Vesicles made completely from diblock copolymers-polymersomes-can be stably
prepared by a wide range of techniques common to liposomes. Processes such
as film rehydration, sonication, and extrusion can generate many-micron gi
ants as well as monodisperse, similar to 100 nm vesicles of PEO-PEE (polyet
hyleneoxide-polyethylethylene) or PEG-PSD (polyethyleneoxide-polybutadiene)
. These thick-walled vesicles of polymer can encapsulate macromolecules jus
t as liposomes can but, unlike many pure liposome systems, these polymersom
es exhibit no in-surface thermal transitions and a subpopulation even survi
ve autoclaving. Suspension in blood plasma has no immediate ill-effect on v
esicle stability, and neither adhesion nor stimulation of phagocytes are ap
parent when giant polymersomes are held in direct, protracted contact. Prol
iferating cells, in addition, are unaffected when cultured for an extended
time with an excess of polymersomes. The effects are consistent with the st
eric stabilization that PEG-lipid can impart to liposomes, but the present
single-component polymersomes are far more stable mechanically and are not
limited by PEG-driven micellization. The results potentiate a broad new cla
ss of technologically useful, polymer-based vesicles. (C) 2001 John Wiley &
Sons, Inc.