Towards microfluidic-based exosome isolation and detection for tumor therapy

被引:166
作者
Wang, Jie [1 ,4 ]
Ma, Peng [1 ,2 ,4 ]
Kim, Daniel H. [3 ,4 ]
Liu, Bi-Feng [2 ]
Demirci, Utkan [1 ,4 ]
机构
[1] Stanford Univ, Canary Ctr Stanford Canc Early Detect, Bioacoust MEMS Med BAMM Lab, Dept Radiol,Sch Med, Palo Alto, CA 94304 USA
[2] Huazhong Univ Sci & Technol, Britton Chance Ctr Biomed Photon, Wuhan Natl Lab Optoelect Hubei Bioinformat & Mol, Dept Biomed Engn,Coll Life Sci & Technol, Wuhan 430074, Peoples R China
[3] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
[4] Stanford Univ, Canary Ctr Stanford Canc Early Detect, Dept Radiol, Sch Med, Palo Alto, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Exosomes; Extracellular vesicles; Microfluidics; Isolation; Detection; Tumor-targeted drug delivery; PLASMON RESONANCE SENSORS; MESENCHYMAL STROMAL CELLS; DRUG-DELIVERY VEHICLES; EXTRACELLULAR VESICLES; QUANTITATIVE DETECTION; CIRCULATING EXOSOMES; ELECTROCHEMICAL DETECTION; RAPID ISOLATION; LIQUID-BIOPSY; ON-CHIP;
D O I
10.1016/j.nantod.2020.101066
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exosomes are a class of cell-secreted, nano-sized extracellular vesicles with a bilayer membrane structure of 30-150 nm in diameter. Their discovery and application have brought breakthroughs in numerous areas, such as liquid biopsies, cancer biology, drug delivery, immunotherapy, tissue repair, and cardiovascular diseases. Isolation of exosomes is the first step in exosome-related research and its applications. Standard benchtop exosome separation and sensing techniques are tedious and challenging, as they require large sample volumes, multi-step operations that are complex and time-consuming, requiring cumbersome and expensive instruments. In contrast, microfluidic platforms have the potential to overcome some of these limitations, owing to their high-precision processing, ability to handle liquids at a microscale, and integrability with various functional units, such as mixers, actuators, reactors, separators, and sensors. These platforms can optimize the detection process on a single device, representing a robust and versatile technique for exosome separation and sensing to attain high purity and high recovery rates with a short processing time. Herein, we overview microfluidic strategies for exosome isolation based on their hydrodynamic properties, size filtration, acoustic fields, immunoaffinity, and dielectrophoretic properties. We focus especially on advances in label-free isolation of exosomes with active biological properties and intact morphological structures. Further, we introduce microfluidic techniques for the detection of exosomal proteins and RNAs with high sensitivity, high specificity, and low detection limits. We summarize the biomedical applications of exosome-mediated therapeutic delivery targeting cancer cells. To highlight the advantages of microfluidic platforms, conventional techniques are included for comparison. Future challenges and prospects of microfluidics towards exosome isolation applications are also discussed. Although the use of exosomes in clinical applications still faces biological, technical, regulatory, and market challenges, in the foreseeable future, recent developments in microfluidic technologies are expected to pave the way for tailoring exosome-related applications in precision medicine. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:27
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共 239 条
  • [1] Self-Assembled Peptide- and Protein-Based Nanomaterials for Antitumor Photodynamic and Photothermal Therapy
    Abbas, Manzar
    Zou, Qianli
    Li, Shukun
    Yan, Xuehai
    [J]. ADVANCED MATERIALS, 2017, 29 (12)
  • [2] Introduction to Extracellular Vesicles: Biogenesis, RNA Cargo Selection, Content, Release, and Uptake
    Abels, Erik R.
    Breakefield, Xandra O.
    [J]. CELLULAR AND MOLECULAR NEUROBIOLOGY, 2016, 36 (03) : 301 - 312
  • [3] Exosome-delivered microRNAs modulate the inflammatory response to endotoxin
    Alexander, Margaret
    Hu, Ruozhen
    Runtsch, Marah C.
    Kagele, Dominique A.
    Mosbruger, Timothy L.
    Tolmachova, Tanya
    Seabra, Miguel C.
    Round, June L.
    Ward, Diane M.
    O'Connell, Ryan M.
    [J]. NATURE COMMUNICATIONS, 2015, 6
  • [4] Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes
    Alvarez-Erviti, Lydia
    Seow, Yiqi
    Yin, HaiFang
    Betts, Corinne
    Lakhal, Samira
    Wood, Matthew J. A.
    [J]. NATURE BIOTECHNOLOGY, 2011, 29 (04) : 341 - U179
  • [5] Microfluidic-integrated DNA nanobiosensors
    Ansari, M. I. Hague
    Hassan, Shabir
    Qurashi, Ahsanulhaq
    Khanday, Firdous Ahmad
    [J]. BIOSENSORS & BIOELECTRONICS, 2016, 85 : 247 - 260
  • [6] Strategic design of extracellular vesicle drug delivery systems
    Armstrong, James P. K.
    Stevens, Molly M.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2018, 130 : 12 - 16
  • [7] Treatment of HER2-positive breast cancer: current status and future perspectives
    Arteaga, Carlos L.
    Sliwkowski, Mark X.
    Osborne, C. Kent
    Perez, Edith A.
    Puglisi, Fabio
    Gianni, Luca
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2012, 9 (01) : 16 - 32
  • [8] Electrokinetically Driven Exosome Separation and Concentration Using Dielectrophoretic-Enhanced PDMS-Based Microfluidics
    Ayala-Mar, Sergio
    Perez-Gonzalez, Victor H.
    Mata-Gomez, Marco A.
    Gallo-Villanueva, Roberto C.
    Gonzalez-Valdez, Jose
    [J]. ANALYTICAL CHEMISTRY, 2019, 91 (23) : 14975 - 14982
  • [9] Mesenchymal Stem Cell-Derived Extracellular Vesicles as Therapeutics and as a Drug Delivery Platform
    Baek, Gyuhyeon
    Choi, Hojun
    Kim, Youngeun
    Lee, Hai-Chon
    Choi, Chulhee
    [J]. STEM CELLS TRANSLATIONAL MEDICINE, 2019, 8 (09) : 880 - 886
  • [10] Nanomaterials: Applications in Cancer Imaging and Therapy
    Barreto, Jose A.
    O'Malley, William
    Kubeil, Manja
    Graham, Bim
    Stephan, Holger
    Spiccia, Leone
    [J]. ADVANCED MATERIALS, 2011, 23 (12) : H18 - H40