Journal
MICROCHIMICA ACTA
Volume 189, Issue 10, Pages -Publisher
SPRINGER WIEN
DOI: 10.1007/s00604-022-05478-0
Keywords
Multiple-channel DNAzymes cycling; Cross-over nucleic structure; PtFe@Co-MOF; Electrochemical aptasensor; AFB1 detection
Categories
Funding
- National Natural Science Foundation of China [81401757]
- Sichuan Province Science and Technology Support Program [2019YJ0367]
- Health Commission of Sichuan Province Project [20PJ173]
- National College Students Innovation and Entrepreneurship Training Program [201913705047, 201713705085]
- Sichuan Provincial Key Laboratory of Development and Regeneration [SYS16-004]
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A novel electrochemical aptasensor with high sensitivity and specificity for the detection of Aflatoxin B1 has been developed in this study. The target-triggered multiple-channel DNAzyme cycling amplified assay and PtFe@Co-MOF as a signal amplifier resulted in enhanced detection signals. This aptasensor shows promise for rapid on-site detection with low cost.
A novel electrochemical aptasensor for the detection of Aflatoxin B1 (AFB1) was developed for the first time by using the target-triggered multiple-channel deoxyribozymes (DNAzymes) cycling amplified assay with Pt Fe doped NH2-Co-MOF (PtFe@Co-M0F) as a signal amplifier. In the presence of AFB1, a self-assembling cross-over nucleic structure could be triggered by AFB1 via two aptamers' structure switching for strand displacement, resulting in four channels of Mg2+-dependent DNAzyme recycling simultaneously to multiply the detection signals. These DNAzymes cyclically split the substrate sequence to release the PtFe@Co-MOF labeled detection probe (DP), which is subsequently hybridized with the capture probes on the Au-deposited glassy carbon electrode. The fabrication procedure was characterized by differential pulse voltammetry, and the results of the morphological and element composition characteristics methods were analyzed to determine the successful preparation of PtFe@Co-MOF. The limit of detection (LOD) for AFB1 detection was 2 pg mL(-1 )with a linear range from 5 pg mL(-1) to 80 ng mL(-1). By comparison, the enhanced detection sensitivity has been found to originate from the efficient shearing of DNAzymes, enhanced peroxidase-like capability, and multiple active sites of PtFe@ Co-MOF. Besides, this aptasensor showed high specificity for AFB1 compared with similar mycotoxins and exhibited high accuracy with low experimental cost and easy operation. Furthermore, the unique design of electrochemical aptasensors could provide a promising platform for the onsite determination of AFB1, as well as other targets by replacing the aptamer and other core recognition sequences.
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