4.7 Article

Enhanced peroxidase-like activity of boron nitride quantum dots anchored porous CeO2 nanorods by aptamer for highly sensitive colorimetric detection of kanamycin

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 330, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2020.129318

关键词

Kanamycin; Nanozymes; BNQDs/CeO2; Aptamer-regulated; Colorimetric sensing

资金

  1. National Natural Science Foundation of China [51521006, 51579096]
  2. Funds for Innovative Province Construction of Hunan Province [2019RS3012]
  3. National Innovative Talent Promotion Program of China
  4. [2017RA2088]

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In this study, a simple and low-cost colorimetric analysis method was developed for highly sensitive determination of KAN by integrating BNQDs/CeO2 nanozyme and aptamer. The method demonstrated promising potential as a universal detection platform for environmental monitoring and food safety through the enhanced catalytic activity and specific recognition of KAN.
Kanamycin (KAN) residue in the environment and food have a huge risk to human health, therefore, designing simple and sensitive determination methods for KAN is in high demand. Here, a simple and low-cost colorimetric analysis was established for highly sensitive determination of KAN through integrating boron nitride quantum dots anchored porous CeO2 nanorods (BNQDs/CeO2) and aptamer. The BNQDs/CeO2 as nanozyme showed prominent peroxidase-like activity, which could effectively catalyze 3,3',5,5' -tetramethylbenzidine (TMB) oxidation by H2O2 because of large surface area and synergetic interaction between BNQDs and CeO2. Moreover, it presented an obviously enhanced catalytic activity after combing with KAN-specific aptamer, resulting from the increased dispersibility and substrate affinity of BNQDs/CeO2 nanozyme. While KAN could restrain such a catalytic enhancement through aptamer-target recognition event. On the basis of aptamer-regulated mimic enzyme activity, the proposed colorimetric method realized quantitative KAN determination ranging from 0.01 nM to 100 nM with an ultralow detection limit of 4.6 pM. This analysis method is facile in design and can be applied to other biomolecular recognition processes, promising as a universal detection platform for environmental monitoring and food safety.

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