Table 2.
Comparison of plant-derived EVs and animal-derived EVs.
| Type studies | Plant-derived EVs | Animal-derived EVs |
|---|---|---|
| Extraction methods | ultracentrifugation and sucrose density gradient centrifugation | ultracentrifugation, sucrose density gradient centrifugation, size-based techniques, precipitation, immunoaffinity capture-based techniques and microfluidics based techniques |
| Particle size | EVs 100−1000 nm | microvesicles100-1000 nm exosomes 30-150 nm |
| Lipids | phosphatidylethanolamine, phosphatidic acid, phosphatidylcholine, no cholesterol | cholesterol, sphingomyelin, ceramide |
| Proteins | less research, contains less than animal-derived EVs, proteins that regulate carbohydrate/lipid metabolism, membrane proteins etc. | rich in variety, mainly targeting fusion proteins, rab family proteins, heat shock proteins family, transmembrane proteins, cytoskeleton proteins etc. |
| RNA | mainly miRNA and small amount of ribosomal RNA | mRNA, miRNA, lncRNA, cirRNA and lack of ribosomal RNA |
| Application | anti-tumor, anti-inflammation, and drug delivery | anti-tumor, anti-inflammation, and biomarkers of diseases |
| Advantages | abundance of plant resources, large-scale production from abundance of plant resources, high biocompatibility and bioavailability with low toxicity, suitable features for a drug delivery system | high homology, can be used as a biomarker of disease, diversity of separation methods |
| limitations | concern about poor biocompatibility from impurities, fewer targeting moieties for mammalian cells | low production, less resources |