Antioxidative and cytoprotective response elicited by molybdenum nanoparticles in human cells

J Colloid Interface Sci. 2015 Nov 1:457:370-7. doi: 10.1016/j.jcis.2015.07.034. Epub 2015 Jul 15.

Abstract

Nanotechnology based therapeutics can offer an alternative platform in a wide variety of biomedical applications. Here we report novel cytotoxicity preventive potential of molybdenum nanoparticles (Mo NPs) in human breast (MCF-7) and fibrosarcoma (HT-1080) cells compromised with oxidant exposure. Physicochemical properties such as size, crystallinity, purity and band gap (an optical characteristic) of Mo NPs were characterized respectively by field emission transmission electron microscopy (FETEM), X-ray diffraction (XRD), energy dispersive spectrum (EDS) and UV-vis absorption spectroscopy. The average size of crystalline Mo NPs was found to be 35 nm with a band gap of 1.4 eV. Potential cytotoxicity of Mo NPs was evaluated by a battery of cell viability and oxidative stress parameters. Cell viability and oxidative stress data suggested Mo NPs to be reasonably non-cytotoxic. Cytotoxic preventive and GSH restoring potential of Mo NPs was determined against cytotoxicity and oxidative stress induced by H2O2 (and ZnO NPs) in two cells. Mo NPs significantly increased GSH level in MCF-7 and HT-1080 cells, an activity that was comparable to antioxidant N-acetyl cysteine (NAC). GSH level was increased 1.56 times in MCF-7 cells and 1.25 times in HT-1080 cells by 100 μg/ml of Mo NPs relative to control cells in 24 h. End-point data clearly suggest that Mo NPs significantly protected cells against cytotoxicity induced by H2O2 and ZnO (NPs) (p<0.05). Our study warrants further investigation about Mo NPs that could be exploited in myriads of nanotechnology applications.

Keywords: Antioxidants NPs; Glutathione; Molybdenum NPs; Nanomedicine; Oxidants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / chemistry
  • Antioxidants / pharmacology*
  • Cell Survival / drug effects
  • Cytoprotection / drug effects*
  • Dose-Response Relationship, Drug
  • Humans
  • Hydrogen Peroxide / chemistry
  • Hydrogen Peroxide / pharmacology
  • MCF-7 Cells
  • Molybdenum / chemistry
  • Molybdenum / pharmacology*
  • Nanoparticles / chemistry*
  • Oxidants / chemistry
  • Oxidants / pharmacology
  • Oxidation-Reduction
  • Oxidative Stress / drug effects
  • Particle Size
  • Structure-Activity Relationship
  • Surface Properties
  • Tumor Cells, Cultured

Substances

  • Antioxidants
  • Oxidants
  • Molybdenum
  • Hydrogen Peroxide