Cytocompatibility evaluation of glycol-chitosan coated boron nitride nanotubes in human endothelial cells

Colloids Surf B Biointerfaces. 2013 Nov 1:111:142-9. doi: 10.1016/j.colsurfb.2013.05.031. Epub 2013 May 25.

Abstract

Boron nitride nanotubes (BNNTs) are intriguing nanomaterials with a wide range of potential biomedical applications. The assessment of BNNT interactions with biological systems, at both the cellular and subcellular levels, is an essential starting point for determining their bio-safety. We explore the effects of increasing concentrations of GC-BNNTs (0-100 μg/mL) on human vein endothelial cells (HUVECs), testing cell toxicity, proliferation, cytoskeleton integrity, cell activation and DNA damage. No significant changes were observed in cell viability, cytoskeleton integrity or DNA damage. Only a modest reduction in cell viability, tested by trypan blue assay, and the increased expression of vascular adhesion molecule-1, a marker of cell activation, were detected at the highest concentration used (100 μg/mL). Taken together, these findings indicate that GC-BNNTs do not affect endothelial cell biology, and are a promising first step in further investigation of their application potential in vascular targeting, imaging, and drug delivery.

Keywords: Boron nitride nanotubes; Cell activation; Endothelial cells; In vitro testing.

MeSH terms

  • Actins / metabolism
  • Boron Compounds / pharmacology*
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Chitosan / pharmacology*
  • Coated Materials, Biocompatible / pharmacology*
  • Endocytosis / drug effects
  • Focal Adhesions / drug effects
  • Focal Adhesions / metabolism
  • Histones / metabolism
  • Human Umbilical Vein Endothelial Cells / cytology*
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Human Umbilical Vein Endothelial Cells / ultrastructure
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Nanotubes / chemistry*
  • Nanotubes / ultrastructure
  • Spectrophotometry, Atomic
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Actins
  • Boron Compounds
  • Coated Materials, Biocompatible
  • H2AX protein, human
  • Histones
  • Vascular Cell Adhesion Molecule-1
  • glycol-chitosan
  • Intercellular Adhesion Molecule-1
  • boron nitride
  • Chitosan