Layered Double Hydroxide as a Vehicle to Increase Toxicity of Gallate Ions against Adenocarcinoma Cells

Molecules. 2016 Jul 16;21(7):928. doi: 10.3390/molecules21070928.

Abstract

The antineoplasic activity of gallic acid has been reported. This compound induces apoptosis and inhibits the growth of several neoplasic cells. However, this molecule is easily oxidized and degraded in the body. The aim of this work was to intercalate gallate ions into layered double hydroxide (LDH) nanoparticles under controlled conditions to reduce oxidation of gallate and to evaluate its toxicity against the A549 adenocarcinoma cell line. An isopropanol medium under nitrogen atmosphere was adequate to intercalate gallate ions with a lesser oxidation degree as detected by electron spin resonance spectroscopy. Concentrations of the hybrid LDH-gallate nanoparticles between 0.39 and 25 µg/mL reduced the cell viability to 67%, while the value reached with the pure gallic acid and LDH was 90% and 78%, respectively, thus proving that the combination of gallate ions with the inorganic nanoparticles increases the toxicity potential within this dose range.

Keywords: gallic; nanocarrier; nanomedicine; nanoparticle.

MeSH terms

  • Adenocarcinoma
  • Antineoplastic Agents, Phytogenic / chemistry*
  • Antineoplastic Agents, Phytogenic / toxicity
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Drug Carriers / chemistry
  • Electron Spin Resonance Spectroscopy
  • Gallic Acid / chemistry*
  • Gallic Acid / toxicity*
  • Humans
  • Hydroxides / chemistry*
  • Ions / chemistry*
  • Nanoparticles / chemistry
  • Nanoparticles / ultrastructure
  • Spectroscopy, Fourier Transform Infrared
  • Thermogravimetry
  • X-Ray Diffraction

Substances

  • Antineoplastic Agents, Phytogenic
  • Drug Carriers
  • Hydroxides
  • Ions
  • Gallic Acid