Journal
SENSORS AND ACTUATORS B-CHEMICAL
Volume 70, Issue 1-3, Pages 222-231Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/S0925-4005(00)00573-6
Keywords
field-effect transistor; ISFET; ENFET; glucose; glucose oxidase; urea; urease; acetylcholine; alpha-chymotrypsin; monolayer; biosensor
Ask authors/readers for more resources
A gate surface of an ion-selective field-effect transistor was modified with a monolayer enzyme array that stimulates biocatalytic reactions that control. the gate potential. Stepwise assemblage of the biocatalytic layer included primary silanization of the Al2O3-gate with 3-aminopropyltriethoxysilane, subsequent activation of the amino groups with glutaric dialdehyde and the covalent attachment of the enzyme to the functionalized gate surface. Urease, glucose oxidase, acetylcholine esterase and alpha -chymotrypsin were used to organize the biocatalytic matrices onto the chip gate. The resulting enzyme-based field-effect transistors, ENFETs, demonstrated capability to sense urea, glucose, acetylcholine and N-acetyl-L-tyrosine ethyl ester, respectively. The mechanism of the biosensing involves the alteration of the pH in the sensing layer by the biocatalytic reactions and the detection of the pH change by the ENFET. The major advantage of the enzyme-thin-layered FET devices as biosensors is the fast response-time (several tens of seconds) of these bioelectronic devices. This advantage over traditional thick-polymer-based ENFETs results from the low diffusion barrier for the substrate penetration to the biocatalytic active sites and minute isolation of the pH-sensitive gate surface from the bulk solution. (C) 2000 Elsevier Science B.V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available