Volume 12 Issue 1
Feb.  2022
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Juan Tan, Shiyue Wu, Qingqing Cai, Yi Wang, Pu Zhang. Reversible regulation of enzyme-like activity of molybdenum disulfide quantum dots for colorimetric pharmaceutical analysis[J]. Journal of Pharmaceutical Analysis, 2022, 12(1): 113-121. doi: 10.1016/j.jpha.2021.03.010
Citation: Juan Tan, Shiyue Wu, Qingqing Cai, Yi Wang, Pu Zhang. Reversible regulation of enzyme-like activity of molybdenum disulfide quantum dots for colorimetric pharmaceutical analysis[J]. Journal of Pharmaceutical Analysis, 2022, 12(1): 113-121. doi: 10.1016/j.jpha.2021.03.010

Reversible regulation of enzyme-like activity of molybdenum disulfide quantum dots for colorimetric pharmaceutical analysis

doi: 10.1016/j.jpha.2021.03.010
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This work was supported by the National Natural Science Foundation of China (Grant Nos.: 21775014 and 81972020) and Open Foundation Project of Engineering Research Center for Biotechnology of Active Substances, Ministry of Education (Grant No.: AS201905). Pu Zhang and Yi Wang were sponsored by the Chongqing Talent Program (Top-notch Youth) and the Chongqing High-level Personnel of Special Support Program (Top-notch Youth), respectively.

  • Received Date: Sep. 09, 2020
  • Accepted Date: Mar. 25, 2021
  • Rev Recd Date: Feb. 24, 2021
  • Publish Date: Mar. 31, 2021
  • Regulating the catalytic activity of nanozymes is significant for their applications in various fields. Here, we demonstrate a new strategy to achieve reversible regulation of the nanozyme's activity for sensing purpose. This strategy involves the use of zero-dimensional MoS2 quantum dots (MQDs) as the building blocks of nanozymes which display very weak peroxidase (POD)-like activity. Interestingly, such POD-like activity of the MQDs largely enhances in the presence of Fe3+ while diminishes with the addition of captopril thereafter. Further investigations identify the mechanism of Fe3+-mediated aggregation-induced enhancement of the POD-like activity and the inhibitory effect of captopril on the enhancement, which is highly dependent on their concentrations. Based on this finding, a colorimetric method for the detection of captopril is developed. This sensing approach exhibits the merits of simplicity, rapidness, reliability, and low cost, which has been successfully applied in quality control of captopril in pharmaceutical products. Moreover, the present sensing platform allows smartphone read-out, which has promising applications in point-of-care testing devices for clinical diagnosis and drug analysis.
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