Synthesis and characterization of Poloxamer 188-grafted heparin copolymer

Drug Dev Ind Pharm. 2010 Jul;36(7):832-8. doi: 10.3109/03639040903520983.

Abstract

Background: Poloxamer 188 is a safe biocompatible polymer that can be used in protein drug delivery system.

Aim: In this study, a new heparin-poloxamer 188 conjugate (HP) was synthesized and its physicochemical properties were investigated. HP structure was confirmed by Fourier transform infrared spectroscopy (FTIR) and Hydrogen-1 nuclear magnetic resonance spectroscopy ((1)H-NMR). Content of the conjugated heparin was analyzed using Toluidine Blue. The critical micelle concentration (CMC) of the copolymer was determined by a fluorescence probe technique. The effect of HP on the gelation of poloxamer 188 was characterized by the rheological properties of the HP-poloxamer hydrogels. Solubility and viscosity of HP were also evaluated compared with poloxamer 188.

Results: From the results, the solubility of the conjugated heparin was increased compared with free heparin. The content of heparin in HP copolymer was 62.9%. The CMC of HP and poloxamer 188 were 0.483 and 0.743 mg/mL, respectively. The gelation temperature of 0.4 g/mL HP was 43.5 degrees C, whereas that of the same concentration of poloxamer 188 was 37.3 degrees C. With HP content in poloxamer 188 solution increasing, a V-shape change of gelation temperature was observed.

Conclusion: Considering the importance of poloxamer 188 in functional material, HP may prove to be a facile temperature-sensitive material for protein drug-targeted therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Carriers
  • Drug Compounding
  • Drug Delivery Systems
  • Heparin / chemistry*
  • Micelles
  • Poloxamer / chemistry*
  • Solubility
  • Technology, Pharmaceutical
  • Viscosity

Substances

  • Drug Carriers
  • Micelles
  • Poloxamer
  • Heparin