Published March 2015 | Version v1
Journal article

Synthesis, photophysical analysis, and in vitro cytotoxicity assessment of the multifunctional (magnetic and luminescent) core@shell nanomaterial based on lanthanide-doped orthovanadates

  • 1. Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland)
  • 2. Adam Mickiewicz University, Department of Behavioural Ecology, Faculty of Biology (Poland)
  • 3. Adam Mickiewicz University, Department of Cell Biology, Faculty of Biology (Poland)

Description

Rare earths orthovanadates (REVO4) doped with luminescent lanthanide ions (Ln3+) play an important role as promising light-emitting materials. Gadolinium orthovanadate exhibits strong absorption of ultraviolet radiation and as a matrix doped with Eu3+ ions is well known for its efficient and intense red emission, induced by energy transfer from the VO43− groups to Eu3+ ions. In the presented study, Fe3O4@SiO2@GdVO4:Eu3+ 5 % nanomaterial was investigated. The core@shell structures demonstrate attractive properties, such as higher thermal stability, enhanced water solubility, increased optical response, higher luminescence, longer decay times, and magnetic properties. Silica coating may protect nanocrystals from the surrounding environment. Therefore, such silica-covered nanoparticles (NPs) are successfully utilized in biomedical research. Multifunctional magnetic nanophosphors are very interesting due to their potential biomedical applications such as magnetic resonance imaging, hyperthermic treatment, and drug delivery. Therefore, the aim of our study was to investigate photophysical, chemical, and biological properties of multifunctional REVO4 doped with Ln3+. Moreover, the studied NPs did not affect erythrocyte sedimentation rate, cell membrane permeability, and morphology of human red blood cells

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Publishing Information

Journal Title
Journal of Nanoparticle Research
Journal Volume
17
Journal Issue
3
Journal Page Range
p. 1-11
ISSN
1388-0764

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Copyright (c) 2015 Springer Science+Business Media Dordrecht