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Nano Lett. 2017 Dec 13;17(12):7207-7212. doi: 10.1021/acs.nanolett.7b02302. Epub 2017 Nov 15.

The Role of Nanoparticle Design in Determining Analytical Performance of Lateral Flow Immunoassays.

Author information

1
Department of Mechanical Engineering, University of Minnesota , 111 Church Street SE, Minneapolis, Minnesota 55455, United States.
2
Institution of Biomaterials and Biomedical Engineering & Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto , 160 College Street, Toronto, Ontario 3E1, Canada.
3
The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Bioinspired Engineering and Biomechanics Center (BEBC), Xi'an Jiaotong University , Xi'an 710049, China.
4
Department of Medicine, Microbiology Research Facility (MRF), University of Minnesota , 689 SE 23rd Avenue, Minneapolis, Minnesota 55455, United States.
5
Department of Biomedical Engineering, University of Minnesota , 312 Church Street SE, Minneapolis, Minnesota 55455, United States.

Abstract

Rapid, simple, and cost-effective diagnostics are needed to improve healthcare at the point of care (POC). However, the most widely used POC diagnostic, the lateral flow immunoassay (LFA), is ∼1000-times less sensitive and has a smaller analytical range than laboratory tests, requiring a confirmatory test to establish truly negative results. Here, a rational and systematic strategy is used to design the LFA contrast label (i.e., gold nanoparticles) to improve the analytical sensitivity, analytical detection range, and antigen quantification of LFAs. Specifically, we discovered that the size (30, 60, or 100 nm) of the gold nanoparticles is a main contributor to the LFA analytical performance through both the degree of receptor interaction and the ultimate visual or thermal contrast signals. Using the optimal LFA design, we demonstrated the ability to improve the analytical sensitivity by 256-fold and expand the analytical detection range from 3 log10 to 6 log10 for diagnosing patients with inflammatory conditions by measuring C-reactive protein. This work demonstrates that, with appropriate design of the contrast label, a simple and commonly used diagnostic technology can compete with more expensive state-of-the-art laboratory tests.

KEYWORDS:

C-reactive protein; Gold nanoparticles; immunoassay; size dependent; thermal contrast

PMID:
29120648
PMCID:
PMC5747258
DOI:
10.1021/acs.nanolett.7b02302
[Indexed for MEDLINE]
Free PMC Article

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