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本文引用的文献

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Inertial microfluidic physics.惯性微流体物理学
Lab Chip. 2014 Aug 7;14(15):2739-61. doi: 10.1039/c4lc00128a. Epub 2014 Jun 10.
2
Inertial focusing in microfluidics.微流控中的惯性聚焦
Annu Rev Biomed Eng. 2014 Jul 11;16:371-96. doi: 10.1146/annurev-bioeng-121813-120704. Epub 2014 May 29.
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Inertial particle separation by differential equilibrium positions in a symmetrical serpentine micro-channel.在对称蛇形微通道中通过差分平衡位置进行惯性颗粒分离。
Sci Rep. 2014 Mar 31;4:4527. doi: 10.1038/srep04527.
4
Microfluidic, marker-free isolation of circulating tumor cells from blood samples.从血液样本中进行微流控、无标记循环肿瘤细胞分离。
Nat Protoc. 2014 Mar;9(3):694-710. doi: 10.1038/nprot.2014.044. Epub 2014 Feb 27.
5
Standing surface acoustic wave (SSAW)-based microfluidic cytometer.基于体声波(SSAW)的微流控细胞分析仪。
Lab Chip. 2014 Mar 7;14(5):916-23. doi: 10.1039/c3lc51139a.
6
Continuous separation of blood cells in spiral microfluidic devices.螺旋微流控装置中血细胞的连续分离。
Biomicrofluidics. 2013 Sep 5;7(5):54101. doi: 10.1063/1.4819275. eCollection 2013.
7
Vortex-aided inertial microfluidic device for continuous particle separation with high size-selectivity, efficiency, and purity.涡旋辅助惯性微流控装置用于连续的具有高尺寸选择性、高效率和高纯度的粒子分离。
Biomicrofluidics. 2013 Aug 21;7(4):44119. doi: 10.1063/1.4818906. eCollection 2013.
8
Sub-micrometer-precision, three-dimensional (3D) hydrodynamic focusing via "microfluidic drifting".亚微米精度的三维(3D)水力聚焦通过“微流漂移”实现。
Lab Chip. 2014 Jan 21;14(2):415-23. doi: 10.1039/c3lc50810b. Epub 2013 Nov 28.
9
Enhanced size-dependent trapping of particles using microvortices.利用微涡旋增强颗粒的尺寸依赖性捕获。
Microfluid Nanofluidics. 2013 Nov 1;15(5). doi: 10.1007/s10404-013-1176-y.
10
Microstructure-induced helical vortices allow single-stream and long-term inertial focusing.微结构诱导的螺旋涡旋允许单流和长期惯性聚焦。
Lab Chip. 2013 Aug 7;13(15):2942-9. doi: 10.1039/c3lc41227j.

直微通道中的单流惯性聚焦

Single stream inertial focusing in a straight microchannel.

作者信息

Wang Xiao, Zandi Matthew, Ho Chia-Chi, Kaval Necati, Papautsky Ian

机构信息

BioMicroSystems Laboratory, Department of Electrical Engineering and Computing Systems, University of Cincinnati, 812 Rhodes Hall, ML030, Cincinnati, OH 45221, USA.

出版信息

Lab Chip. 2015 Apr 21;15(8):1812-21. doi: 10.1039/c4lc01462f.

DOI:10.1039/c4lc01462f
PMID:25761900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4388233/
Abstract

In the past two decades, microfluidics has become of great value in precisely aligning cells or microparticles within fluids. Microfluidic techniques use either external forces or sheath flow to focus particulate samples, and face the challenges of complex instrumentation design and limited throughput. The burgeoning field of inertial microfluidics brings single-position focusing functionality at throughput orders of magnitude higher than previously available. However, most inertial microfluidic focusers rely on cross-sectional flow-induced drag force to achieve single-position focusing, which inevitably complicates the device design and operation. In this work, we present an inertial microfluidic focuser that uses inertial lift force as the only driving force to focus microparticles into a single position. We demonstrate single-position focusing of different sized microbeads and cells with 95-100% efficiency, without the need for secondary flow, sheath flow or external forces. We further integrate this device with a laser counting system to form a sheathless flow cytometer, and demonstrated counting of microbeads with 2200 beads s(-1) throughput and 7% coefficient of variation. Cells can be completely recovered and remain viable after passing our integrated cytometry system. Our approach offers a number of benefits, including simplicity in fundamental principle and geometry, convenience in design, modification and integration, flexibility in focusing of different samples, high compatibility with real-world cellular samples as well as high-precision and high-throughput single-position focusing.

摘要

在过去二十年中,微流控技术在精确排列流体中的细胞或微粒方面变得极具价值。微流控技术利用外力或鞘流来聚焦颗粒样本,面临着复杂仪器设计和通量有限的挑战。新兴的惯性微流控领域带来了单位置聚焦功能,其通量比以前高出几个数量级。然而,大多数惯性微流控聚焦器依靠横截面流动诱导的拖曳力来实现单位置聚焦,这不可避免地使设备设计和操作变得复杂。在这项工作中,我们展示了一种惯性微流控聚焦器,它使用惯性升力作为唯一驱动力将微粒聚焦到单个位置。我们展示了不同尺寸微珠和细胞的单位置聚焦,效率为95%-100%,无需二次流、鞘流或外力。我们进一步将该设备与激光计数系统集成,形成了一种无鞘流式细胞仪,并展示了以2200个微珠每秒的通量和7%的变异系数对微珠进行计数。细胞通过我们的集成流式细胞仪系统后可以完全回收并保持活力。我们的方法具有许多优点,包括基本原理和几何结构简单、设计、修改和集成方便、不同样本聚焦灵活、与真实细胞样本高度兼容以及高精度和高通量单位置聚焦。