Manipulation of Polymer Chain Entanglement and Self-Assembly for DNA Capillary Electrophoresis

2005 ◽  
Vol 227 (1) ◽  
pp. 77-88 ◽  
Author(s):  
Benjamin Chu ◽  
Qicong Ying ◽  
Yanmei Wang ◽  
Jun Zhang
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>


2020 ◽  
Vol 11 (8) ◽  
pp. 1514-1524 ◽  
Author(s):  
Rintaro Takahashi ◽  
Shotaro Miwa ◽  
Fabian H. Sobotta ◽  
Ji Ha Lee ◽  
Shota Fujii ◽  
...  

Upon extending a hydrophobic polymer chain from the end of a preceding hydrophilic chain in aqueous solutions, the resultant block copolymers may eventually undergo self-assembly.


2014 ◽  
Vol 16 (37) ◽  
pp. 20190-20201 ◽  
Author(s):  
Josmin P. Jose ◽  
Sabu Thomas

Transport mechanism through binary (A & C) and ternary hybrid (AC) XLPE nanocomposites.


1978 ◽  
Vol 16 (4) ◽  
pp. 157-160 ◽  
Author(s):  
J. H. Southern ◽  
R. L. Ballman ◽  
J. A. Burroughs ◽  
D. R. Paul

2018 ◽  
Vol 14 (5) ◽  
pp. 1748-1749
Author(s):  
Jianhao Wang ◽  
Chencheng Zhang ◽  
Li Yang ◽  
Yaqin Gu ◽  
Jianpeng Wang ◽  
...  

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