Synthesis and Electrografting of Dendron Anchored OEGylated Surfaces and Their Protein Adsorption Resistance

被引:9
作者
Felipe, Mary Jane L.
Ponnapati, Ramakrishna R.
Pernites, Roderick B.
Dutta, Pampa
Advincula, Rigoberto C. [1 ]
机构
[1] Univ Houston, Dept Chem, Houston, TX 77204 USA
基金
美国国家科学基金会;
关键词
electrografting; PEG; OEG; protein resistance; electrochemical; adsorption; SPR; SELF-ASSEMBLED MONOLAYERS; GOLD; CARBAZOLE; POLYMERS; BRUSHES; GLYCOL); WATER;
D O I
10.1021/am100737s
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
In this study, a series of electrochemically active oligo(ethylene glycol) (OEG) linear dendrons have been synthesized and grated onto electrode surfaces by cyclic voltammetry (CV) to improve protein resistance. Dendronized molecules with peripheral carbazole functionality and branching architecture enabled tethering of the poly(ethylene glycol), (PEG) or OEG group with a predictable number of electrochemical reactive groups affecting OEG distribution and orientation. It is possible that ample spacing between the OEG chains affects the intrinsic hydration of these layers and thus surface protein resistance. The films were characterized by CV, surface plasmon resonance (SPR) static contact angle measurements, and atomic force microscopy (AFM). This approach should enable improved nonbiofouling properties on biorelevant electrode surfaces (metal or metal oxides) by potentiostatic or potentio-dynamic electrochemical methods providing an alternative to the self-assemble monolayer (SAM) approach for anchoring PEG layers.
引用
收藏
页码:3401 / 3405
页数:5
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