by-nc-nd/3.0/es/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Atribución-NoComercial-SinDerivadas 3.0 España</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Electrochemical immunoplatform to help managing pancreatic cancer</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods></metadata></record></GetRecord></OAI-PMH>