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Macromol Biosci ; 11(4): 535-48, 2011 Apr 08.
Artigo em Inglês | MEDLINE | ID: mdl-21259436

RESUMO

An efficient and metal-catalyst free method of glycopolymer synthesis via thiol/para-fluorine "click" reaction was used to graft acetylated 1-thio-ß-D-glucopyranose and 1-thio-ß-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.


Assuntos
Materiais Revestidos Biocompatíveis/química , Fibroblastos/citologia , Polímeros de Fluorcarboneto/química , Poliestirenos/química , Células 3T3 , Animais , Adesão Celular , Polímeros de Fluorcarboneto/síntese química , Teste de Materiais/métodos , Camundongos , Poliestirenos/síntese química
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