Table 1.
Isolation Technique | Principle | Recovery (%) | Pros | Cons | References |
---|---|---|---|---|---|
Ultracentrifugation | Sedimentation rate | 5–20 | High sample capacity and low cost | Time-consuming and low purity | [9,10] |
Density gradient ultracentrifugation | Density, size, shape | 10–40 | High purity and protein concentration | Long run time and low yield | [9,11,12] |
Polymer-based precipitation | Sedimentation rate | 90+ | High yield | Low purity | [13,14,15] |
Ultrafiltration | Size | 30 | Maintains integrity; simple and low-cost | Moderate purity; low yield due to exosome trapping in filter pores | [9,16,17] |
Size-exclusion chromatography | Size | 40–80 | High purity, integrity, and functionality; reduction of exosome aggregation | Low extraction volume | [9,18] |
Immunoaffinity chromatography | Surface marker | 90+ | Maintain integrity | Low capacity and low yield | [9,19,20] |
Microfluidics | Surface marker | 40–90 | Low cost and low input sample required | Low sample capacity; cargo may be modified | [9,21,22] |
Magnetic bead isolation | Surface marker | 80+ | Maintain integrity | Possible impurities |
[23,24] |