4.8 Article

Ultrabright Fluorescence Readout of an Inkjet-Printed Immunoassay Using Plasmonic Nanogap Cavities

Journal

NANO LETTERS
Volume 20, Issue 6, Pages 4330-4336

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.0c01051

Keywords

Plasmonics; Nanocube; Nanogap; Immunoassay; Point-of-Care

Funding

  1. National Institute of Health (NIH) [5R01-HL144928-02]
  2. Research Corporation for Science Advancement
  3. United States Special Operations Command [W81XWH-16-C-0219]
  4. Combat Casualty Care Research Program (JPC-6) [W81XWH-17-2-0045]
  5. National Council for the Improvement of Higher Education-CAPES (the Science without Borders project)

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Fluorescence-based microarrays are promising diagnostic tools due to their high throughput, small sample volume requirements, and multiplexing capabilities. However, their low fluorescence output has limited their implementation for in vitro diagnostics applications in point-of-care (POC) settings. Here, by integration of a sandwich immunoassay microarray within a plasmonic nanogap cavity, we demonstrate strongly enhanced fluorescence which is critical for readout by inexpensive POC detectors. The immunoassay consists of inkjet-printed antibodies on a polymer brush which is grown on a gold film. Colloidally synthesized silver nanocubes are placed on top and interact with the underlying gold film creating high local electromagnetic field enhancements. By varying the thickness of the brush from 5 to 20 nm, up to a 151-fold increase in fluorescence and 14-fold improvement in the limit-of-detection is observed for the cardiac biomarker B-type natriuretic peptide (BNP) compared to the unenhanced assay, paving the way for a new generation of POC clinical diagnostics.

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