Synergistic anticancer effects achieved by co-delivery of TRAIL and paclitaxel using cationic polymeric micelles

Macromol Biosci. 2011 Feb 11;11(2):296-307. doi: 10.1002/mabi.201000332. Epub 2010 Dec 8.

Abstract

Cationic micellar nanoparticles self-assembled from a biodegradable amphiphilic copolymer have been used to deliver human TRAIL and paclitaxel simultaneously. Polyplexes formed between paclitaxel-loaded nanoparticles and TRAIL are stable with a size of ≈180 nm and a zeta potential at ≈75 mV. Anticancer effects and apoptotic pathway mechanisms of this drug-and-protein co-delivery system are investigated in various human breast cancer cell lines with different TRAIL sensitivity. The co-delivery nanoparticulate system induces synergistic anti-cancer activities with limited toxicity in non-cancerous cells. An advantage of this co-delivery is a significantly higher anti-cancer effect as compared to free drug and protein formulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Caspases / metabolism
  • Cations
  • Cell Cycle / drug effects
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Drug Synergism
  • Electrophoretic Mobility Shift Assay
  • Humans
  • Micelles*
  • Nanoparticles / chemistry
  • Paclitaxel / chemistry
  • Paclitaxel / pharmacology*
  • Particle Size
  • Polymers / chemistry
  • Polymers / pharmacology*
  • Static Electricity
  • TNF-Related Apoptosis-Inducing Ligand / pharmacology*
  • Time Factors
  • Tumor Stem Cell Assay

Substances

  • Antineoplastic Agents
  • Cations
  • Micelles
  • Polymers
  • TNF-Related Apoptosis-Inducing Ligand
  • Caspases
  • Paclitaxel