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A Fibronectin Peptide‐Coupled Biopolymer Nanofibrous Matrix to Speed Up Initial Cellular Events
Author(s) -
Kim JiEun,
Noh KyungTae,
Yu HyeSun,
Lee HyeYoung,
Jang JunHyeog,
Kim HaeWon
Publication year - 2010
Publication title -
advanced engineering materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 114
eISSN - 1527-2648
pISSN - 1438-1656
DOI - 10.1002/adem.200980008
Subject(s) - nanofiber , peptide , materials science , fibronectin , cell adhesion , carbodiimide , electrospinning , tissue engineering , adhesion , polymer , biopolymer , biophysics , extracellular matrix , oligopeptide , biomolecule , polymer chemistry , nanotechnology , biochemistry , chemistry , biomedical engineering , composite material , medicine , biology
Abstract Degradable polymer nanofibers produced by electrospinning are attractive for use in cell culture and tissue repair. However, the hydrophobicity and initial poor cell adhesion of synthetic polymers have limited their use in tissue regeneration. Herein, the surface of a poly(lactide‐co‐caprolactone) Arg‐Gly‐Asp sequence of nanofiber was tailored with a fibronectin peptide (FN10), which was designed to retain the central cell‐binding domain. The electrospun nanofibers are first treated with an alkaline solution to reveal the carboxyl groups on the surface, which is followed by coupling with an FN10 solution in conjunction with a carbodiimide‐based agent. Peptide coupling occurs effectively with saturation within 1 h, and the coupled peptide maintains its stability for several days. The peptide‐coupled nanofibers show significant improvements in initial cell adhesion and spreading compared with the untreated one, confirming the role of the FN10 peptide in the initial cell events. This methodology may be useful in tailoring the surface of polymeric nanofibers with biomolecules targeted for specific tissue responses.