PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES
PAPER|Updated:2023-01-03
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PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES
PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES
Chinese Journal of Polymer Science2013年31卷第3期 页码:495-502
Affiliations:
a.Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China
b.College of Chemistry and Material Sciences, South-Central University for Nationalities, Wuhan 430074, China
Author bio:
**Zhao-qiang Wu (武照强), E-mail: wzqwhu@suda.edu.cn
Funds:
Fundamental Research Funds for the Central Universities and Research Program of Introducing Talents of Discipline of University(B08021);Fundamental Research Funds for the Central Universities
Wei-fang Tong, Xiao-li Liu, Fei Pan, 等. PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES[J]. Chinese Journal of Polymer Science, 2013,31(3):495-502.
Wei-fang Tong, Xiao-li Liu, Fei Pan, et al. PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES[J]. Chinese Journal of Polymer Science, 2013, 31(3): 495-502.
Wei-fang Tong, Xiao-li Liu, Fei Pan, 等. PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES[J]. Chinese Journal of Polymer Science, 2013,31(3):495-502.DOI: 10.1007/s10118-013-1210-2.
Wei-fang Tong, Xiao-li Liu, Fei Pan, et al. PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES[J]. Chinese Journal of Polymer Science, 2013, 31(3): 495-502.DOI: 10.1007/s10118-013-1210-2.
PROTEIN ADSORPTION AND CELL ADHESION ON RGD-FUNCTIONALIZED SILICON SUBSTRATE SURFACES
A method was developed to modify silicon surfaces with good protein resistance and specific cell attachment. A silicon surface was initially deposited using a block copolymer of
N
-vinylpyrrolidone (NVP) and 2-hydroxyethyl methacrylate (HEMA) (PVP-
b
-PHEMA) film through surface-initiated atom transfer radical polymerization and then further immobilized using a short arginine-glycine-aspartate (RGD) peptide. Our results demonstrate that the RGD-modified surfaces (Si-RGD) can suppress non-specific adsorption of proteins and induce the adhesion of L929 cells. The Si-RGD surface exhibited higher cell proliferation rates than the unmodified silicon surface. This research established a simple method for the fabrication of dual-functional silicon surface that combines antifouling and cell attachment promotion.
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