Study on the drug release property of cholesteryl end-functionalized poly(epsilon-caprolactone) microspheres

J Biomed Mater Res B Appl Biomater. 2006 Apr;77(1):39-46. doi: 10.1002/jbm.b.30395.

Abstract

End-functionalized poly/oligo(epsilon-caprolactone)s were synthesized through the ring-opening polymerization of epsilon-caprolactone initiated by cholesterol with a hydroxyl group. Using the end-functionalized poly/oligo(epsilon-caprolactone)s with different molecular weights, the microsphere drug delivery systems were fabricated using a convenient melting-emulsion method. The drug release properties of microspheres were investigated with the presence of an enzyme, Pseudomonas cepacia lipase, as well as in the absence of the enzyme. The release profiles can be fitted nicely by the classical empirical exponential expression. Under the hydrolytic condition, the drug release is mainly controlled by Fickian diffusion, and the high molecular weight of the matrix results in a slower drug release rate. Under the enzymatic condition, the drug release is dominated by combined degradation and diffusion mechanism, and the high molecular weight sample exhibits a faster release rate that is mainly caused by the higher degradation rate of the sample with lower cholesteryl moiety content.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocompatible Materials / chemistry*
  • Burkholderia cepacia / enzymology
  • Cholesterol* / chemistry
  • Cholesterol* / metabolism
  • Delayed-Action Preparations
  • Drug Carriers* / chemistry
  • Drug Carriers* / metabolism
  • Drug Delivery Systems
  • Lipase / metabolism
  • Materials Testing
  • Microspheres*
  • Molecular Structure
  • Molecular Weight
  • Polyesters* / chemistry
  • Polyesters* / metabolism

Substances

  • Biocompatible Materials
  • Delayed-Action Preparations
  • Drug Carriers
  • Polyesters
  • polycaprolactone
  • Cholesterol
  • Lipase