Liposome retention in size exclusion chromatography

BMC Biotechnol. 2005 May 10;5:11. doi: 10.1186/1472-6750-5-11.


Background: Size exclusion chromatography is the method of choice for separating free from liposome-encapsulated molecules. However, if the column is not presaturated with lipids this type of chromatography causes a significant loss of lipid material. To date, the mechanism of lipid retention is poorly understood. It has been speculated that lipid binds to the column material or the entire liposome is entrapped inside the void.

Results: Here we show that intact liposomes and their contents are retained in the exclusion gel. Retention depends on the pore size, the smaller the pores, the higher the retention. Retained liposomes are not tightly fixed to the beads and are slowly released from the gels upon direct or inverted eluent flow, long washing steps or column repacking. Further addition of free liposomes leads to the elution of part of the gel-trapped liposomes, showing that the retention is transitory. Trapping reversibility should be related to a mechanism of partitioning of the liposomes between the stationary phase, water-swelled polymeric gel, and the mobile aqueous phase.

Conclusion: Retention of liposomes by size exclusion gels is a dynamic and reversible process, which should be accounted for to control lipid loss and sample contamination during chromatography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / chemistry
  • Animals
  • Biotechnology / methods*
  • Chemistry, Physical / methods
  • Chromatography / methods*
  • Chromatography, Gel / methods
  • Drosophila melanogaster / enzymology
  • Drug Carriers / chemistry
  • Fluoresceins / chemistry
  • Gels / chemistry
  • Kinetics
  • Lipids / chemistry
  • Liposomes / chemistry*
  • Membranes, Artificial
  • Microscopy, Electron, Scanning
  • Microscopy, Fluorescence
  • Permeability


  • Drug Carriers
  • Fluoresceins
  • Gels
  • Lipids
  • Liposomes
  • Membranes, Artificial
  • Acetylcholinesterase
  • fluorexon