Hydrogen-Bonded Layer-by-Layer Temperature-Triggered Release Films†

Langmuir ◽  
2009 ◽  
Vol 25 (24) ◽  
pp. 14025-14029 ◽  
Author(s):  
Aliaksandr Zhuk ◽  
Svetlana Pavlukhina ◽  
Svetlana A. Sukhishvili
Soft Matter ◽  
2019 ◽  
Vol 15 (45) ◽  
pp. 9318-9324
Author(s):  
Liliana Maldonado ◽  
Gabriel Debais ◽  
Federico Davia ◽  
Lucila P. Méndez De Leo ◽  
Mario Tagliazucchi

Poly(sulfonic acid)s and poly(ethylene oxide) unexpectedly form novel hydrogen-bonded interpolymer complexes in aqueous solution and on surfaces by layer-by-layer deposition.


2019 ◽  
Vol 52 (12) ◽  
pp. 4432-4440 ◽  
Author(s):  
Victor Selin ◽  
Aliaksei Aliakseyeu ◽  
John F. Ankner ◽  
Svetlana A. Sukhishvili

2020 ◽  
Vol 2 (12) ◽  
pp. 5398-5405
Author(s):  
Nithya Joseph ◽  
Maarten A. Mees ◽  
Maarten Vergaelen ◽  
Brecht Valley ◽  
Hanne Marien ◽  
...  

ChemPhysChem ◽  
2007 ◽  
Vol 8 (3) ◽  
pp. 418-424 ◽  
Author(s):  
Shuguang Yang ◽  
Yongjun Zhang ◽  
Xiaoyan Zhang ◽  
Ying Guan ◽  
Jian Xu ◽  
...  

2010 ◽  
Vol 20 (8) ◽  
pp. 1546-1552 ◽  
Author(s):  
Kentaro Yoshida ◽  
Katsuhiko Sato ◽  
Jun-ichi Anzai

2020 ◽  
Vol 12 (7) ◽  
pp. 890-900
Author(s):  
Hua Wei ◽  
Hua Zhang ◽  
Yang Zhou ◽  
Zongbao Wang ◽  
Rong Wang ◽  
...  

This study demonstrated the feasibility of polymer brushes-modified plate substrate as template to construct multilayer thin films via layer-by-layer hydrogen bonded assembly. The anchored chains via controlled surface-initiated atom transfer radical polymerization (SI-ATRP). The anchored poly(4-vinylpyridine) brushes functions as a multivalent H-acceptor to regulate the following hydrogen bonded assembly with H-donors to construct multilayer thin films via layer-by-layer deposition technique. The growth mechanism and film natures of multilayer films mediated by hydrogen bonded assembly from a polymer brushes-grafted surface were fully investigated.


2015 ◽  
Vol 6 ◽  
pp. 2504-2512 ◽  
Author(s):  
Manuel Häuser ◽  
Klaus Langer ◽  
Monika Schönhoff

Nanoparticles (NP) of poly(lactic-co-glycolic acid) (PLGA) represent a promising biodegradable drug delivery system. We suggest here a two-step release system of PLGA nanoparticles with a pH-tunable polymeric shell, providing an initial pH-triggered step, releasing a membrane-toxic cationic compound. PLGA nanoparticles are coated by polyelectrolytes using the layer-by-layer self-assembly technique, employing poly(acrylic acid) (PAA) as a pH-sensitive component and poly(diallyldimethylammonium chloride) (PDADMAC) as the releasable polycation. The pH during multilayer deposition plays a major role and influences the titration curve of the layer system. The pH-tunability of PAA is intensively investigated with regard to the pH region, in which the particle system becomes uncharged. The isoelectric point can be shifted by employing suitable deposition pH values. The release is investigated by quantitative 1H NMR, yielding a pH-dependent release curve. A release of PDADMAC is initiated by a decrease of the pH value. The released amount of polymer, as quantified by 1H NMR analysis, clearly depends on the pH value and thus on the state of deprotonation of the pH-sensitive PAA layer. Subsequent incubation of the nanoparticles with high concentrations of sodium chloride shows no further release and thus demonstrates the pH-driven release to be quantitative.


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