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Updated: Aug 15, 2026

Fluorescence-quenching of a Liposomal-encapsulated Near-infrared Fluorophore as a Tool for In Vivo Optical Imaging
Published on: January 5, 2015
Liposome biodistribution by time resolved fluorimetry of lipophilic europium complexes
Nathalie Mignet1, Quentin le Masne de Chermont, Tatiana Randrianarivelo
1CNRS-UMR8151; INSERM U640, Laboratoire Pharmacol. Chim. Genet., Université René Descartes Paris, 4, avenue de l' Observatoire, 75270 Paris cedex 06, France. Nathalie.mignet@univ-paris5.fr
Abstract:
The use of conventional fluorophores suffers from some limitations in biological fluids due to low signal/background ratio. Today, this sensitivity issue might be reasonably improved thanks to lanthanide chelates, by selective detection of long decay fluorescence. Use of pulsed light source time-resolved fluorimetry takes into account the fluorescence decay time of the lanthanide chelates to gain sensitivity in biological media. Lipid-DTPA: Eu compounds have been prepared and incorporated into liposomes to evaluate europium based detection of liposomes in biological media. Fluorescence emission was not modified by this incorporation. Europium labelled liposomes were used for biodistribution studies and showed their use in this context.

