Design and simulation of biomimetic microfluidic designs to achieve uniform flow and DNA capture for high-throughput multiplexing†

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-02-05 DOI:10.1039/D4LC01023J
Enas Osman, Jonathan L'Heureux-Hache, Phoebe Li and Leyla Soleymani
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引用次数: 0

Abstract

High-throughput multi-analyte point-of-care detection is often constrained by the limited number of analytes that can be effectively monitored. This study introduces bio-inspired microfluidic designs optimized for multi-analyte detection using 38–42 biosensors. Drawing inspiration from the human spinal cord and leaf vein networks, these perfusion-oriented designs ensure uniform flow velocity and consistent molecular capture while maintaining spatial separation to prevent cross-talk. In silico optimizations achieved velocity profile uniformity with coefficients of variance of 0.89% and 0.86% for the spine- and leaf-inspired designs, respectively. However, simulations revealed that velocity uniformity alone is insufficient for accurate molecular capture prediction without consistent reaction site channel dimensions. The bio-inspired designs demonstrated superior performance, stabilizing—coefficient of variance below 20%—in DNA capture within 10 minutes, compared to 68 minutes for a simple branched design. This work underscores the potential of bio-inspired microfluidics to enable scalable, uniform, and high-performance systems for multi-analyte detection.

Abstract Image

设计和模拟仿生微流体设计,以实现高通量复用的均匀流动和DNA捕获。
高通量多分析物即时检测通常受到可有效监测的分析物数量有限的限制。本研究介绍了利用38-42个生物传感器优化的多分析物检测的仿生微流控设计。从人类脊髓和叶静脉网络中汲取灵感,这些以灌注为导向的设计确保了均匀的流速和一致的分子捕获,同时保持了空间分离以防止串扰。通过计算机优化,脊柱和叶片设计的速度分布均匀性分别达到0.89%和0.86%。然而,模拟表明,如果没有一致的反应位点通道尺寸,仅速度均匀性不足以准确预测分子捕获。与简单的分支设计需要68分钟相比,生物启发设计在10分钟内显示出卓越的性能,稳定的变异系数低于20%。这项工作强调了生物启发微流体的潜力,使多分析物检测的可扩展,均匀和高性能系统成为可能。
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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