scholarly journals The combination of block copolymers and phospholipids to form giant hybrid unilamellar vesicles (GHUVs) does not systematically lead to “intermediate” membrane properties

Soft Matter ◽  
2018 ◽  
Vol 14 (31) ◽  
pp. 6476-6484 ◽  
Author(s):  
T. P. T. Dao ◽  
F. Fernandes ◽  
M. Fauquignon ◽  
E. Ibarboure ◽  
M. Prieto ◽  
...  

The combination of a triblock copolymer and phospholipids to form GHUVs leads to an unexpected decrease of vesicle toughness.

2021 ◽  
Vol 12 (37) ◽  
pp. 5377-5389
Author(s):  
Riccardo Wehr ◽  
Elena C. dos Santos ◽  
Moritz S. Muthwill ◽  
Vittoria Chimisso ◽  
Jens Gaitzsch ◽  
...  

Analysis of the membrane properties and stability of fully amorphous small and giant unilamellar vesicles composed of atactic or isotactic poly(butylene oxide)-block-poly(glycidol) (PBO-b-PG) amphiphilic diblock copolymers.


2013 ◽  
Vol 166 ◽  
pp. 303 ◽  
Author(s):  
Regina Schöps ◽  
Elkin Amado ◽  
Sophie S. Müller ◽  
Holger Frey ◽  
Jörg Kressler

RSC Advances ◽  
2015 ◽  
Vol 5 (64) ◽  
pp. 52105-52120 ◽  
Author(s):  
E. Villar-Alvarez ◽  
E. Figueroa-Ochoa ◽  
S. Barbosa ◽  
J. F. A. Soltero ◽  
P. Taboada ◽  
...  

Reverse triblock copolymer micelles with lengthy polyethylene oxide blocks as efficient sustained dual drug-loaded nanocarriers.


2003 ◽  
Vol 788 ◽  
Author(s):  
Hui-suk Yun ◽  
Makoto Kuwabara ◽  
Haoshen Zhou ◽  
Itaru Honma

ABSTRACTHexagonally mesostructured 12-phosphotungstic acid (PWA) thin films with both large pore size and hierarchical structures have been successfully prepared by using triblock copolymer templates for the first time. The films is composed by three kind of structures; PWA Keggin anion, monoclinic crystal structure consisting of PWA Keggin anion and organic part (hydrophilic component) of block copolymers, and the hexagonal mesostructure of self-arrayed PWA and block copolymers. The calcined PWA films show better electrochemical properties such as a faster faradic processes and larger specific capacity than normal P WA clusters.


Soft Matter ◽  
2011 ◽  
Vol 7 (18) ◽  
pp. 8100 ◽  
Author(s):  
Matthias Schulz ◽  
Daniela Glatte ◽  
Annette Meister ◽  
Peggy Scholtysek ◽  
Andreas Kerth ◽  
...  

2010 ◽  
Vol 663-665 ◽  
pp. 880-882
Author(s):  
Xin De Tang ◽  
Jing Xu

The behavior of amphiphilic block copolymers in solution has attracted considerable attention in recent years. In this paper, the self-assembly behaviors of the amphiphilic fluorinated ABC-type triblock copolymer (MeOPEO16-PSt220-PFHEA22) in different mixed solutions were studied. Also, the effect of ionic concentration on the self-assembly aggregates of the copolymer in toluene-ethanol-water was studied.


2002 ◽  
Vol 67 (2) ◽  
pp. 267-278 ◽  
Author(s):  
Jan Lokaj ◽  
Libuše Brožová ◽  
Petr Holler ◽  
Zbyněk Pientka

Radical copolymerization of a mixture of styrene (S) and acrylonitrile (AN) at azeotropic composition (63 mole % of S and 37 mole % of AN) at 125 °C in the presence of dibenzoyl peroxide and 2,2,6,6-tetramethylpiperidin-1-yloxyl (TEMPO) gave TEMPO-terminated S-AN copolymers with narrow molecular weight distributions. Both the linear semilogarithmic time-conversion and molecular weight-conversion dependences indicated a quasiliving copolymerization process. Polymerization of styrene initiated with the synthesized macroinitiators containing reversibly bound terminal TEMPO groups yielded film-forming poly(styrene-co-acrylonitrile)-block-polystyrene copolymers. Using the resulting diblock copolymer as a macroinitiator in copolymerization of S and AN, a triblock copolymer of the A-B-A type was obtained. Films of the block copolymers were prepared by casting chloroform solutions and their permeabilities (P) to nitrogen, oxygen, methane, carbon dioxide, and hydrogen were determined. The films showed high selectivities to oxygen (PO2/PN2 > 6). The block copolymers behaved as single-phase homogeneous materials.


2018 ◽  
Vol 9 (44) ◽  
pp. 5385-5394 ◽  
Author(s):  
Emeline Rideau ◽  
Frederik R. Wurm ◽  
Katharina Landfester

Polybutadiene-block-poly(ethyl ethylene phosphate) can reproducibly self-assemble in large number into giant unilamellar vesicles (GUVs) by non-assisted film hydration, representing a stepping stone for better liposomes – substitutes towards the generation of artificial cells.


2015 ◽  
Vol 6 (11) ◽  
pp. 1986-1996 ◽  
Author(s):  
Eva Annika Weiber ◽  
David Meis ◽  
Patric Jannasch

The use of methylhydroquinones enables the preparation of block copolymers having phenylene rings with precisely 2, 3 or 4 quaternary ammonium groups. Membrane properties show the importance of controlling the local ionic distribution to reach high anion conductivity.


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