Thermally responsive gels formed from highly branched poly(N-isopropyl acrylamide)s with either carboxylic acid or trihistidine end groups

RSC Advances ◽  
2013 ◽  
Vol 3 (39) ◽  
pp. 18107 ◽  
Author(s):  
James W. Lapworth ◽  
Paul V. Hatton ◽  
Stephen Rimmer
RSC Advances ◽  
2016 ◽  
Vol 6 (75) ◽  
pp. 71345-71350 ◽  
Author(s):  
T. Swift ◽  
J. Lapworth ◽  
K. Swindells ◽  
L. Swanson ◽  
S. Rimmer

Thermally responsive highly branched poly(N-isopropyl acrylamide)s (HB-PNIPAM) were prepared and end-functionalised to give polymers with acid or trihistidine end groups. ​The ionisation of the end groups affects the swelling of desolvated globules.


2019 ◽  
Vol 156 ◽  
pp. 44-49 ◽  
Author(s):  
Saurabh Saxena ◽  
Prateek Malik ◽  
Ajay K. Tyagi ◽  
Geetha Seshadri ◽  
Uttam Kumar Mandal

2006 ◽  
Vol 4 (12) ◽  
pp. 117-126 ◽  
Author(s):  
John Collett ◽  
Aileen Crawford ◽  
Paul V Hatton ◽  
Mark Geoghegan ◽  
Stephen Rimmer

Hydrogel brushes are materials composed of a water-swollen network, which contains polymer chains that are grafted with another polymer. Using a thermally responsive polymer, poly( N -isopropyl acrylamide) (polyNIPAM), as the graft component we are able to maintain the critical solution temperature ( T crit ), independent of the overall composition of the material, at approximately 32°C. The change in swelling at T crit is a function of the amount of polyNIPAM in the system. However, there is a much smaller change in the surface contact angles at T crit . PolyNIPAM-based materials have generated considerable interest, as ‘smart’ substrates for the culture of cells and here, we show the utility of hydrogel brushes in cell culture. Chondrocytes attached to the hydrogel brushes and yielded viable cell cultures. Moreover, the chondrocytes could be released from the hydrogel brushes without the use of proteases by reducing the temperature of the cultures to below T crit to induce a change in the conformation of the polyNIPAM chain at T crit . The importance of the crosslink hydrogel component is illustrated by significant changes in cell attachment/cell viability as the crosslink density is changed.


1996 ◽  
Vol 457 ◽  
Author(s):  
Phillip B. Messersmith ◽  
F. Znidarsich

ABSTRACTStimuli responsive polymeric hydrogel composites were synthesized by room temperature copolymerization of N-isopropyl acrylamide and methylene bisacrylamide (crosslinking monomer) in an aqueous suspension of Na-montmorillonite. Hydrogels containing 3.5 weight % of montmorillonite exhibited a lower critical solution temperature (LCST) similar to unmodified PNIPAM hydrogel (approximately 32°C), and underwent a reversible 60–70% volume shrinkage when heated from ambient temperature to above the LCST. However, hydrogels containing 10 weight% montmorillonite did not exhibit a measurable LCST, and underwent considerably less shrinkage when heated. A solvent exchange reaction was used to replace the water with an acrylic monomer, which was polymerized in-situ to create a delaminated montmorillonite/polymer nanocomposite.


2017 ◽  
Vol 111 ◽  
pp. 79-87 ◽  
Author(s):  
Pavel Kucharczyk ◽  
Jiri Zednik ◽  
Petr Humpolicek ◽  
Zdenka Capakova ◽  
Vladimir Sedlarik

2015 ◽  
Vol 11 ◽  
pp. 638-646 ◽  
Author(s):  
Joana Salta ◽  
Jens Dernedde ◽  
Hans-Ulrich Reissig

In this article a series of divalent and trivalent carbohydrate mimetics on the basis of an enantiopure aminopyran and of serinol is described. These aminopolyols are connected by amide bonds to carboxylic acid derived spacer units either by Schotten–Baumann acylation or by coupling employing HATU as reagent. The O-sulfation employing the SO3·DMF complex was optimized. It was crucial to follow this process by 700 MHz 1H NMR spectroscopy to ensure full conversion and to use a refined neutralization and purification protocol. Many of the compounds could not be tested as L-selectin inhibitor by SPR due to their insolubility in water, nevertheless, a divalent and a trivalent amide showed surprisingly good activities with IC50 values in the low micromolar range.


2016 ◽  
Vol 88 (12) ◽  
pp. 1117-1128 ◽  
Author(s):  
Bruno Sena da Fonseca ◽  
Susana Piçarra ◽  
Ana Paula Ferreira Pinto ◽  
Maria de Fátima Montemor

AbstractThe overall performance of alkoxysilanes as stone consolidants is constrained by stone mineralogy (particularly in the carbonate varieties) and by their tendency to crack during drying. In an attempt to overcome these problems, polyethylene glycol “chains” with two carboxylic acid end-groups (PEG-CA) were introduced in siloxane sols obtained by sol-gel chemistry using tetraethoxysilane (TEOS) as precursor. Different pre-condensation degrees (by varying the stirring times of sol-gel reaction: 10 min, 2, and 24 h) and PEG-CA chains with different molecular weights were studied as variables affecting the initial efficacy of the consolidants when applied into a limestone. The sol containing siloxanes with the lowest pre-condensation degree (10 min stirring) was quite susceptible to the carbonate media and thus a poor consolidation was achieved. The sol with the highest pre-condensation degree (24 h stirring) together with the PEG-CA chains with intermediate molecular weight produced significant and uniform strength gains along the stone depth. The consolidation also showed to be highly dependent on the molecular weight of the PEG-CA chains, the PEG-CA with highest molecular weight produced a non-uniform strength increase with potential harmful side effects. The results confirmed the role of carboxylic acid end-groups as efficient sol-gel catalysts and their ability to be incorporated into the silica matrix in the presence of carbonate stone.


1971 ◽  
Vol 49 (17) ◽  
pp. 2916-2917 ◽  
Author(s):  
M. Day ◽  
D. M. Wiles

The liquid phase photolysis of undiluted di-n-butyl terephthalate yields 1-butene and carboxylic acid end groups as a result of a Norrish Type II photochemical rearrangement reaction. Quantum yields for the production of these two products have been determined and found to be [Formula: see text] and [Formula: see text] in vacuum and [Formula: see text] and [Formula: see text] in air.


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