Skip to main content

Table 1 The comparison of methods for exosome isolation

From: Immune cells: potential carriers or agents for drug delivery to the central nervous system

Isolation method

Advantages

Disadvantages

Differential ultracentrifugation

Low cost

Low contamination risk with extra isolation reagents

Suitable for large volume preparation

High equipment requirement

Time consuming

Labor intensive

Potential mechanical damage due to high-speed centrifugation

Protein aggregation

Not suitable for small volume diagnosis

Low portability

Density gradient ultracentrifugation

High purity of products

Allowing separation of the subpopulation of exosomes

Lower volume processability

High equipment requirement

Time consuming

Labor intensive

Potential mechanical damage due to high-speed centrifugation

Not suitable for small volume diagnosis

Low portability

Ultrafiltration

Low equipment cost

Fast procedure

Good portability

Moderate purity

Potential deterioration induced by shear stress

Possible loss due to clogging and membrane trapping

Immuno-affinity-based isolation method

Suitable for separating exosomes of specific origin

High-purity exosomes

Easy to use

No chemical contamination

High-cost antibodies

Exosome markers must be optimized

Low processing volume and yields

Extra step for exosome elution may damage native exosome structure