4.3 Article

Development of fluorescent nanoparticle-labeled lateral flow assay for the detection of nucleic acids

Journal

BIOMEDICAL MICRODEVICES
Volume 15, Issue 5, Pages 751-758

Publisher

SPRINGER
DOI: 10.1007/s10544-013-9760-1

Keywords

Ru(bpy)(3)(2+)-doped silica nanoparticle; DNA probe; Fluorescence; Nucleic acid; Lateral flow

Funding

  1. USDA [2010-34637-20985]
  2. UMass Amherst Center for Hierarchical Manufacturing, a nanoscience shared facility
  3. National Science Foundation [CMMI-1025020]

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The rapid, specific and sensitive detection of nucleic acids is of utmost importance for the identification of infectious agents, diagnosis and treatment of genetic diseases, and the detection of pathogens related to human health and safety. Here we report the development of a simple and sensitive nucleic acid sequence-based and Ru(bpy)(3)(2+)-doped silica nanoparticle-labeled lateral flow assay which achieves low limit of detection by using fluorescencent nanoparticles. The detection of the synthetic nucleic acid sequences representative of Trypanosoma mRNA, the causative agent for African sleeping sickness, was utilized to demonstrate this assay. The 30 nm spherical Ru(bpy)(3)(2+)-doped silica nanoparticles were prepared in aqueous medium by a novel method recently reported. The nanoparticles were modified by 3-glycidoxypropyl trimeth oxysilane in order to conjugate to amine-capped oligonucleotide reporter probes. The fluorescent intensities of the fluorescent assays were quantified on a mictrotiter plate reader using a custom holder. The experimental results showed that the lateral flow fluorescent assay developed was more sensitive compared with the traditional colloidal gold test strips. The limit of detection for the fluorescent lateral flow assay developed is approximately 0.066 fmols as compared to approximately 15 fmols for the colloidal gold. The limit of detection can further be reduced about one order of magnitude when dipstick format was used.

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