Abstract
A rapid and simple near-infrared (NIR) luminescence quenching method for the detection of phenolic compounds based on combining the unique property of N-acetyl-l-cysteine-protected gold nanoparticles (NAC-AuNPs) and tyrosinase (Tyr) enzymatic reactions is described. This method relies on the luminescence quenching of NAC-AuNPs-tyrosinase (NAC-AuNPs-Tyr) hybrid material by phenolic compounds. The quinone intermediates produced from enzymatic catalytic oxidation of phenolic compounds were believed to play a major role in the luminescence quenching. Dynamic quenching mechanism was confirmed by using time-resolved luminescence spectroscopy. Optimization of the experimental parameters including the concentration of NAC-AuNPs-Tyr (20 μg/mL), excitation wavelength (450 nm), pH (6.0), and temperature (20 °C) has been determined. A linear range 0.5 μM to 1.0 mM and a detection limit 0.1 μM of catechol were obtained under optimal conditions. The sensitivity of different phenolic compounds was compared and follows the trend: catechol > p-cresol > phenol. The proposed NIR luminescence quenching method exhibits high sensitivity, good repeatability, and long-term stability, demonstrating potential for further development to NIR luminescence phenol biosensors.
Original language | English |
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Pages (from-to) | 1043-1048 |
Number of pages | 6 |
Journal | Biosensors and Bioelectronics |
Volume | 25 |
Issue number | 5 |
DOIs | |
Publication status | Published - 15 Jan 2010 |
Scopus Subject Areas
- Biotechnology
- Biophysics
- Biomedical Engineering
- Electrochemistry
User-Defined Keywords
- Gold nanoparticles
- Near-infrared fluorescence
- Phenolic compounds
- Tyrosinase