Microfluidics for exosome isolation and analysis: enabling liquid biopsy for personalized medicine

被引:532
作者
Contreras-Naranjo, Jose C. [1 ]
Wu, Hung-Jen [1 ]
Ugaz, Victor M. [1 ,2 ]
机构
[1] Texas A&M Univ, Artie McFerrin Dept Chem Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
基金
美国国家卫生研究院;
关键词
TUMOR-DERIVED EXOSOMES; HUMAN-BODY FLUIDS; EXTRACELLULAR VESICLES; CIRCULATING EXOSOMES; PROTEOMIC ANALYSIS; LATERAL DISPLACEMENT; PARTICLE SEPARATION; CANCER; MICROVESICLES; QUANTIFICATION;
D O I
10.1039/c7lc00592j
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Exosomes, the smallest sized extracellular vesicles (similar to 30-150 nm) packaged with lipids, proteins, functional messenger RNAs and microRNAs, and double-stranded DNA from their cells of origin, have emerged as key players in intercellular communication. Their presence in bodily fluids, where they protect their cargo from degradation, makes them attractive candidates for clinical application as innovative diagnostic and therapeutic tools. But routine isolation and analysis of high purity exosomes in clinical settings is challenging, with conventional methods facing a number of drawbacks including low yield and/or purity, long processing times, high cost, and difficulties in standardization. Here we review a promising solution, microfluidic-based technologies that have incorporated a host of separation and sensing capabilities for exosome isolation, detection, and analysis, with emphasis on point-of-care and clinical applications. These new capabilities promise to advance fundamental research while paving the way toward routine exosome-based liquid biopsy for personalized medicine.
引用
收藏
页码:3558 / 3577
页数:20
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