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. Author manuscript; available in PMC: 2021 Aug 26.
Published in final edited form as: Lab Chip. 2020 Aug 26;20(17):3187–3201. doi: 10.1039/d0lc00609b

Table 2.

A survey of existing microfluidic exosome separation methods

Type Methods Throughput Recovery rate of exosomes Purity of recovered exosomes Biological samples used in the study Reference
Label-free (size-based) Nano-DLD 0.012 μL /h N/A N/A Human urine 48
Acoustics 240 μL/h 82% 98.4% Whole blood, cell culture medium 47
Pinched-flow fractionation 1200 μL/h N/A N/A Cell culture medium 45
AF4 267–1333 μL /h N/A N/A Cell culture medium 49
Nanowire trapping 600 μL /h 10% N/A Mixture of BSA, liposome and beads 46
Viscoelastic 200 μL/h >80% > 90% Cell culture medium, pure serum 31
ExoTIC 5000 μL /h >90% N/A Plasma, urine, lavage, cell culture medium 24
Double filtration 2400 μL/h 92% N/A Cell culture medium, urine 25
Exodisc-B/P 180–900 μL/h 76–88% N/A Whole blood, plasma, and cell culture medium 26
FerroChip 60–180 μL/h 94.3% 87.9% Cell culture medium and serum This work
Label-based iMER 240 μL / h 93% N/A Serum 44
CD63-modified herringbone groves ∼ 800 μL / h 42–94% N/A Serum and cell culture medium 42
CD41-modified mica surface 72 μL / h N/A N/A Human plasma, 41
ExoChip 240 μL / h N/A N/A Serum 17
nPLEX 500 μL / h N/A N/A Ascites fluid 43
Nano-IMEX 3 μL / h N/A N/A Diluted plasma 19