Preparation of ZnFe2O4 nanoparticles in the template of silk-fibroin peptide and their neuro-cytocompability in PC12 cells

Colloids Surf B Biointerfaces. 2013 Jul 1:107:19-26. doi: 10.1016/j.colsurfb.2013.01.072. Epub 2013 Feb 13.

Abstract

There is an urgency to prepare non-neurotoxic nanoparticles (NPs) as MRI contrast agent. We prepared ZnFe2O4 NPs with monocrystal structure in the template of silk-fibroin (SF) peptide at room temperature. Analyses of their crystallite size and NPs diameter after the growth of 1 d and 8 d indicated that SF peptide could promote nucleation, growth and dispersion of NPs. Results of EDS, Raman and TG proved that there was 4 wt% of the chemical composition of SF in as-prepared NPs. A possible growth mechanism of ZnFe2O4 NPs in the template of SF is proposed. The saturation magnetizations of NPs with SF (SF-NPs) were about 15 and 30 emu/g for 1 and 8 d, respectively. SF-NPs obviously promoted the viability of PC12 cells at NPs concentration of 0.0625 mg/mL in 2 d and 5 d of co-culture. Analysis of neurite length indicated no significant decreases of the experimental groups at different SF-NPs concentrations (from 0.0625 to 0.5 mg/mL) after 5 d cell co-culture, because SF peptide coating could slow the release of iron/zinc ions from NPs. Furthermore, SF-NPs did not destroy the organelles, karyotheca and the neurite using the observation in the cell ultrathin sections. Based on their good magnetic property and neuro-cytocompatibility, the potential application of ZnFe2O4 NPs with SF as MRI contrast agents would be envisioned.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Ferric Compounds / chemistry*
  • Fibroins / pharmacology*
  • Minerals / chemistry
  • Nanoparticles / chemistry*
  • Nanoparticles / ultrastructure
  • Neurites / drug effects
  • Neurites / metabolism
  • Neurites / ultrastructure
  • Neurons / cytology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / ultrastructure
  • Oxides / chemistry*
  • PC12 Cells
  • Peptides / pharmacology*
  • Rats
  • Spectrum Analysis, Raman
  • Time Factors
  • X-Ray Diffraction
  • Zinc / pharmacology*
  • Zinc Compounds / chemistry*

Substances

  • Ferric Compounds
  • Minerals
  • Oxides
  • Peptides
  • Zinc Compounds
  • Fibroins
  • Zinc