Surface plasmon resonance-induced photoactivation of gold nanoparticles as mitochondria-targeted therapeutic agents for pancreatic cancer

Expert Opin Ther Targets. 2013 Dec;17(12):1383-93. doi: 10.1517/14728222.2013.855200. Epub 2013 Nov 5.

Abstract

Background: Noble metal nanoparticles such as gold nanoparticles can strongly absorb light in the visible region by inducing coherent collective oscillation of conduction band electrons in strong resonance with visible frequencies of light. This phenomenon is frequently termed as surface plasmon resonance (SPR).

Objectives: The main objective was to study the effects of laser photoactivated gold nanoparticles (by means of SPR) on human pancreatic cancer cells.

Results: Gold nanoparticles obtained using standard wet chemical methods (with sodium borohydride as a reducing agent) underwent photoexcitation using 2w 808 nm laser and further administered to 1.4E7 pancreatic cancer cell lines. Flow cytometry, transmission electron microscopy, phase contrast microscopy, quantitative proteomics and confocal microscopy combined with immunochemical staining were used to examine the interaction between photo excited gold nanoparticles and pancreatic cancer cells.

Conclusion: The study shows that phonon-phonon interactions following laser photoexcitation of gold nanoparticles exhibit increased intracellular uptake, as well as mitochondrial swelling, closely followed by mitochondrial inner membrane permeabilization and depolarization. This unique data may represent a major step in mitochondria-targeted anticancer therapies using laser-activated gold nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / radiation effects
  • Antineoplastic Agents / therapeutic use*
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Gold / pharmacology
  • Gold / radiation effects
  • Gold / therapeutic use*
  • Humans
  • Lasers
  • Membrane Potential, Mitochondrial / drug effects
  • Metal Nanoparticles / radiation effects
  • Metal Nanoparticles / therapeutic use*
  • Metal Nanoparticles / ultrastructure
  • Microscopy, Electron, Transmission
  • Mitochondria / drug effects
  • Mitochondria / physiology
  • Mitochondria / ultrastructure
  • Oxidative Stress
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / physiopathology
  • Pancreatic Neoplasms / ultrastructure
  • Surface Plasmon Resonance*

Substances

  • Antineoplastic Agents
  • Gold