| Literature DB >> 21259436 |
Krzysztof Babiuch1, C Remzi Becer, Michael Gottschaldt, Joseph T Delaney, Jürgen Weisser, Birgitt Beer, Ralf Wyrwa, Matthias Schnabelrauch, Ulrich S Schubert.
Abstract
An efficient and metal-catalyst free method of glycopolymer synthesis via thiol/para-fluorine "click" reaction was used to graft acetylated 1-thio-β-D-glucopyranose and 1-thio-β-D-galactopyranose onto a homopolymer of pentafluorostyrene (PFS) as well as onto a block copolymer of styrene and PFS. Subsequent deprotection of the carbohydrate moieties yielded well-defined, sugar-modified polymers (PDI < 1.2). The prepared polymers were not cytotoxic against 3T3 fibroblasts and MC3T3-E1 preosteoblasts. Furthermore, the water-insoluble copolymers were drop-cast and examined as synthetic biocompatible coatings on poly(propylene) substrates for culturing the investigated cell types. Both fibro- and preosteoblasts showed stable adhesion and proliferation on the glycopolymer-coated surfaces.Entities:
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Year: 2011 PMID: 21259436 DOI: 10.1002/mabi.201000374
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979