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微流控通道内的表面导向接枝聚合。

Surface-directed, graft polymerization within microfluidic channels.

作者信息

Hu Shuwen, Ren Xueqin, Bachman Mark, Sims Christopher E, Li G P, Allbritton Nancy L

机构信息

Center for Biomedical Engineering, Integrated Nanosystems Research Facility, Department of Electrical and Computer Engineering, and Department of Physiology and Biophysics, University of California, Irvine, CA 92697, USA.

出版信息

Anal Chem. 2004 Apr 1;76(7):1865-70. doi: 10.1021/ac049937z.

Abstract

We demonstrate a simple procedure to coat the surfaces of enclosed PDMS microchannels by UV-mediated graft polymerization. In prior applications, only disassembled channels could be coated by this method. This limited the utility of the method to coatings that could easily and tightly seal with themselves. By preadsorbing a photoinitiator onto the surface of PDMS microchannels, the rate of polymer formation at the surface was greatly accelerated compared to that in solution. Thus, a gel did not form in the lumen of enclosed microchannels. We demonstrate that the photoinitiator benzophenone remained on the surface of PDMS even after extensive washing. After addition of a variety of monomer solutions (acrylic acid, poly(ethylene glycol) monomethoxyl acrylate, or poly(ethylene glycol) diacrylate) and illumination with UV light, a stable, covalently attached surface coating formed in the microchannels. The electroosmotic mobility was stable in response to air exposure and to repeated cycles of hydration-dehydration of the coating. These surfaces also supported the electrophoretic separation of two model analytes. Placement of an opaque mask over a portion of the channel permitted photopatterning of the microchannels with a resolution of approximately 100 microm. By using an appropriate mixture of monomers combined with masks, it should be possible to fabricate PDMS microfluidic devices with distinct surface properties in different regions or channels.

摘要

我们展示了一种通过紫外线介导的接枝聚合来包覆封闭的聚二甲基硅氧烷(PDMS)微通道表面的简单方法。在先前的应用中,该方法只能用于包覆拆解后的通道。这限制了该方法的实用性,使其仅适用于能够轻松紧密自密封的涂层。通过将光引发剂预吸附到PDMS微通道表面,与溶液中相比,表面聚合物形成的速率大大加快。因此,在封闭微通道的内腔中没有形成凝胶。我们证明,即使经过大量洗涤,光引发剂二苯甲酮仍保留在PDMS表面。加入各种单体溶液(丙烯酸、聚(乙二醇)单甲氧基丙烯酸酯或聚(乙二醇)二丙烯酸酯)并经紫外线照射后,微通道中形成了稳定的、共价连接的表面涂层。涂层在暴露于空气以及反复的水合-脱水循环过程中,其电渗迁移率保持稳定。这些表面还支持两种模型分析物的电泳分离。在通道的一部分上方放置一个不透明掩膜,可以实现微通道的光刻图案化,分辨率约为100微米。通过使用适当的单体混合物并结合掩膜,应该能够制造出在不同区域或通道具有不同表面性质的PDMS微流控装置。

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