Jm. Vanalstine et al., POLY(ETHYLENE GLYCOL) AMPHIPHILE ADSORPTION AND LIPOSOME PARTITION, Journal of chromatography B. Biomedical applications, 680(1-2), 1996, pp. 145-155
Citations number
64
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Journal of chromatography B. Biomedical applications
Surface localized poly(ethylene glycol) (PEG) amphiphiles of type C-16
:0-EO(151) and C-18:2-EO(1.51) were studied via ellipsometry at macros
copic, hat methylated silica (MeSi), phosphatidic acid (PA), and phosp
hatidylcholine (PC) surfaces. At these surfaces the amphiphiles adsorb
similarly, in a non-cooperative manner, achieving a plateau (approxim
ate to 0.1 PEG chains/nm(2)) well below amphiphile critical micelle co
ncentration (CMC). The resultant PEG-enriched layers were 10-15 nm thi
ck, with a polymer concentration (approximate to 0.07 g/cm(3)) greater
than the PEG-enriched phase of many dextran, PEG aqueous two-phase sy
stems. PEG-amphiphile adsorption (mg/m(2)) at hydrophobic and phosphol
ipid flat surfaces correlated with changes in the partition (log K) of
PC liposomes in such two-phase systems. PEG-amphiphile adsorption at
macroscopic surfaces appears to represent a balance between hydrophobi
c attraction and repulsive intra-chain interactions which promote chai
n elongation normal to the surface.