| Literature DB >> 19072234 |
Clément Houga1, Joanna Giermanska, Sébastien Lecommandoux, Redouane Borsali, Daniel Taton, Yves Gnanou, Jean-François Le Meins.
Abstract
The self-assembly of dextran-block-polystyrene (dex-b-PS) block copolymers was investigated in solution. The hydrophobic PS weight fraction in these block copolymers ranges from 7 to 92% w/w, whereas the average number molar mass of dextran was kept constant at 6600 gmol(-1). Self-assembly by direct dissolution in water could be performed only for block copolymers with a low hydrophobic content (7% w/w), whereas mixtures of tetrahydrofuran and dimethylsulfoxide were required for higher PS content, before transferring the structures into water. Core-shell micelles, ovoïds, and vesicles could be identified upon characterization by light and neutrons scattering, atomic force microscopy, and transmission electron microscopy. Most of the morphologies observed were not expected considering the chemical composition of the block copolymers. Finally, the size and shape of these nanoparticles were fixed upon cross-linking the dextran block through reaction of the hydroxyl groups with divinylsulfone. The role of the dextran conformation on the self-assembly process is discussed.Entities:
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Year: 2009 PMID: 19072234 DOI: 10.1021/bm800778n
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988