Facile synthesis of multicompartment micelles based on biocompatible poly(3-hydroxyalkanoate)

Macromol Rapid Commun. 2013 Feb 25;34(4):362-8. doi: 10.1002/marc.201200692. Epub 2012 Dec 12.

Abstract

In this paper, a straightforward method to produce poly(3-hydroxyalkanoate)-based multicompartment micelles (MCMs) is presented. Thiol-ene addition is used to graft sequentially perfluorooctyl chains and poly(ethylene glycol) oligomers onto poly(3-hydroxyoctanoate-co-hydroxyundecenoate) oligomers backbone. Well-defined copolymers are obtained as shown by ¹H NMR and size-exclusion chromatography. After nanoprecipitation in water, novel PHA-based MCMs are evidenced by cryo-transmission electron microscopy. Moreover, the cytocompatibility of MCMs is demonstrated in vitro via cell viability assay.

MeSH terms

  • Alkenes / chemistry
  • Animals
  • Biocompatible Materials / chemical synthesis
  • Biocompatible Materials / chemistry*
  • Biocompatible Materials / toxicity
  • Cell Survival / drug effects
  • Light
  • Mice
  • Micelles*
  • NIH 3T3 Cells
  • Nanostructures / chemistry
  • Polyhydroxyalkanoates / chemistry*
  • Polyhydroxyalkanoates / toxicity
  • Scattering, Radiation
  • Sulfhydryl Compounds / chemistry

Substances

  • Alkenes
  • Biocompatible Materials
  • Micelles
  • Polyhydroxyalkanoates
  • Sulfhydryl Compounds