Potentiometric, spectrophotometric and calorimetric study on iron(III) and copper(II) complexes with 1,2-dimethyl-3-hydroxy-4-pyridinone

J Inorg Biochem. 2008 Apr;102(4):684-92. doi: 10.1016/j.jinorgbio.2007.10.012. Epub 2007 Oct 30.

Abstract

The iron(III)-1,2-dimethyl-3-hydroxy-4-pyridinone (Deferiprone) system is carefully characterized by a combined potentiometric-spectrophotometric procedure at 25 and 37 degrees C at different ionic strengths, and by thermochemical and quantum-chemical studies. The main purpose of this work was to determine how the temperature dependence of both complex-formation and protonation constants can affect the pFe values on going from 25 degrees C (pFe is normally calculated using 25 degrees C stability constants) to the physiological temperature of 37 degrees C at which chelating agents are active in vivo. The copper(II)-Deferiprone system is also studied and the iron(III)-Deferiprone distribution diagrams in presence of variable copper(II) amounts are shown so as to explain possible side effects due to a competing metal ion during the chelating therapy of iron overload.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry / methods*
  • Copper / chemistry*
  • Deferiprone
  • Electrochemistry / methods*
  • Ferric Compounds / chemistry*
  • Pyridones / chemistry*
  • Spectrum Analysis / methods*

Substances

  • Ferric Compounds
  • Pyridones
  • Deferiprone
  • Copper