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Extracellular vesicles (EVs) are lipid bilayer-delimited particles [1] that are naturally released from almost all types of cells but, unlike a cell, cannot replicate. EVs range in diameter from near the size of the smallest physically possible unilamellar liposome (around 20-30 nanometers) to as large as 10 microns or more, although the vast majority of EVs are smaller than 200 nm.
Exosomes are extracellular vesicles having a unique biogenesis pathway via multivesicular bodies. Exosome formation starts with the invagination of the multi-vesicular bodies (MVBs) or late endosomes to generate intraluminal vesicles (ILVs). [57] There are various proposed mechanisms for formation of MVBs, vesicle budding, and sorting.
However, due to exosomes being small in size (30-150 nm), present in various biological fluids (such as blood, urine, saliva), sensitivity to environmental factors (such temperature, pH), complexity of drug loading efficiency, there are challenges associated with isolation, purification, delivery and drug payload.
The International Society for Extracellular Vesicles (ISEV) is an international scientific organization that focuses on advancing global extracellular vesicle (EV) research. [1] These membrane-bound particles are released from all known cells and include exosomes , ectosomes , exophers, oncosomes, and more.
The Journal of Extracellular Vesicles, JEV, is a peer-reviewed open-access scientific journal of the International Society for Extracellular Vesicles (ISEV). As one of two official journals of ISEV, the other being the Journal of Extracellular Biology, JEV covers research on lipid bilayer-delimited particles known as extracellular vesicles (EVs).
Vesicles can also fuse with other organelles within the cell. A vesicle released from the cell is known as an extracellular vesicle. Vesicles perform a variety of functions. Because it is separated from the cytosol, the inside of the vesicle can be made to be different from the cytosolic environment. For this reason, vesicles are a basic tool ...
An experimental nasal spray has helped clear toxic protein buildups in the brains of mouse models of Alzheimer's. Its developers believe the spray may help delay Alzheimer's by at least a decade.
A similar approach can be exploited in the biodetoxification of drugs by injecting empty liposomes with a transmembrane pH gradient. In this case the vesicles act as sinks to scavenge the drug in the blood circulation and prevent its toxic effect. [25] Another strategy for liposome drug delivery is to target endocytosis events.