Accelerated blood clearance was not induced for a gadolinium-containing PEG-poly(L-lysine)-based polymeric micelle in mice

Pharm Res. 2010 Feb;27(2):296-302. doi: 10.1007/s11095-009-0018-9. Epub 2009 Dec 25.

Abstract

Purpose: Accelerated blood clearance (ABC) is induced by repeated injections of PEGylated liposomes. In this study, the ABC was investigated for a gadolinium-containing PEG-poly(L-lysine)-based polymeric micelle (Gd-micelle) and PEGylated liposome (Gd-liposome) in mice.

Materials and methods: Effects of the first injection of Gd-micelle on the tissue distribution of the second dose of Gd-micelle were studied. Additionally, effects of the first injection of Gd-micelle, Gd-liposome, empty liposome, polyethyleneglycol (PEG(500,000)), and PEG-lipid on the distribution of the second dose of the Gd-liposome were evaluated.

Results: Results indicated that the tissue distribution of the second injection of the Gd-micelle at a dose of 33, 5, or 2 micromol Gd/kg was not affected by the first injection of the Gd-micelle at different doses and time intervals or of the empty PEGylated liposome 7 days before. ABC of Gd-liposome at a dose of 2.3 micromol Gd/kg (corresponding to 10 micromol lipids/kg) was observed when the empty PEGylated liposome or Gd-liposome, but not the Gd-micelle, PEG(500,000) or PEG-lipid, was pre-administered.

Conclusions: The hydrophobic core of the micelle or lipid bilayer of PEGylated liposome has a major effect on this phenomenon. These studies have significant implications for the evaluation of PEG-poly(L-lysine)-based micellar formulation of Gd-based contrast agents.

Publication types

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

MeSH terms

  • Animals
  • Drug Carriers / chemistry
  • Drug Carriers / pharmacokinetics
  • Female
  • Gadolinium / administration & dosage*
  • Gadolinium / blood
  • Gadolinium / chemistry
  • Metabolic Clearance Rate / drug effects
  • Metabolic Clearance Rate / physiology
  • Mice
  • Micelles*
  • Polyethylene Glycols / administration & dosage
  • Polyethylene Glycols / metabolism*
  • Polyethylene Glycols / pharmacokinetics
  • Polylysine / administration & dosage
  • Polylysine / analogs & derivatives*
  • Polylysine / blood*
  • Polylysine / pharmacokinetics
  • Polymers / administration & dosage
  • Polymers / chemistry
  • Polymers / pharmacokinetics
  • Time Factors
  • Tissue Distribution / drug effects
  • Tissue Distribution / physiology

Substances

  • Drug Carriers
  • Micelles
  • Polymers
  • polylysine-graft-(poly(ethylene glycol))
  • Polylysine
  • Polyethylene Glycols
  • Gadolinium