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用于微流控芯片等电聚焦应用的多孔聚二甲基硅氧烷膜的简单制备方法。

A simple method for preparation of macroporous polydimethylsiloxane membrane for microfluidic chip-based isoelectric focusing applications.

机构信息

Department of Mechanical and Mechatronics Engineering, University of Waterloo, 200 University Ave West, Waterloo, Ontario, N2L 3G1 Canada.

出版信息

Anal Chim Acta. 2010 Mar 10;662(2):200-5. doi: 10.1016/j.aca.2010.01.010. Epub 2010 Jan 11.

Abstract

A new, simple method was reported to prepare PDMS membranes with micrometer size pores for microfluidic chip applications. The pores were formed by adding polystyrene and toluene into PDMS prepolymer solution prior to spin-coating and curing. The resulting PDMS membrane has a thickness of around 10 microm and macropores with a diameter ranging from 1 to 2 microm measured using scanning electron microscope (SEM) imaging. This PDMS membrane was validated by integrating it with PDMS microfluidic chips for protein separation using isoelectric focusing mechanism coupled with whole channel imaging detection (IEF-WCID). It has been shown that five standard pI markers and a mixture of two proteins, myoglobin and beta-lactoglobulin, can be separated using these chips. The results indicated that this macroporous PDMS membrane can replace the dialysis membrane in PDMS chips for the IEF-WCID technique. The preparation method of macroporous PDMS membrane may be potentially applied in other fields of microfluidic chips.

摘要

一种新的简单方法被报道用于制备用于微流控芯片应用的具有微米级孔径的 PDMS 膜。在旋涂和固化之前,将聚苯乙烯和甲苯加入 PDMS 预聚物溶液中以形成孔。使用扫描电子显微镜 (SEM) 成像测量得到的 PDMS 膜的厚度约为 10 微米,并且具有直径为 1 至 2 微米的大孔。通过将其与 PDMS 微流控芯片集成,使用等电聚焦机制结合全通道成像检测 (IEF-WCID) 来验证这种 PDMS 膜进行蛋白质分离。已经表明,使用这些芯片可以分离五个标准 pI 标记物和肌红蛋白和β-乳球蛋白两种蛋白质的混合物。结果表明,这种多孔 PDMS 膜可以替代 PDMS 芯片中的透析膜用于 IEF-WCID 技术。这种大孔 PDMS 膜的制备方法可能在微流控芯片的其他领域具有潜在的应用。

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