Thienopyrrole-expanded BODIPY as a potential NIR photosensitizer for photodynamic therapy

Chem Commun (Camb). 2013 May 11;49(38):3940-2. doi: 10.1039/c3cc40746b. Epub 2013 Mar 27.

Abstract

The synthesis and characterization of a highly photostable bromo-substituted BODIPY dye (I) fused-ring-expanded with thienopyrrole moieties is reported. The results of MTT assays and flow cytometric analyses in living HeLa cells demonstrate that I has a high singlet oxygen quantum yield (ΦΔ = 0.63) and exhibits photocytotoxicity upon irradiation in the NIR region making it potentially suitable for use in PDT.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron Compounds / chemistry
  • Boron Compounds / therapeutic use*
  • Cell Survival / drug effects
  • Cell Survival / radiation effects
  • HeLa Cells
  • Humans
  • Neoplasms / drug therapy*
  • Photochemotherapy* / methods
  • Photosensitizing Agents / chemistry
  • Photosensitizing Agents / therapeutic use*
  • Pyrroles / chemistry
  • Pyrroles / therapeutic use*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Photosensitizing Agents
  • Pyrroles
  • thienopyrrole