• Title of article

    Enhanced stability of enzyme organophosphate hydrolase interfaced on the carbon nanotubes

  • Author/Authors

    Pedrosa، نويسنده , , Valber A. and Paliwal، نويسنده , , Sheetal and Balasubramanian، نويسنده , , Shankar and Nepal، نويسنده , , Dhriti and Davis، نويسنده , , Virginia and Wild، نويسنده , , James and Ramanculov، نويسنده , , Erlan and Simonian، نويسنده , , Aleksandr، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2010
  • Pages
    6
  • From page
    69
  • To page
    74
  • Abstract
    In this paper we demonstrate that SWNTs and a covalent immobilization strategy enable very sensitive sensors with excellent long term stability. Organophosphorus hydrolase (OPH) functionalized single and multi-walled carbon nanotube (CNT) conjugates were exploited for direct amperometric detection of paraoxon, a model organophosphate. The catalytic hydrolysis of paraoxon produces equimoles of p-nitrophenol; oxidation was monitored amperometrically in real time under flow-injection (FIA) mode. OPH covalently immobilized on single-walled carbon nanotubes (SWNTs) demonstrated much higher activity than OPH conjugated to multi-walled carbon nanotubes (MWNTs). The dynamic concentration range for SWNT-OPH was 0.5–8.5 μmol L−1 with a detection limit of 0.01 μmol L−1 (S/N = 3). In addition to this high sensitivity, the immobilized OPH retained a significant degree of enzymatic activity, and displayed remarkable stability with only 25% signal loss over 7 months. These results suggest that covalent immobilization of OPH on CNTs can be used for specific immobilization with advantages of long term stability, high sensitivity, and simplicity.
  • Keywords
    Organophosphate , Carbon nanotubes , Covalent immobilization
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Serial Year
    2010
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Record number

    1971239