4D smart porous scaffolds based on polyHIPE architecture and electroactive PEDOT

2021 ◽  
Author(s):  
Ana Ferrandez-Montero ◽  
Bastien Carlier ◽  
Rémy AGNIEL ◽  
johanne Leroy-dudal ◽  
Cedric Vancaeyzeele ◽  
...  
Keyword(s):  
Polymeric Materials ◽  
Porous Scaffolds ◽  
Stimuli Responsive ◽  
Responsive Materials ◽  
Wide Range ◽  
Passive Materials

3D porous polymeric materials have a wide range of applications and can be obtained from different approaches as passive materials, permanently set after fabrication. Stimuli-responsive materials gives the opportunity to...

scholarly journals Natural Polysaccharide Carriers in Brain Delivery: Challenge and Perspective

Pharmaceutics ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 1183
Author(s):  
Manuela Curcio ◽  
Giuseppe Cirillo ◽  
Jourdin R. C. Rouaen ◽  
Federica Saletta ◽  
Fiore Pasquale Nicoletta ◽  
...  
Keyword(s):  
Blood Brain Barrier ◽  
Brain Barrier ◽  
Brain Diseases ◽  
Stimuli Responsive ◽  
Drug Bioavailability ◽  
Responsive Materials ◽  
Blood Brain ◽  
Wide Range ◽  
Materials Used ◽  
The Brain

Targeted drug delivery systems represent valuable tools to enhance the accumulation of therapeutics in the brain. Here, the presence of the blood brain barrier strongly hinders the passage of foreign substances, often limiting the effectiveness of pharmacological therapies. Among the plethora of materials used for the development of these systems, natural polysaccharides are attracting growing interest because of their biocompatibility, muco-adhesion, and chemical versatility which allow a wide range of carriers with tailored physico-chemical features to be synthetized. This review describes the state of the art in the field of targeted carriers based on natural polysaccharides over the last five years, focusing on the main targeting strategies, namely passive and active transport, stimuli-responsive materials and the administration route. In addition, in the last section, the efficacy of the reviewed carriers in each specific brain diseases is summarized and commented on in terms of enhancement of either blood brain barrier (BBB) permeation ability or drug bioavailability in the brain.

scholarly journals From Appendage to Crosslinker – Unusual Swelling Behavior in Spiropyran-Modified Hydrogels

2021 ◽  
Author(s):  
Michael M. Lerch ◽  
Ankita Shastri ◽  
Thomas B.H. Schroeder ◽  
Amos Meeks ◽  
Shucong Li ◽  
...  
Keyword(s):  
Polymeric Materials ◽  
Crosslinking Density ◽  
Stimuli Responsive ◽  
Solution Ph ◽  
Responsive Materials ◽  
Cooperative Effects ◽  
Isomer Distribution ◽  
Vis Spectroscopy ◽  
Swelling Studies ◽  
Hydrogel Swelling

Stimuli-responsive materials typically contain responsive molecular units that couple an external trigger to a defined macroscale response. Ongoing efforts to boost the versatility and complexity of these responses increasingly focus on multi-stimuli-responsive molecular units and crosslinkers, as these bear the potential to impart self-regulatory behaviors building on cooperative effects and feedback mechanisms. Herein, we study a stimuli-responsive platform consisting of polyacrylamide-based hydrogels with well-known multi-responsive spiropyrans covalently bound as pendant groups or ´non-innocent´ crosslinkers. Surprisingly, as compared to their appended counterparts, spiropyran crosslinkers cause up to two-fold larger hydrogel swelling in methylenebisacrylamide-crosslinked poly(acrylamide-co-acrylic acid) hydrogels, despite their increased relative crosslinking density. We seek the origin of this unexpected behavior by employing nanoindentation, swelling studies, and UV-vis spectroscopy to study changes in mechanical properties and in spiropyran isomer distribution as a function of solution pH, co-monomer chemistry, and swelling-induced polymer strain. We then estimate the osmotic counterion pressures as a function of spiropyran isomer distribution but find that such pressures alone are insufficient to explain the observed behavior. Charge complexation, cooperative effects between the hydrogel´s mechanics and chemistry, and aggregate formation may all be invoked to explain features of the observed ´non-innocence´ of spiropyran crosslinkers. Taken together, these insights will aid rational implementation of such responsive crosslinkers in materials design and extend the functionality of existing polymeric materials towards more complex and better tunable behaviors.

CO2-responsive polymeric materials: synthesis, self-assembly, and functional applications

2016 ◽  
Vol 45 (15) ◽  
pp. 4391-4436 ◽  
Author(s):  
Ali Darabi ◽  
Philip G. Jessop ◽  
Michael F. Cunningham
Keyword(s):  
Self Assembly ◽  
Polymeric Materials ◽  
Stimuli Responsive ◽  
Materials Synthesis ◽  
Responsive Materials ◽  
Functional Applications ◽  
System P

CO2is an ideal trigger for switchable or stimuli-responsive materials because it is benign, inexpensive, green, abundant, and does not accumulate in the system.

Smart and Intelligent Stimuli Responsive Materials: An Innovative Step in Drug Delivery System

2020 ◽  
Vol 6 (1) ◽  
pp. 41-52 ◽  
Author(s):  
Arijit Guha ◽  
Md. Adil Shaharyar ◽  
Kazi Asraf Ali ◽  
Sanjit Kr. Roy ◽  
Ketousetuo Kuotsu
Keyword(s):  
Drug Delivery ◽  
Smart Materials ◽  
Intelligent Systems ◽  
Stimuli Responsive ◽  
Design Development ◽  
Scientific Review ◽  
Responsive Materials ◽  
Wide Range ◽  
Current Scenario ◽  
Niche Area

Background: In the field of drug delivery, smart and intelligent approaches have gained significant attention among researchers in order to improve the efficacy of conventional dosage forms. Material science has played a key role in developing these intelligent systems that can deliver therapeutic cargo on-demand. Stimuli responsive material based drug delivery systems have emerged as one of the most promising innovative tools for site-specific delivery. Several endogenous and exogenous stimuli have been exploited to devise “stimuli-responsive” materials for targeted drug delivery. Methods: For better understanding, these novel systems have been broadly classified into two categories: Internally Regulated Systems (pH, ionic strength, glucose, enzymes, and endogenous receptors) and Externally Regulated Systems (Light, magnetic field, electric field, ultrasound, and temperature). This review has followed a systematic approach through separately describing the design, development, and applications of each stimuli-responsive system in a constructive manner. Results: The development includes synthesis and characterization of each system, which has been discussed in a structured manner. From advantages to drawbacks, a detailed description has been included for each smart stimuli responsive material. For a complete review in this niche area of drug delivery, a wide range of therapeutic applications including recent advancement of these smart materials have been incorporated. Conclusion: From the current scenario to future development, a precise overview of each type of system has been discussed in this article. In summary, it is expected that researchers working in this novel area will be highly benefited from this scientific review.

Gold/Silver-Polymer Hybrid Nanostructures as Thermoreversible Optical Sensors and Probes for the Quantification Radical Compounds

2015 ◽  
Vol 1802 ◽  
pp. 41-44 ◽  
Author(s):  
Eun Chul Cho ◽  
Ju A La ◽  
Sora Lim ◽  
Ji Eun Song
Keyword(s):  
Optical Sensors ◽  
Polymeric Materials ◽  
Hybrid Nanostructures ◽  
Stimuli Responsive ◽  
Ag Nps ◽  
Au Nps ◽  
Optical Signals ◽  
Gold Silver ◽  
Wide Range ◽  
Color Switching

ABSTRACTWe present gold (Au) and silver (Ag) nanoparticles (NPs) could be used not only for stimuli-responsive optical sensors but also for the quantification of radical compounds when these nanoparticles are suitably combined with polymeric materials. When Au NPs are assembled 2-dimensionally on the surface of hydrogel NPs which respond to temperatures, the hybrid NPs displayed thermoreversible multiple color switching. Accordingly, optical bandwidths of the hybrid NPs are reversibly changed with temperatures: with hybrid NPs assembled with 51 nm Au NPs, prominent optical signals are recorded at 900 nm at 50 °C while most of extinction signals are shown below 600 nm at room temperatures. In addition, we demonstrate the modification of Ag NPs’ surfaces (nanocubes and nanospheres) with polyelectrolytes (either positive or negative) could extend the quantifiable detection ranges of radical compounds. Through the surface modification of Ag NPs, the polyelectrolytes protect the Ag NPs by probably either retarding (forming diffusion barriers) or preventing (blocking/entrapping/scavenging) the arrival of radicals to Ag NPs or both. The roles of the polyelectrolytes are demonstrated by using radical compounds produced from tetrahydrofuran and H2O2. From the results, we could obtain calibration curves for the wide-range quantification of radical compounds.

Smart Polymers and their Applications: A Review

2017 ◽  
Vol 8 (03) ◽  
Author(s):  
Gore S. A. ◽  
Gholve S. B. ◽  
Savalsure S. M. ◽  
Ghodake K. B. ◽  
Bhusnure O. G. ◽  
...  
Keyword(s):  
Oil Recovery ◽  
Water Soluble ◽  
Solution Temperature ◽  
Smart Polymers ◽  
Stimuli Responsive ◽  
Responsive Materials ◽  
Water Soluble Polymers ◽  
Commercial Applications ◽  
Stimuli Sensitive ◽  
External Stimuli

Smart polymers are materials that respond to small external stimuli. These are also referred as stimuli responsive materials or intelligent materials. Smart polymers that can exhibit stimuli-sensitive properties are becoming important in many commercial applications. These polymers can change shape, strength and pore size based on external factors such as temperature, pH and stress. The stimuli include salt, UV irradiation, temperature, pH, magnetic or electric field, ionic factors etc. Smart polymers are very promising applicants in drug delivery, tissue engineering, cell culture, gene carriers, textile engineering, oil recovery, radioactive wastage and protein purification. The study is focused on the entire features of smart polymers and their most recent and relevant applications. Water soluble polymers with tunable lower critical solution temperature (LCST) are of increasing interest for biological applications such as cell patterning, smart drug release, DNA sequencing etc.

Sensitive Mechanocontrolled Luminescence in Cross-Linked Polymer Films

2019 ◽  
Author(s):  
Ayumu Karimata ◽  
Pradnya Patil ◽  
Eugene Khaskin ◽  
Sébastien Lapointe ◽  
robert fayzullin ◽  
...  
Keyword(s):  
Mechanical Stress ◽  
Polymer Films ◽  
Soft Matter ◽  
Small Strain ◽  
Visual Methods ◽  
Photoluminescence Intensity ◽  
Stimuli Responsive ◽  
Responsive Materials ◽  
Highly Sensitive ◽  
Mechanical Stretching

Direct translation of mechanical force into changes in chemical behavior on a molecular level has important implication not only for the fundamental understanding of mechanochemical processes, but also for the development of new stimuli-responsive materials. In particular, detection of mechanical stress in polymers via non-destructive methods is important in order to prevent material failure and to study the mechanical properties of soft matter. Herein, we report that highly sensitive changes in photoluminescence intensity can be observed in response to the mechanical stretching of cross-linked polymer films when using stable, (pyridinophane)Cu-based dynamic mechanophores. Upon stretching, the luminescence intensity increases in a fast and reversible manner even at small strain (< 50%) and applied stress (< 0.1 MPa) values. Such sensitivity is unprecedented when compared to previously reported systems based on organic mechanophores. The system also allows for the detection of weak mechanical stress by spectroscopic measurements or by direct visual methods.<br>

scholarly journals Thermo- and Photoresponsive Behaviors of Dual-Stimuli-Responsive Organogels Consisting of Homopolymers of Coumarin-Containing Methacrylate

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 329
Author(s):  
Seidai Okada ◽  
Eriko Sato
Keyword(s):  
Functional Group ◽  
Solution Temperature ◽  
Stimuli Responsive ◽  
Critical Solution Temperature ◽  
Equilibrium Degree ◽  
Stimuli Responsive Polymers ◽  
Responsive Polymers ◽  
Dual Functional ◽  
Wide Range ◽  
Increasing Temperature

Coumarin-containing vinyl homopolymers, such as poly(7-methacryloyloxycoumarin) (P1a) and poly(7-(2′-methacryloyloxyethoxy)coumarin) (P1b), show a lower critical solution temperature (LCST) in chloroform, which can be controlled by the [2 + 2] photochemical cycloaddition of the coumarin moiety, and they are recognized as monofunctional dual-stimuli-responsive polymers. A single functional group of monofunctional dual-stimuli-responsive polymers responds to dual stimuli and can be introduced more uniformly and densely than those of dual-functional dual-stimuli-responsive polymers. In this study, considering a wide range of applications, organogels consisting of P1a and P1b, i.e., P1a-gel and P1b-gel, respectively, were synthesized, and their thermo- and photoresponsive behaviors in chloroform were investigated in detail. P1a-gel and P1b-gel in a swollen state (transparent) exhibited phase separation (turbid) through a temperature jump and reached a shrunken state (transparent), i.e., an equilibrium state, over time. Moreover, the equilibrium degree of swelling decreased non-linearly with increasing temperature. Furthermore, different thermoresponsive sites were photopatterned on the organogel through the photodimerization of the coumarin unit. The organogels consisting of homopolymers of coumarin-containing methacrylate exhibited unique thermo- and photoresponsivities and behaved as monofunctional dual-stimuli-responsive organogels.

scholarly journals Review of Functional Treatments for Modified Wood

Coatings ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 327
Author(s):  
Morwenna J. Spear ◽  
Simon F. Curling ◽  
Athanasios Dimitriou ◽  
Graham A. Ormondroyd
Keyword(s):  
High Performance ◽  
Responsive Materials ◽  
Wood Modification ◽  
Wide Range ◽  
Natural Wood ◽  
Impregnation Modification ◽  
New Applications ◽  
New Generation ◽  
Dimensional Instability ◽  
Modified Wood

Wood modification is now widely recognized as offering enhanced properties of wood and overcoming issues such as dimensional instability and biodegradability which affect natural wood. Typical wood modification systems use chemical modification, impregnation modification or thermal modification, and these vary in the properties achieved. As control and understanding of the wood modification systems has progressed, further opportunities have arisen to add extra functionalities to the modified wood. These include UV stabilisation, fire retardancy, or enhanced suitability for paints and coatings. Thus, wood may become a multi-functional material through a series of modifications, treatments or reactions, to create a high-performance material with previously impossible properties. In this paper we review systems that combine the well-established wood modification procedures with secondary techniques or modifications to deliver emerging technologies with multi-functionality. The new applications targeted using this additional functionality are diverse and range from increased electrical conductivity, creation of sensors or responsive materials, improvement of wellbeing in the built environment, and enhanced fire and flame protection. We identified two parallel and connected themes: (1) the functionalisation of modified timber and (2) the modification of timber to provide (multi)-functionality. A wide range of nanotechnology concepts have been harnessed by this new generation of wood modifications and wood treatments. As this field is rapidly expanding, we also include within the review trends from current research in order to gauge the state of the art, and likely direction of travel of the industry.

scholarly journals Recent Advances in Fabrication of Non-Isocyanate Polyurethane-Based Composite Materials

Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3497
Author(s):  
Piotr Stachak ◽  
Izabela Łukaszewska ◽  
Edyta Hebda ◽  
Krzysztof Pielichowski
Keyword(s):  
Raw Materials ◽  
Synthesis Method ◽  
Polymeric Materials ◽  
Original Research ◽  
Significant Group ◽  
Oh Groups ◽  
New Class ◽  
Hazardous Chemical ◽  
Wide Range

Polyurethanes (PUs) are a significant group of polymeric materials that, due to their outstanding mechanical, chemical, and physical properties, are used in a wide range of applications. Conventionally, PUs are obtained in polyaddition reactions between diisocyanates and polyols. Due to the toxicity of isocyanate raw materials and their synthesis method utilizing phosgene, new cleaner synthetic routes for polyurethanes without using isocyanates have attracted increasing attention in recent years. Among different attempts to replace the conventional process, polyaddition of cyclic carbonates (CCs) and polyfunctional amines seems to be the most promising way to obtain non-isocyanate polyurethanes (NIPUs) or, more precisely, polyhydroxyurethanes (PHUs), while primary and secondary –OH groups are being formed alongside urethane linkages. Such an approach eliminates hazardous chemical compounds from the synthesis and leads to the fabrication of polymeric materials with unique and tunable properties. The main advantages include better chemical, mechanical, and thermal resistance, and the process itself is invulnerable to moisture, which is an essential technological feature. NIPUs can be modified via copolymerization or used as matrices to fabricate polymer composites with different additives, similar to their conventional counterparts. Hence, non-isocyanate polyurethanes are a new class of environmentally friendly polymeric materials. Many papers on the matter above have been published, including both original research and extensive reviews. However, they do not provide collected information on NIPU composites fabrication and processing. Hence, this review describes the latest progress in non-isocyanate polyurethane synthesis, modification, and finally processing. While focusing primarily on the carbonate/amine route, methods of obtaining NIPU are described, and their properties are presented. Ways of incorporating various compounds into NIPU matrices are characterized by the role of PHU materials in copolymeric materials or as an additive. Finally, diverse processing methods of non-isocyanate polyurethanes are presented, including electrospinning or 3D printing.

Sign in / Sign up

Export Citation Format

Share Document