Isolation of exosomes from whole blood by integrating acoustics and microfluidics

被引:669
|
作者
Wu, Mengxi [1 ,2 ]
Ouyang, Yingshi [3 ]
Wang, Zeyu [1 ]
Zhang, Rui [2 ]
Huang, Po-Hsun [1 ]
Chen, Chuyi [1 ]
Li, Hui [3 ,4 ]
Li, Peng [1 ,5 ]
Quinn, David [6 ]
Dao, Ming [7 ]
Suresh, Subra [8 ]
Sadovsky, Yoel [3 ,9 ]
Huang, Tony Jun [1 ]
机构
[1] Duke Univ, Dept Mech Engn & Mat Sci, Durham, NC 27708 USA
[2] Penn State Univ, Dept Engn Sci & Mech, 227 Hammond Bldg, University Pk, PA 16802 USA
[3] Univ Pittsburgh, Magee Womens Res Inst, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[4] Cent S Univ, Xiangya Hosp 3, Changsha 410000, Hunan, Peoples R China
[5] West Virginia Univ, Eugene Bennett Dept Chem, Morgantown, WV 26506 USA
[6] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[7] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[8] Nanyang Technol Univ, Singapore 639798, Singapore
[9] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
extracellular vesicles; exosomes; blood-borne vesicles; surface acoustic waves; acoustic tweezers; EXTRACELLULAR VESICLES; CELLS; SEPARATION; ERYTHROPOIESIS; BIOMARKERS; PROTEOMICS; PARTICLES; MICRORNAS; MEMBRANE; SENSOR;
D O I
10.1073/pnas.1709210114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exosomes are nanoscale extracellular vesicles that play an important role in many biological processes, including intercellular communications, antigen presentation, and the transport of proteins, RNA, and other molecules. Recently there has been significant interest in exosome-related fundamental research, seeking new exosome-based biomarkers for health monitoring and disease diagnoses. Here, we report a separation method based on acoustofluidics (i.e., the integration of acoustics and microfluidics) to isolate exosomes directly from whole blood in a label-free and contact-free manner. This acoustofluidic platform consists of two modules: a microscale cell-removal module that first removes larger blood components, followed by extracellular vesicle subgroup separation in the exosome-isolation module. In the cell-removal module, we demonstrate the isolation of 110-nm particles from a mixture of micro-and nanosized particles with a yield greater than 99%. In the exosome-isolation module, we isolate exosomes from an extracellular vesicle mixture with a purity of 98.4%. Integrating the two acoustofluidic modules onto a single chip, we isolated exosomes from whole blood with a blood cell removal rate of over 99.999%. With its ability to perform rapid, biocompatible, label-free, contact-free, and continuous-flow exosome isolation, the integrated acoustofluidic device offers a unique approach to investigate the role of exosomes in the onset and progression of human diseases with potential applications in health monitoring, medical diagnosis, targeted drug delivery, and personalized medicine.
引用
收藏
页码:10584 / 10589
页数:6
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