Topotecan-loaded mesoporous silica nanoparticles for reversing multi-drug resistance by synergetic chemoradiotherapy

Chem Asian J. 2015 Feb;10(2):344-8. doi: 10.1002/asia.201403117. Epub 2014 Nov 20.

Abstract

Multi-drug resistance (MDR) has become a major challenge for the further improvement of chemotherapy. Thus, more effective strategies for further enhancing the treatment against cancer by overcoming MDR are warranted. In this study, by the encapsulation of the radiosensitizing drug TPT into mesoporous silica nanoparticles (MSNs), the combined use of drug-delivered chemotherapy and high-energy X-ray induced radiotherapy could produce synergetic chemoradiotherapeutic effects to kill multi-drug resistant cells through significant DNA damage, thus leading to an efficient circumvention of MDR. We hope that this synergetic dual-mode treatment strategy may achieve higher oncolytic efficacy and find use in future clinical anti-MDR applications.

Keywords: DNA damage; cancer; chemoradiotherapy; mesoporous materials; multi-drug resistance; radiosensitization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / drug effects
  • Cell Survival / radiation effects
  • DNA Damage / drug effects
  • DNA Damage / radiation effects
  • Drug Carriers / chemistry
  • Drug Resistance, Neoplasm / drug effects
  • Drug Resistance, Neoplasm / radiation effects
  • Humans
  • MCF-7 Cells
  • Nanoparticles / chemistry*
  • Neoplasms / drug therapy
  • Neoplasms / radiotherapy
  • Polyethylene Glycols / chemistry
  • Porosity
  • Radiation, Ionizing
  • Silicon Dioxide / chemistry*
  • Topoisomerase I Inhibitors / administration & dosage
  • Topoisomerase I Inhibitors / chemistry*
  • Topoisomerase I Inhibitors / toxicity
  • Topotecan / administration & dosage
  • Topotecan / chemistry*
  • Topotecan / toxicity

Substances

  • Drug Carriers
  • Topoisomerase I Inhibitors
  • Polyethylene Glycols
  • Silicon Dioxide
  • Topotecan