Immunological assay using a solid-state pore with a low limit of detection.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
19 Jul 2024
Historique:
received: 27 12 2023
accepted: 08 07 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: epublish

Résumé

Emerging infectious diseases, cancer, and other diseases are quickly tested mainly via immune reactions based on specific molecular recognition between antigens and antibodies. By changing the diameter of solid-state pores, biomolecules of various sizes can be rapidly detected at the single-molecule level. The combination of immunoreactions and solid-state pores paves the way for an efficient testing method with high specificity and sensitivity. The challenge in developing this method is achieving quantitative analysis using solid-state pores. Here, we demonstrate a method with a low limit of detection for testing tumor markers using a combination of immunoreactions and solid-state pore technology. Quantitative analysis of the mixing ratio of two and three beads with different diameters was achieved with an error rate of up to 4.7%. The hybrid solid-state pore and immunoreaction methods with prostate-specific antigen (PSA) and anti-PSA antibody-modified beads achieved a detection limit of 24.9 fM PSA in 30 min. The hybrid solid-state pore and immunoreaction enabled the rapid development of easy-to-use tests with lower limit of detection and greater throughput than commercially available immunoassay for point-of-care testing.

Identifiants

pubmed: 39030274
doi: 10.1038/s41598-024-67112-8
pii: 10.1038/s41598-024-67112-8
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77
Biomarkers, Tumor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

16686

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : #JP21zf0127004

Informations de copyright

© 2024. The Author(s).

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Auteurs

Hiroyasu Takei (H)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Tomoko Nakada (T)

SANKEN, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka, 567-0047, Japan.

Lat Wai Leong (LW)

SANKEN, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka, 567-0047, Japan.

Atsuki Ito (A)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Kakeru Hanada (K)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Hinako Maeda (H)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Muhammad Shan Sohail (MS)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Kazuhiko Tomiyasu (K)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Osamu Sakamoto (O)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Norihiko Naono (N)

Aipore Inc., 26-1 Sakuragaokacho, Shibuya, Tokyo, 150-8512, Japan.

Masateru Taniguchi (M)

SANKEN, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka, 567-0047, Japan. taniguti@sanken.osaka-u.ac.jp.

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