Preparation and function of poly(acrylic acid)s modified by supramolecular complex composed of porphinatoiron and a cyclodextrin dimer that bind diatomic molecules (O2 and CO) in aqueous solution

Chem Asian J. 2011 Nov 4;6(11):2946-55. doi: 10.1002/asia.201100354. Epub 2011 Sep 9.

Abstract

Poly(acrylic acid) (PAA) is modified by 5-(4-β-alanylaminophenyl)-10,15,20-tris(4-sulfonatophenyl) porphinatoiron(III) to yield iron porphyrin-bearing PAAs (FeP(n)s) through a condensation reaction. FeP(n)s were further functionalized by Py3CD, which is a per-O-methylated β-cyclodextrin (CD) dimer with a pyridine linker and includes the porphyrin pendants to form ferric hemoCD-P(n)s. Ferrous hemoCD-P(3), having three porphyrin chromophores in a polymer chain, is shown to bind molecular oxygen (P(1/2)=7.9±1.4 Torr) in aqueous solution at pH 7.0 and 25 °C, affording oxy-hemoCD-P(3). Oxy-hemoCD-P(3) is biphasically autoxidized to ferric hemoCD-P(3), with 27% of the dioxygen adducts being rapidly oxidized. The rate of autoxidation of oxy-hemoCD-P(15), having 15 porphyrin chromophores in a polymer chain, was much faster than that of oxy-hemoCD-P(3), thus suggesting self-catalyzed autoxidation of oxy-hemoCD-P(n)s. Oxy-hemoCD-P(n)s are markedly stabilized by catalase, thereby indicating that hydrogen peroxide generated from oxy-hemoCD-P(n) accelerates the autoxidation. Most of the hemoCD-P(3) molecules injected into the femoral vein of a rat remained in the body, though about 16% of the hemoCD-P(3) molecules were excreted in the urine as a carbon monoxide adduct.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylates
  • Animals
  • Blood Substitutes / analysis
  • Blood Substitutes / chemical synthesis
  • Blood Substitutes / pharmacokinetics
  • Blood Substitutes / pharmacology
  • Carbon Monoxide / chemistry*
  • Carbon Monoxide / metabolism
  • Catalase / chemistry
  • Catalase / metabolism
  • Delayed-Action Preparations / analysis
  • Delayed-Action Preparations / chemical synthesis*
  • Delayed-Action Preparations / pharmacokinetics
  • Delayed-Action Preparations / pharmacology
  • Diatoms / chemistry*
  • Diatoms / metabolism
  • Hydrogen-Ion Concentration
  • Iron / chemistry
  • Iron / metabolism
  • Magnetic Resonance Imaging
  • Male
  • Metalloporphyrins / analysis
  • Metalloporphyrins / chemical synthesis*
  • Metalloporphyrins / chemistry
  • Metalloporphyrins / metabolism
  • Oxidation-Reduction
  • Oxygen / chemistry*
  • Oxygen / metabolism
  • Polymers / analysis
  • Polymers / chemistry
  • Pyridines / chemistry
  • Rats
  • Solutions / chemistry
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Superoxides / chemistry
  • Superoxides / metabolism
  • Water / chemistry
  • beta-Cyclodextrins / chemical synthesis*
  • beta-Cyclodextrins / chemistry

Substances

  • Acrylates
  • Blood Substitutes
  • Delayed-Action Preparations
  • Metalloporphyrins
  • Polymers
  • Pyridines
  • Solutions
  • beta-Cyclodextrins
  • Water
  • Superoxides
  • Carbon Monoxide
  • Iron
  • Catalase
  • Oxygen