带横流微过滤器的自驱动螺旋微通道流中的迪恩涡流增强血浆分离。

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS
Biomicrofluidics Pub Date : 2024-02-07 eCollection Date: 2024-01-01 DOI:10.1063/5.0189413
Yudong Wang, Niladri Talukder, Bharath Babu Nunna, Eon Soo Lee
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引用次数: 0

摘要

近年来,护理点(POC)诊断设备发展迅速,但它们主要使用唾液而不是血液作为测试样本。为了扩大床旁诊断设备的应用范围,需要一种无需动力系统的高效自流分离技术。微过滤是一种很有前途的血浆分离技术,但由于血细胞堵塞而受到限制,导致分离速度和效率降低。造成这些限制的主要原因是血流中的高粘度和血细胞比容。血液中的血细胞比容稍有增加,就会大大增加微过滤器分离血浆所需的压力,降低分离速度和效率。为应对这一挑战,本研究探讨了在微流体设备内稀释全血而无需外部动力系统的可行性。这项研究利用惯性聚焦和迪恩涡流效应,在螺旋微通道中聚焦红细胞,提取血细胞比容较低的血液。首先通过实验研究了颗粒在毛细管流动过程中的惯性迁移;在优化的 350 × 60 μm(横截面积,长宽比 5.8)微通道中,最多有 88% 的颗粒迁移到底部和顶部的平衡位置。在优化的微通道尺寸下,对生理血细胞比容范围内的全血样本进行了实验,在 350 × 60 μm 的微通道中,外分支出口和内分支出口的血细胞比容降低了 10%以上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dean vortex-enhanced blood plasma separation in self-driven spiral microchannel flow with cross-flow microfilters.

Point-of-care (POC) diagnostic devices have been developing rapidly in recent years, but they are mainly using saliva instead of blood as a test sample. A highly efficient self-separation during the self-driven flow without power systems is desired for expanding the point-of-care diagnostic devices. Microfiltration stands out as a promising technique for blood plasma separation but faces limitations due to blood cell clogging, resulting in reduced separation speed and efficiency. These limitations are mainly caused by the high viscosity and hematocrit in the blood flow. A small increment in the hematocrit of the blood significantly increases the pressure needed for the blood plasma separation in the micro-filters and decreases the separation speed and efficiency. Addressing this challenge, this study explores the feasibility of diluting whole blood within a microfluidic device without external power systems. This study implemented a spiral microchannel utilizing the inertial focusing and Dean vortex effects to focus the red blood cells and extract the blood with lower hematocrit. The inertial migration of the particles during the capillary flow was first investigated experimentally; a maximum of 88% of the particles migrated to the bottom and top equilibrium positions in the optimized 350 × 60 μm (cross-sectional area, 5.8 aspect ratio) microchannel. With the optimized dimension of the microchannel, the whole blood samples within the physiological hematocrit range were tested in the experiments, and more than 10% of the hematocrit reduction was compared between the outer branch outlet and inner branch outlet in the 350 × 60 μm microchannel.

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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...
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