Direct electrochemistry and electrochemical catalysis of myoglobin- TiO sub(2) coated multiwalled carbon nanotubes modified electrode

TiO sub(2) nanoparticles were homogeneously coated on multiwalled carbon nanotubes (MWCNTs) by hydrothermal deposition, and this nanocomposite might be a promising material for myoglobin (Mb) immobilization in view of its high biocompatibility and large surface. The glassy carbon (GC) electrode modi...

Full description

Saved in:
Bibliographic Details
Published inBioelectrochemistry (Amsterdam, Netherlands) Vol. 74; no. 1; pp. 157 - 163
Main Authors Zhang, Lei, Tian, Dan-Bi, Zhu, Jun-Jie
Format Journal Article
LanguageEnglish
Published 01.11.2008
Online AccessGet full text

Cover

Loading…
More Information
Summary:TiO sub(2) nanoparticles were homogeneously coated on multiwalled carbon nanotubes (MWCNTs) by hydrothermal deposition, and this nanocomposite might be a promising material for myoglobin (Mb) immobilization in view of its high biocompatibility and large surface. The glassy carbon (GC) electrode modified with Mb-TiO sub(2)/MWCNTs films exhibited a pair of well-defined, stable and nearly reversible cycle voltammetric peaks. The formal potential of Mb in TiO sub(2)/MWCNTs film was linearly varied in the range of pH 3-10 with a slope of 48.65 mV/pH, indicating that the electron transfer was accompanied by single proton transportation. The electron transfer between Mb and electrode surface, k sub(s) of 3.08 s super(- 1), was greatly facilitated in the TiO sub(2)/MWCNTs film. The electrocatalytic reductions of hydrogen peroxide were also studied, and the apparent Michaelis-Menten constant is calculated to be 83.10 mu M, which shows a large catalytic activity of Mb in the TiO sub(2)/MWCNTs film to H sub(2)O sub(2). The modified GC electrode shows good analytical performance for amperometric determination of hydrogen peroxide. The resultant Mb-TiO sub(2)/MWCNTs modified glassy carbon electrode exhibited fast amperometric response to hydrogen peroxide reduction, long term life and excellent stability. Finally the activity of the sensor for nitric oxide reduction was also investigated.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Feature-2
ISSN:1567-5394
DOI:10.1016/j.bioelechem.2008.07.003