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Received April 9, 2008
Accepted May 30, 2008
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Simple fabrication of functionalized surface with polyethylene glycol microstructure and glycidyl methacrylate moiety for the selective immobilization of proteins and cells
Department of Chemical Engineering, Chungnam National University, 220 Gung-dong, Yu-Seong gu, Daejeon 305-764, Korea
rhadum@cnu.ac.kr
Korean Journal of Chemical Engineering, November 2008, 25(6), 1467-1472(6), 10.1007/s11814-008-0241-9
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Abstract
This study reported simple surface modification for the immobilization of biomolecules such as proteins and cells onto desired area at micron-scale level. First, thin film composed of glycidyl methacrylate (GMA) was prepared by UV-photopolymerization. Then, the polyethylene glycol (PEG) microstructures which played a role in the prevention of nonspecific binding of biomolecules were fabricated by using micromolding in capillaries (MIMIC). Thus, we could easily obtain an orthogonal surface having biomolecular attraction and repulsion areas. In addition, we could control of the height of prepared PEG microstructures with spin coating or not. For the investigation of feasibility of biomolecule patterning onto the functionalized surface, FITC-BSA and HEK 293 were examined as representative biomolecule models. A functionalized surface with GMA promotes the strong adhesion of biomolecules, and PEG microstructures located on the background prevent nonspecific binding of biomolecules at micron-scale level._x000D_
The orthogonal difference in surface functionality showed strong possibility of simple patterning of biomolecules. In addition, the proposed method could easily control the size, shape, and height of patterns. It will be useful platform technology for the construction of a biomolecule array.
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Suh KY, Jon S, Langmuir, 21(15), 6836 (2005)
Kim P, Lee SE, Jung HS, Lee HY, Kawai T, Suh KY, Lab. Chip., 6, 54 (2006)
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Revzin A, Russell RJ, Yadavalli VK, Koh WG, Deister C, Hile DD, Mellott MB, Pishko MV, Langmuir, 17(18), 5440 (2001)
Ostuni E, Kane R, Chen CS, Ingber DE, Whitesides GM, Langmuir, 16(20), 7811 (2000)
Shim HW, Lee JH, Hwang TS, Rhee YW, Bae YM, Choi JS, Han J, Lee CS, Biosens. Bioelectron., 22, 3188 (2007)
Viswanathan K, Ozhalici H, Elkins CL, Heisey C, Ward TC, Long TE, Langmuir, 22(3), 1099 (2006)