Cu-BTC Derived Mesoporous CuS Nanomaterial as Nanozyme for Colorimetric Detection of Glutathione

Molecules. 2024 May 3;29(9):2117. doi: 10.3390/molecules29092117.

Abstract

In this paper, Cu-BTC derived mesoporous CuS nanomaterial (m-CuS) was synthesized via a two-step process involving carbonization and sulfidation of Cu-BTC for colorimetric glutathione detection. The Cu-BTC was constructed by 1,3,5-benzenetri-carboxylic acid (H3BTC) and Cu2+ ions. The obtained m-CuS showed a large specific surface area (55.751 m2/g), pore volume (0.153 cm3/g), and pore diameter (15.380 nm). In addition, the synthesized m-CuS exhibited high peroxidase-like activity and could catalyze oxidation of the colorless substrate 3,3',5,5'-tetramethylbenzidine to a blue product. Peroxidase-like activity mechanism studies using terephthalic acid as a fluorescent probe proved that m-CuS assists H2O2 decomposition to reactive oxygen species, which are responsible for TMB oxidation. However, the catalytic activity of m-CuS for the oxidation of TMB by H2O2 could be potently inhibited in the presence of glutathione. Based on this phenomenon, the colorimetric detection of glutathione was demonstrated with good selectivity and high sensitivity. The linear range was 1-20 μM and 20-300 μM with a detection limit of 0.1 μM. The m-CuS showing good stability and robust peroxidase catalytic activity was applied for the detection of glutathione in human urine samples.

Keywords: Cu-BTC; colorimetric detection; glutathione; mesoporous CuS nanomaterial; nanozyme.

MeSH terms

  • Benzidines / chemistry
  • Catalysis
  • Colorimetry* / methods
  • Copper* / chemistry
  • Glutathione* / analysis
  • Glutathione* / chemistry
  • Humans
  • Hydrogen Peroxide* / analysis
  • Hydrogen Peroxide* / chemistry
  • Limit of Detection
  • Nanostructures* / chemistry
  • Oxidation-Reduction
  • Phthalic Acids / chemistry
  • Porosity

Substances

  • Glutathione
  • Copper
  • Hydrogen Peroxide
  • Phthalic Acids
  • 3,3',5,5'-tetramethylbenzidine
  • Benzidines
  • terephthalic acid