The performance of Capillary Electrophoresis applied to the analysis of pro
teins can be considerably improved by using a pre-treated capillary present
ing a permanent hydrophilic layer immobilised on the capillary surface. The
protein/surface interactions are then reduced or eliminated, resulting in
an increased efficiency of separation. Some difficult analyses become possi
ble, such as the analysis of basic proteins which are irreversibly adsorbed
on a silica wall, The use of pre-treated tubes allows to improve the repro
ducibility of the analyses, as the electroosmotic flow is better controlled
in a broader range of pH. This review examines the various processes used
to modify permanently the wall of a silica capillary. Two different approac
hes are possible: i/ adsorption and immobilisation of a hydrophilic layer,
ii/ covalent bonding of a stationary phase (ligand or macromolecule) having
no affinity with the proteins analysed.