Spin-coated Au-nanohole arrays engineered by nanosphere lithography for a Staphylococcus aureus 16S rRNA electrochemical sensor

Biosens Bioelectron. 2016 Mar 15:77:1086-94. doi: 10.1016/j.bios.2015.10.094. Epub 2015 Nov 2.

Abstract

The nanopatterning of gold nanoparticle (AuNP) arrays on an indium tin oxide (ITO) electrode using efficient and low-cost methods is described. This process used nanosphere lithography (NSL) encompassing the deposition of monolayered Polystyrene (PS) followed by a convective self-assembly drop coating protocol onto the ITO substrate that further acted as the mask after the AuNP assembly. The results showed that spin-coating allowed AuNPs to follow the contour and adhere to the PS nanospheres. The final products, after etching the PS, generated a highly ordered Au-nanohole array on an ITO substrate. The Au-nanohole arrays on the ITO electrode provided a greater surface area and successfully enhanced the peak current of electrochemical measurements by 82% compared with bare ITO and was used to detect Staphylococcus aureus 16S rRNA hybridization. In contrast to non-templated AuNP structures, the Au-nanohole arrays on the ITO electrode contributed to an optimum sensitivity improvement in DNA hybridization detection by 23%, along with an impressive limit of detection (LOD) of 10 pM. The high specificity of this distinguished structure was also achieved in the hybridization measurements of multi-analyte pathogens. These findings indicate that the combination of PS nanosphere lithography, followed by the spin-coating of AuNPs, leads to an inexpensive and simple engineering process that effectively generates uniform Au-nanohole arrays on ITO, which provides a greater surface area to optimize the electrochemical performance of the DNA biosensor.

Keywords: 16S rRNA; Au-nanohole array; Electrochemical sensor; Nanosphere lithography (NSL); Spin-coated AuNPs; Staphylococcus aureus.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques / instrumentation*
  • Equipment Design
  • Equipment Failure Analysis
  • Gold / chemistry
  • Metal Nanoparticles / chemistry*
  • Molecular Imprinting / methods
  • Nanopores / ultrastructure*
  • RNA, Ribosomal, 16S / analysis
  • RNA, Ribosomal, 16S / genetics*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Staphylococcus aureus / genetics*
  • Staphylococcus aureus / isolation & purification*

Substances

  • RNA, Ribosomal, 16S
  • Gold