Covalent micropatterning of poly(dimethylsiloxane) by photografting through a mask

被引:122
作者
Wang, YL
Lai, HH
Bachman, M
Sims, CE
Li, GP [1 ]
Allbritton, NL
机构
[1] Univ Calif Irvine, Integrated Nanosyst Res Facil, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Elect Engn & Comp Sci, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Mat Sci & Chem Engn, Irvine, CA 92697 USA
关键词
D O I
10.1021/ac0509915
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new photografting method to micropattern a covalent surface modification on poly(dimethylsiloxane) (PDMS) provides advantages in simplicity and efficiency. To accomplish the entire process on the benchtop, the PDMS was initially treated with benzophenone dissolved in a water/acetone mixture. This process permitted limited diffusion of the photoinitiator into the PDMS surface. Polymerization of acrylic acid was initiated by exposure of the benzophenone-implanted PDMS to UV radiation through a photomask with a thin aqueous layer of acrylic acid sandwiched between the PDMS and photomask. This procedure resulted in patterned poly(acrylic acid) (PAA) on the PDMS surface. In the modified regions, PAA and PDMS formed an interpenetrating polymer network extending 50 mu m into the PDMS with an X-Y spatial resolution of 5 mu m. The carboxyl groups of the PAA graft could be derivatized to covalently bond other molecules to the patterned PAA. Two bioanalytical applications of this micropatterned surface were demonstrated: (1) a guide for cell attachment and growth and (2) a substrate for immunoassays. 3T3 cells were shown to selectively localize to modified surface regions where they could be cultured for up to 7 days. Additionally, the micropatterned surface was used to immobilize either protein A or antibody for heterogeneous immunoassays.
引用
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页码:7539 / 7546
页数:8
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