Introducing RGD Peptides on PHBV Films through PEG-Containing Cross-Linkers to Improve the Biocompatibility

被引:79
作者
Wang, Yan-Yan [1 ]
Lue, Lan-Xin [1 ]
Shi, Jun-Cai [1 ]
Wang, Hai-Feng [1 ]
Xiao, Zhong-Dang [1 ]
Huang, Ning-Ping [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Peoples R China
基金
美国国家科学基金会;
关键词
HUMAN-ENDOTHELIAL-CELLS; POLY(L-LYSINE)-G-POLY(ETHYLENE GLYCOL); FIBRINOGEN ADSORPTION; SURFACE MODIFICATION; PROTEIN ADSORPTION; PLASMA TREATMENT; POLY(3-HYDROXYBUTYRATE-CO-3-HYDROXYVALERATE); BIOMATERIALS; AMINOLYSIS; SCAFFOLDS;
D O I
10.1021/bm100886w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), a biodegradable polyester, has been a good candidate of biomaterial employed in tissue engineering. However, the PHBV film is hydrophobic and has no recognition sites for cell attachment. In this study, PHBV films are activated by ammonia plasma treatment to produce amino groups on the surface, followed by sequential reactions with a heterobifunctional cross-linker containing a segment of poly(ethylene glycol) (PEG) and further with RGD-containing peptides. XPS analyses of modified surfaces after each reaction step reveal that the RGD-containing peptides have been covalently grafted onto PHBV films. The result of cell viability assay indicates that the RGD-modified PHBV films exhibit a distinctly unproved cellular compatibility. Moreover, according to the results of serum adsorption tests by optical waveguide lightmode spectroscopy (OWLS) and fibrinogen adsorption tests by enzyme-linked immunosorbent assay (ELISA) on unmodified and modified PHBV surfaces, the introduced PEG chains can significantly decrease the nonspecific adsorption of proteins from serum and fibrinogen from plasma, thus decreasing the risk of thrombus formation and improving the blood compatibility of implanted materials.
引用
收藏
页码:551 / 559
页数:9
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