Magnetic functionalised carbon nanotubes as drug vehicles for cancer lymph node metastasis treatment

Eur J Cancer. 2011 Aug;47(12):1873-82. doi: 10.1016/j.ejca.2011.03.018. Epub 2011 Apr 13.

Abstract

Strategies using carbon-based nanomaterials as carriers for delivering chemotherapeutic drugs to cancers have been described well. Here a novel magnetic lymphatic-targeting drug-delivery system, based on functionalised carbon nanotubes (fCNTs), is presented with the aim of improving the outcome of cancer with lymph node involvement. The potential therapeutic effect of gemcitabine (GEM) loading magnetic multiwalled carbon nanotubes (mMWNTs) was compared with that of GEM loading magnetic-activated carbon particles (mACs) in vitro and in vivo. mMWNTs-GEM and mACs-GEM both had high anti-tumour activity in vitro similar to free drug. Subcutaneous administration of GEM loading magnetic nanoparticles resulted in successful regression and inhibition of lymph node metastasis under the magnetic field, with mMWNTs-GEM superior to mACs-GEM, and more effectively in the high-dose versus low-dose groups. The successful application of intra-lymphatic delivery of chemotherapeutics using mMWNTs highlights the clinical potential of fCNTs for future cancer metastasis treatment with high efficacy and minimum side-effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimetabolites, Antineoplastic / administration & dosage
  • Antimetabolites, Antineoplastic / pharmacology
  • Apoptosis
  • Biomarkers, Tumor / analysis*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Disease Models, Animal
  • Drug Carriers
  • Gemcitabine
  • Humans
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Lymph Nodes / pathology*
  • Lymphatic Metastasis
  • Magnetite Nanoparticles*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Microscopy, Electron, Transmission
  • Nanotubes, Carbon*
  • Necrosis
  • Pancreatic Neoplasms / chemistry
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / pathology*

Substances

  • Antimetabolites, Antineoplastic
  • Biomarkers, Tumor
  • Drug Carriers
  • Magnetite Nanoparticles
  • Nanotubes, Carbon
  • Deoxycytidine
  • Gemcitabine