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微流控无流动化学浓度梯度生成

Microfluidic flow-free generation of chemical concentration gradients.

作者信息

Zhou Yao, Lin Qiao

机构信息

Department of Mechanical Engineering, Columbia University, New York, NY 10027, USA.

出版信息

Sens Actuators B Chem. 2014 Jan;190:334-341. doi: 10.1016/j.snb.2013.08.073. Epub 2013 Sep 3.

DOI:10.1016/j.snb.2013.08.073
PMID:30505071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6268163/
Abstract

This paper presents a class of novel microfluidic concentration gradient generation (CGG) devices that create temporally stable chemical concentration gradients with complex shapes in a flow-free environment. The devices feature a two-layer channel design and the incorporation of a semipermeable membrane, which effectively segregates the concentration gradient region in the lower layer from the flow of reagent sample (simply "sample" onward) and buffer in the upper layer. In the mean time, free diffusion across the membrane constantly replenishes sample and buffer to maintain a stable concentration. The shapes of the concentration gradients are controlled by the geometries of the micro-channels and chambers. Concentration gradients with complex shapes can be achieved by piecewise combining constituent gradients with elementary shapes. Capable of generating concentration gradients in a flow-free environment, our devices eliminate undesirable flow stimulation on biological cells under investigation, while maintaining a stable chemical environment for cell studies.

摘要

本文介绍了一类新型的微流控浓度梯度生成(CGG)装置,该装置可在无流动环境中创建具有复杂形状的时间稳定化学浓度梯度。这些装置采用双层通道设计,并结合了半透膜,可有效将下层的浓度梯度区域与上层的试剂样品(以下简称“样品”)和缓冲液流隔离开来。同时,通过膜的自由扩散不断补充样品和缓冲液以维持稳定的浓度。浓度梯度的形状由微通道和腔室的几何形状控制。通过将具有基本形状的组成梯度进行分段组合,可实现具有复杂形状的浓度梯度。我们的装置能够在无流动环境中生成浓度梯度,消除了对所研究生物细胞的不良流动刺激,同时为细胞研究维持稳定的化学环境。

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本文引用的文献

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Electrophoresis. 2011 Nov;32(22):3133-7. doi: 10.1002/elps.201100161. Epub 2011 Aug 23.
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Generation of complex concentration profiles by partial diffusive mixing in multi-stream laminar flow.通过多股层流中的部分扩散混合生成复杂浓度分布
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A platform for assessing chemotactic migration within a spatiotemporally defined 3D microenvironment.
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Screening applications in drug discovery based on microfluidic technology.基于微流控技术的药物发现筛选应用。
Biomicrofluidics. 2016 Jan 28;10(1):011502. doi: 10.1063/1.4940886. eCollection 2016 Jan.
5
Microfluidic study of the chemotactic response of Escherichia coli to amino acids, signaling molecules and secondary metabolites.大肠杆菌对氨基酸、信号分子和次生代谢产物趋化反应的微流控研究
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一个用于在时空定义的3D微环境中评估趋化性迁移的平台。
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4
Generation of stable complex gradients across two-dimensional surfaces and three-dimensional gels.在二维表面和三维凝胶上生成稳定的复合梯度。
Langmuir. 2007 Oct 23;23(22):10910-2. doi: 10.1021/la7026835. Epub 2007 Oct 2.
5
MAPK-mediated bimodal gene expression and adaptive gradient sensing in yeast.丝裂原活化蛋白激酶介导的酵母双峰基因表达及适应性梯度感知
Nature. 2007 Mar 1;446(7131):46-51. doi: 10.1038/nature05561. Epub 2007 Feb 18.
6
Generation of complex, static solution gradients in microfluidic channels.在微流控通道中生成复杂的静态溶液梯度。
J Am Chem Soc. 2006 Apr 5;128(13):4194-5. doi: 10.1021/ja058530o.
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Characterization of a membrane-based gradient generator for use in cell-signaling studies.用于细胞信号研究的基于膜的梯度发生器的特性描述。
Lab Chip. 2006 Mar;6(3):389-93. doi: 10.1039/b514133h. Epub 2006 Feb 1.
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