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Electrochemical Immunosensing of ST2: A Checkpoint Target in Cancer Diseases

dc.contributor.authorTorrente Rodríguez, Rebeca Magnolia
dc.contributor.authorMuñoz San Martín, Cristina
dc.contributor.authorGamella Carballo, María
dc.contributor.authorPedrero Muñoz, María
dc.contributor.authorMartínez-Bosch, Neus
dc.contributor.authorNavarro, Pilar
dc.contributor.authorGarcía de Frutos, Pablo
dc.contributor.authorPingarrón Carrazón, José Manuel
dc.contributor.authorCampuzano Ruiz, Susana
dc.date.accessioned2023-06-17T08:22:51Z
dc.date.available2023-06-17T08:22:51Z
dc.date.issued2021-06-21
dc.description.abstractA magnetic beads (MB)-involved amperometric immunosensor for the determination of ST2, a member of the IL1 receptor family, is reported in this work. The method utilizes a sandwich immunoassay and disposable screen-printed carbon electrodes (SPCEs). Magnetic immunoconjugates built on the surface of carboxylic acid-microsized magnetic particles (HOOC-MBs) were used to selectively capture ST2. A biotinylated secondary antibody further conjugated with a streptavidin peroxidase conjugate (Strep-HRP) was used to accomplish the sandwiching of the target protein. The immune platform exhibits great selectivity and a low limit of detection (39.6 pg mL−1) for ST2, allowing the determination of soluble ST2 (sST2) in plasma samples from healthy individuals and patients diagnosed with pancreatic ductal adenocarcinoma (PDAC) in only 45 min once the immunoconjugates have been prepared. The good correlation of the obtained results with those provided by an ELISA kit performed using the same immunoreagents demonstrates the potential of the developed strategy for early diagnosis and/or prognosis of the fatal PDAC disease.
dc.description.departmentDepto. de Química Analítica
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (MICINN)
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII)/FEDER
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/70833
dc.identifier.doi10.3390/bios11060202
dc.identifier.issn2079-6374
dc.identifier.officialurlhttps://doi.org/10.3390/bios11060202
dc.identifier.relatedurlhttps://www.mdpi.com/2079-6374/11/6/202/htm
dc.identifier.urihttps://hdl.handle.net/20.500.14352/6870
dc.issue.number6
dc.journal.titleBiosensors
dc.language.isoeng
dc.page.initial202
dc.publisherMPDI
dc.relation.projectID(PID2019-103899RB-I00, RTI2018-095672-B-I00)
dc.relation.projectIDPI20/00625.
dc.relation.projectIDS2018/NMT-4349
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordelectrochemical immune platform
dc.subject.keywordhuman ST2
dc.subject.keywordplasma
dc.subject.keywordpancreatic cancer
dc.subject.ucmOncología
dc.subject.unesco3201.01 Oncología
dc.titleElectrochemical Immunosensing of ST2: A Checkpoint Target in Cancer Diseases
dc.typejournal article
dc.volume.number11
dspace.entity.typePublication
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