Label-Free Isolation of Exosomes Using Microfluidic Technologies

微泡 微流控 外体 纳米技术 微尺度化学 计算机科学 分离(微生物学) 材料科学 生化工程 计算生物学 生物 生物信息学 小RNA 工程类 生物化学 基因 数学教育 数学
作者
Sara Hassanpour Tamrin,Amir Sanati‐Nezhad,Arindom Sen
出处
期刊:ACS Nano [American Chemical Society]
卷期号:15 (11): 17047-17079 被引量:144
标识
DOI:10.1021/acsnano.1c03469
摘要

Exosomes are cell-derived structures packaged with lipids, proteins, and nucleic acids. They exist in diverse bodily fluids and are involved in physiological and pathological processes. Although their potential for clinical application as diagnostic and therapeutic tools has been revealed, a huge bottleneck impeding the development of applications in the rapidly burgeoning field of exosome research is an inability to efficiently isolate pure exosomes from other unwanted components present in bodily fluids. To date, several approaches have been proposed and investigated for exosome separation, with the leading candidate being microfluidic technology due to its relative simplicity, cost-effectiveness, precise and fast processing at the microscale, and amenability to automation. Notably, avoiding the need for exosome labeling represents a significant advance in terms of process simplicity, time, and cost as well as protecting the biological activities of exosomes. Despite the exciting progress in microfluidic strategies for exosome isolation and the countless benefits of label-free approaches for clinical applications, current microfluidic platforms for isolation of exosomes are still facing a series of problems and challenges that prevent their use for clinical sample processing. This review focuses on the recent microfluidic platforms developed for label-free isolation of exosomes including those based on sieving, deterministic lateral displacement, field flow, and pinched flow fractionation as well as viscoelastic, acoustic, inertial, electrical, and centrifugal forces. Further, we discuss advantages and disadvantages of these strategies with highlights of current challenges and outlook of label-free microfluidics toward the clinical utility of exosomes.
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