研究目的
To fabricate and characterize a localized surface plasmon resonance-based biosensor for detecting glutamate using gold nanoparticles on an optical fiber substrate.
研究成果
The fabricated LSPR-based glutamate sensor demonstrated high sensitivity and selectivity, with advantages such as low cost, immunity to electromagnetic interference, and capability for online monitoring and remote sensing.
研究不足
The sensor's performance is limited by the amounts of enzyme and co-enzyme immobilized on the AuNPs, which constrain the conversion of glutamate into α-ketoglutarate at higher concentrations.
1:Experimental Design and Method Selection:
The sensor was designed to operate according to an intensity modulation scheme where the absorbance changed as the glutamate concentration varied in the sample around the probe.
2:Sample Selection and Data Sources:
Glutamate solutions were prepared with concentrations ranging from 1 to 10 mM using 50 mM phosphate buffer at pH
3:List of Experimental Equipment and Materials:
Optical fiber (core diameter =600 μm, numerical aperture =
4:37), gold nanoparticles, enzyme glutamate dehydrogenase, coenzyme nicotinamide adenine dinucleotide, and various chemicals for synthesis and immobilization. Experimental Procedures and Operational Workflow:
The probe was fabricated by decorating AuNPs on an unclad portion of an optical fiber and co-immobilizing the enzyme and coenzyme over the AuNPs. The performance was evaluated in terms of calibration curve, specificity, sensitivity, and limit of detection.
5:Data Analysis Methods:
The absorbance spectra were recorded and analyzed to determine the sensor's performance parameters.
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