Fabrication of microchannels with patterned bio-active layers

R. Iwama, Lap Man Lee, E. S. Cho, Y. Zohar
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引用次数: 2

Abstract

Patterns of bio-active coatings on the inner surfaces of microchannels have been realized using a novel low-temperature, UV-epoxy glass-to-silicon bonding technique. Sucrose is applied as a protection layer for the immobilized bio-functional films during the bonding step. The bio-functional layer is composed of antibody patterns, for binding specific targets, next to polyethylene glycol (PEG) coated regions for preventing non-specific absorption. The activity of the patterned bio layer is tested, after the removal of the sucrose protection layer, utilizing fluorescent microscopy. A solution of fluorescent-labelled antigens is injected into the microchannels for incubation with the immobilized antibodies. Upon exposure to proper radiation, light is emitted only from the antibody patterns while the PEG regions remain dark. Hence, the sucrose-protection and UV-bonding techniques have not significantly compromised the functionality of the patterned antibodies, in binding to their counter receptors, and PEG molecules, in preventing non-specific adsorption, at the end of the fabrication process.
具有图案生物活性层的微通道的制备
利用一种新型的低温紫外环氧玻璃-硅键合技术,在微通道内表面实现了生物活性涂层的图案。在键合过程中,蔗糖作为固定化生物功能膜的保护层。生物功能层由抗体模式组成,用于结合特定目标,靠近聚乙二醇(PEG)包被区域,以防止非特异性吸收。在去除蔗糖保护层后,利用荧光显微镜测试图案生物层的活性。将荧光标记抗原溶液注射到微通道中,与固定抗体孵育。暴露在适当的辐射下,光仅从抗体模式发射,而PEG区域保持黑暗。因此,蔗糖保护和紫外线键合技术并没有显著损害图案抗体的功能,在制造过程结束时,与它们的对抗受体和PEG分子结合,防止非特异性吸附。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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