Interactions of the beta-blocker drug, propranolol, with detergents, beta-cyclodextrin and living cells studied using fluorescence spectroscopy and imaging

R. H. Bisby, S. W. Botchway, A. G. Crisostomo, J. Karolin, A. W. Parker, L. Schroeder

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Interactions of the beta-blocker drug, propranolol, with amphipathic systems have been studied using fluorescence spectroscopy. The results show a strong binding of propranolol with micelles of sodium dodecyl sulfate revealed through changes in the fluorescence spectrum and an increase in fluorescence lifetime. Quenching of propranolol fluorescence by iodide is used to demonstrate interaction with beta-cyclodextrin. At high concentrations, self-quenching of propranolol fluorescence was also observed with kappa(q), = 2.5 x 10(9) dm(3) mol(-1) s(-1). Two-photon excited (630 nm) fluorescence lifetime imaging of propranolol in cells showed propranolol to be widely distributed in the cell cytoplasm, with fluorescence lifetimes shorter than in solution. The results suggest that intracellular propranolol is mainly confined within the aqueous cytoplasm and rather than membrane associated.

Original languageEnglish
Pages (from-to)137-142
Number of pages6
JournalSpectroscopy
Volume24
Issue number1-2
DOIs
Publication statusPublished - 2010

Keywords

  • propranolol
  • fluorescence
  • lifetime
  • quenching
  • micelle
  • cyclodextrin
  • imaging
  • live cell
  • binding
  • water

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