Abstract
Split aptamers are fragments of the parent aptamer which still possess binding ability to its target. They have shown great potential in the development of aptasensors. In this study, a fluorescence aptasensor was constructed employing the split aptamer as a cooperative recognition molecular probe and Graphene Oxide nanosheets (GO) as a quencher for rapid detection of kanamycin in chilled pork. Under optimal conditions,the proposed biosensor showed a good linear relationship in the range of 0.5–50 nM with the detection limit of 0.36 nM. The recoveries of the actual samples ranged from 97.6 to 103.5%. Furthermore, the test can be completed in 25 min. This study provides good reference for developing simple, economical, and rapid assay for other small molecular targets detection.
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Acknowledgements
This work was financially supported by the Natural Science Foundation of Jiangsu Province [Grant No. BK20201452], Nanjing Pukou District Social Development Project [Grant No. S2020-17], Hebei Agricultural Science and Technology Achievement Transformation Fund [Grant No. 20822906D].
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Ye, H., Wan, T., Li, X. et al. Rapid detection of kanamycin using cooperative recognition split aptamer and graphene oxide nanosheets. Food Measure 17, 2144–2151 (2023). https://doi.org/10.1007/s11694-022-01781-9
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DOI: https://doi.org/10.1007/s11694-022-01781-9