L-Lysine-modified Fe3O4 nanoparticles for magnetic cell labeling

Colloids Surf B Biointerfaces. 2020 Jun:190:110879. doi: 10.1016/j.colsurfb.2020.110879. Epub 2020 Feb 19.

Abstract

The efficiency of magnetic labeling with L-Lys-modified Fe3O4 magnetic nanoparticles (MNPs) and the stability of magnetization of rat adipose-derived mesenchymal stem cells, lineage-negative (Lin(-)) hematopoietic progenitor cells from mouse bone marrow and human leukemia K562 cells were studied. For this purpose, covalent modification of MNPs with 3-aminopropylsilane and N-di-Fmoc-L-lysine followed by removal of N-protecting groups was carried out. Since the degree of hydroxylation of the surface of the starting nanoparticles plays a crucial role in the silanization reaction and the possibility of obtaining stable colloidal solutions. In present work we for the first time performed a comparative qualitative and quantitative evaluation of the number of adsorbed water molecules and hydroxyl groups on the surface of chemically and physically obtained Fe3O4 MNPs using comprehensive FTIR spectroscopy and thermogravimetric analysis. The results obtained can be further used for magnetic labeling of cells in experiments in vitro and in vivo.

Keywords: Hematopoietic; Human leukemia cells; L-Lysine; Magnetic labeling; Magnetic nanoparticles; Mesenchymal stem cells; Progenitor cells.

MeSH terms

  • Animals
  • Cells, Cultured
  • Ferric Compounds / chemistry*
  • Humans
  • K562 Cells
  • Lysine / chemistry*
  • Magnetic Phenomena
  • Magnetite Nanoparticles / chemistry*
  • Particle Size
  • Rats
  • Surface Properties

Substances

  • Ferric Compounds
  • Magnetite Nanoparticles
  • ferric oxide
  • Lysine