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一种将毛细管嵌入微流控装置的简化方法——以基于溶胶-凝胶的预浓缩为例。

A simplified method for capillary embedment into microfluidic devices - exemplified by sol-gel-based preconcentration.

作者信息

Thorslund Sara, Johannesson Nina, Nikolajeff Fredrik, Bergquist Jonas

机构信息

Department of Engineering Sciences, Angström Laboratory, Uppsala University, Uppsala, Sweden.

出版信息

Electrophoresis. 2007 Dec;28(24):4758-64. doi: 10.1002/elps.200700221.

Abstract

We here describe an alternative method of embedding functionalized capillaries into microdevices fabricated in PDMS. The capillaries have square-shaped outer dimensions and fit into elastic PDMS channel networks of similar dimensions. By modifying the capillary off-chip, the technique makes it possible to integrate a new chip function without risking contamination of already existing chemically patterned areas because of new reagent solutions. Leak-free insertion of these capillaries has earlier been reported, where a thin layer of uncured PDMS bonded the capillary to the microchannel and the lid structure. In this new approach, oxygen plasma is used to bond the square capillary to the PDMS, eliminating the risk of clogging the microsystem with uncured prepolymer. The new embedding technique was exemplified and evaluated by inserting a square capillary piece containing monolithic sol-gel for sample preconcentration application. The assembled microdevice was run with mass spectrometric detection, showing that peptides were preconcentrated without leakage from either the sol-gel itself or around the inserted capillary. Repeated preconcentration runs showed migration times better than 3% for all peptides. We believe that the presented microchip assembling technique greatly simplifies the insertion of functionalized capillary pieces, e.g., an initial preconcentrator to a PDMS device containing other downstream modules.

摘要

我们在此描述一种将功能化毛细管嵌入聚二甲基硅氧烷(PDMS)制成的微器件中的替代方法。这些毛细管具有方形的外部尺寸,可适配到尺寸相似的弹性PDMS通道网络中。通过在芯片外对毛细管进行改性,该技术能够集成新的芯片功能,而不会因新的试剂溶液而有污染已有化学图案区域的风险。此前已有关于这些毛细管无泄漏插入的报道,其中未固化的PDMS薄层将毛细管与微通道和盖子结构粘结在一起。在这种新方法中,使用氧等离子体将方形毛细管粘结到PDMS上,消除了未固化预聚物堵塞微系统的风险。通过插入包含整体式溶胶 - 凝胶用于样品预浓缩应用的方形毛细管片段,对新的嵌入技术进行了举例说明和评估。组装好的微器件采用质谱检测运行,结果表明肽段得到了预浓缩,且溶胶 - 凝胶本身或插入毛细管周围均无泄漏。重复进行预浓缩运行显示,所有肽段的迁移时间偏差优于3%。我们认为,所展示的微芯片组装技术极大地简化了功能化毛细管片段的插入过程,例如将初始预浓缩器插入到包含其他下游模块的PDMS器件中。

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