Dean-Flow-Coupled Elasto-Inertial Focusing Accelerates Exosome Purification to Facilitate Single Vesicle Profiling

被引:23
|
作者
Bai, Jun-Jie [2 ]
Zhang, Xuan [2 ]
Wei, Xing [2 ]
Wang, Yu [2 ]
Du, Cheng [1 ]
Wang, Ze-Jun [2 ]
Chen, Ming-Li [2 ]
Wang, Jian-Hua [2 ]
机构
[1] Gen Hosp Northern Theater Command, Dept Oncol, Shenyang 110819, Liaoning, Peoples R China
[2] Northeastern Univ, Coll Sci, Res Ctr Analyt Sci, Dept Chem, Shenyang 110819, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
EXTRACELLULAR VESICLES; SPIRAL MICROCHANNEL; MICROFLUIDICS; PROGRESS; SEPARATION;
D O I
10.1021/acs.analchem.2c04898
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Exosomes are recognized as noteworthy biomarkers playing unprecedented roles in intercellular communication and disease diagnosis and treatment. It is a prerequisite to obtain high purity exosomes for the comprehension of exosome biochemistry and further illustration of their functionality/mechanisms. However, the isolation of nanoscale exosomes from endogenous proteins is particularly challenging for small-volume biological samples. Herein, a Dean-flow-coupled elasto-inertial microfluidic chip (DEIC) was developed. It consists of a spiral microchannel with dimensional confined concave structures and facilitates elastoinertial separation of exosomes with lower protein contaminants from cell culture medium and human serum. The presence of 0.15% (w/v) poly-(oxyethylene) controls the elastic lift force acting on suspended nanoscale particles and makes it feasible for field-free purification of integrity exosomes with a 70.6% recovery and a 91.4% removal rate for proteins. As a proof of concept, the technique demonstrated the individual-vesicle-level biomarker (EpCAM and PD-L1) profiling in combination with simultaneous aptamer-mediated analysis to disclose the sensibility for immune response. Overall, DEIC enables the collection of high-purity exosomes and exhibits potential in integration with downstream analyses of exosomes.
引用
收藏
页码:2523 / 2531
页数:9
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