Chemical speciation of copper(II) diaminediamide derivative of pentacycloundecane--a potential anti-inflammatory agent

Dalton Trans. 2007 Mar 21:(11):1140-9. doi: 10.1039/b614878f. Epub 2007 Feb 8.

Abstract

Formation constants of copper(ii), zinc(ii) and calcium(ii) with 3,5-diaminodiamido-4-oxahexacyclododecane (cageL) has been studied by glass electrode potentiometry at 25 degrees C and an ionic strength of 0.15 mol dm(-3). Copper(ii) forms more stable complexes with cageL than zinc(ii) and calcium(ii). Metal ion complexation promotes deprotonation and coordination of the amide nitrogens resulting in overall tetragonal coordination of Cu(2+) suggested by the UV-visible electronic spectra. Speciation calculations using a blood plasma model suggest that zinc(ii) and calcium(ii) are good competitors of copper(ii) in vivo. Bio-distribution experiments using (64)Cu-labelled Cu(ii)-cageL show that about 50% dose of the complex is retained in the body after 24 h.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry*
  • Anti-Inflammatory Agents / pharmacokinetics
  • Bridged-Ring Compounds / chemistry*
  • Bridged-Ring Compounds / pharmacokinetics
  • Copper / chemistry*
  • Copper / pharmacokinetics
  • Diamide / chemistry*
  • Diamines / chemistry*
  • Mice
  • Mice, Inbred BALB C
  • Potentiometry
  • Superoxide Dismutase / metabolism
  • Tissue Distribution
  • Zinc / chemistry*
  • Zinc / pharmacokinetics

Substances

  • Anti-Inflammatory Agents
  • Bridged-Ring Compounds
  • Diamines
  • Diamide
  • Copper
  • Superoxide Dismutase
  • Zinc