Solvent Regulation Induced Cathode Aggregation-Induced Electrochemiluminescence of Tetraphenylethylene Nanoaggregates for Ultrasensitive Zearalenone Analysis

Anal Chem. 2024 Jun 4;96(22):9043-9050. doi: 10.1021/acs.analchem.4c00430. Epub 2024 May 22.

Abstract

Zearalenone (ZEN) is an extremely hazardous chemical widely existing in cereals, and its high-sensitivity detection possesses significant significance to human health. Here, the cathodic aggregation-induced electrochemiluminescence (AIECL) performance of tetraphenylethylene nanoaggregates (TPE NAs) was modulated by solvent regulation, based on which an electrochemiluminescence (ECL) aptasensor was constructed for sensitive detection of ZEN. The aggregation state and AIECL of TPE NAs were directly and simply controlled by adjusting the type of organic solvent and the fraction of water, which solved the current shortcomings of low strength and weak stability of the cathode ECL signal for TPE. Impressively, in a tetrahydrofuran-water mixed solution (volume ratio, 6:4), the relative ECL efficiency of TPE NAs reached 16.03%, which was 9.2 times that in pure water conditions, and the maximum ECL spectral wavelength was obviously red-shifted to 617 nm. In addition, "H"-shape DNA structure-mediated dual-catalyzed hairpin self-assembly (H-D-CHA) with higher efficiency by the synergistic effect between the two CHA reactions was utilized to construct a sensitive ECL aptasensor for ZEN analysis with a low detection limit of 0.362 fg/mL. In conclusion, solvent regulation was a simple and efficient method for improving the performance of AIECL materials, and the proposed ECL aptasensor had great potential for ZEN monitoring in food safety.

MeSH terms

  • Aptamers, Nucleotide / chemistry
  • Biosensing Techniques
  • Electrochemical Techniques*
  • Electrodes*
  • Limit of Detection
  • Luminescent Measurements*
  • Solvents* / chemistry
  • Stilbenes / chemistry
  • Zearalenone* / analysis
  • Zearalenone* / chemistry

Substances

  • Zearalenone
  • Solvents
  • tetraphenylethylene
  • Stilbenes
  • Aptamers, Nucleotide