Chromatographie d'exclusion stérique

Size-exclusion chromatography separates molecules based on their size using a stationary phase containing uniform pores. Large molecules cannot enter the pores and elute first, while small molecules penetrate deeply into the pores and elute last. Intermediate-sized molecules are separated in the retention window, with retention time directly influenced by molecular size.

Gel filtration uses hydrophilic packing materials and is applied to water-soluble samples, while gel permeation chromatography uses hydrophobic packing materials for substances soluble in less-polar organic solvents. Both methods separate polymers and macromolecules effectively. The choice of packing depends on the solvent compatibility and sample polarity requirements.

Size-exclusion chromatography uses two main stationary phase types: silica particles and cross-linked polymer resin beads. Silica particles offer rigidity and stability with various solvent compatibility. Polymer beads come in different pore sizes and can be hydrophilic for aqueous separations or hydrophobic for non-polar solvents like polystyrene-divinylbenzene.

An experimental calibration curve is prepared using standard substances with known molecular weights. This curve relates retention time or volume to molecular size. The calibration curve is then used to estimate the unknown molecular mass of sample molecules by comparing their retention behavior to the standards.

Smaller solutes spend more time within the pores of the stationary phase, resulting in longer elution times and greater retention volumes. The retention volume for a solute depends on its distribution ratio, which ranges from 0 at the exclusion limit to 1 at the inclusion limit. This reflects how well the solute penetrates the pores.

Yes, size-exclusion chromatography can be carried out using conventional high performance liquid chromatography instrumentation by replacing the HPLC column with an appropriate size-exclusion column. A UV/Vis detector is typically used to obtain chromatograms. This approach allows researchers to adapt existing equipment for SEC applications.

Silica particles used for size exclusion are deactivated to prevent unwanted interactions between the sample molecules and the stationary phase surface. Deactivation ensures that separation is based solely on molecular size and pore penetration rather than chemical interactions. In contrast, polymer resins are synthesized without exchange sites to achieve the same goal.