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Title: Block copolymer vesicles
Author(s): Opsteen, J.A. (306279517)
Cornelissen, J.J.L.M. (230245234)
Hest, J.C.M. van (147373069)
Publication year: 2004
Document type: Article / Letter to editor
Journal: Pure and Applied Chemistry
ISSN: 0033-4545
Volume: vol. 76
Issue: iss. 7-8
Start page: p. 1309
End page: p. 1319
Abstract: Amphiphilic block copolymers have the ability to assemble into multiple morphologies in solution. Depending on the length of the hydrophilic block, the morphology can vary from spherical micelles, rods, and vesicles to large compound micelles (LCMs). Vesicle formation is favored upon an increase in total molecular weight of the block copolymer, that is, an increasing bending modulus (K). Owing to the polymeric character of this type of vesicle (also called polymersomes), they possess remarkable properties. The diffusion of (polymeric) amphiphiles in these vesicles is very low compared to liposomes and for high-molecular-weight chain entanglements even lead to reptation-type motions, which make it possible to trap near-equilibrium and metastable morphologies. Additionally, in contrast to liposomes, membrane thicknesses can exceed 200 nm. As a consequence, this increased membrane thickness, in combination with the conformational freedom of the polymer chains, leads to a much lower permeability for water of block copolymer vesicles compared to liposomes. The enhanced toughness and reduced permeability of polymersomes makes them, therefore, very suitable as stable nanocontainers, which can be used, for example, as reactors or drug delivery vehicles.
Subject: Bio-Organic Chemistry
Organization: Bio-organic Chemistry
Physical Organic Chemistry
Organization (former): Physical Organic and Supramolecular Chemistry
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/57533

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