Multifunctional doxorubicin loaded superparamagnetic iron oxide nanoparticles for chemotherapy and magnetic resonance imaging in liver cancer

Biomaterials. 2010 Jun;31(18):4995-5006. doi: 10.1016/j.biomaterials.2010.02.068. Epub 2010 Mar 26.

Abstract

To develop a drug delivery system with enhanced efficacy and minimized adverse effects, we synthesized a novel polymeric nanoparticles, (YCC-DOX) composed of poly (ethylene oxide)-trimellitic anhydride chloride-folate (PEO-TMA-FA), doxorubicin (DOX) and superparamagnetic iron oxide (Fe(3)O(4)) and folate. The efficacy of the nanoparticles was evaluated in rats and rabbits with liver cancer, in comparison with free-DOX (FD) and a commercial liposome drug, DOXIL. YCC-DOX showed the anticancer efficacy and specifically targeted folate receptor (FR)-expressing tumors, thereby increasing the bioavailability and efficacy of DOX. The relative tumor volume of the YCC-DOX group was decreased two- and four-fold compared with the FD and DOXIL groups in the rat and rabbit models, respectively. Furthermore, YCC-DOX showed higher MRI sensitivity comparable to a conventional MRI contrast agent (Resovist), even in its lower iron content. In the immunohistochemical analysis, YCC-DOX group showed the lower expression of CD34 and Ki-67, markers of angiogenesis and cell proliferation, respectively, while apoptotic cells were significantly rich in the YCC-DOX group in terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. These results indicate that YCC-DOX is a promising candidate for treating liver cancer and monitoring the progress of the cancer using MRI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / administration & dosage*
  • Antibiotics, Antineoplastic / therapeutic use
  • Apoptosis / drug effects
  • Carrier Proteins / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Doxorubicin / administration & dosage*
  • Doxorubicin / therapeutic use
  • Ferric Compounds* / chemistry
  • Folate Receptors, GPI-Anchored
  • Humans
  • Liver Neoplasms / diagnosis*
  • Liver Neoplasms / drug therapy*
  • Magnetic Resonance Imaging / methods*
  • Magnetics
  • Male
  • Nanoparticles* / chemistry
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cell Surface / metabolism

Substances

  • Antibiotics, Antineoplastic
  • Carrier Proteins
  • Ferric Compounds
  • Folate Receptors, GPI-Anchored
  • Receptors, Cell Surface
  • ferric oxide
  • Doxorubicin