Suppressing parasitic flow in membraneless diffusion-based microfluidic gradient generators†

IF 5.4 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-03-03 DOI:10.1039/D4LC00956H
Vahid Khandan, Ryan C. Chiechi, Elisabeth Verpoorte and Klaus Mathwig
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引用次数: 0

Abstract

Diffusion-based microfluidic gradient generators (DMGGs) are essential for various in vitro studies due to their ability to provide a convection-free concentration gradient. However, these systems, often referred to as membrane-based DMGGs, exhibit delayed gradient formation due to the incorporated flow-resistant membrane. This limitation substantially hinders their application in dynamic and time-sensitive studies. Here, we accelerate the gradient response in DMGGs by removing the membrane and implementing new geometrical configurations to compensate for the membrane's role in suppressing parasitic flows. We introduce these novel configurations into two microfluidic designs: the H-junction and the Y-junction. In the H-junction design, parasitic flow is redirected through a bypass channel following the gradient region. The Y-junction design features a shared discharge channel that allows converging discharge flow streams, preventing the buildup of parasitic pressure downstream of the gradient region. Using hydraulic circuit analysis and fluid dynamics simulations, we demonstrate the effectiveness of the H-junction and Y-junction designs in suppressing parasitic pressure flows. These computational results, supported by experimental data from particle image velocimetry, confirm the capability of our designs to generate a highly stable, accurate, and convection-free gradient with rapid formation. These advantages make the H-junction and Y-junction designs ideal experimental platforms for a wide range of in vitro studies, including drug testing, cell chemotaxis, and stem cell differentiation.

Abstract Image

抑制无膜扩散微流体梯度发生器中的寄生流。
基于扩散的微流体梯度发生器(DMGGs)是各种体外研究必不可少的,因为它们能够提供无对流的浓度梯度。然而,这些通常被称为膜基dmgg的系统,由于掺入了抗流膜,呈现出延迟的梯度形成。这一限制极大地阻碍了它们在动态和时间敏感研究中的应用。在这里,我们通过去除膜和实现新的几何结构来补偿膜在抑制寄生流中的作用,从而加速dmgg中的梯度响应。我们将这些新的结构引入到两种微流控设计中:h结和y结。在h结设计中,寄生流通过沿梯度区域的旁路通道重新定向。y型结的设计特点是共享排放通道,允许汇聚排放流,防止梯度区域下游的寄生压力积聚。通过液压回路分析和流体动力学仿真,我们证明了h结和y结设计在抑制寄生压力流动方面的有效性。这些计算结果得到了粒子图像测速实验数据的支持,证实了我们的设计能够快速生成高度稳定、准确和无对流的梯度。这些优点使h结和y结设计成为广泛的体外研究的理想实验平台,包括药物测试,细胞趋化性和干细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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