Electrochemical immunoplatform to help managing pancreatic cancer
dc.contributor.author | Pérez Ginés, Víctor | |
dc.contributor.author | Torrente Rodríguez, Rebeca Magnolia | |
dc.contributor.author | Pedrero Muñoz, María | |
dc.contributor.author | Martínez-Bosch, Neus | |
dc.contributor.author | García de Frutos, Pablo | |
dc.contributor.author | Navarro, Pilar | |
dc.contributor.author | Pingarrón Carrazón, José Manuel | |
dc.contributor.author | Campuzano Ruiz, Susana | |
dc.date.accessioned | 2023-06-22T12:43:21Z | |
dc.date.available | 2023-06-22T12:43:21Z | |
dc.date.issued | 2023 | |
dc.description.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. | |
dc.description.department | Depto. de Química Analítica | |
dc.description.faculty | Fac. de Ciencias Químicas | |
dc.description.refereed | TRUE | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/77048 | |
dc.identifier.doi | 10.1016/j.jelechem.2023.117312 | |
dc.identifier.essn | 1873-2569 | |
dc.identifier.issn | 1572-6657 | |
dc.identifier.officialurl | https://doi.org/10.1016/j.jelechem.2023.117312 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/73095 | |
dc.journal.title | Journal of Electroanalytical Chemistry | |
dc.language.iso | spa | |
dc.page.initial | 117312 | |
dc.publisher | Elsevier | |
dc.relation.hasversion | VoR | |
dc.relation.projectID | PID2019-103899RB-I00 | |
dc.relation.projectID | S2018/NMT-4349 | |
dc.relation.projectID | PI20/00625 | |
dc.relation.projectID | TRANSNANOAVANSENS-CM Program | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 España | |
dc.rights.accessRights | open access | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/es/ | |
dc.subject.cdu | 543 | |
dc.subject.keyword | Immunoplatform | |
dc.subject.keyword | Amperometrym | |
dc.subject.keyword | CA19-9 | |
dc.subject.keyword | Pancreatic cancer | |
dc.subject.keyword | Serum samples | |
dc.subject.ucm | Química | |
dc.subject.ucm | Química analítica (Química) | |
dc.subject.unesco | 23 Química | |
dc.subject.unesco | 2301 Química Analítica | |
dc.title | Electrochemical immunoplatform to help managing pancreatic cancer | |
dc.type | journal article | |
dc.volume.number | 935 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | d0f6938e-07a1-4ad4-a231-b847cc6f0aa4 | |
relation.isAuthorOfPublication | f4569700-ddad-4754-a155-145a8107c215 | |
relation.isAuthorOfPublication | 422f8844-54d1-4615-98e8-ef5a0c7e3519 | |
relation.isAuthorOfPublication | 8808f99c-5f56-4562-839a-517626c76dad | |
relation.isAuthorOfPublication | 6945fb1e-9c48-459d-b994-e64328c3e79b | |
relation.isAuthorOfPublication.latestForDiscovery | 6945fb1e-9c48-459d-b994-e64328c3e79b |
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