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用于生物/化学分析的液体塞微处理。

Microprocessing of liquid plugs for bio/chemical analyses.

作者信息

Sassa Fumihiro, Fukuda Junji, Suzuki Hiroaki

机构信息

Graduate School of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8573, Japan.

出版信息

Anal Chem. 2008 Aug 15;80(16):6206-13. doi: 10.1021/ac800492v. Epub 2008 Jul 16.

Abstract

A microfluidic device and operation to handle liquid plugs for biochemical analyses were developed for efficient handling of plugs of many solutions. A major part of the device was a T-junction consisting of a main flow channel and a handling flow channel. Unit operations including attachment of plugs, division of a plug, sorting of plugs, and formation of plugs of various lengths enabled controlled sequential reactions in a microflow channel. Rapid mixing could easily be achieved by moving a plug formed by merging two plugs back and forth. The device could be used for efficient characterization of performance in bio/chemical sensing. In experiments using L-glutamate oxidase, plugs containing an enzyme or a substrate were formed, mixed sequentially, and the intensity of fluorescence from plugs of different concentrations of L-glutamate or pHs could be measured simultaneously. Cross-contamination of plugs by neighboring plugs poses a problem in using the same flow channel repeatedly. However, the influence could be minimized by using a cleansing plug placed between them in a sufficiently hydrophobic flow channel and by processing the plugs at a low velocity. The device can be a critical component for microprocessing in various bio/chemical analyses.

摘要

为了高效处理多种溶液的液塞,开发了一种用于生化分析的微流控装置及其操作方法,以处理液塞。该装置的主要部分是一个由主流道和处理流道组成的T型接头。包括液塞附着、液塞分割、液塞分选以及形成各种长度液塞的单元操作,能够在微流道中实现受控的顺序反应。通过前后移动由两个液塞合并形成的液塞,可以轻松实现快速混合。该装置可用于生物/化学传感中性能的高效表征。在使用L-谷氨酸氧化酶的实验中,形成了含有酶或底物的液塞,依次混合,并可同时测量不同浓度L-谷氨酸或pH值的液塞的荧光强度。在重复使用同一流道时,相邻液塞的交叉污染是一个问题。然而,通过在足够疏水的流道中在它们之间放置一个清洁液塞,并以低速处理液塞,可以将这种影响降至最低。该装置可以成为各种生物/化学分析中微处理的关键组件。

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