Abstract
Recently attention in liposome preparation
technology has been focused on the preparation of
liposomes with a large number of bilayers.
These liposomes offer the possibility to encapsulate
large amounts of hydrophobic drugs. All
methods used to prepare these vesicles are modifications
of the method used to produce reversephase
evaporation vesicles (REV), as described
first by Szoka and Papahadjopoulos
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multilamellar vesicle