4.7 Article

Substituent Effects Impact Surface Charge and Aggregation of Thiophenol-Labeled Gold Nanoparticles for SERS Biosensors

Journal

BIOSENSORS-BASEL
Volume 12, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/bios12010025

Keywords

SERS; immunoassay; nanoparticles; multiplexing; Raman reporter molecules; aggregation

Funding

  1. National Institutes of Health STTR grant [R41CA213718]
  2. National Institutes of Health grants [U01CA200466]

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SERS immunoassay biosensors have great potential for clinical diagnostics due to their high sensitivity and the growing interest in multi-marker panels. However, difficulties in designing compatible extrinsic Raman labels have hindered their development. Previous studies have focused on selecting Raman reporter molecules (RRMs) based on their spectroscopic characteristics for multiplexing, as well-differentiated spectra are essential for simultaneous detection. However, these candidates often induce aggregation of SERS nanotags made of gold nanoparticles. Therefore, a better understanding of factors affecting the aggregation of RRM-coated gold nanoparticles is needed.
SERS immunoassay biosensors hold immense potential for clinical diagnostics due to their high sensitivity and growing interest in multi-marker panels. However, their development has been hindered by difficulties in designing compatible extrinsic Raman labels. Prior studies have largely focused on spectroscopic characteristics in selecting Raman reporter molecules (RRMs) for multiplexing since the presence of well-differentiated spectra is essential for simultaneous detection. However, these candidates often induce aggregation of the gold nanoparticles used as SERS nanotags despite their similarity to other effective RRMs. Thus, an improved understanding of factors affecting the aggregation of RRM-coated gold nanoparticles is needed. Substituent electronic effects on particle stability were investigated using various para-substituted thiophenols. The inductive and resonant effects of functional group modifications were strongly correlated with nanoparticle surface charge and hence their stability. Treatment with thiophenols diminished the negative surface charge of citrate-stabilized gold nanoparticles, but electron-withdrawing substituents limited the magnitude of this diminishment. It is proposed that this phenomenon arises by affecting the interplay of competing sulfur binding modes. This has wide-reaching implications for the design of biosensors using thiol-modified gold surfaces. A proof-of-concept multiplexed SERS biosensor was designed according to these findings using the two thiophenol compounds with the most electron-withdrawing substitutions: NO2 and CN.

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