Please use this identifier to cite or link to this item: https://doi.org/10.1021/am100591t
Title: Glucose biosensor from covalent immobilization of chitosan-coupled carbon nanotubes on polyaniline-modified gold electrode
Authors: Wan, D.
Yuan, S.
Li, G.L.
Neoh, K.G. 
Kang, E.T. 
Keywords: Au electrode
carbon nanotubes
chitosan
glucose biosensor
polyaniline
Issue Date: 24-Nov-2010
Citation: Wan, D., Yuan, S., Li, G.L., Neoh, K.G., Kang, E.T. (2010-11-24). Glucose biosensor from covalent immobilization of chitosan-coupled carbon nanotubes on polyaniline-modified gold electrode. ACS Applied Materials and Interfaces 2 (11) : 3083-3091. ScholarBank@NUS Repository. https://doi.org/10.1021/am100591t
Abstract: An amperometric glucose biosensor was prepared using polyaniline (PANI) and chitosan-coupled carbon nanotubes (CS-CNTs) as the signal amplifiers and glucose oxidase (GOD) as the glucose detector on a gold electrode (the Au-g-PANI-c-(CS-CNTs)-GOD biosensor). The PANI layer was prepared via oxidative graft polymerization of aniline from the gold electrode surface premodified by self-assembled monolayer of 4-aminothiophenol. CS-CNTs were covalently coupled to the PANI-modified gold substrate using glutaradehyde as a bifunctional linker. GOD was then covalently bonded to the pendant hydroxyl groups of chitosan using 1,4-carbonyldiimidazole as the bifunctional linker. The surface functionalization processes were ascertained by X-ray photoelectron spectroscopy (XPS) analyses. The field emission scanning electron microscopy (FESEM) images of the Au-g-PANI-c-(CS-CNTs) electrode revealed the formation of a three-dimensional surface network structure. The electrode could thus provide a more spatially biocompatible microenvironment to enhance the amount and biocatalytic activity of the immobilized enzyme and to better mediate the electron transfer. The resulting Au-g-PANI-c-(CS-CNTs)-GOD biosensor exhibited a linear response to glucose in the concentration range of 1-20 mM, good sensitivity (21 μA/(mM•cm2)), good reproducibility, and retention of >80% of the initial response current after 2 months of storage. © 2010 American Chemical Society.
Source Title: ACS Applied Materials and Interfaces
URI: http://scholarbank.nus.edu.sg/handle/10635/89013
ISSN: 19448244
DOI: 10.1021/am100591t
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