Toxicity of functional nano-micro zinc oxide tetrapods: impact of cell culture conditions, cellular age and material properties

PLoS One. 2014 Jan 13;9(1):e84983. doi: 10.1371/journal.pone.0084983. eCollection 2014.

Abstract

With increasing production and applications of nanostructured zinc oxide, e.g., for biomedical and consumer products, the question of safety is getting more and more important. Different morphologies of zinc oxide structures have been synthesized and accordingly investigated. In this study, we have particularly focused on nano-micro ZnO tetrapods (ZnO-T), because their large scale fabrication has been made possible by a newly introduced flame transport synthesis approach which will probably lead to several new applications. Moreover, ZnO-T provide a completely different morphology then classical spherical ZnO nanoparticles. To get a better understanding of parameters that affect the interactions between ZnO-T and mammalian cells, and thus their biocompatibility, we have examined the impact of cell culture conditions as well as of material properties on cytotoxicity. Our results demonstrate that the cell density of fibroblasts in culture along with their age, i.e., the number of preceding cell divisions, strongly affect the cytotoxic potency of ZnO-T. Concerning the material properties, the toxic potency of ZnO-T is found to be significantly lower than that of spherical ZnO nanoparticles. Furthermore, the morphology of the ZnO-T influenced cellular toxicity in contrast to surface charges modified by UV illumination or O2 treatment and to the material age. Finally, we have observed that direct contact between tetrapods and cells increases their toxicity compared to transwell culture models which allow only an indirect effect via released zinc ions. The results reveal several parameters that can be of importance for the assessment of ZnO-T toxicity in cell cultures and for particle development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Count
  • Cell Culture Techniques
  • Cell Death / drug effects
  • Cell Shape / drug effects
  • Cell Survival / drug effects
  • Cellular Senescence / drug effects*
  • Dermis / cytology
  • Fibroblasts / cytology*
  • Fibroblasts / drug effects
  • Humans
  • Nanoparticles / toxicity*
  • Nanoparticles / ultrastructure
  • Particle Size*
  • Zinc Oxide / chemistry*
  • Zinc Oxide / toxicity*

Substances

  • Zinc Oxide

Grants and funding

Authors HP, EM and CR would like to acknowledge a grant from Medical Faculty (Christiana Albertina University Kiel). Authors also thank the German Research Foundation (DFG) for financial support under schemes SFB 855-A5 and Ad/183/10-1. YKM acknowledges the Humboldt Foundation for postdoctoral grant. ME thanks to DFG for SFB 677 and EL554/1-1. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.