PSMA-targeting iron oxide magnetic nanoparticles enhance MRI of preclinical prostate cancer

Nanomedicine (Lond). 2015 Feb;10(3):375-86. doi: 10.2217/nnm.14.122. Epub 2014 Nov 19.

Abstract

Aim: To evaluate the potential of newly-developed, biocompatible iron oxide magnetic nanoparticles (MNPs) conjugated with J591, an antibody to an extracellular epitope of PSMA, to enhance MRI of prostate cancer.

Materials & methods: Specific binding to PSMA by J591-MNP was investigated in vitro. MRI studies were performed on orthotopic tumor-bearing NOD.SCID mice 2 h and 24 h after intravenous injection of J591-MNPs, or non-targeting MNPs.

Results & conclusion: In vitro, MNPs did not affect prostate cancer cell viability, and conjugation to J591 did not compromise antibody specificity and enhanced cellular iron uptake. Magnetic resonance contrast of tumors was increased in vivo using PSMA-targeting MNPs, but not by non-targeting MNPs. This provides proof-of-concept that PSMA-targeting MNPs have potential to enhance magnetic resonance detection/localization of prostate cancer.

Keywords: MRI; cancer imaging; iron oxide magnetic nanoparticles (MNPs); prostate cancer; prostate specific membrane antigen (PSMA); targeted imaging; targeted nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Surface / analysis*
  • Cell Line, Tumor
  • Contrast Media*
  • Ferric Compounds*
  • Glutamate Carboxypeptidase II / analysis*
  • Humans
  • Magnetic Resonance Imaging
  • Magnetite Nanoparticles*
  • Male
  • Mice, Inbred NOD
  • Mice, SCID
  • Prostate / pathology
  • Prostatic Neoplasms / diagnosis*

Substances

  • Antigens, Surface
  • Contrast Media
  • Ferric Compounds
  • Magnetite Nanoparticles
  • ferric oxide
  • FOLH1 protein, human
  • Glutamate Carboxypeptidase II