DMAP-BODIPY alkynes: a convenient tool for labeling biomolecules for bimodal PET-optical imaging

Chemistry. 2014 Sep 26;20(40):12933-44. doi: 10.1002/chem.201402379. Epub 2014 Aug 21.

Abstract

Several new boron dipyrromethene/N,N-dimethylaminopyridine (BODIPY-DMAP) assemblies were synthesized as precursors for bimodal imaging probes (optical imaging, OI/positron emission tomography, PET). The photophysical properties of the new compounds were also studied. The first proof-of-concept was obtained with the preparation of several new BODIPY-labeled bombesins and evaluation of the affinity for bombesin receptors by using a competition binding assay. Fluorination reactions were investigated on DMAP-BODIPY precursors as well as on DMAP-BODIPY-labeled bombesins. Chemical modifications on the BODIPY core were also performed to obtain luminescent dyes emitting in the therapeutic window (650-900 nm), suitable for in vivo imaging, making these compounds promising precursors for PET/optical dual-modality imaging agents.

Keywords: alkynes; click chemistry; fluorine; imaging agents; luminescence; radiochemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemical synthesis
  • Alkynes / chemistry*
  • Bombesin / analysis
  • Bombesin / metabolism
  • Boron Compounds / chemical synthesis
  • Boron Compounds / chemistry*
  • Click Chemistry
  • Halogenation
  • Luminescent Agents / chemical synthesis
  • Luminescent Agents / chemistry*
  • Optical Imaging / methods
  • Positron-Emission Tomography / methods
  • Pyridines / chemical synthesis
  • Pyridines / chemistry*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • 4-(dimethylamine)pyridine
  • Alkynes
  • Boron Compounds
  • Luminescent Agents
  • Pyridines
  • Bombesin