Abstract
The direct electrochemistry of glucose oxidase (GOD) immobilized on a hexagonal mesoporous silica modified glassy carbon electrode was investigated. The adsorbed GOD displayed a pair of redox peaks with a formal potential of - 417 mV in 0.1 M pH 6.1 phosphate buffer solution (PBS). The response showed a diffusion-controlled electrode process with a two-electron transfer coupled with a two-proton transfer reaction process. GOD immobilized on a hexagonal mesoporous silica retained its bioactivity and stability. In addition, the immobilized GOD could electrocatalyze the oxidation of glucose to gluconlactone by taking ferrocene monocarboxylic acid (FMCA) as a mediator in N2 saturated solutions, indicating that the electrode may have the potential application in biosensors to analyze glucose. The sensor could exclude the interference of commonly coexisted uric acid, p-acetaminophenol and ascorbic acid and diagnose diabetes very fast and sensitively. This work demonstrated that the mesoporous silica provided a novel matrix for protein immobilization and the construction of biosensors.
Original language | English |
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Pages (from-to) | 250-256 |
Number of pages | 7 |
Journal | Bioelectrochemistry |
Volume | 70 |
Issue number | 2 |
DOIs | |
State | Published - May 2007 |
Externally published | Yes |
Keywords
- Biosensors
- Chemically modified electrode
- Direct electrochemistry
- Glucose
- Glucose oxidase
- Hexagonal mesoporous silica