scholarly journals Synthesis and characterization of copolymer hydrogels of chitosan, itaconic acid and N-isopropilacrylamide

2011 ◽  
Vol 65 (6) ◽  
pp. 657-666
Author(s):  
Nedeljko Milosavljevic ◽  
Nikola Milasinovic ◽  
Jovanka Filipovic ◽  
Melina Kalagasidis-Krusic
Keyword(s):  
Itaconic Acid ◽  
Polymer Chains ◽  
Solution Temperature ◽  
Critical Solution Temperature ◽  
Ionic Groups ◽  
Reaction Solution ◽  
Degree Of Swelling ◽  
The Matrix ◽  
Higher Temperature

This paper deals with synthesis of copolymer hydrogels of N-isopropilacrylamide, itaconic acid and chitosan. During synthesis, pH of the reaction solution and temperature were varied. It was found that reaction at higher temperature, above lower critical solution temperature (LCST) value of N-isopropilacrylamide resulted in a formation of polymer rich domains or aggregates in the matrix of loosely tied network, which cause a higher degree of swelling. Moreover, reaction pH also affects the degree of swelling and contraction of hydrogels owing to the different ionization of the ionic groups presence in hydrogel. The values of diffusion exponent, n, indicate non-Fickian kinetics corresponding to diffusion and relaxation of polymer chains. These hydrogels could be classified as macroporous hydrogels. Hence, it is possible to synthetize hydrogels of desired functionality which allow their application in different fields.

scholarly journals Synthesis and characterization of PIL/pNIPAAm hybrid hydrogels

2016 ◽  
Vol 2 (1) ◽  
pp. 1-4
Author(s):  
Sylvia Pfensig ◽  
Daniela Arbeiter ◽  
Klaus-Peter Schmitz ◽  
Niels Grabow ◽  
Thomas Eickner ◽  
...  
Keyword(s):  
Mechanical Characterization ◽  
Heating Temperature ◽  
Controlled Drug Release ◽  
Solution Temperature ◽  
Scanning Calorimetry ◽  
Critical Solution Temperature ◽  
Temperature Range ◽  
Hybrid Hydrogels ◽  
Higher Temperature

AbstractIn this study, varying amounts of NIPAAm and an ionic liquid (IL), namely 1-vinyl-3-isopropylimidazolium bromide ([ViPrIm]+[Br]−), have been used to synthesize hybrid hydrogels by radical emulsion polymerization. Amounts of 70/30%, 50/50%, 30/70%, 15/85% and 5/95% (wt/wt) of PIL/pNIPAAm were used to produce hybrid hydrogels as well as the parental hydrogels. The adhesive strength was investigated and evaluated for mechanical characterization. Thermal properties of resulting hydrogels have been investigated using differential scanning calorimetry (DSC) in a default heating temperature range (heating rate 10 K min−1). The presence of poly ionic liquids (PIL) in the polymer matrix leads to a moved LCST (lower critical solution temperature) to a higher temperature range for certain hybrid hydrogels PIL/pNIPAAm. While pNIPAAm exhibits an LCST at 33.9 ± 0.3°C, PIL/pNIPAAm 5/95% and PIL/pNIPAAm 15/85% were found to have LCSTs at 37.6 ± 0.9°C and 52 ± 2°C, respectively. This could be used for controlled drug release that goes along with increasing body temperature in response to an implantation caused infection.

scholarly journals Effects of the Hydrophilic–Lipophilic Balance of Alternating Peptides on Self-Assembly and Thermo-Responsive Behaviors

2019 ◽  
Vol 20 (18) ◽  
pp. 4604 ◽  
Author(s):  
Ihsan ◽  
Nargis ◽  
Koyama
Keyword(s):  
Aqueous Solutions ◽  
Self Assembly ◽  
Polymer Chains ◽  
Systematic Evaluation ◽  
Solution Temperature ◽  
Critical Solution Temperature ◽  
Hydrophilic Lipophilic Balance ◽  
Upper Critical Solution Temperature ◽  
Cloud Points ◽  
Micellization Behavior

A series of N-substituted poly(Gly–alter–Val) peptides were successfully synthesized for the systematic evaluation of the micellization behavior of alternating peptides. Three-component polymerization employing an aldehyde, a primary ammonium chloride, and potassium isocyanoacetate afforded four alternating peptides in excellent yields. We investigated the dependence of the hydrophilic–lipophilic balance of alternating peptides on the micellization behavior. All the aqueous solutions of alternating peptides exhibited upper critical solution temperature (UCST) behaviors, strongly indicating that the alternating binary pattern would mainly contribute to the UCST behaviors. The cloud points of alternating peptides shifted to higher temperatures as the side chains became more hydrophilic, which is opposite to the trend of typical surfactants. Such unusual micellization behaviors appeared to be dependent on the quasi-stable structure of single polymer chains formed in water.

Synthesis and Characterization of Comb-Type Grafted Hydrogels

2012 ◽  
Vol 602-604 ◽  
pp. 1274-1284
Author(s):  
Ping Zhang ◽  
Shi Pu Li ◽  
Xin Yu Wang ◽  
Hong Lian Dai
Keyword(s):  
Aqueous Solution ◽  
Fluorescence Spectroscopy ◽  
Lower Critical Solution Temperature ◽  
Ammonium Persulfate ◽  
Solution Temperature ◽  
Synthesis And Characterization ◽  
Critical Solution Temperature

The grafted hydrogels of N-isopropylacrylamide (IPAAm) with 2-hydroxyethylacrylate (HEA) was prepared in an aqueous solution using ammonium persulfate (APS) and N,N,N’,N’-tetramethylethylene diamine (TEMED) as an accelerator. Lower critical solution temperature (LCST) and swelling ratios were measured as a function of temperature. The properties of the hydrogels contained pyrenyl probe in water were investigated by fluorescence spectroscopy.

scholarly journals Thermally responsive polymeric hydrogel brushes: synthesis, physical properties and use for the culture of chondrocytes

2006 ◽  
Vol 4 (12) ◽  
pp. 117-126 ◽  
Author(s):  
John Collett ◽  
Aileen Crawford ◽  
Paul V Hatton ◽  
Mark Geoghegan ◽  
Stephen Rimmer
Keyword(s):  
Crosslink Density ◽  
Cell Attachment ◽  
Viable Cell ◽  
Contact Angles ◽  
Polymer Chains ◽  
Solution Temperature ◽  
Critical Solution Temperature ◽  
Thermally Responsive ◽  
Isopropyl Acrylamide ◽  
Responsive Polymer

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.

scholarly journals Constrained thermoresponsive polymers – new insights into fundamentals and applications

2021 ◽  
Vol 17 ◽  
pp. 2123-2163
Author(s):  
Patricia Flemming ◽  
Alexander S Münch ◽  
Andreas Fery ◽  
Petra Uhlmann
Keyword(s):  
Phase Transition ◽  
Current Knowledge ◽  
Polymer Chains ◽  
Switching Behavior ◽  
Solution Temperature ◽  
Miscibility Gap ◽  
Underlying Structure ◽  
Thermoresponsive Polymers ◽  
Critical Solution Temperature ◽  
Stimuli Responsive Polymers

In the last decades, numerous stimuli-responsive polymers have been developed and investigated regarding their switching properties. In particular, thermoresponsive polymers, which form a miscibility gap with the ambient solvent with a lower or upper critical demixing point depending on the temperature, have been intensively studied in solution. For the application of such polymers in novel sensors, drug delivery systems or as multifunctional coatings, they typically have to be transferred into specific arrangements, such as micelles, polymer films or grafted nanoparticles. However, it turns out that the thermodynamic concept for the phase transition of free polymer chains fails, when thermoresponsive polymers are assembled into such sterically confined architectures. Whereas many published studies focus on synthetic aspects as well as individual applications of thermoresponsive polymers, the underlying structure–property relationships governing the thermoresponse of sterically constrained assemblies, are still poorly understood. Furthermore, the clear majority of publications deals with polymers that exhibit a lower critical solution temperature (LCST) behavior, with PNIPAAM as their main representative. In contrast, for polymer arrangements with an upper critical solution temperature (UCST), there is only limited knowledge about preparation, application and precise physical understanding of the phase transition. This review article provides an overview about the current knowledge of thermoresponsive polymers with limited mobility focusing on UCST behavior and the possibilities for influencing their thermoresponsive switching characteristics. It comprises star polymers, micelles as well as polymer chains grafted to flat substrates and particulate inorganic surfaces. The elaboration of the physicochemical interplay between the architecture of the polymer assembly and the resulting thermoresponsive switching behavior will be in the foreground of this consideration.

Pyrene-labeled amphiphilic poly-(N-isopropylacrylamides) prepared by using a lipophilic radical initiator: synthesis, solution properties in water, and interactions with liposomes

1995 ◽  
Vol 73 (11) ◽  
pp. 2030-2040 ◽  
Author(s):  
Françoise M. Winnik ◽  
Alexander Adronov ◽  
Hiromi Kitano
Keyword(s):  
Polymeric Micelles ◽  
Polymer Concentration ◽  
Polymer Chains ◽  
Solution Temperature ◽  
Solution Properties ◽  
Excimer Emission ◽  
Elastic Light Scattering ◽  
Critical Solution Temperature ◽  
Liposome Suspension ◽  
Hydrophobic Tail

Fluorescently labeled amphiphilic poly-(N-isopropylacrylamides) (PNIPAM) substituted with a N-[4-(1-pyrenyl)butyl]-N-n-octadecyl group at the chain end were prepared by free-radical polymerization in dioxane of N-isopropylacrylamide (NIPAM) using 4,4′-azobis{4-cyano-N,N-[4-(1-pyrenyl)butyl]-n-octadecyl}pentanamide as the initiator. The solution properties of the polymers in water were studied as a function of polymer concentration and temperature. Quasi-elastic light-scattering measurements and fluorescence experiments monitoring the pyrene excimer and pyrene monomer emissions revealed the presence of multimolecular polymeric micelles below the lower critical solution temperature (LCST) of PNIPAM. These underwent partial, reversible reorganization as they were heated above the LCST. The interactions of the pyrene-labeled amphiphilic PNIPAM with dimyristoylphosphatidylcholine (DMPC) liposomes have been examined in water at 25 °C. From fluorescence experiments it was established that the polymeric micelles are disrupted irreversibly upon contact with the liposomes. The anchoring of the polymer chains occurs by insertion of their hydrophobic tail within the phospholipidic bilayer, as evidenced from a large decrease of the pyrene excimer emission relative to pyrene monomer emission. The copolymers remained anchored within the bilayer as the temperature of the copolymer–liposome suspension was raised above the LCST of PNIPAM. Keywords: liposome, poly-(N-isopropylacrylamide), fluorescence, micelles.

Superabsorbent Nanohydrogels of Poly (N-Isopropyl Acrylamide-Co-Itaconic Acid) Grafted on Starch — Synthesis and Swelling Study

Nano LIFE ◽  
2016 ◽  
Vol 06 (02) ◽  
pp. 1650005 ◽  
Author(s):  
Karim Pourjamal ◽  
Marziyeh Fathi ◽  
Ali Akbar Entezami ◽  
Mohammad Hasanzadeh ◽  
Nasrin Shadjou
Keyword(s):  
Itaconic Acid ◽  
Starch Synthesis ◽  
Ammonium Persulfate ◽  
Solution Temperature ◽  
Scanning Calorimetry ◽  
Critical Solution Temperature ◽  
Dsc Studies ◽  
Isopropyl Acrylamide ◽  
Effects Of Ph

Biopolymer-based superabsorbent nanohydrogel consisting of N-isopropylacrylamide and itaconic acid (IA) was grafted on to starch backbone in an aqueous solution in the absence of the cross-linker agents. The copolymerization reaction occurred in the presence of ammonium persulfate (APS) as an initiator. The effect of N-isopropylacrylamide-to-IA ratio and different concentrations of initiator were investigated. The nanohydrogel composition was characterized by Fourier transform infrared spectroscopy (FTIR). The thermal stability was analyzed by Thermogravimetric analysis (TGA). Differential scanning calorimetry (DSC) studies were employed for determination of lower critical solution temperature in hydrogels. Dynamic light scattering analysis showed a narrow size distribution around 70–200[Formula: see text]nm for the synthesized nanohydrogels. The effects of pH on swelling behavior of the hydrogel were investigated. The obtained nanohydrogels, due to their pH and thermo dual sensitive properties, have the potential to be used in the drug delivery systems.

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