Fluorescent non-porous silica nanoparticles for long-term cell monitoring: cytotoxicity and particle functionality

Acta Biomater. 2013 Nov;9(11):9183-93. doi: 10.1016/j.actbio.2013.04.026. Epub 2013 May 9.

Abstract

Inorganic nanoparticles such as silica particles offer many exciting possibilities for biomedical applications. However, the possible toxicity of these particles remains an issue of debate that seriously impedes their full exploitation. In the present work, commercially available fluorescent silica nanoparticles 25, 45 and 75 nm in diameter optimized for cell labelling (C-Spec® particles) are evaluated with regard to their effects on cultured cells using a novel multiparametric setup. The particles show clear concentration and size-dependent effects, where toxicity is caused by the number and total surface area of cell-associated particles. Cell-associated particles generate a short burst of oxidative stress that, next to inducing cell death, affects cell signalling and impedes cell functionality. For cell labelling purposes, 45 nm diameter silica particles were found to be optimally suited and no adverse effects were noticeable at concentrations of 50 μg ml(-1) or below. At this safe concentration, the particles were found to still allow fluorescence tracking of cultured cells over longer time periods. In conclusion, the data shown here provide a suitable concentration of silica particles for fluorescent cell labelling and demonstrate that at safe levels, silica particles remain perfectly suitable for fluorescent cell studies.

Keywords: Cell labelling; Cytotoxicity; Nanotoxicity; Silica nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Shape / drug effects
  • Cell Survival / drug effects
  • Cell Tracking / methods*
  • Endocytosis / drug effects
  • Exocytosis / drug effects
  • Fluorescence
  • Human Umbilical Vein Endothelial Cells / cytology
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Nanoparticles / chemistry*
  • Nanoparticles / toxicity*
  • PC12 Cells
  • Particle Size
  • Porosity
  • Rats
  • Reactive Oxygen Species / metabolism
  • Silicon Dioxide / toxicity*
  • Time Factors

Substances

  • Reactive Oxygen Species
  • Silicon Dioxide