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dc.contributor.authorJamshaid, Talhaes_ES
dc.contributor.authorTenório-Neto, Ernandes Taveiraes_ES
dc.contributor.authorBaraket, Abdellatifes_ES
dc.contributor.authorLebaz, Noureddinees_ES
dc.contributor.authorElaissari, Abdelhamides_ES
dc.contributor.authorSanchís Villariz, Anaes_ES
dc.contributor.authorSalvador, Juan Pabloes_ES
dc.contributor.authorMarco, María Pilares_ES
dc.contributor.authorBausells, Joanes_ES
dc.contributor.authorErrachid, Abdelhamides_ES
dc.contributor.authorZine, Nadiaes_ES
dc.date.accessioned2020-04-22T08:02:38Z-
dc.date.available2020-04-22T08:02:38Z-
dc.date.issued2020-04-21-
dc.identifier.citationBiosensors 10 (4): 43 (2020)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/208554-
dc.description.abstractIn this work, we report the development of a highly sensitive biosensor for sulfapyridine detection based on an integrated bio micro-electromechanical system (Bio-MEMS) containing four gold working electrodes (WEs), a platinum counter electrode (CE), and a reference electrode (RE). Firstly, the cleaned WEs were modified with 4-aminophenylacetic acid (CMA). Then, (5-[4-(amino)phenylsulfonamide]-5-oxopentanoic acid (SA2BSA) was immobilized onto the transducers surface by carbodiimide chemistry. The analyte was quantified by competitive detection with SA2BSA immobilized on the WE toward a mixture of Ab155 antibody (with fixed concentration) and sulfapyridine. In order to obtain a highly sensitive biosensor, Ab155 was immobilized onto magnetic latex nanoparticles surface to create a 3D architecture (Ab-MLNp). Using electrochemical impedance spectroscopy (EIS), we investigated the influence of the Ab-MLNp on the sensitivity of our approach. The optimized system was analyzed, as competitive assay, with different concentrations of sulfapyridine (40 µM, 4 µM, and 2 nM) and with phosphate buffer solution. From data fitting calculations and graphs, it was observed that the EIS showed more linearity when Ab-MLNp was used. This result indicates that the magnetic latex nanoparticles increased the sensitivity of the biosensor.es_ES
dc.description.sponsorshipThe authors acknowledge the financial support from the projects European Communities Seventh Framework Program: SEA-on-a-CHIP (FP7-OCEAN-2013) under the grant agreement N° 614168, and funding from the European Union’s Horizon 2020 research and innovation program entitled KardiaTool under grant agreement N° 643694, and the fellowship from Science Without Borders program—Conselho Nacional de Desenvolvimento Ciêntífico Tenológico (CNPq)–Brazil grant N° 249056/2013-5.es_ES
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institutees_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectBiosensorses_ES
dc.subjectSulfapyridinees_ES
dc.subjectSA2BSAes_ES
dc.subjectBioMEMSes_ES
dc.subjectMagnetic nanoparticleses_ES
dc.subjectCompetitive assayes_ES
dc.titleDevelopment of Novel Magneto-Biosensor for Sulfapyridine Detectiones_ES
dc.typeartículoes_ES
dc.identifier.doi10.3390/bios10040043-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/bios10040043es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.contributor.orcidSalvador, Juan Pablo [0000-0002-3608-0634]es_ES
dc.contributor.orcidMarco, María Pilar [0000-0002-2237-7197]es_ES
dc.identifier.pmid32326302-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypeartículo-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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