• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

微流控平台中自驱动流动过程中的血浆自分离技术。

Blood Plasma Self-Separation Technologies during the Self-Driven Flow in Microfluidic Platforms.

作者信息

Wang Yudong, Nunna Bharath Babu, Talukder Niladri, Etienne Ernst Emmanuel, Lee Eon Soo

机构信息

Advanced Energy Systems and Microdevices Laboratory, Department of Mechanical and Industrial Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.

Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Harvard University, Cambridge, MA 02139, USA.

出版信息

Bioengineering (Basel). 2021 Jul 3;8(7):94. doi: 10.3390/bioengineering8070094.

DOI:10.3390/bioengineering8070094
PMID:34356201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8301051/
Abstract

Blood plasma is the most commonly used biofluid in disease diagnostic and biomedical analysis due to it contains various biomarkers. The majority of the blood plasma separation is still handled with centrifugation, which is off-chip and time-consuming. Therefore, in the Lab-on-a-chip (LOC) field, an effective microfluidic blood plasma separation platform attracts researchers' attention globally. Blood plasma self-separation technologies are usually divided into two categories: active self-separation and passive self-separation. Passive self-separation technologies, in contrast with active self-separation, only rely on microchannel geometry, microfluidic phenomena and hydrodynamic forces. Passive self-separation devices are driven by the capillary flow, which is generated due to the characteristics of the surface of the channel and its interaction with the fluid. Comparing to the active plasma separation techniques, passive plasma separation methods are more considered in the microfluidic platform, owing to their ease of fabrication, portable, user-friendly features. We propose an extensive review of mechanisms of passive self-separation technologies and enumerate some experimental details and devices to exploit these effects. The performances, limitations and challenges of these technologies and devices are also compared and discussed.

摘要

由于血浆含有各种生物标志物,因此它是疾病诊断和生物医学分析中最常用的生物流体。大多数血浆分离仍通过离心进行,这是一种芯片外且耗时的方法。因此,在芯片实验室(LOC)领域,一个有效的微流控血浆分离平台吸引了全球研究人员的关注。血浆自分离技术通常分为两类:主动自分离和被动自分离。与主动自分离相比,被动自分离技术仅依赖于微通道几何形状、微流体现象和流体动力。被动自分离装置由毛细管流驱动,毛细管流是由于通道表面的特性及其与流体的相互作用而产生的。与主动血浆分离技术相比,被动血浆分离方法因其易于制造、便携、用户友好等特点而在微流控平台中更受关注。我们对被动自分离技术的机制进行了广泛综述,并列举了一些利用这些效应的实验细节和装置。还对这些技术和装置的性能、局限性和挑战进行了比较和讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/68018b046fdc/bioengineering-08-00094-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/dcf3baa8674c/bioengineering-08-00094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/f183f3ebfb97/bioengineering-08-00094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/f2a6b0d8483b/bioengineering-08-00094-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/abb0a442e07d/bioengineering-08-00094-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/7711a8d4169d/bioengineering-08-00094-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/61f8331e7a31/bioengineering-08-00094-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/0d4ebd7073ed/bioengineering-08-00094-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/0f19d81c34b8/bioengineering-08-00094-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/81d088bb027e/bioengineering-08-00094-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/020e99b90d85/bioengineering-08-00094-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/73c8f6b694b7/bioengineering-08-00094-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/953349b02996/bioengineering-08-00094-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/859b1d4abc1b/bioengineering-08-00094-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/5b1a9de2e0d5/bioengineering-08-00094-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/57467b5b583d/bioengineering-08-00094-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/68018b046fdc/bioengineering-08-00094-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/dcf3baa8674c/bioengineering-08-00094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/f183f3ebfb97/bioengineering-08-00094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/f2a6b0d8483b/bioengineering-08-00094-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/abb0a442e07d/bioengineering-08-00094-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/7711a8d4169d/bioengineering-08-00094-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/61f8331e7a31/bioengineering-08-00094-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/0d4ebd7073ed/bioengineering-08-00094-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/0f19d81c34b8/bioengineering-08-00094-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/81d088bb027e/bioengineering-08-00094-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/020e99b90d85/bioengineering-08-00094-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/73c8f6b694b7/bioengineering-08-00094-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/953349b02996/bioengineering-08-00094-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/859b1d4abc1b/bioengineering-08-00094-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/5b1a9de2e0d5/bioengineering-08-00094-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/57467b5b583d/bioengineering-08-00094-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c05/8301051/68018b046fdc/bioengineering-08-00094-g016.jpg

相似文献

1
Blood Plasma Self-Separation Technologies during the Self-Driven Flow in Microfluidic Platforms.微流控平台中自驱动流动过程中的血浆自分离技术。
Bioengineering (Basel). 2021 Jul 3;8(7):94. doi: 10.3390/bioengineering8070094.
2
Passive microfluidic devices for cell separation.被动式微流控芯片细胞分离技术。
Biotechnol Adv. 2024 Mar-Apr;71:108317. doi: 10.1016/j.biotechadv.2024.108317. Epub 2024 Jan 12.
3
Dean vortex-enhanced blood plasma separation in self-driven spiral microchannel flow with cross-flow microfilters.Dean 涡流增强在带有错流微滤器的自驱动螺旋微通道流中的血浆分离。
Biomicrofluidics. 2024 Feb 7;18(1):014104. doi: 10.1063/5.0189413. eCollection 2024 Jan.
4
Continuous particle separation in spiral microchannels using Dean flows and differential migration.利用迪恩流和差异迁移在螺旋微通道中进行连续粒子分离
Lab Chip. 2008 Nov;8(11):1906-14. doi: 10.1039/b807107a. Epub 2008 Sep 24.
5
An experimental study of centrifugal microfluidic platforms for magnetic-inertial separation of circulating tumor cells using contraction-expansion and zigzag arrays.使用收缩-扩张和之字形阵列的离心微流控平台用于磁惯性分离循环肿瘤细胞的实验研究。
J Chromatogr A. 2023 Sep 13;1706:464249. doi: 10.1016/j.chroma.2023.464249. Epub 2023 Jul 29.
6
High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section.高通量、无需标记的全血中白细胞的平行螺旋微通道 U 型横截面分离
Biosensors (Basel). 2021 Oct 20;11(11):406. doi: 10.3390/bios11110406.
7
A hydrodynamic-based dual-function microfluidic chip for high throughput discriminating tumor cells.基于流体动力学的双功能微流控芯片,用于高通量肿瘤细胞鉴别。
Talanta. 2024 Jun 1;273:125884. doi: 10.1016/j.talanta.2024.125884. Epub 2024 Mar 13.
8
Latest advances and perspectives of liquid biopsy for cancer diagnostics driven by microfluidic on-chip assays.微流控芯片分析驱动的液体活检在癌症诊断中的最新进展和展望。
Lab Chip. 2023 Jun 28;23(13):2922-2941. doi: 10.1039/d2lc00837h.
9
A review of active and passive hybrid systems based on Dielectrophoresis for the manipulation of microparticles.基于介电泳的主动和被动混合系统综述用于微粒子操控。
J Chromatogr A. 2022 Aug 2;1676:463268. doi: 10.1016/j.chroma.2022.463268. Epub 2022 Jun 21.
10
Development of a microfluidic device for cell concentration and blood cell-plasma separation.用于细胞浓缩和血细胞-血浆分离的微流控装置的开发。
Biomed Microdevices. 2015 Dec;17(6):115. doi: 10.1007/s10544-015-0017-z.

引用本文的文献

1
An energy-embodied paralleled liquid manipulation for equipment-free, quantitative multiplexed liver function monitoring.一种用于无设备、定量多重肝功能监测的能量体现并行液体操控技术。
Sci Adv. 2025 Aug 8;11(32):eadx0092. doi: 10.1126/sciadv.adx0092.
2
Intelligent Microfluidics for Plasma Separation: Integrating Computational Fluid Dynamics and Machine Learning for Optimized Microchannel Design.用于血浆分离的智能微流体技术:整合计算流体动力学和机器学习以优化微通道设计
Biosensors (Basel). 2025 Feb 6;15(2):94. doi: 10.3390/bios15020094.
3
Enhanced Stability and Sensitivity for CA-125 Detection Under Microfluidic Shear Flow Using Polyethylene Glycol-Coated Biosensor.

本文引用的文献

1
A new microchannel capillary flow assay (MCFA) platform with lyophilized chemiluminescence reagents for a smartphone-based POCT detecting malaria.一种新型微通道毛细管流动分析(MCFA)平台,带有冻干化学发光试剂,用于基于智能手机的即时检测疟疾。
Microsyst Nanoeng. 2020 Jan 27;6:5. doi: 10.1038/s41378-019-0108-8. eCollection 2020.
2
Modeling Focused-Ultrasound Response for Non-Invasive Treatment Using Machine Learning.使用机器学习对聚焦超声无创治疗反应进行建模
Bioengineering (Basel). 2021 Jun 1;8(6):74. doi: 10.3390/bioengineering8060074.
3
Solvent-Induced Formation of Novel Ni(II) Complexes Derived from Bis-Thiosemicarbazone Ligand: An Insight from Experimental and Theoretical Investigations.
使用聚乙二醇涂层生物传感器在微流控剪切流下增强CA-125检测的稳定性和灵敏度。
ACS Omega. 2024 Dec 20;10(1):692-702. doi: 10.1021/acsomega.4c07596. eCollection 2025 Jan 14.
4
Polydimethylsiloxane Surface Modification of Microfluidic Devices for Blood Plasma Separation.用于血浆分离的微流控装置的聚二甲基硅氧烷表面改性
Polymers (Basel). 2024 May 16;16(10):1416. doi: 10.3390/polym16101416.
5
Impact of Sample Type on D-Dimer Screening.样本类型对D-二聚体筛查的影响
Malays J Med Sci. 2024 Apr;31(2):153-158. doi: 10.21315/mjms2024.31.2.13. Epub 2024 Apr 23.
6
Protein-Centric Analysis of Personalized Antibody Repertoires Using LC-MS-Based Fab-Profiling on a timsTOF.基于 timsTOF 上的 LC-MS 技术的 Fab 谱分析,实现个性化抗体库的蛋白组学分析。
J Am Soc Mass Spectrom. 2024 Jun 5;35(6):1292-1300. doi: 10.1021/jasms.4c00076. Epub 2024 Apr 25.
7
Dean vortex-enhanced blood plasma separation in self-driven spiral microchannel flow with cross-flow microfilters.Dean 涡流增强在带有错流微滤器的自驱动螺旋微通道流中的血浆分离。
Biomicrofluidics. 2024 Feb 7;18(1):014104. doi: 10.1063/5.0189413. eCollection 2024 Jan.
8
Microfluidic Blood Separation: Key Technologies and Critical Figures of Merit.微流控血液分离:关键技术与关键性能指标
Micromachines (Basel). 2023 Nov 18;14(11):2117. doi: 10.3390/mi14112117.
9
Intensity-Based Camera Setup for Refractometric and Biomolecular Sensing with a Photonic Crystal Microfluidic Chip.基于强度的光子晶体微流控芯片折光和生物分子传感相机设置。
Biosensors (Basel). 2023 Jun 27;13(7):687. doi: 10.3390/bios13070687.
10
Efficient and Simple Paper-Based Assay for Plasma Separation Using Universal Anti-H Agglutinating Antibody.使用通用抗-H凝集抗体进行血浆分离的高效简易纸质检测法。
ACS Omega. 2022 Oct 28;7(44):40109-40115. doi: 10.1021/acsomega.2c04908. eCollection 2022 Nov 8.
溶剂诱导的新型 Ni(II)配合物的形成:来自双硫代缩氨基脲配体的实验和理论研究的见解。
Int J Mol Sci. 2021 May 19;22(10):5337. doi: 10.3390/ijms22105337.
4
Numerical and experimental analysis of a high-throughput blood plasma separator for point-of-care applications.用于即时应用的高通量血浆分离器的数值和实验分析。
Anal Bioanal Chem. 2021 May;413(11):2867-2878. doi: 10.1007/s00216-021-03190-1. Epub 2021 Mar 8.
5
Ultrahigh throughput beehive-like device for blood plasma separation.用于血浆分离的超高通量蜂窝状装置。
Electrophoresis. 2020 Dec;41(24):2136-2143. doi: 10.1002/elps.202000202. Epub 2020 Oct 26.
6
Synthetic Paper Separates Plasma from Whole Blood with Low Protein Loss.合成纸可实现低蛋白丢失量的全血与血浆分离。
Anal Chem. 2020 May 5;92(9):6194-6199. doi: 10.1021/acs.analchem.0c01474. Epub 2020 Apr 27.
7
investigations of red blood cell phase separation in a complex microchannel network.复杂微通道网络中红细胞相分离的研究
Biomicrofluidics. 2020 Jan 2;14(1):014101. doi: 10.1063/1.5127840. eCollection 2020 Jan.
8
Wettability patterning in microfluidic devices using thermally-enhanced hydrophobic recovery of PDMS.利用 PDMS 热增强疏水性恢复在微流控装置中进行润湿性图案化。
Soft Matter. 2019 Dec 7;15(45):9253-9260. doi: 10.1039/c9sm01792e. Epub 2019 Oct 28.
9
Factors affecting sedimentational separation of bacteria from blood.影响从血液中沉淀分离细菌的因素。
Biotechnol Prog. 2020 Jan;36(1):e2892. doi: 10.1002/btpr.2892. Epub 2019 Sep 10.
10
Thermopneumatic suction integrated microfluidic blood analysis system.热气动抽吸集成微流控血液分析系统。
PLoS One. 2019 Mar 7;14(3):e0208676. doi: 10.1371/journal.pone.0208676. eCollection 2019.