We demonstrate here the formation of compartmentalized
polymersomes
with an internal “gelly” cavity using an original and
versatile process. Nanosize polymersomes of poly(trimethylene carbonate)-b-poly(l-glutamic acid) (PTMC-b-PGA), formed by a solvent displacement method are encapsulated with
a rough “cytoplasm mimic” in giant polymersomes of poly(butadiene)-b-poly(ethylene oxide) PB-b-PEO by emulsion–centrifugation.
Such a system constitutes a first step toward the challenge of structural
cell mimicry with both “organelles” and “cytoplasm
mimics”. The structure is demonstrated with fluorescence labeling
and confocal microscopy imaging with movies featuring the motion of
the inner nanosize polymersomes in larger vesicles. Without “cytoplasm
mimic”, the motion was confirmed to be Brownian by particle
tracking analysis. The inner nanosize polymersomes motion was blocked
in the presence of alginate, but only hindered in the presence of
dextran. With the use of such high molecular weight and concentrated
polysaccharides, the crowded internal volume of cells, responsible
for the so-called “macromolecular crowding” effect influencing
every intracellular macromolecular association, seems to be efficiently
mimicked. This study constitutes major progress in the field of structural
biomimicry and will certainly enable the rise of new, highly interesting
properties in the field of high-added value soft matter