Carbohydrate plasma expanders for passive tumor targeting: in vitro and in vivo studies

Carbohydr Polym. 2013 Jun 5;95(1):404-13. doi: 10.1016/j.carbpol.2013.03.033. Epub 2013 Mar 15.

Abstract

The objective of this study was to investigate the suitability of carbohydrate plasma volume expanders as a novel polymer platform for tumor targeting. Many synthetic polymers have already been synthesized for targeted tumor therapy, but potential advantages of these carbohydrates include inexpensive synthesis, constant availability, a good safety profile, biodegradability and the long clinical use as plasma expanders. Three polymers have been tested for cytotoxicity and cytokine activation in cell cultures and conjugated with a near-infrared fluorescent dye: hydroxyethyl starches (HES 200 kDa and HES 450 kDa) and dextran (DEX 500 kDa). Particle size and molecular weight distribution were determined by asymmetric flow field-flow fractionation (AF4). The biodistribution was investigated non-invasively in nude mice using multispectral optical imaging. The most promising polymer conjugate was characterized in human colon carcinoma xenograft bearing nude mice. A tumor specific accumulation of HES 450 was observed, which proves it's potential as carrier for passive tumor targeting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Cells, Cultured
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Cytokines / metabolism
  • Dextrans / administration & dosage*
  • Dextrans / chemistry
  • Dextrans / pharmacokinetics
  • Female
  • Hep G2 Cells
  • Humans
  • Hydroxyethyl Starch Derivatives / administration & dosage*
  • Hydroxyethyl Starch Derivatives / chemistry
  • Hydroxyethyl Starch Derivatives / pharmacokinetics
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Mice
  • Mice, Nude
  • Plasma Substitutes / administration & dosage*
  • Plasma Substitutes / chemistry
  • Plasma Substitutes / pharmacokinetics
  • Tissue Distribution
  • Tumor Burden / drug effects
  • Xenograft Model Antitumor Assays

Substances

  • Cytokines
  • Dextrans
  • Hydroxyethyl Starch Derivatives
  • Plasma Substitutes