Near-IR absorbing BODIPY derivatives as glutathione-activated photosensitizers for selective photodynamic action

Chemistry. 2014 Dec 1;20(49):16088-92. doi: 10.1002/chem.201405450. Epub 2014 Oct 24.

Abstract

Enhanced spatiotemporal selectivity in photonic sensitization of dissolved molecular oxygen is an important target for improving the potential and the practical applications of photodynamic therapy. Considering the high intracellular glutathione concentrations within cancer cells, a series of BODIPY-based sensitizers that can generate cytotoxic singlet oxygen only after glutathione-mediated cleavage of the electron-sink module were designed and synthesized. Cell culture studies not only validate our design, but also suggest an additional role for the relatively hydrophobic quencher module in the internalization of the photosensitizer.

Keywords: BODIPY dyes; photochemistry; photodynamic action; photosensitizers; singlet oxygen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron Compounds / chemistry*
  • Boron Compounds / metabolism
  • Boron Compounds / pharmacology*
  • Cell Line, Tumor
  • Glutathione / metabolism*
  • Humans
  • Infrared Rays
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Photochemotherapy
  • Photosensitizing Agents / chemistry*
  • Photosensitizing Agents / metabolism
  • Photosensitizing Agents / pharmacology
  • Singlet Oxygen / metabolism

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Photosensitizing Agents
  • Singlet Oxygen
  • Glutathione