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
Link To Document :
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