Abstract
WS2nanotubes functionalized with carboxylic acid functions (WS2-COOH) were used for improved immobilization of the enzyme tyrosinase in order to form an electrochemical biosensor towards catechol and dopamine. The nanotubes were deposited on glassy carbon electrodes using a dispersion-filtration-transfer procedure to assure the reproducibility of the deposits. After the electrochemical and morphological characterization of these WS2-COOH nanotube deposits, the formed biosensors showed very satisfying performance towards catechol detection with a linear range of 0.6-70 µmol L-1and a sensitivity of 10.7 ± 0.2 mA L mol-1. The apparent Michaelis Menten constant of this system is slightly lower than theKMvalue of tyrosinase in solution, reflecting an excellent accessibility of the active site of the enzyme combined with a good mass transport of the target molecule through the deposit. For dopamine detection, we observed an accumulation of this substrate due to electrostatic interactions between the amine function of dopamine and the carboxylic acid groups of the nanotubes. This led to improved signal capture at low dopamine concentrations. With linear ranges of 0.5-10 µmol L-1and 10-40 µmol L-1, and respective sensitivities of 6.2 ± 0.7 mA L mol-1and 3.4 ± 0.4 mA L mol-1, the overall sensor performance is within the average of comparable results using carbon nanotubes. Nonetheless, the simplified handling of these nanotubes and their reduced environmental impact make these WS2-COOH nanotubes a promising nanomaterial for biosensing applications.
Original language | English |
---|---|
Pages (from-to) | 3566-3573 |
Number of pages | 8 |
Journal | Journal of Materials Chemistry B |
Volume | 8 |
Issue number | 16 |
DOIs | |
State | Published - 28 Apr 2020 |
Bibliographical note
Funding Information:We gratefully acknowledge the University Grenoble Alpes (Contrats Doctoraux thématiques UJF 2014) for the PhD fellowship funding of Quentin Palomar, and the CNRS PICS program 6344 France Israel for further support. The authors wish also to acknowledge the support from the platform Chimie NanoBio ICMG FR 2607 (PCN-ICMG), from the LabEx ARCANE (ANR-11-LABX-0003-01 and CBH-EUR-GS, ANR-17-EURE-0003), and from the Institut Carnot PolyNat (CARN 0007-01).
Funding Information:
We gratefully acknowledge the University Grenoble Alpes (Contrats Doctoraux th?matiques UJF 2014) for the PhD fellowship funding of Quentin Palomar, and the CNRS PICS program 6344 France Israel for further support. The authors wish also to acknowledge the support from the platform Chimie NanoBio ICMG FR 2607 (PCN-ICMG), from the LabEx ARCANE (ANR-11-LABX-0003-01 and CBH-EUR-GS, ANR-17-EURE-0003), and from the Institut Carnot PolyNat (CARN 0007-01).
Publisher Copyright:
© The Royal Society of Chemistry 2019.