Vertical Flow Immunoassay Based on Carbon Black Nanoparticles for the Detection of IgG against SARS-CoV-2 Spike Protein in Human Serum: Proof-of-Concept.


Journal

Biosensors
ISSN: 2079-6374
Titre abrégé: Biosensors (Basel)
Pays: Switzerland
ID NLM: 101609191

Informations de publication

Date de publication:
29 Aug 2023
Historique:
received: 07 08 2023
revised: 25 08 2023
accepted: 28 08 2023
medline: 28 9 2023
pubmed: 27 9 2023
entrez: 27 9 2023
Statut: epublish

Résumé

Point-of-care tests play an important role in serological diagnostics of infectious diseases and post-vaccination immunity monitoring, including in COVID-19. Currently, lateral flow tests dominate in this area and show good analytical performance. However, studies to improve the effectiveness of such tests remain important. In comparison with lateral flow tests, vertical flow immunoassays allow for a reduction in assay duration and the influence of the hook effect. Additionally, the use of carbon black nanoparticles (CNPs) as a color label can provide a lower detection limit (LOD) compared to conventional colloidal gold. Therefore, we have developed a vertical flow immunoassay for the detection of IgG against SARS-CoV-2 spike protein in human serum samples by applying a conjugate of CNPs with anti-human IgG mouse monoclonal antibodies (CNP@MAb). The vertical flow assay device consists of a plastic cassette with a hole on its top containing a nitrocellulose membrane coated with spike protein and an absorbent pad. The serum sample, washing buffer, and CNP@MAb flow vertically through the nitrocellulose membrane and absorbent pads, reducing assay time and simplifying the procedure. In positive samples, the interaction of CNP@MAb with anti-spike antibodies leads to the appearance of black spots, which can be visually detected. The developed method allows for rapid visual detection (5-7 min) of IgG vs. spike protein, with a LOD of 7.81 BAU/mL. It has been shown that an untrained operator can perform the assay and visually evaluate its results. Thus, the presented assay can be used in the further development of test systems for the serological diagnostics of COVID-19 or post-vaccination immunity monitoring.

Identifiants

pubmed: 37754091
pii: bios13090857
doi: 10.3390/bios13090857
pmc: PMC10526127
pii:
doi:

Substances chimiques

spike protein, SARS-CoV-2 0
Spike Glycoprotein, Coronavirus 0
Collodion 9004-70-0
Soot 0
Immunoglobulin G 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Russian Science Foundation
ID : 22-24-20091
Organisme : The Government of Perm krai
ID : 22-24-20091

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Auteurs

Maria Kropaneva (M)

Institute of Ecology and Genetics of Microorganisms, Ural Branch of Russian Academy of Sciences, 614081 Perm, Russia.
Biology Faculty, Perm State University, 614990 Perm, Russia.

Pavel Khramtsov (P)

Institute of Ecology and Genetics of Microorganisms, Ural Branch of Russian Academy of Sciences, 614081 Perm, Russia.
Biology Faculty, Perm State University, 614990 Perm, Russia.

Maria Bochkova (M)

Institute of Ecology and Genetics of Microorganisms, Ural Branch of Russian Academy of Sciences, 614081 Perm, Russia.
Biology Faculty, Perm State University, 614990 Perm, Russia.

Sergey Lazarev (S)

Institute of Ecology and Genetics of Microorganisms, Ural Branch of Russian Academy of Sciences, 614081 Perm, Russia.
Biology Faculty, Perm State University, 614990 Perm, Russia.

Dmitriy Kiselkov (D)

Institute of Technical Chemistry, Ural Branch of Russian Academy of Sciences, 614013 Perm, Russia.

Mikhail Rayev (M)

Institute of Ecology and Genetics of Microorganisms, Ural Branch of Russian Academy of Sciences, 614081 Perm, Russia.
Biology Faculty, Perm State University, 614990 Perm, Russia.

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Classifications MeSH