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Heteroatom-Doped Magneto-Fluorescent Carbon Dots, a Potent Agent for Multimodal Imaging Publisher Pubmed



Kajani AA1 ; Pouresmaeili A1 ; Mehrgardi MA2 ; Javanmard SH3, 4
Authors
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Authors Affiliations
  1. 1. Department of Biotechnology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, 81746-73441, Iran
  2. 2. Department of Chemistry, University of Isfahan, Isfahan, 81746-73441, Iran
  3. 3. Personalized Medicine Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Applied Physiology Research Center, Cardiovascular Research Institute, Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Scientific Reports Published:2024


Abstract

A simple, one-pot and green method is reported for hydrothermal synthesis of highly fluorescent and magnetic carbon dots (CDs) by using D-glucose, as the carbon source. CDs were fully characterized by the UV-Vis and fluorescence spectroscopy, DLS, FTIR, TEM, EDS, XRD, and VSM. The nitrogen doping of different diamines significantly improved the fluorescence quantum yield (QY) of CDs with the maximum effect obtained by using m-phenylenediamine (mPDA). Temperature and reaction time also affected the QY of CDs with the best results obtained at 150 °C for 3 h. The heteroatom doping by innovative use of different metal sulfates including FeSO4, MnSO4, CuSO4, MgSO4, and ZnSO4, further improved the optical properties of CDs. Interestingly, the magnetic and multicolor CDs with high colloidal stability and QYs of 17.7, 16.5, and 53.9% at 460, 490, and 515 nm, respectively, were synthesized by using 0.1 M of glucose, mPDA and MnSO4. The resulted Mn-, S-, N-doped CDs represented rapid uptake and high-quality fluorescence imaging of the human fibroblast and umbilical vein endothelial cells in vitro, without significant toxicity. The CDs also displayed high r1 relaxivity of 32.3 mM− 1 s− 1 and were used for high-contrast MR and fluorescence imaging of mouse tumor models, in vivo. © The Author(s) 2024.