Electrospun nanofibers surface-modified with fluorescent proteins

被引:43
作者
Choi, Ji Suk
Yoo, Hyuk Sang [1 ]
机构
[1] Kangwon Natl Univ, Sch Biosci & Bioengn, Dept Biomat Engn, Chunchon 200701, South Korea
[2] Kangwon Natl Univ, Inst Biosci & Biotechnol, Chunchon, South Korea
关键词
nanofibers; electrospinning; PCL; PEG; wound healing; surface modification; protein modified surfaces; tissue regeneration scaffolds; tissue engineering; PLC-PEG copolymers; NORMAL HUMAN KERATINOCYTES; ADHESIVE RGD PEPTIDE; IN-VITRO; SCAFFOLD; POLYMER; MEMBRANES; CHITOSAN; CELLS; DIFFERENTIATION; IMMOBILIZATION;
D O I
10.1177/0883911507081101
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Electrospun nanofiber surfaces are modified with proteins to control protein release. A mixture of poly(E-caprolactone) (PCL) and PCL-PEG block copolymers is electrospun to prepare amine-terminated block copolymers. The amount of surface exposed amine groups increases as the blend ratio of block copolymer increases. Cell attachments on the nanofibers change according to the ratio of the block copolymer in the blend; this indicates that the PEG moiety plays a significant role in enhancing and decreasing biocompatibility of nanofibers. Fluorescent proteins are immobilized on the surface of nanofibers by conjugating activated carboxylic groups of the protein to the surface exposed amine groups of nanofibers in an aqueous environment. The number of amine groups increases as the ratio of block copolymers increases. Proteins that are chemically associated with the nanofibers show an attenuated release profile while most of the proteins physically associated with the nanofibers are released in 1 day. These results show that the protein-immobilized nanofibers can be potentially applied to tissue engineering scaffolds and wound healing materials with bioactive protein being slowly released over a long period of time.
引用
收藏
页码:508 / 524
页数:17
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