In vitro characterization of a targeted, dye-loaded nanodevice for intraoperative tumor delineation

Neurosurgery. 2009 May;64(5):965-71; discussion 971-2. doi: 10.1227/01.NEU.0000344150.81021.AA.

Abstract

Objective: To synthesize and complete in vitro characterization of a novel, tumor-targeted nanodevice for visible intraoperative delineation of brain tumors.

Methods: The ability of dye-loaded polyacrylamide nanoparticles (NP) containing methylene blue, Coomassie blue, or indocyanine green to cause color change in the 9L glioma cell lines was evaluated. Cells were incubated with dye-loaded NPs, photographed, and analyzed colorimetrically. Confocal microscopy was used to determine subcellular localization of NPs in treated cells.

Results: Incubation of glioma cell lines with dye-loaded NPs resulted in clearly visible, quantifiable cell tagging in a dose- and time-dependent manner. Dye-loaded NPs were observed to bind to the surface and become internalized by glioma cells. Coating the NP surface with F3, a peptide that binds to the tumor cell surface receptor nucleolin, significantly increased NP affinity for glioma cells. F3 targeting also significantly increased the rate of cell tagging by dye-loaded NPs. Finally, F3-targeted NPs demonstrated specificity for targeting various cancer cell lines based on their surface expression of cell surface nucleolin.

Conclusion: F3-targeted dye-loaded NPs efficiently cause definitive color change in glioma cells. This report represents the first use of targeted NPs to cause a visible color change in tumor cell lines. Similar nanodevices may be used in the future to enable visible intraoperative tumor delineation during tumor resection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylic Resins / administration & dosage*
  • Acrylic Resins / metabolism
  • Cell Line, Tumor
  • Colorimetry / methods
  • Dose-Response Relationship, Drug
  • Epitopes
  • Fluorescent Dyes
  • Glioma / metabolism*
  • Glioma / pathology
  • Glioma / ultrastructure
  • Humans
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning / methods
  • Nanoparticles / administration & dosage*
  • Nucleolin
  • Phosphoproteins / metabolism
  • RNA-Binding Proteins / metabolism
  • Subcellular Fractions / metabolism
  • Time Factors

Substances

  • Acrylic Resins
  • Epitopes
  • F3 epitope
  • Fluorescent Dyes
  • Phosphoproteins
  • RNA-Binding Proteins
  • polyacrylamide