In vitro cytotoxicity of a library of BODIPY-anthracene and -pyrene dyads for application in photodynamic therapy

Photochem Photobiol Sci. 2019 Feb 13;18(2):495-504. doi: 10.1039/c8pp00402a.

Abstract

The facile synthesis and in vitro activity of a library of heavy atom-free BODIPY-anthracene, -pyrene dyads (BAD-13-BPyrD-19) and a control (BODIPY 20) are reported. We demonstrate that singlet oxygen produced from dyad triplet states formed from charge-separated states is sufficient to induce cytotoxicity in human breast cancer cells (MDA-MB-468) at micromolar concentrations. The compounds in this series are promising candidates for photodynamic therapy, especially BAD-17 which displays significant photocytotoxicity (15% cell viability) at a concentration of 5 × 10-7 M, with minimal toxicity (89% cell viability) in the absence of light.

MeSH terms

  • Anthracenes / chemistry*
  • Boron Compounds / chemistry*
  • Boron Compounds / pharmacology*
  • Cell Line
  • Cell Survival / drug effects
  • Cell Survival / radiation effects
  • Photochemotherapy / methods*
  • Photosensitizing Agents / chemistry*
  • Photosensitizing Agents / pharmacology*
  • Pyrenes / chemistry*
  • Singlet Oxygen / metabolism

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Anthracenes
  • Boron Compounds
  • Photosensitizing Agents
  • Pyrenes
  • Singlet Oxygen
  • pyrene
  • anthracene