George Peter A, Donose Bogdan C, Cooper-White Justin J
Australian National Fabrication Facility (QLD Node), University of Queensland, Bld 75, Cnr Cooper and College Rds, Brisbane, QLD 4072, Australia.
Biomaterials. 2009 May;30(13):2449-56. doi: 10.1016/j.biomaterials.2009.01.012. Epub 2009 Feb 6.
In this paper we report a method for biomaterial surface modification that utilizes the self-assembly of block copolymers of poly(styrene-block-ethylene oxide) (PS-PEO) to generate micro-phase separated surfaces with varying density PEO domains. These PS-PEO self-assembled surfaces showed a significant reduction in protein adsorption compared to control polystyrene surfaces. The adhesion of NIH-3T3 fibroblast cells was shown to be significantly affected by the surface coverage of PEO nano-domains formed by copolymer self-assembly. These nano-domains, when presented at high number density (almost 1000 domains per square micron), were shown to completely prevent cellular attachment, even though small amounts of protein were able to bind to the surface.
在本文中,我们报告了一种生物材料表面改性方法,该方法利用聚(苯乙烯 - 嵌段 - 环氧乙烷)(PS - PEO)嵌段共聚物的自组装来生成具有不同密度PEO域的微相分离表面。与对照聚苯乙烯表面相比,这些PS - PEO自组装表面的蛋白质吸附显著减少。NIH - 3T3成纤维细胞的粘附显示出受到共聚物自组装形成的PEO纳米域表面覆盖率的显著影响。这些纳米域,当以高密度出现(每平方微米几乎有1000个域)时,即使少量蛋白质能够结合到表面,也显示出能完全阻止细胞附着。