Enhanced Particle Trap: Design and Simulation of Pillar-Based Contactless Dielectrophoresis Microfluidic Devices

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Peyman Torky Harchegani, Mohsen Mashhadi Keshtiban, Mahdi Moghimi Zand, Zahra Azizi
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Abstract

Contactless and conventional dielectrophoresis (DEP) microfluidic devices are extensively utilized in lab-on-a-chip applications, particularly for cell isolation and analysis. Nonetheless, these devices typically operate at low throughput and require high applied voltages, posing limitations for microfluidic cell isolation and separation. Addressing these challenges, this study explores the utilization of diverse micro-pillar geometries within the microfluidic device to augment THP-1 cell trapping efficiency numerically using FEM modeling. Furthermore, the simulations examine the influence of pillar gap and quantity on cell trapping efficiency in a contactless DEP device. Notably, elliptical pillars demonstrate superior cell trapping efficiency at elevated flow rates compared to alternative configurations, making the microchip more amenable for high-throughput cell separation, trapping, and isolation applications. Remarkably, employing elliptical pillars in a contactless DEP microfluidic chip yields nearly 100% cell trapping efficiency at higher flow rates. Ellipse configuration showed 122% higher cell trap efficiency at the maximum flowrate compare to the previous study with circular configuration. Additionally, it is observed that reducing the gap between pillars correlates with enhanced cell trapping efficiency. Simulation outcomes indicate that employing two rows of elliptical pillars with a 40-µm gap achieves optimal performance. The findings of this investigation underscore the importance of pillars in contactless DEP devices and provide valuable insights for future designs of such microfluidic devices.

增强粒子阱:基于柱的非接触介电微流控装置的设计与仿真。
非接触式和传统的介质电泳(DEP)微流控装置广泛应用于芯片上的实验室应用,特别是细胞分离和分析。尽管如此,这些设备通常以低通量运行,并且需要高施加电压,这对微流体细胞的分离和分离造成了限制。为了解决这些挑战,本研究探索了微流控装置中不同微柱几何形状的利用,通过有限元模拟来提高THP-1细胞的捕获效率。在此基础上,仿真研究了非接触式DEP器件中柱隙和柱量对电池捕获效率的影响。值得注意的是,与其他配置相比,椭圆柱在高流速下表现出优越的细胞捕获效率,使微芯片更适合高通量细胞分离、捕获和隔离应用。值得注意的是,在非接触式DEP微流控芯片中采用椭圆柱,在较高的流速下,电池捕获效率接近100%。在最大流速下,椭圆结构的电池阱效率比圆形结构的电池阱效率高122%。此外,还观察到减少柱之间的间隙与增强的细胞捕获效率相关。仿真结果表明,采用两排间距为40 μ m的椭圆柱可获得最佳性能。本研究结果强调了柱在非接触式DEP器件中的重要性,并为未来此类微流体器件的设计提供了有价值的见解。
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
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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