Microfluidic Approaches for Affinity-Based Exosome Separation

被引:27
|
作者
Theel, Eike K. [1 ]
Schwaminger, Sebastian P. [1 ,2 ]
机构
[1] Tech Univ Munich, Sch Engn & Design, Bioseparat Engn Grp, Boltzmannstr 15, D-85748 Garching, Germany
[2] Med Univ Graz, Otto Loewi Res Ctr, Div Med Chem, Neue Stiftingtalstr 6, A-8010 Graz, Austria
关键词
exosomes; affinity separation; microfluidic chamber; purification; extracellular vesicles; mu TAS; LOC; EXTRACELLULAR VESICLES; CIRCULATING EXOSOMES; MICROVESICLES; RELEASE; ULTRACENTRIFUGATION; IDENTIFICATION; TETRASPANINS; DIAGNOSTICS; CONVERSION; BIOMARKERS;
D O I
10.3390/ijms23169004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As a subspecies of extracellular vesicles (EVs), exosomes have provided promising results in diagnostic and theranostic applications in recent years. The nanometer-sized exosomes can be extracted by liquid biopsy from almost all body fluids, making them especially suitable for mainly non-invasive point-of-care (POC) applications. To achieve this, exosomes must first be separated from the respective biofluid. Impurities with similar properties, heterogeneity of exosome characteristics, and time-related biofouling complicate the separation. This practical review presents the state-of-the-art methods available for the separation of exosomes. Furthermore, it is shown how new separation methods can be developed. A particular focus lies on the fabrication and design of microfluidic devices using highly selective affinity separation. Due to their compactness, quick analysis time and portable form factor, these microfluidic devices are particularly suitable to deliver fast and reliable results for POC applications. For these devices, new manufacturing methods (e.g., laminating, replica molding and 3D printing) that use low-cost materials and do not require clean rooms are presented. Additionally, special flow routes and patterns that increase contact surfaces, as well as residence time, and thus improve affinity purification are displayed. Finally, various analyses are shown that can be used to evaluate the separation results of a newly developed device. Overall, this review paper provides a toolbox for developing new microfluidic affinity devices for exosome separation.
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页数:22
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