Table 2.
Strategy | Principle | Advantages | Disadvantages |
---|---|---|---|
Ultracentrifugation | Density, size, and shape | Low cost Low risk of pollution Fast Scalable |
Low purity Damages membrane integrity Time consuming Labor intensive |
Immunoaffinity capture | Specific recognition of exosome markers by corresponding immobilized antibodies |
Suitable for separating exosomes of specific origin High purity |
High cost Low yield Damages membrane integrity |
Polymeric precipitation | High hydrophilic water-excluding polymers |
Low cost Scalable Simple |
Low purity Protein aggregates remain |
Tangential flow ultrafiltration | Size and shape | High purity Fast Scalable Simple |
Low purity Membrane-fouling High cost |
Microfluidics techniques | Immunoaffinity, size, and density | Low cost Fast Simple Easily automated and integrated with diagnosis |
Low sensitivity and specificity Small sample size |
Size-exclusion chromatography | Size | High purity Fast Maintains membrane integrity |
High cost Needs specialized equipment and filler |