English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Vesicles of double hydrophilic pullulan and poly(acrylamide) block copolymers : a combination of synthetic- and bio-derived blocks

MPS-Authors
/persons/resource/persons198575

Willersinn,  Jochen
Bernhard Schmidt, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

/persons/resource/persons179930

Schmidt,  Bernhard V. K. J.
Bernhard Schmidt, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

2382762.pdf
(Publisher version), 5MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Willersinn, J., Bogomolova, A., Brunet Cabré, M., & Schmidt, B. V. K. J. (2017). Vesicles of double hydrophilic pullulan and poly(acrylamide) block copolymers: a combination of synthetic- and bio-derived blocks. Polymer Chemistry, 8(7), 1244-1254. doi:10.1039/C6PY02212J.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002C-3FBC-5
Abstract
The formation of vesicular structures with average diameters from 200 to 300 nm consisting of double hydrophilic diblock copolymers pullulan-b-poly(N,N-dimethylacrylamide) (Pull-b-PDMA) and pullulan-b-poly(N-ethylacrylamide) (Pull-b-PEA) in aqueous solution is described. Bio-derived pullulan was depolymerized and functionalized with alkyne endgroups. Furthermore, azide end functionalized acrylamide blocks PDMA and PEA were synthesized via RAFT polymerization. Individual blocks were conjugated via copper catalyzed azide alkyne cycloaddition (CuAAC) to afford defined double hydrophilic block copolymers. Aqueous solutions of the synthesized block copolymers showed formation of completely hydrophilic vesicles that were observed via various techniques including dynamic light scattering (DLS), static light scattering (SLS), laser scanning confocal microscopy (LSCM), and cryogenic scanning electron microscopy (SEM).