4.7 Article

Selective Colorimetric Detection of Cancer Cells Based on Iron/Copper Nanocatalyst Peroxidase Activity

Journal

IEEE SENSORS JOURNAL
Volume 22, Issue 11, Pages 10492-10499

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/JSEN.2022.3168301

Keywords

peroxidase-like activity; nanozymes; cancer cell detection; iron oxide; copper oxide; therapeutic effect

Funding

  1. Natural Science Foundation of Shandong Province [ZR2020QC061]
  2. Double-Hundred Talent Plan of Shandong Province
  3. Liaocheng University [318051901, 31805180301, 31805180326]

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In this study, a novel nanostructured hybrid enzyme was developed as an artificial enzyme for detecting and treating cancer cells. The hybrid enzyme showed enhanced peroxidase-like activity and selective interaction with GLUT overexpressed cancer cells, making it a promising candidate for clinical cancer diagnosis and therapy.
Nanomaterial based enzyme i.e., nanozymes have the potential to overcome natural enzymes' major shortcomings, hence the development of effective artificial enzymes is a burgeoning topic in nanobiotechnology. A novel nanostructured hybrid enzyme was constructed as a mimetic enzyme for in vitro cancer cell detection and therapeutic treatment in the current study. The iron-copper (FeCu) nanocatalyst was prepared and immobilized with 2-DG, as cancer cell targeting ligand 2-DG can interact with the GLUT receptor overexpressed in several cancer cells. FeCu@2-DG showed enhanced peroxidase-like activity and oxidized the substrate 3,3',5,5'-tetramethylbenzidine (TMB) into blue color product in the presence of hydrogen peroxide (H2O2). Peroxidase activity of nanocatalyst can be well utilized as selective and quantitative colorimetric sensor for detection of liver cancer cells (HepG2). Sensor is shown to detect HepG2 cells in linear range of 50-1000 cells/mL, with detection limit of 20 cells/mL. Additionally, nanocatalyst can also be used as H2O2 and ascorbic acid mediated therapeutic effect in cancer cells. Phloretin (GLUT in hibitor)treated cells showed the negligible interaction with particle in comparison of control non-treated cells. Thus, confirming the selective interaction of synthesized particle with GLUT overexpressed cancer cells. Based on the simple peroxidase function, the developed hybrid might be a promising candidate for clinical cancer diagnosis and therapy.

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