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Fluorescence Anisotropy Cytosensing of Folate Receptor Positive Tumor Cells Using 3D Polyurethane-Go-Foams Modified With Folic Acid: Molecular Dynamics and in Vitro Studies Publisher Pubmed



Esmaeili Y1 ; Mohammadi Z1 ; Khavani M2 ; Sanati A1 ; Shariati L3, 4 ; Seyedhosseini Ghaheh H5 ; Bidram E1, 3 ; Zarrabi A6
Authors
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Authors Affiliations
  1. 1. Biosensor Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, University of California Berkeley, Berkeley, 94720, CA, United States
  3. 3. Department of Biomaterials, Nanotechnology and Tissue Engineering, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Applied Physiology Research Center, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Hezarjerib Ave, Isfahan, 8174673461, Iran
  5. 5. Department of Pharmaceutical Biotechnology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. Department of Biomedical Engineering, Faculty of Engineering and Natural Sciences, Istinye University, Istanbul, 34396, Turkey

Source: Microchimica Acta Published:2023


Abstract

Integrated polyurethane (PU)–based foams modified with PEGylated graphene oxide and folic acid (PU@GO-PEG-FA) were developed with the goal of capturing and detecting tumor cells with precision. The detection of the modified PU@GO-PEG surface through FA against folate receptor-overexpressed tumor cells is the basis for tumor cell capture. Molecular dynamics (MD) simulations were applied to study the strength of FA interactions with the folate receptor. Based on the obtained results, the folate receptor has intense interactions with FA, which leads to the reduction in the FA interactions with PEG, and so decreases the fluorescence intensity of the biosensor. The synergistic interactions offer the FA-modified foams a high efficiency for capturing the tumor cell. Using a turn-off fluorescence technique based on the complicated interaction of FA-folate receptor generated by target recognition, the enhanced capture tumor cells could be directly read out at excitation-emission wavelengths of 380–450 nm. The working range is between 1×10 2to 2×10 4cells mL -1 with a detection limit of 25 cells mL -1 and good reproducibility with relative standard deviation of 2.35%. Overall, findings demonstrate that the fluorescence-based biosensor has a significant advantage for early tumor cell diagnosis. Graphical Abstract: [Figure not available: see fulltext.]. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.