Table 2.
Methods of EV characterization.
| Method | Identify projects | Advantages | Disadvantages | References |
|---|---|---|---|---|
| Nanoparticle tracking analysis | Size and concentration | Assays that do not rely on specific markers; direct quantification | High equipment costs; determination of non-exosomal contaminants | (44, 55, 58) |
| Dynamic light scattering | Size and concentration | High sensitivity; simple sample preparation | Harsh imaging conditions; low flux | (69, 70) |
| Western blotting | Expression of specific proteins in EVs | Large analysis capacity; distinguishing EV-specific proteins; high sensitivity | Cannot distinguish between dissociated proteins; long consumption time; requires known antibodies | (51, 52) |
| Transmission electron microscope | EV morphology | Visualization of EV morphology | Vacuum environment required | (42, 46) |
| Scanning electron microscope | EV morphology | Visualization of EV morphology | Destroys the specimen | (45) |
| Flow cytometry | Individual EV size and protein mass spectrometry analysis | Accurate realization of multi-parameter analysis of individual EVs | Long consumption time; requires special equipment | (39, 63, 65) |
EV, extracellular vesicle.