Reversion of multidrug resistance by co-encapsulation of doxorubicin and cyclosporin A in polyalkylcyanoacrylate nanoparticles

Biomaterials. 2000 Jan;21(1):1-7. doi: 10.1016/s0142-9612(99)00125-8.

Abstract

Individual and combined polyalkylcyanoacrylate nanoparticle formulation of cyclosporin A and doxorubicin were prepared and evaluated in an attempt to show improved growth inhibition efficacy in a resistant cell culture line. The drug loaded nanoparticles were prepared using the well established emulsion polymerization process without using any modification for the hydrophilic doxorubicin drug whereas the incorporation of cyclosporin A needed to wait a moment after the polymerization reaction started. This was necessary to avoid cyclosporin A precipitation and polymer aggregation. Cyclosporin A release from the nanoparticles was rapid probably because the drug was adsorbed onto the nanoparticles surface rather than embedded into the polymeric core. Doxorubicin displayed also a burst effect but with a slower second phase probably related with the nanoparticles bioerosion rate owing to its entrapment in the polymeric network. Finally, it was shown in resistant cell culture experiments that the association of both cyclosporin A and doxorubicin within a single nanoparticle formulation elicited the most effective growth rate inhibition as compared to other combinations of both drugs while using a lower amount of polymer compared to separated nanoparticle formulations. This result was probably due to the synergistic effect achieved by combining the chemo-sensitizing compound cyclosporin A, with an effective cytotoxic drug like doxorubicin.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / chemistry
  • Capsules
  • Cell Division / drug effects
  • Cyanoacrylates / administration & dosage*
  • Cyanoacrylates / chemistry
  • Cyclosporine / administration & dosage*
  • Cyclosporine / chemistry
  • Cyclosporine / toxicity
  • Doxorubicin / administration & dosage*
  • Doxorubicin / chemistry
  • Doxorubicin / toxicity
  • Drug Resistance, Multiple*
  • Drug Resistance, Neoplasm
  • Growth Inhibitors / administration & dosage
  • Growth Inhibitors / chemistry
  • Growth Inhibitors / toxicity
  • Leukemia P388
  • Particle Size
  • Tumor Cells, Cultured

Substances

  • Capsules
  • Cyanoacrylates
  • Growth Inhibitors
  • Doxorubicin
  • Cyclosporine