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Amperometric l-ascorbic acid biosensors equipped with enzyme micelle membrane
Xiuyun Wang1, Hiroaki Watanabe, Shunichi Uchiyama
1Department of Materials & Science, Graduate School of Engineering, Saitama Institute of Technology, Fukaya, Saitama 369-0293, Japan.
Stable ascorbate oxidase (ASOD) micelle membranes on electrodes enable sensitive amperometric detection of l-ascorbic acid (AsA). This method offers rapid, interference-free sensing of AsA at cathodic potentials.
Area of Science:
- Biomedical Engineering
- Electrochemistry
- Biosensors
Background:
- Ascorbate oxidase (ASOD) is an enzyme that catalyzes the oxidation of l-ascorbic acid (AsA).
- Developing stable and sensitive biosensors for AsA detection is crucial for various applications.
- Polymaleimidostyrene (PMS) can form stable micelle structures with enzymes.
Purpose of the Study:
- To develop a stable and sensitive amperometric biosensor for l-ascorbic acid (AsA) detection.
- To utilize ascorbate oxidase (ASOD) immobilized in a polymaleimidostyrene (PMS) membrane.
- To investigate the performance of the biosensor on different electrode materials.
Main Methods:
- Immobilization of ASOD within a PMS membrane to form a stable micelle structure.
- Coating the ASOD-PMS membrane onto aminated glassy carbon electrodes (AGCE) and gold electrodes (AuE).
- Amperometric detection of AsA based on oxygen consumption at a cathodic applied potential (-0.5V vs. Ag/AgCl).
Main Results:
- The ASOD-PMS membrane formed a stable, oxygen-permeable hydrophobic layer on the electrodes.
- The developed AsA sensors exhibited good sensitivity and rapid response times (within 1 minute).
- A linear relationship between current and AsA concentration was observed from 5µM to 0.4mM using AGCE.
Conclusions:
- The ASOD-PMS biosensor provides a sensitive and selective method for AsA detection.
- The use of cathodic potential effectively avoids interference from other reducing agents.
- This approach offers a promising platform for developing robust amperometric biosensors.
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