Controlled Protein Absorption and Cell Adhesion on
Polymer-Brush-Grafted Poly(3,4-ethylenedioxythiophene) Films
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Abstract
Tailoring the surface of biometallic
implants with protein-resistant polymer brushes represents an efficient
approach to improve the biocompability and mechanical compliance with
soft human tissues. A general approach utilizing electropolymerization
to form initiating group (-Br) containing poly(3,4-ethylenedioxythiophen)s
(poly(EDOT)s) is described. After the conducting polymer is deposited,
neutral poly((oligo(ethylene glycol) methacrylate), poly(OEGMA), and
zwitterionic poly([2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium
hydroxide), poly(SBMA), brushes are grafted by surface-initiated atom
transfer radical polymerization. Quartz crystal microbalance (QCM)
experiments confirm protein resistance of poly(OEGMA) and poly(SBMA)-grafted
poly(EDOT)s. The protein binding properties of the surface are modulated
by the density of polymer brushes, which is controlled by the feed
content of initiator-containing monomer (EDOT-Br) in the monomer mixture
solution for electropolymerization. Furthermore, these polymer-grafted
poly(EDOT)s also prevent cells to adhere on the surface