Amplified electrochemical determination of UO22+ based on the cleavage of the DNAzyme and DNA-modified gold nanoparticle network structure
A superior electrochemical biosensor was designed for the determination of UO 2 2+ in aqueous solution by integration of DNAzyme and DNA-modified gold nanoparticle (DNA-AuNP) network structure. Key features of this method include UO 2 2+ inducing the cleavage of the DNAzyme and signal amplification...
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Veröffentlicht in: | Mikrochimica acta (1966) 2020-05, Vol.187 (5), p.311-311, Article 311 |
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Sprache: | eng |
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Zusammenfassung: | A superior electrochemical biosensor was designed for the determination of UO
2
2+
in aqueous solution by integration of DNAzyme and DNA-modified gold nanoparticle (DNA-AuNP) network structure. Key features of this method include UO
2
2+
inducing the cleavage of the DNAzyme and signal amplification of DNA-AuNP network structure. In this electrochemical method, the DNA-AuNP network structure can be effectively modified on the surface of gold electrode and then employed as an ideal signal amplification unit to generate amplified electrochemical response by inserting a large amount of electrochemically active indicator methylene blue (MB). In the presence of UO
2
2+
, the specific sites on DNA-AuNP network structure can be cleaved by UO
2
2+
, releasing the DNA-AuNP network structure with detectable reduction of electrochemical response intensity. The electrochemical response intensity is related to the concentration of UO
2
2+
. The logarithm of electrochemical response intensity and UO
2
2+
concentration showed a wide linear range of 10~100 pM, and the detection limit reached 8.1 pM (S/
N
= 3). This method is successfully used for determination of UO
2
2+
in water samples.
Graphical abstract
Fabricated DNAzyme network structure for enhanced electrical signal. Numerical experiments show that the current signal decreases as the concentration of UO
2
2+
increases. It can be seen that the biosensors could be used to detect UO
2
2+
in aqueous solution effectively. |
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ISSN: | 0026-3672 1436-5073 |
DOI: | 10.1007/s00604-020-04263-1 |