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Functionalized gold nanoflowers on carbon screen-printed electrodes: an electrochemical platform for biosensing hemagglutinin protein of influenza A H1N1 virus
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Physical Chemistry.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology. Uppsala University, Science for Life Laboratory, SciLifeLab.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology. Uppsala University, Science for Life Laboratory, SciLifeLab.
Uppsala University, Science for Life Laboratory, SciLifeLab. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology.
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2025 (English)In: Beilstein Journal of Nanotechnology, ISSN 2190-4286, Vol. 16, p. 540-550Article in journal (Refereed) Published
Abstract [en]

An electrochemical biosensor based on modified carbon screen-printed electrodes was developed for the detection of hemagglutinin of influenza A H1N1 virus (H1). Gold nanoflowers were electrodeposited on the electrode to increase conductivity and surface area. The electrochemical signal was amplified by functionalization of the gold nanoflowers with 4-aminothiophenol, which resulted in a 100-fold decrease of the charge transfer resistance due to a tunneling effect. Subsequently, monoclonal antibodies against H1 were immobilized on the surface via covalent amide bond formation, followed by blocking with bovine serum albumin to minimize nonspecific hydrophobic binding. The electrodes were characterized by cyclic voltammetry and electrochemical impedance spectroscopy experiments in the presence of [Fe(CN)6]3-/4-. Differential pulse voltammetry was used to measure the change in current across the electrode as a function of H1 concentration. This was performed on a series of samples of artificial saliva containing H1 protein in a clinically relevant concentration range. In these experiments, the biosensor showed a limit of detection of 19 pg/mL. Finally, the biosensor platform was coupled to an automated microfluidics system, and no significant decrease of the electrochemical signal was observed.

Place, publisher, year, edition, pages
Beilstein Institut , 2025. Vol. 16, p. 540-550
Keywords [en]
charge transfer, cyclic voltammetry, differential pulse voltammetry, electrochemical impedance spectroscopy, electrodeposition
National Category
Analytical Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-555792DOI: 10.3762/bjnano.16.42ISI: 001470359600001PubMedID: 40275987Scopus ID: 2-s2.0-105003816165OAI: oai:DiVA.org:uu-555792DiVA, id: diva2:1958126
Funder
Swedish Research Council, 2020-02258Available from: 2025-05-13 Created: 2025-05-13 Last updated: 2025-05-13Bibliographically approved

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Torres Mendez, Carlos EnriqueMestres, GemmaKamali-Moghaddam, Masood

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Torres Mendez, Carlos EnriqueMestres, GemmaKamali-Moghaddam, Masood
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Physical ChemistryDepartment of Immunology, Genetics and PathologyScience for Life Laboratory, SciLifeLabDepartment of Materials Science and EngineeringMolecular Tools and Functional Genomics
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Beilstein Journal of Nanotechnology
Analytical Chemistry

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