直接微流体通道中的血液成分分离。

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS Biomicrofluidics Pub Date : 2023-10-16 eCollection Date: 2023-09-01 DOI:10.1063/5.0176457
Lap Man Lee, Ketan H Bhatt, Dustin W Haithcock, Balabhaskar Prabhakarpandian
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引用次数: 0

摘要

在许多诊断应用和血液处理中需要分离血液成分。在实验室中,血液通常通过手动操作进行分离,包括大量离心设备,这大大增加了物流负担。如果不使用微流体技术,就无法容易地在现场和资源有限的环境中进行血样处理。在这项研究中,我们开发了一种占地面积小、快速、被动的微流体通道装置,该装置依靠边缘化和惯性聚焦效应进行血液成分分离。不需要血液稀释、裂解或标记步骤来保持样品的完整性。这项工作的一个主要创新是在出口处插入流体限制器,以将分离界面转移到指定的出口通道中。因此,与以前的工作相比,分离效率显著提高。我们展示了不同的操作模式,从人类全血中提取血小板或血浆,到通过操作出口流体阻力从富含血小板的血浆中浓缩血小板。使用具有高纵横比矩形横截面的直微流体通道,我们证明了从人类全血中提取的血小板纯度为95.4%。在血浆提取中,红细胞去除率达到99.9%。我们还证明了2.6倍浓度的富含血小板的血浆溶液可以生产浓缩血小板。与使用过滤膜或基于亲和性的纯化方法的其他血液分级方法相比,通过连续和无堵塞的再循环操作,提取效率和通过率是可扩展的。我们的微流体血液分离方法具有高度可调性和通用性,易于集成到多步骤血液处理和先进的样品制备工作流程中。
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Blood component separation in straight microfluidic channels.

Separation of blood components is required in many diagnostic applications and blood processes. In laboratories, blood is usually fractionated by manual operation involving a bulk centrifugation equipment, which significantly increases logistic burden. Blood sample processing in the field and resource-limited settings cannot be readily implemented without the use of microfluidic technology. In this study, we developed a small footprint, rapid, and passive microfluidic channel device that relied on margination and inertial focusing effects for blood component separation. No blood dilution, lysis, or labeling step was needed as to preserve sample integrity. One main innovation of this work was the insertion of fluidic restrictors at outlet ports to divert the separation interface into designated outlet channels. Thus, separation efficiency was significantly improved in comparison to previous works. We demonstrated different operation modes ranging from platelet or plasma extraction from human whole blood to platelet concentration from platelet-rich plasma through the manipulation of outlet port fluidic resistance. Using straight microfluidic channels with a high aspect ratio rectangular cross section, we demonstrated 95.4% platelet purity extracted from human whole blood. In plasma extraction, 99.9% RBC removal rate was achieved. We also demonstrated 2.6× concentration of platelet-rich plasma solution to produce platelet concentrate. The extraction efficiency and throughput rate are scalable with continuous and clog-free recirculation operation, in contrast to other blood fractionation approaches using filtration membranes or affinity-based purification methods. Our microfluidic blood separation method is highly tunable and versatile, and easy to be integrated into multi-step blood processing and advanced sample preparation workflows.

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来源期刊
Biomicrofluidics
Biomicrofluidics 生物-纳米科技
CiteScore
5.80
自引率
3.10%
发文量
68
审稿时长
1.3 months
期刊介绍: Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications. BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics. Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary) Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification) Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation) Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles) Cell culture and analysis(single cell assays, stimuli response, stem cell transfection) Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays) Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers) Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...
期刊最新文献
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