Vesicles can be made from various polymers, from modified biological to who
lly synthetic, in media ranging from complex to neat organics and water. Al
though the canonical form of polymers that have the ability to assemble int
o encapsulating vesicles is an amphiphilic H-P (hydrophobic-polar) diblock,
additional block copolymers from triblocks to pentablocks have also been s
hown to assemble into vesicles. Polydispersity seems to have a minimal effe
ct, but solvent requirements may well depend on the proportion of H to P as
well as the molecular weight. What is clear from all of the ultrastructura
l characterization done on polymer vesicles is that the 'universal' thickne
ss of 3-4 nm, which is well-known for natural lipid vesicles, reflects no p
hysical limitation on the amphiphilic assembly at the nano-scale. Emerging
material characterizations emphasize the dominance of the two-dimensional H
-P interface and the unnatural robustness possible in the responses of poly
mer membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.