E. Osterberg et al., PROTEIN-REJECTING ABILITY OF SURFACE-BOUND DEXTRAN IN END-ON AND SIDE-ON CONFIGURATIONS - COMPARISON TO PEG, Journal of biomedical materials research, 29(6), 1995, pp. 741-747
There is much interest in attaching, polyethylene glycol (PEG) and oth
er hydrophilic, neutral polymers to surfaces to reduce the extent of p
rotein and cell adsorption. Interestingly, these same surface-bound po
lymers are effective in masking surface charge and reducing electrokin
etic effects such as particle electrophoretic mobility, streaming pote
ntial, and electroosmosis. It is apparent that similar molecular prope
rties are responsible for both protein and cell rejection and reductio
n of electrokinetic effects. In this work we compared the fibrinogen-r
ejecting ability and the effect on electrophoretic mobility of three p
olymer coatings bound to polystyrene. The three polymers were side-bou
nd dextran, end-bound dextran, and end-bound PEG. The results of these
measurements were used to elucidate the importance of polymer packing
density and polymer layer thickness on protein adsorption and reducti
on of electrokinetic effects. Protein adsorption appears not to be sen
sitive to polymer layer thickness or the presence of dilute polymer ta
ils in a surface coating, while electrokinetic effects are. Protein ad
sorption is, however, very sensitive to the availability of exposed su
rface. Finally, the unique effectiveness of PEG is apparent in this re
search as in previous studies. (C) 1995 John Wiley & Sons, Inc.