Hyperbranched polycaprolactone-click-poly(N-vinylcaprolactam) amphiphilic copolymers and their applications as temperature-responsive membranes

2014 ◽  
Vol 2 (7) ◽  
pp. 814-825 ◽  
Author(s):  
Tao Cai ◽  
Min Li ◽  
Bin Zhang ◽  
Koon-Gee Neoh ◽  
En-Tang Kang
Soft Matter ◽  
2017 ◽  
Vol 13 (40) ◽  
pp. 7441-7452 ◽  
Author(s):  
Ruggero Foralosso ◽  
Lee Moir ◽  
Francesca Mastrotto ◽  
Luana Sasso ◽  
Aleksandra Tchoryk ◽  
...  

Blends of amphiphilic copolymers and mixtures of their nanoparticles can be tuned for temperature-responsive behaviour.


2016 ◽  
Vol 40 (10) ◽  
pp. 8397-8407 ◽  
Author(s):  
Beibei Lu ◽  
Lei Li ◽  
Jianning Wu ◽  
Lulu Wei ◽  
Jun Hou ◽  
...  

Well-defined dual pH and temperature responsive triblock star-shaped amphiphilic copolymers of β-CD-g-(PHEMA-b-PNIPAM-b-PDMAEMA)3 were synthesized by the combination of RAFT polymerizations.


2015 ◽  
Vol 23 (8) ◽  
pp. 1283-1290 ◽  
Author(s):  
Yanlei Su ◽  
Yuan Liu ◽  
Xueting Zhao ◽  
Yafei Li ◽  
Zhongyi Jiang

2016 ◽  
Author(s):  
Arjen Gebraad ◽  
Teuvo Hentunen ◽  
Tiina Laitala-Leinonen

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>


2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>


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