Ultrathin poly(ethylene glycol) films for silicon-based microdevices

被引:59
作者
Sharma, S
Johnson, RW
Desai, TA [1 ]
机构
[1] Univ Illinois, Dept Bioengn, Chicago, IL 60607 USA
[2] Abbott Labs, Struct Chem, Abbott Pk, IL 60064 USA
[3] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
基金
美国国家科学基金会;
关键词
poly(ethylene glycol); silicon; microdevices; thin films; covalent coupling;
D O I
10.1016/S0169-4332(02)01220-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Development of poly(ethylene glycol) (PEG) films that are ultrathin, uniform, conformal and stable in vivo-like environments is extremely desirable for biocompatible silicon-based microdevices. To this end, we have characterized PEG thin films, created by chemical coupling, at different PEG concentrations for various immobilization times, using the techniques of X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), ellipsometry and contact angle measurement. A continuous increase in film thickness and contact angle was measured with increase in PEG concentration and immobilization time (30-120 min). The surface roughness had a minimum value for 1.0% PEG (immobilization time = 60 min). The biocompatibility of ultrathin PEG films was also tested using fluorescein isothiocyanate (FITC)-labeled bovine serum albumin (BSA). Results indicated PEG-modified silicon surfaces to be more resistant to protein adsorption. The stability of ultrathin PEG films over time in dry and aqueous in vivo-like environments was also examined. While ultrathin PEG films were extremely stable in dry conditions, their stability was compromised in aqueous in vivo-like environments (PBS, 37 degreesC, pH 7.4, 5% CO2). Nevertheless, ultrathin PEG films retained their efficacy to control protein fouling for the period investigated. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:218 / 229
页数:12
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