Kinetics of avidin-induced clearance of biotinylated bimodal liposomes for improved MR molecular imaging

Magn Reson Med. 2008 Dec;60(6):1444-56. doi: 10.1002/mrm.21780.

Abstract

Dual labeled liposomes, carrying both paramagnetic and fluorescent lipids, were recently proposed as potent contrast agents for MR molecular imaging. These nanoparticles are coated with poly(ethylene glycol) (PEG) to increase their blood circulation half-life, which should allow extensive accumulation at the targeted site. To eliminate nonspecific blood pool signal from the MR images, the circulating liposomes should ideally be cleared from the circulation when sufficient target-specific contrast enhancement is obtained. To that aim, we designed an avidin chase that allowed controlled and rapid clearance of paramagnetic biotinylated liposomes from the blood circulation in C57BL/6 mice. Avidin-induced alterations in blood clearance kinetics and tissue distribution were studied quantitatively by determination of the Gd content in blood and tissue samples ex vivo. Intrinsic liposomal blood clearance showed bi-exponential behavior with half-lives t(1/2alpha) = 2.1 +/- 1.1 and t(1/2beta) = 15.1 +/- 5.4 hours, respectively. In contrast, the contrast agent was cleared from the blood by the avidin infusion to <1% of the initial dose within 4 hours. Avidin-induced liposomal blood clearance was also demonstrated in vivo by dynamic T(1)-weighted MRI. The ability to rapidly clear circulating contrast agents opens up exciting possibilities to study targeting kinetics, to increase the specificity of molecular MRI and to optimize nanoparticulate contrast agent formulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avidin / administration & dosage*
  • Biotinylation / methods
  • Contrast Media / pharmacokinetics*
  • Image Enhancement / methods*
  • Kinetics
  • Liposomes / pharmacokinetics*
  • Magnetic Resonance Imaging / methods*
  • Metabolic Clearance Rate / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Molecular Probe Techniques*
  • Organ Specificity / drug effects
  • Tissue Distribution / drug effects

Substances

  • Contrast Media
  • Liposomes
  • Avidin