| Literature DB >> 26444914 |
Nina Yu Kostina1, Ognen Pop-Georgievski1, Michael Bachmann2, Neda Neykova3,4, Michael Bruns5, Jiří Michálek1, Martin Bastmeyer6,7, Cesar Rodriguez-Emmenegger8.
Abstract
Poly(ϵ-caprolactone) (PCL) nanofibers are very attractive materials for tissue engineering (TE) due to their degradability and structural similarity to the extracellular matrix (ECM). However, upon exposure to biological media, their surface is rapidly fouled by proteins and cells, which may lead to inflammation and foreign body reaction. In this study, an approach for the modification of PCL nanofibers to prevent protein fouling from biological fluids and subsequent cell adhesion is introduced. A biomimetic polydopamine (PDA) layer was deposited on the surface of the PCL nanofibers and four types of antifouling polymer brushes were grown by surface-initiated atom transfer radical polymerization (SI-ATRP) from initiator moieties covalently attached to the PDA layer. Cell adhesion was assessed with mouse embryonic fibroblasts (MEFs). MEFs rapidly adhered and formed cell-matrix adhesions (CMAs) with PCL and PCL-PDA nanofibers. Importantly, the nanofibers modified with antifouling polymer brushes were able to suppress non-specific protein adsorption and thereby cell adhesion.Entities:
Keywords: antifouling; cell adhesion; nanofibers; polymer brushes; surface-initiated atom transfer radical polymerization (SI-ATRP)
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Year: 2015 PMID: 26444914 DOI: 10.1002/mabi.201500252
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979