Premium
Control of protein adsorption on functionalized electrospun fibers
Author(s) -
Grafahrend Dirk,
Calvet Julia Lleixa,
Klinkhammer Kristina,
Salber Jochen,
Dalton Paul D.,
Möller Martin,
Klee Doris
Publication year - 2008
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.21928
Subject(s) - ethylene glycol , protein adsorption , electrospinning , peg ratio , adsorption , chemical engineering , surface modification , materials science , contact angle , copolymer , amphiphile , polymer chemistry , polymer , chemistry , organic chemistry , composite material , engineering , economics , finance
Electrospun fibers that are protein resistant and functionalized with bioactive signals were produced by solution electrospinning amphiphilic block copolymers. Poly (ethylene glycol)‐ block ‐poly( D , L ‐lactide) (PEG‐ b ‐PDLLA) was synthesized in two steps, with a PEG segment of 10 kDa, while the PDLLA block ranged from 20 to 60 kDa. Depending on the PEG and PDLLA segment ratio, as well as solvent selection, the hydrophilicity and protein adsorption could be altered on the electrospun mesh. Furthermore, an α‐acetal PEG‐ b ‐PDLLA was synthesized that allowed the conjugation of active molecules, resulting in surface functionalization of the electrospun fiber. Electrospun material with varying morphologies and diameter were electrospun from 10, 20, and 30 wt.% solutions. Sessile drop measurements showed a reduction in the contact angle from 120° for pure poly( D , L ‐lactide) with increasing PEG/PDLLA ratio. All electrospun block PEG‐ b ‐PDLLA fibers had hydrophilic properties, with contact angles below 45°. The fibers were collected onto six‐arm star‐poly(ethylene glycol) (star‐PEG) coated silicon wafers and incubated with fluorescently labeled proteins. All PEG‐ b ‐PDLLA fibers showed no detectable adsorption of bovine serum albumin (BSA) independent of their composition while a dependence between hydrophobic block length was observed for streptavidin adsorption. Fibers of block copolymers with PDLLA blocks smaller than 39 kDa showed no adsorption of BSA or streptavidin, indicating good non‐fouling properties. Fibers were surface functionalized with N ε ‐(+)‐biotinyl‐ L ‐lysine (biocytin) or RGD peptide by attaching the molecule to the PEG block during synthesis. Protein adsorption measurements, and the controlled interaction of biocytin with fluorescently labeled streptavidin, showed that the electrospun fibers were both resistant to protein adsorption and are functionalized. Fibroblast adhesion was contrasting between the unfunctionalized and RGD‐coupled electrospun fabrics, confirming that the surface of the fibers was functionalized. The PEG‐ b ‐PDLLA surface functionalized electrospun fibers are promising substrates for controlling cell–material interactions, particularly for tissue‐engineering applications. Biotechnol. Bioeng. 2008;101: 609–621. © 2008 Wiley Periodicals, Inc.