Preparation of micropatterned hydrogel substrate via surface graft polymerization combined with photolithography for biosensor application

被引:46
作者
Lee, Woojin [1 ]
Choi, Dongkil [1 ]
Lee, Yeol [1 ]
Kim, Dae-Nyun [1 ]
Park, Jinwon [1 ]
Koh, Won-Gun [1 ]
机构
[1] Yonsei Univ, Dept Chem Engn, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
poly(ethylene glycol) hydrogels; surface graft polymerization; photolithography; benzophenone; poly(acrylic acid) micropatterns;
D O I
10.1016/j.snb.2007.09.085
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper presents a simple method to create protein micropattern on the poly(ethylene glycol) (PEG) hydrogels through the surface graft polymerization and photolithography. The modification of the protein-repellent PEG hydrogel surface was achieved by a two-step process using immobilization of benzophenone on the PEG hydrogel as surface initiator and subsequent surface-initiated polymerization of acrylic acid by UV irradiation. Surface modification of PEG hydrogels was demonstrated with FTIR/ATR spectroscopy and XPS by confirming the presence of carboxyl groups in the poly(acrylic acid) (PAA). The photograft polymerization through the designed photomask produced well-defined, pH-responsive PAA micropatterns with diameters ranging from 50 to 300 mu m on the PEG hydrogels. The size of PAA micropatterns was controlled by changing the environmental pH, such that a 300 pm diameter and 17 mu m thick PAA micropattern at pH 4 swelled to 480 mu m diameter and 80 mu m thick at pH 7. Activation of the carboxyl groups in PAA allowed covalent immobilization of proteins only on the PAA micropatterns due to the nonadhesivity of PEG. Based on these results, biotin was micropatterned on the PEG hydrogels and binding of streptavidin was qualitatively and quantitatively investigated, demonstrating the possibility of micropatterned PEG hydrogels for various biosensor systems. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:841 / 849
页数:9
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