Preparation, characterization and anti-cancer activity of graphene oxide-‑silver nanocomposite

J Photochem Photobiol B. 2020 Sep:210:111984. doi: 10.1016/j.jphotobiol.2020.111984. Epub 2020 Jul 30.

Abstract

This work reported the preparation, characterization, cytotoxicity of green synthesized Lespedeza cuneate mediated silver nanoparticles (Lc-AgNPs) and graphene oxide‑silver nanocomposite (GO-AgNComp) using Lc-AgNPs. The UV absorption spectrum at 419 nm indicated the successful formation of GO-AgNComp. The TEM analysis displayed the thin sheet of graphene decorated Lc-AgNPs in GO-AgNComp. Zeta potential was -13.2 mV for Lc-AgNPs and -30.5 mV for GO-AgNComp. The photothermal conversion efficiency was calculated as 31.09% for GO-AgNComp. The negatively charged zeta potential of GO-AgNComp enhanced its cellular penetration through enhanced permeability and retention (EPR) effect. The near-infrared laser (NIR) induced the anticancer activity of Lc-AgNPs and GO-AgNComp in human lung cancer cells (A549) and brain tumour (LN229). The results indicated that about 50% of A549 cells and LN229 cells were ablated by treatment of 24.73 ± 2.98 μg/mL and 27.34 ± 1.62 μg/mL of Lc-AgNPs, as well by 15.46 ± 2.31 μg/mL and 20.95 ± 1.35 μg/mL of GO-AgNComp respectively. Moreover, GO-AgNComp was not cytotoxic to normal mouse fibroblast cells (NIH3T3), but it caused the cancer cell death in A549 and LN229 through ROS generation, nuclear damage, and mitochondrial membrane potential (∆ψm) loss. This work reported the anticancer potential of GO-AgNComp, which deserves further study on the molecular elucidation of GO-AgNComp mediated human lung and tumour therapy.

Keywords: Graphene oxide; Lespedeza cuneata; Nanocomposite; Photothermolysis.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Graphite / chemistry*
  • Green Chemistry Technology
  • Humans
  • Lespedeza / chemistry
  • Lespedeza / metabolism
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • NIH 3T3 Cells
  • Nanocomposites / chemistry*
  • Nanocomposites / therapeutic use
  • Nanocomposites / toxicity
  • Particle Size
  • Plant Extracts / chemistry
  • Reactive Oxygen Species / metabolism
  • Silver / chemistry*

Substances

  • Antineoplastic Agents
  • Plant Extracts
  • Reactive Oxygen Species
  • graphene oxide
  • Silver
  • Graphite