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. Author manuscript; available in PMC: 2022 Apr 1.
Published in final edited form as: Nano Today. 2021 Jan 13;37:101066. doi: 10.1016/j.nantod.2020.101066

Table 1.

Current conventional exosome isolation methods.

Isolation technique Principle Time Advantages Disadvantages

Differential ultracentrifugation
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Particles with various size and density demonstrate various sediment speed under centrifugation 5–18 hours ✓ Suitable for large volume preparation ➣Require expensive equipment
➣Potential damage because of the high-speed centrifugation
➣Time-consuming
Size
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Separate with specific molecular size exclusion 2–4 hours ✓ Isolate native exosomes ➣ Exosomes and proteins clogging on nanopores
➣ Potential isolate other nanovesicles in similar size with exosomes
Bead
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On the basis of interaction between antibodies/ligan ds and exosome markers 2–6 hours ✓ High-purity
✓ Useful for isolating specific exosomes from target origin
➣Expensive antibodies functionalization
➣Low yields
and processing volume
➣Exosome markers must be optimized
Polymer
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High hydrophilic water-excluding polymers changes the solubility of exosomes 0.5–12 hours ✓ Available for all types of samples
✓ Easy to use
➣Potential polymeric, protein aggregates, and other extracellular vesicles contaminants.