Polymers are widely used for a large range of medical devices used as bioma
terials on a temporary, intermittent, and long-term basis. II is now well a
ccepted that the initial rapid adsorption of proteins to polymeric surfaces
affects the performance of these biomaterials. However, protein adsorption
to a polymer surface can be modulated by an appropriate design of the inte
rface. Extensive study has shown that these interactions can be minimized b
y coating with a highly hydrated layer (hydrogel), by grafting on the surfa
ce different biomolecules, or by creating domains with chemical functions (
charges, hydrophilic groups). Our laboratory has investigated the latter ap
proach over the past 2 decades, in particular the synthesis and the biologi
cal activities of polymers to improve the biocompatibility of blood-contact
ing devices. These soluble and insoluble polymers were obtained by chemical
substitution of macromolecular chains with suitable groups able to develop
specific interactions with biological components. Applied to compatibility
with the blood and the immune systems, this concept has been extended to i
nteractions of polymeric biomaterials with eukaryotic and prokaryotic cells
. The design of new biomaterials with low bacteria attachment is thus under
intensive study. After a brief overview of current trends in the surface m
odifications of biocompatible materials, we will describe how biospecific p
olymers can be obtained and review our recent results on the inhibition of
bacterial adhesion using one type of functionalized polymer obtained by ran
dom substitution. This strategy applied to existing or new materials, seems
promising for thr limitation of biomaterial-associated infections (Infect
Control Hosp Epidemiol 2000;21: 104-110).