用于三维微流体的 5 轴数控微铣床

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Lab on a Chip Pub Date : 2024-11-04 DOI:10.1039/d4lc00496e
Mitchell Modarelli, Devin Kot-Thompson, Kazunori Hoshino
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引用次数: 0

摘要

微流体制造技术的黄金标准--SU-8 图形化,需要光刻设备和设施,不适合三维微流体。三维打印机更为方便,可实现与传统光刻技术相当的高分辨率,但只能用于特定材料。另外,五轴计算机数控(CNC)微铣床可以有效地利用各种材料制作具有高分辨率、高纵横比和非平面几何形状的结构原型。然而,这些机器并不适合实验室小批量微流体开发,研究人员基本上无法使用。在本文中,我们介绍了一种新型五轴数控微铣床,专为三维微流体通道原型设计,研究人员和实验室都能负担得起。该机器由商用产品和定制部件组装而成,占地 0.72 立方米,完全通过计算机辅助设计(CAD)和制造(CAM)软件运行。五轴数控微铣床实现了亚微米级双向重复精度(≤0.23微米),可加工特征<20微米,工作容积为50 x 50 x 68毫米。工具兼容性和铣削参数的设计几乎可以加工任何可铣削的材料,包括铝、黄铜、不锈钢和钛合金等金属。为了演示高分辨率和高纵横比的铣削,我们用 360 黄铜铣削出了宽度为 18.1 微米、纵横比约为 50:1 的薄壁。我们还演示了用 360 黄铜制造非平面几何形状的模具,以创建聚二甲基硅氧烷(PDMS)微流体通道。其中包括一个 90° 边缘的通道和一个曲率半径为 250 微米的圆形边缘通道。我们的五轴数控微铣床具有高分辨率、几何复杂性、大工作容积和广泛的材料兼容性,是用户友好型台式系统中功能最齐全的微流控原型机。
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5-axis CNC micro-milling machine for three-dimensional microfluidics
The gold standard of microfluidic fabrication techniques, SU-8 patterning, requires photolithography equipment and facilities and is not suitable for 3D microfluidics. A 3D printer is more convenient and may achieve high resolutions comparable to conventional photolithography, but only with select materials. Alternatively, 5-axis computer numerical control (CNC) micro-milling machines can efficiently prototype structures with high resolutions, high aspect ratios, and non-planar geometries from a variety of materials. These machines, however, have not been catered for laboratory-based, small-batch microfluidics development and are largely inaccessible to researchers. In this paper, we present a new 5-axis CNC micro-milling machine specifically designed for prototyping 3D microfluidic channels, made affordable for research and laboratories. The machine is assembled from commercially available products and custom-build parts, occupying 0.72 cubic meters, and operating entirely from computer aided design (CAD) and manufacturing (CAM) software. The 5-axis CNC micro-milling machine achieves sub-µm bidirectional repeatability (≤0.23 µm), machinable features <20 µm, and a work volume of 50 x 50 x 68 mm. The tool compatibility and milling parameters were designed to enable fabrication of virtually any mill-able material including metals like aluminum, brass, stainless steel, and titanium alloys. To demonstrate milling high resolution and high aspect ratios, we milled a thin wall from 360 brass with a width of 18.1 µm and an aspect ratio of ~50:1. We also demonstrated fabricating molds from 360 brass with non-planar geometries to create polydimethylsiloxane (PDMS) microfluidic channels. These included a channel on a 90° edge and a channel on a rounded edge with a 250-µm radius of curvature. Our 5-axis CNC micro-milling machine offers the most versatility in prototyping microfluidics by enabling high resolutions, geometric complexity, a large work volume, and broad material compatibility, all within a user-friendly benchtop system.
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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.
期刊最新文献
Automated Dynamic Inlet Microfluidics (ADIM) system: cost-effective biaxial nanoliter droplet on demand generation platform and its application in agglutination assays. Data storage based on the absence of nucleotides using a bacteriophage abortive infection system reverse transcriptase. Stitched textile-based microfluidics for wearable devices. A nanobody-based microfluidic chip for fast and automated purification of protein complexes. Detecting telomerase activity at the single-cell level using a CRISPR-Cas12a-based chip.
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