Contributing to the management of viral infections through simple immunosensing of the arachidonic acid serum level

A trendsetting direct competitive-based biosensing tool has been developed and implemented for the determination of the polyunsaturated fatty acid arachidonic acid (ARA), a highly significant biological regulator with decisive roles in viral infections. The designed methodology involves a competitiv...

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Detalles Bibliográficos
Autores: Torrente Rodríguez, Rebeca Magnolia, Ruiz Valdepeñas Montiel, Víctor, Iftimie, Simona, Montero Calle, Ana, Pingarrón Carrazón, José Manuel, Castro, Antoni, Camps, Jordi, Barderas Manchado, Rodrigo, Campuzano Ruiz, Susana, Joven, Jorge
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/123885
Acceso en línea:https://hdl.handle.net/20.500.14352/123885
Access Level:acceso abierto
Palabra clave:543
Electrochemical bioplatform
Amperometry
Screen-printed carbon electrode
Arachidonic acid
Serum samples
SARS-CoV-2
RSV
Ciencias
23 Química
Descripción
Sumario:A trendsetting direct competitive-based biosensing tool has been developed and implemented for the determination of the polyunsaturated fatty acid arachidonic acid (ARA), a highly significant biological regulator with decisive roles in viral infections. The designed methodology involves a competitive reaction between the target endogenous ARA and a biotin-ARA competitor for the recognition sites of anti-ARA antibodies covalently attached to the surface of carboxylic acid-coated magnetic microbeads (HOOC-MμBs), followed by the enzymatic label of the biotin-ARA residues with streptavidin-horseradish peroxidase (Strep-HRP) conjugate. The resulting bioconjugates were magnetically trapped onto the sensing surface of disposable screen-printed carbon transducers (SPCEs) to monitor the extent of the biorecognition reaction through amperometry. The operational functioning of the exhaustively optimized and characterized immunosensing bioplatform was highly convenient for the quantitative determination of ARA in serum samples from severe acute respiratory syndrome coronavirus 2 (SARSCoV-2-) and respiratory syncytial virus (RSV)-infected individuals in a rapid, affordable, trustful, and sensitive manner.