Effect of Polymer Brush Architecture on Antibiofouling Properties

被引:153
作者
Gunkel, Gesine [1 ]
Weinhart, Marie [2 ]
Becherer, Tobias [2 ]
Haag, Rainer [2 ]
Huck, Wilhelm T. S. [1 ,3 ]
机构
[1] Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England
[2] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
[3] Radboud Univ Nijmegen, Inst Mol & Mat, NL-6525 AJ Nijmegen, Netherlands
关键词
SELF-ASSEMBLED MONOLAYERS; SURFACE-INITIATED POLYMERIZATIONS; PROTEIN ADSORPTION; BLOOD-PLASMA; POLYGLYCEROL; DERIVATIVES; RESISTANCE; THICKNESS; DENDRONS; DESIGN;
D O I
10.1021/bm200943m
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Polymer brushes show great promise in next-generation antibiofouling surfaces. Here, we have studied the influence of polymer brush architecture on protein resistance. By carefully optimizing reaction conditions, we were able to polymerize oligoglycerol-based brushes with sterically demanding linear or dendronized side chains on gold surfaces. Protein adsorption from serum and plasma was analyzed by surface plasmon resonance. Our findings reveal a pronounced dependence of biofouling on brush architecture. Bulky yet flexible side chains as in dendronized brushes provide an ideal environment to repel protein-possibly through formation of a hydration layer, which can be further enhanced by presenting free hydroxyl groups on the polymer brushes. A deeper understanding of how brush architecture influences protein resistance will ultimately enable fabrication of surface coatings tailored to specific requirements in biomedical applications.
引用
收藏
页码:4169 / 4172
页数:4
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