Formation of polymer vesicles by simultaneous chain growth and self-assembly of amphiphilic block copolymers

2009 ◽  
pp. 2887 ◽  
Author(s):  
Guillaume Delaittre ◽  
Charlotte Dire ◽  
Jutta Rieger ◽  
Jean-Luc Putaux ◽  
Bernadette Charleux
Soft Matter ◽  
2021 ◽  
Author(s):  
Mazarine Houbrechts ◽  
Lucas Caire da Silva ◽  
Anitha Ethirajan ◽  
Katharina Landfester

Polymer vesicles that mimic the function of cell membranes can be obtained through the self-assembly of amphiphilic block copolymers. The cell-like characteristics of polymer vesicles, such as the core-shell structure,...


2021 ◽  
Vol 9 (1) ◽  
pp. 38-50
Author(s):  
Hien Phan ◽  
Vincenzo Taresco ◽  
Jacques Penelle ◽  
Benoit Couturaud

Stimuli-responsive amphiphilic block copolymers obtained by PISA have emerged as promising nanocarriers for enhancing site-specific and on-demand drug release in response to a range of stimuli such as pH, redox agents, light or temperature.


2021 ◽  
Author(s):  
Valene Wang ◽  
Jiwon Kim ◽  
Junyoung Kim ◽  
Seul Woo Lee ◽  
Kyoung Taek Kim

The shape control of nanostructures formed by the solution self-assembly of block copolymers is of significance for drug delivery. In particular, site-specific perturbation resulting in the conformational change of the...


2007 ◽  
Vol 43 (7) ◽  
pp. 2891-2900 ◽  
Author(s):  
Xiaoju Lu ◽  
Shuling Gong ◽  
Lingzhi Meng ◽  
Cheng Li ◽  
Feng Liang ◽  
...  

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2572
Author(s):  
Jaleesa Bresseleers ◽  
Mahsa Bagheri ◽  
Coralie Lebleu ◽  
Sébastien Lecommandoux ◽  
Olivier Sandre ◽  
...  

The careful design of nanoparticles, in terms of size and morphology, is of great importance to developing effective drug delivery systems. The ability to precisely tailor nanoparticles in size and morphology during polymer self-assembly was therefore investigated. Four poly(ethylene glycol)-b-poly(N-2-benzoyloxypropyl methacrylamide) mPEG-b-p(HPMA-Bz) block copolymers with a fixed hydrophilic block of mPEG 5 kDa and a varying molecular weight of the hydrophobic p(HPMA-Bz) block (A: 17.1, B: 10.0, C: 5.2 and D: 2.7 kDa) were self-assembled into nanoparticles by nanoprecipitation under well-defined flow conditions, using microfluidics, at different concentrations. The nanoparticles from polymer A, increased in size from 55 to 90 nm using lower polymer concentrations and slower flow rates and even polymer vesicles were formed along with micelles. Similarly, nanoparticles from polymer D increased in size from 35 to 70 nm at slower flow rates and also formed vesicles along with micelles, regardless of the used concentration. Differently, polymers B and C mainly self-assembled into micelles at the different applied flow rates with negligible size difference. In conclusion, this study demonstrates that the self-assembly of mPEG-b-p(HPMA-Bz) block copolymers can be easily tailored in size and morphology using microfluidics and is therefore an attractive option for further scaled-up production activities.


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