RGD peptide-conjugated multimodal NaGdF4:Yb3+/Er3+ nanophosphors for upconversion luminescence, MR, and PET imaging of tumor angiogenesis

J Nucl Med. 2013 Jan;54(1):96-103. doi: 10.2967/jnumed.112.108043. Epub 2012 Dec 11.

Abstract

Multimodal nanoparticles have been extensively studied for target-specific imaging and therapy of various diseases, including cancer. In this study, radiolabeled arginine-glycine-aspartic acid (RGD)-functionalized Er(3+)/Yb(3+) co-doped NaGdF(4) upconversion nanophosphors (UCNPs) were synthesized and evaluated as a multimodal PET/MR/optical probe with tumor angiogenesis-specific targeting properties.

Methods: A dimeric cyclic RGDyk ((cRGDyk)(2)) peptide was conjugated to polyacrylic acid-coated NaGdF(4):Yb(3+)/Er(3+) UCNPs along with polyethylene glycol molecules and was consecutively radiolabeled with (124)I. In vitro cytotoxicity testing was performed for 3 d. Upconversion luminescence imaging of (cRGDyk)(2)-UCNP was performed on U87MG cells with a laboratory-made confocal microscope. In vivo small-animal PET and clinical 3-T T1-weighted MR imaging of (124)I-labeled RGD-functionalized UCNPs was acquired with or without blocking of cyclic RGD peptide in a U87MG tumor model. Inductively coupled plasma mass spectrometry and biologic transmission electron microscopy were done to evaluate gadolinium concentration and UCNP localization, respectively.

Results: Polymer-coated UCNPs and dimeric RGD-conjugated UCNPs were monodispersely synthesized, and those of hydrodynamic size were 30 ± 8 nm and 32 ± 9 nm, respectively. (cRGDyk)(2)-UCNPs have a low cytotoxic effect on cells. Upconversion luminescence signals of (cRGDyk)(2)-UCNP were specifically localized on the surface of U87MG cells. (124)I-c(RGDyk)(2)-UCNPs specifically accumulated in U87MG tumors (2.8 ± 0.8 vs. 1.3 ± 0.4 percentage injected dose per gram in the blocking experiment), and T1-weighted MR images showed significant positive contrast enhancement in U87MG tumors. Tumor localization of (124)I-c(RGDyk)(2)-UCNPs was confirmed by inductively coupled plasma mass spectrometry and biologic transmission electron microscopy analysis.

Conclusion: These results suggest that (124)I-labeled RGD-functionalized UCNPs have high specificity for α(v)β(3) integrin-expressing U87MG tumor cells and xenografted tumor models. Multimodal UCNPs can be used as a platform nanoparticle with multimodal imaging for cancer-specific diagnoses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Dimerization
  • Erbium / chemistry*
  • Feasibility Studies
  • Fluorides / chemistry*
  • Gadolinium / chemistry*
  • Glioblastoma / blood supply*
  • Glioblastoma / diagnosis
  • Glioblastoma / diagnostic imaging
  • Glioblastoma / pathology
  • Humans
  • Integrin alphaVbeta3 / metabolism
  • Iodine Radioisotopes
  • Luminescent Agents / chemistry
  • Luminescent Measurements
  • Magnetic Resonance Imaging
  • Mice
  • Molecular Imaging / methods*
  • Nanostructures* / toxicity
  • Neovascularization, Pathologic
  • Oligopeptides / chemistry*
  • Oligopeptides / toxicity
  • Polyethylene Glycols / chemistry
  • Positron-Emission Tomography
  • Ytterbium / chemistry*

Substances

  • Integrin alphaVbeta3
  • Iodine Radioisotopes
  • Luminescent Agents
  • Oligopeptides
  • Polyethylene Glycols
  • Erbium
  • arginyl-glycyl-aspartic acid
  • Gadolinium
  • Ytterbium
  • Fluorides