Tuning the Gold Nanoparticle Colorimetric Assay by Nanoparticle Size, Concentration, and Size Combinations for Oligonucleotide Detection

Varsha Sanjay Godakhindi, Peiyuan Kang, Maud Serre, Naga Aravind Revuru, Jesse Minghao Zou, Michael R. Roner, Ruth Levitz, Jeffrey Kahn, Jaona Randrianalisoa, Zhenpeng Qin

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Gold nanoparticle (GNP)-based aggregation assay is simple, fast, and employs a colorimetric detection method. Although previous studies have reported using GNP-based colorimetric assay to detect biological and chemical targets, a mechanistic and quantitative understanding of the assay and effects of GNP parameters on the assay performance is lacking. In this work, we investigated this important aspect of the GNP aggregation assay including effects of GNP concentration and size on the assay performance to detect malarial DNA. Our findings lead us to propose three major competing factors that determine the final assay performance including the nanoparticle aggregation rate, plasmonic coupling strength, and background signal. First, increasing nanoparticle size reduces the Brownian motion and thus aggregation rate, but significantly increases plasmonic coupling strength. We found that larger GNP leads to stronger signal and improved limit of detection (LOD), suggesting a dominating effect of plasmonic coupling strength. Second, higher nanoparticle concentration increases the probability of nanoparticle interactions and thus aggregation rate, but also increases the background extinction signal. We observed that higher GNP concentration leads to stronger signal at high target concentrations due to higher aggregation rate. However, the fact the optimal LOD was found at intermediate GNP concentrations suggests a balance of two competing mechanisms between aggregation rate and signal/background ratio. In summary, our work provides new guidelines to design GNP aggregation-based POC devices to meet the signal and sensitivity needs for infectious disease diagnosis and other applications.

Original languageEnglish (US)
Pages (from-to)1627-1636
Number of pages10
JournalACS Sensors
Volume2
Issue number11
DOIs
StatePublished - Nov 22 2017

Fingerprint

oligonucleotides
Oligonucleotides
Gold
Assays
Tuning
tuning
gold
Nanoparticles
nanoparticles
Agglomeration
Brownian movement
infectious diseases
extinction
DNA
deoxyribonucleic acid

Keywords

  • cross-linking aggregation
  • gold nanoparticle
  • infectious diseases
  • nanoparticle aggregation
  • point-of-care (POC) diagnosis

ASJC Scopus subject areas

  • Bioengineering
  • Fluid Flow and Transfer Processes
  • Process Chemistry and Technology
  • Instrumentation

Cite this

Tuning the Gold Nanoparticle Colorimetric Assay by Nanoparticle Size, Concentration, and Size Combinations for Oligonucleotide Detection. / Godakhindi, Varsha Sanjay; Kang, Peiyuan; Serre, Maud; Revuru, Naga Aravind; Zou, Jesse Minghao; Roner, Michael R.; Levitz, Ruth; Kahn, Jeffrey; Randrianalisoa, Jaona; Qin, Zhenpeng.

In: ACS Sensors, Vol. 2, No. 11, 22.11.2017, p. 1627-1636.

Research output: Contribution to journalArticle

Godakhindi, VS, Kang, P, Serre, M, Revuru, NA, Zou, JM, Roner, MR, Levitz, R, Kahn, J, Randrianalisoa, J & Qin, Z 2017, 'Tuning the Gold Nanoparticle Colorimetric Assay by Nanoparticle Size, Concentration, and Size Combinations for Oligonucleotide Detection', ACS Sensors, vol. 2, no. 11, pp. 1627-1636. https://doi.org/10.1021/acssensors.7b00482
Godakhindi, Varsha Sanjay ; Kang, Peiyuan ; Serre, Maud ; Revuru, Naga Aravind ; Zou, Jesse Minghao ; Roner, Michael R. ; Levitz, Ruth ; Kahn, Jeffrey ; Randrianalisoa, Jaona ; Qin, Zhenpeng. / Tuning the Gold Nanoparticle Colorimetric Assay by Nanoparticle Size, Concentration, and Size Combinations for Oligonucleotide Detection. In: ACS Sensors. 2017 ; Vol. 2, No. 11. pp. 1627-1636.
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