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

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...

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Autores principales: Amogha Tadimety, Ziqian Wu, John H. Molinski, Russell Beckerman, Congran Jin, Lauren Zhang, Timothy J. Palinski, John X. J. Zhang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/a72440af4ecf4005bc860c43fe105cc9
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spelling oai:doaj.org-article:a72440af4ecf4005bc860c43fe105cc92021-12-02T15:23:08ZRational design of on-chip gold plasmonic nanoparticles towards ctDNA screening10.1038/s41598-021-93207-72045-2322https://doaj.org/article/a72440af4ecf4005bc860c43fe105cc92021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-93207-7https://doaj.org/toc/2045-2322Abstract 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.Amogha TadimetyZiqian WuJohn H. MolinskiRussell BeckermanCongran JinLauren ZhangTimothy J. PalinskiJohn X. J. ZhangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Amogha Tadimety
Ziqian Wu
John H. Molinski
Russell Beckerman
Congran Jin
Lauren Zhang
Timothy J. Palinski
John X. J. Zhang
Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
description 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.
format article
author Amogha Tadimety
Ziqian Wu
John H. Molinski
Russell Beckerman
Congran Jin
Lauren Zhang
Timothy J. Palinski
John X. J. Zhang
author_facet Amogha Tadimety
Ziqian Wu
John H. Molinski
Russell Beckerman
Congran Jin
Lauren Zhang
Timothy J. Palinski
John X. J. Zhang
author_sort Amogha Tadimety
title Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
title_short Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
title_full Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
title_fullStr Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
title_full_unstemmed Rational design of on-chip gold plasmonic nanoparticles towards ctDNA screening
title_sort rational design of on-chip gold plasmonic nanoparticles towards ctdna screening
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a72440af4ecf4005bc860c43fe105cc9
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