posted on 2015-05-19, 00:00authored byPasquale Benvenuto, Miguel
A. D. Neves, Christophe Blaszykowski, Alexander Romaschin, Timothy Chung, Sa Rang Kim, Michael Thompson
This work describes the straightforward
surface modification of
316L stainless steel with BTS, S-(11-trichlorosilylundecanyl)-benzenethiosulfonate,
a thiol-reactive trichlorosilane cross-linker molecule designed to
form intermediary coatings with subsequent biofunctionalization capability.
The strategy is more specifically exemplified with the immobilization
of intact antibodies and their Fab′ fragments. Both surface
derivatization steps are thoroughly characterized by means of X-ray
photoelectron spectroscopy. The antigen binding capability of both
types of biofunctionalized surfaces is subsequently assessed by fluorescence
microscopy. It was determined that BTS adlayers achieve robust immobilization
of both intact and fragmented antibodies, while preserving antigen
binding activity. Another key finding was the observation that the
Fab′ fragment immobilization strategy would constitute a preferential
option over that involving intact antibodies in the context of in vivo capture of endothelial progenitor cells in stent
applications.