Chiral pH-Responsive Amphiphilic Polymer Co-networks: Preparation, Chiral Recognition, and Release Abilities

2013 ◽  
Vol 214 (12) ◽  
pp. 1375-1383 ◽  
Author(s):  
Lu Shi ◽  
Peng Xie ◽  
Zhimin Li ◽  
Youping Wu ◽  
Jianping Deng
2017 ◽  
Vol 8 (1) ◽  
pp. 245-259 ◽  
Author(s):  
Elina N. Kitiri ◽  
Costas S. Patrickios ◽  
Chrysovalantis Voutouri ◽  
Triantafyllos Stylianopoulos ◽  
Ingo Hoffmann ◽  
...  

Double-networks based on amphiphilic polymer conetworks synthesized using RAFT polymerization were prepared, exhibiting pH-responsiveness, nanophase separation and enhanced mechanical properties.


Soft Matter ◽  
2017 ◽  
Vol 13 (20) ◽  
pp. 3690-3700 ◽  
Author(s):  
Sivaramakrishnan Ramadurai ◽  
Marco Werner ◽  
Nigel K. H. Slater ◽  
Aaron Martin ◽  
Vladimir A. Baulin ◽  
...  

2018 ◽  
Vol 9 (4) ◽  
pp. 463-471 ◽  
Author(s):  
Qingwei Li ◽  
Ziquan Cao ◽  
Guojie Wang

A multiple-stimuli-responsive polymer nanocarrier has been self-assembled for NIR/UV light- and pH-controlled cargo release.


RSC Advances ◽  
2016 ◽  
Vol 6 (46) ◽  
pp. 40312-40322 ◽  
Author(s):  
Liyi Fu ◽  
Le Liu ◽  
Zheng Ruan ◽  
Houbing Zhang ◽  
Lifeng Yan

A novel folic acid targeted pH-responsive amphiphilic polymer conjugated with near infrared (NIR) probe has been synthesized by the combination of RAFT polymerization, ring-opening polymerization of N-carboxy anhydride (NCA) and click reaction.


2020 ◽  
Vol 3 (3) ◽  
pp. 2104-2117 ◽  
Author(s):  
Shivshankar R. Mane ◽  
Ashlin Sathyan ◽  
Raja Shunmugam

2019 ◽  
Author(s):  
Qingfeng Hou ◽  
Xiaobo Zheng ◽  
Donghong Guo ◽  
Youyi Zhu ◽  
Hui Yang ◽  
...  

2015 ◽  
Vol 6 (39) ◽  
pp. 7053-7059 ◽  
Author(s):  
Shota Fujii ◽  
Makoto Kido ◽  
Masanao Sato ◽  
Yuji Higaki ◽  
Tomoyasu Hirai ◽  
...  

An amphiphilic polymer bearing glutamic acid in the polymer side chain was used as a surface modifier to produce an amino acid-based zwitterionic surface with pH-responsive and selective protein properties.


2019 ◽  
Author(s):  
Nancy Watfa ◽  
Weimin Xuan ◽  
Zoe Sinclair ◽  
Robert Pow ◽  
Yousef Abul-Haija ◽  
...  

Investigations of chiral host guest chemistry are important to explore recognition in confined environments. Here, by synthesizing water-soluble chiral porous nanocapsule based on the inorganic metal-oxo Keplerate-type cluster, {Mo<sub>132</sub>} with chiral lactate ligands with the composition [Mo<sub>132</sub>O<sub>372</sub>(H<sub>2</sub>O)<sub>72</sub>(<i>x-</i>Lactate)<sub>30</sub>]<sup>42-</sup> (<i>x</i> = D or L), it was possible to study the interaction with a chiral guest, L/D-carnitine and (<i>R</i>/<i>S</i>)-2-butanol in aqueous solution. The enantioselective recognition was studied by quantitative <sup>1</sup>H NMR and <sup>1</sup>H DOSY NMR which highlighted that the chiral recognition is regulated by two distinct sites. Differences in the association constants (K) of L- and D-carnitine, which, due to their charge, are generally restricted from entering the interior of the host, are observed, indicating that their recognition predominantly occurs at the surface pores of the structure. Conversely, a larger difference in association constants (K<i><sub>S</sub></i>/K<i><sub>R</sub></i> = 3) is observed for recognition within the capsule interior of (<i>R</i>)- and (<i>S</i>)-2-butanol.


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