Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening

Sci Rep. 2021 Jul 9;11(1):14185. doi: 10.1038/s41598-021-93207-7.

Abstract

This paper demonstrates the design, synthesis, simulation, and testing of three distinct geometries of plasmonic gold nanoparticles for on-chip DNA screening towards liquid biopsy. By employing a seed-mediated growth method, we have synthesized gold nanospheres, nanorods, and nanobipyramids. In parallel, we developed numerical simulations to understand the effects of nanoparticle geometry on the resonance features and refractive index sensitivity. Both experimental and simulation results were compared through a series of studies including in-solution and on-chip tests. We have thoroughly characterized the impact of nanoparticle geometry on the sensitivity to circulating tumor DNA, with immediate implications for liquid biopsy. The results agree well with theoretical predictions and simulations, including both bulk refractive index sensitivity and thin film sensitivity. Importantly, this work quantitatively establishes the link between nanoparticle geometry and efficacy in detecting rare circulating biomarkers. The nanobipyramids provided the highest sensitivity, approximately doubling the sensitivity compared to nanorods. To the best of our knowledge this is the first report carrying through geometric effects of simulation to clinically relevant biosensing. We put forth here synthesis and testing of three nanoparticle geometries, and a framework for both experimental and theoretical validation of plasmonic sensitivities towards liquid biopsy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circulating Tumor DNA / analysis
  • Circulating Tumor DNA / blood*
  • Gold / chemistry*
  • Humans
  • Metal Nanoparticles / chemistry*
  • Nanotubes / chemistry
  • Oligonucleotide Array Sequence Analysis / instrumentation
  • Surface Plasmon Resonance / instrumentation

Substances

  • Circulating Tumor DNA
  • Gold