Journal
MICROCHIMICA ACTA
Volume 189, Issue 5, Pages -Publisher
SPRINGER WIEN
DOI: 10.1007/s00604-022-05266-w
Keywords
Aptamer; Photocurrent; Antibiotic; Metal-organic frameworks; Self-enhancement; Copper sheet
Categories
Funding
- National Natural Science Foundation of China [21575073]
- Open Foundation from the Academic Division of Chemistry, Qingdao University of Science and Technology [QUSTHX201907]
- Laoshan Scholar Program of Qingdao University of Science and Technology [201802685]
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Based on the self-enhanced photoelectrochemical quality of Cu-MOF-NH2, a photoelectrochemical biosensor for kanamycin detection was developed. The biosensor exploited the low electron hole recombination rate of Cu-MOF-NH2 and achieved self-enhancement through the oxidation of kanamycin by the amino group in Cu-MOF-NH2. The sensor showed a dynamic monitoring range of 0.5 to 650 nM and a detection limit of 0.1 nM. It demonstrated successful application in the determination of kanamycin in fish samples.
Based on the self-enhanced photoelectrochemical quality of Cu-MOF-NH2, a photoelectrochemical biosensor for kanamycin detection with a Cu-MOF-NH(2 )modified electrode was constructed. This biosensor took full advantage of the low electron hole recombination rate due to the ligand-to-metal charge-transfer mechanism of excited electron transfer in Cu-MOF-NH2. The kanamycin aptamer was modified onto Cu-MOF-NH2 by Schiff base reaction. In the presence of kanamycin, the holes on the amino group in Cu-MOF-NH2 oxidize kanamycin, making kanamycin itself as a signal enhancement substance, and achieving the effect of self-enhancement. The dynamic monitoring range for kanamycin is 0.5 to 650 nM, and the detection limit is 0.1 nM. The sensor has been successfully applied to the determination of kanamycin in fish with recoveries of 95.7-105.0% and RSD of 1.5-4.0%. This work provides a broad path for the development of self-enhanced photoelectrochemical sensors.
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