Hydroxylation of multi-walled carbon nanotubes: Enhanced biocompatibility through reduction of oxidative stress initiated cell membrane damage, cell cycle arrestment and extrinsic apoptotic pathway

Environ Toxicol Pharmacol. 2016 Oct:47:124-130. doi: 10.1016/j.etap.2016.09.013. Epub 2016 Sep 21.

Abstract

Modification of CNTs with hydroxyl group promotes their applications in biomedical area. However, the impact of hydroxylation on their biocompatibility is far from being completely understood. In this study, we carried out a comprehensive evaluation of hydroxylated multi-walled carbon nanotubes (MWCNTs-OH) on the human normal liver L02 cell line, and compared it with that of pristine multi-walled carbon nanotubes (p-MWCNTs). Results demonstrated that compared with p-MWCNTs, MWCNTs-OH induced significantly lower oxidative stress as indicated by the level of intracellular antioxidant glutathione (GSH), subsequently lead to less cell membrane damage as demonstrated by lactate dehydrogenase (LDH) leakage assay, and showed slightly decreased arrestment of cell cycle distribution at G0/G1. More interestingly, MWCNTs-OH exhibited significantly lower tendency to activate caspase-8, a key molecule involved in the extrinsic apoptotic pathway. All these in vitro results demonstrated that hydroxylation of MWCNTs enhanced their biocompatibility compare with p-MWCNTs.

Keywords: Cell cycle arrestment; Cell membrane integrity; Extrinsic apoptotic pathway; Multi-walled carbon nanotubes; Oxidative stress.

MeSH terms

  • Apoptosis / drug effects
  • Caspase 8 / metabolism
  • Cell Cycle Checkpoints / drug effects*
  • Cell Line
  • Cell Membrane / drug effects*
  • Glutathione / metabolism
  • Humans
  • Hydroxylation
  • Liver / cytology
  • Liver / drug effects
  • Materials Testing
  • Microscopy, Electron, Scanning
  • Microscopy, Electron, Transmission
  • Nanotubes, Carbon / chemistry*
  • Oxidative Stress / drug effects*

Substances

  • Nanotubes, Carbon
  • Caspase 8
  • Glutathione