A plasmon-enhanced fluorescence-based antibody-aptamer biosensor — consisting of gold nanoparticles randomly immobilized onto a glass substrate via electrostatic self-assembly — is described for specific detection of proteins in whole blood. Analyte recognition is realized through a sandwich scheme with a capture bioreceptor layer of antibodies — covalently immobilized onto the gold nanoparticle surface in upright orientation and close-packed configuration by photochemical immobilization technique (PIT) — and a top bioreceptor layer of fluorescently labelled aptamers. Such a sandwich configuration warrants not only extremely high specificity, but also an ideal fluorophore-nanostructure distance (approximately 10–15 nm) for achieving strong fluorescence amplification. For a specific application, we tested the biosensor performance in a case study for the detection of malaria-related marker Plasmodium falciparum lactate dehydrogenase (PfLDH). The proposed biosensor can specifically detect PfLDH in spiked whole blood down to 10 pM (0.3 ng/mL) without any sample pretreatment. The combination of simple and scalable fabrication, potentially high-throughput analysis, and excellent sensing performance provides a new approach to biosensing with significant advantages compared to conventional fluorescence immunoassays. Graphical abstract: [Figure not available: see fulltext.]

Randomly positioned gold nanoparticles as fluorescence enhancers in apta-immunosensor for malaria test / Minopoli, A.; Della Ventura, B.; Campanile, R.; Tanner, J. A.; Offenhausser, A.; Mayer, D.; Velotta, R.. - In: MIKROCHIMICA ACTA. - ISSN 0026-3672. - 188:3(2021), p. 88. [10.1007/s00604-021-04746-9]

Randomly positioned gold nanoparticles as fluorescence enhancers in apta-immunosensor for malaria test

Minopoli A.
Primo
;
Della Ventura B.;Campanile R.;Velotta R.
Ultimo
2021

Abstract

A plasmon-enhanced fluorescence-based antibody-aptamer biosensor — consisting of gold nanoparticles randomly immobilized onto a glass substrate via electrostatic self-assembly — is described for specific detection of proteins in whole blood. Analyte recognition is realized through a sandwich scheme with a capture bioreceptor layer of antibodies — covalently immobilized onto the gold nanoparticle surface in upright orientation and close-packed configuration by photochemical immobilization technique (PIT) — and a top bioreceptor layer of fluorescently labelled aptamers. Such a sandwich configuration warrants not only extremely high specificity, but also an ideal fluorophore-nanostructure distance (approximately 10–15 nm) for achieving strong fluorescence amplification. For a specific application, we tested the biosensor performance in a case study for the detection of malaria-related marker Plasmodium falciparum lactate dehydrogenase (PfLDH). The proposed biosensor can specifically detect PfLDH in spiked whole blood down to 10 pM (0.3 ng/mL) without any sample pretreatment. The combination of simple and scalable fabrication, potentially high-throughput analysis, and excellent sensing performance provides a new approach to biosensing with significant advantages compared to conventional fluorescence immunoassays. Graphical abstract: [Figure not available: see fulltext.]
2021
Randomly positioned gold nanoparticles as fluorescence enhancers in apta-immunosensor for malaria test / Minopoli, A.; Della Ventura, B.; Campanile, R.; Tanner, J. A.; Offenhausser, A.; Mayer, D.; Velotta, R.. - In: MIKROCHIMICA ACTA. - ISSN 0026-3672. - 188:3(2021), p. 88. [10.1007/s00604-021-04746-9]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/847651
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