M. Malmsten et Jm. Vanalstine, ADSORPTION OF POLY(ETHYLENE GLYCOL) AMPHIPHILES TO FORM COATINGS WHICH INHIBIT PROTEIN ADSORPTION, Journal of colloid and interface science, 177(2), 1996, pp. 502-512
The adsorption of poly(ethylene glycol) (PEG)-esterified fatty acids a
t methylated silica, phosphatidic acid, and phosphatidylcholine surfac
es was investigated with in situ ellipsometry. For a series of PEG-fat
ty acid esters of ethoxy groups and acyl tails of type C-i:j-EO(151) (
16 less than or equal to i less than or equal to 18, 0 less than or eq
ual to j less than or equal to 2)adsorption at methylated silica was i
ndependent of bulk micellization, and a plateau was reached below the
critical micellization concentration (CMC). The plateau adsorbed amoun
t for the investigated fatty acid esters was only weakly dependent on
the nature of the hydrophobic moiety. Instead, saturation adsorption w
as largely determined by the interactions between PEG chains. Adsorpti
on isotherms were therefore essentially identical on all three of the
quite different surfaces. At saturation adsorption, the adsorbed layer
thickness was 10-15 nm, while the average adsorbed layer concentratio
n was 0.07 g/cm(3). Formation of the PEG-surfactant coatings thus appe
ared to involve significant molecular alterations of PEG from a random
coil, The ability of the PEG-ester coatings to inhibit protein adsorp
tion was also investigated. At the adsorption plateau, all coatings in
vestigated displayed quite good ability to inhibit adsorption by a num
ber of serum proteins. For the surfaces studied this ability decreased
below 0.2 CMC. These findings are discussed in relation to the abilit
y of PEG-derivatized lipids to control the in vivo fate of colloidal d
rug carriers. (C) Academic Press, Inc.