Ionic complexes of biosynthetic poly(malic acid) and poly(glutamic acid) as prospective drug-delivery systems

Macromol Biosci. 2007 Jul 9;7(7):897-906. doi: 10.1002/mabi.200700025.

Abstract

The hydrolytic degradability and erythromycin release from stoichiometric ionic complexes of biotechnological poly(beta,L-malic acid)s and poly(gamma,D-glutamic acid)s with alkyltrimethylammonium surfactants were investigated. The influence of pH, temperature and antibiotic load on hydrolysis rate was examined. It was found that poly(malic acid) complexes degraded by a surface erosion mechanism at a higher rate than poly(glutamic acid) complexes, which eroded in bulk. Erythromycin was lodged in the paraffinic subphase of the complexes and upon aging it was delivered according to a sigmoidal profile that appeared to be independent on the antibiotic load.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Carriers / chemistry
  • Drug Carriers / pharmacokinetics*
  • Erythromycin / administration & dosage
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • Ions
  • Kinetics
  • Malates*
  • Materials Testing
  • Polyglutamic Acid*
  • Polymers*
  • Temperature

Substances

  • Drug Carriers
  • Ions
  • Malates
  • Polymers
  • poly(malic acid)
  • Polyglutamic Acid
  • Erythromycin