4.8 Article

Metal enhanced fluorescence on nanoporous gold leaf-based assay platform for virus detection

Journal

BIOSENSORS & BIOELECTRONICS
Volume 58, Issue -, Pages 33-39

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2014.02.039

Keywords

Nanoporous gold leaf; Surface roughness; Fluorescence enhancement; Quantum dot; Influenza A virus

Funding

  1. Korea Healthcare Technology RD Project [A110191]
  2. Ministry for Health, Welfare & Family Affairs, Republic of Korea
  3. National Fisheries Research & Development Institute [RP-2012-BT-030]
  4. Civil & Military Technology Cooperation Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2013M3C1A9055407]
  5. Financial Supporting Project of Long-term Overseas Dispatch of PNU's Tenure-track Faculty
  6. Promotion of Nanobio-Technology Research
  7. Ministry of Education, Culture, Sports, Science and Technology, Japan
  8. Grants-in-Aid for Scientific Research [25246029] Funding Source: KAKEN

Ask authors/readers for more resources

In the present study, a rapid, sensitive and quantitative detection of influenza A virus targeting hemagglutinin (HA) was developed using hybrid structure of quantum dots (QDs) and nanoporous gold leaf (NPGL). NPGL film was prepared by dealloying bimetallic film where its surface morphology and roughness were fairly controlled. Anti-influenza A virus HA antibody (ab66189) was bound with NPGL and amine (-NH2) terminated QDs. These biofunctionalized NPGL and QDs formed a complex with the influenza virus A/Beijing/262/95 (H1N1) and the photoluminescence (PL) intensities of QDs were linearly correlated with the concentrations of the virus up to 1 ng/mL while no PL was observed in the absence of the virus, or in bovine serum albumin (BSA, 1 mu g/mL) alone. In addition, it was demonstrated that this assay detected successfully influenza virus A/Yokohama/110/2009 (H3N2) that is isolated from a clinical sample, at a concentration of ca. 50 plaque forming units (PFU)/mL. This detection limit is 2-order more sensitive than a commercially available rapid influenza diagnostic test. From these results, the proposed assay may offer a new strategy to monitor influenza virus for public health. (c) 2014 Elsevier B.V. All rights reserved.

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