A novel micellar PEGylated hyperbranched polyester as a prospective drug delivery system for paclitaxel

Macromol Biosci. 2008 Sep 9;8(9):871-81. doi: 10.1002/mabi.200800015.

Abstract

A hyperbranched aliphatic polyester has been functionalized with PEG chains to afford a novel water-soluble BH40-PEG polymer which exhibits unimolecular micellar properties, and is therefore appropriate for application as a drug-delivery system. The solubility of the anticancer drug paclitaxel was enhanced by a factor of 35, 110, 230, and 355 in aqueous solutions of BH40-PEG of 10, 30, 60, and 90 mg x mL(-1), respectively. More than 50% of the drug is released at a steady rate and release is almost complete within 10 h. The toxicity of BH40-PEG was assessed in vitro with A549 human lung carcinoma cells and found to be nontoxic for 3 h incubation up to a 1.75 mg x mL(-1) concentration while LD50 was 3.5 mg x mL(-1). Finally, it was efficiently internalized in cells, primarily in the absence of foetal bovine serum, while confocal microscopy revealed the preferential localization of the compound in cell nuclei. [Figure: see text].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Membrane Permeability
  • Cell Nucleus / metabolism
  • Drug Delivery Systems
  • Humans
  • Micelles
  • Paclitaxel / administration & dosage*
  • Polyesters / chemistry*
  • Polyesters / pharmacokinetics
  • Polyesters / toxicity
  • Polyethylene Glycols
  • Solubility

Substances

  • Micelles
  • Polyesters
  • Polyethylene Glycols
  • Paclitaxel