Blockchain Papers

Abdallah Almahmoud, Harendra S. Parekh, Brett M. Paterson, Karnaker R. Tupally · 8 authors

No abstract is available for this record.

Soumya Narayana, B.H. Jaswanth Gowda, Umme Hani, Mohammed Gulzar Ahmed · 6 authors

Hydrogels are innovative materials characterized by a water-swollen, crosslinked polymeric network capable of retaining substantial amounts of water while maintaining structural integrity. Their unique ability to swell or contract in response to environmental stimuli makes them integral to biomedical applications, including drug delivery, tissue engineering, and wound healing. Among these, "smart" hydrogels, sensitive to stimuli such as pH, temperature, and light, showcase reversible transitions between liquid and semi-solid states. Thermoresponsive hydrogels, exemplified by poly(N-isopropylacrylamide) (PNIPAM), are particularly notable for their sensitivity to temperature changes, transitioning near their lower critical solution temperature (LCST) of approximately 32 °C in water. Structurally, PNIPAM-based hydrogels (PNIPAM-HYDs) are chemically versatile, allowing for modifications that enhance biocompatibility and functional adaptability. These properties enable their application in diverse therapeutic areas such as cancer therapy, phototherapy, wound healing, and tissue engineering. In this review, the unique properties and behavior of smart PNIPAM are explored, with an emphasis on diverse synthesis methods and a brief note on biocompatibility. Furthermore, the structural and functional modifications of PNIPAM-HYDs are detailed, along with their biomedical applications in cancer therapy, phototherapy, wound healing, tissue engineering, skin conditions, ocular diseases, etc. Various delivery routes and patents highlighting therapeutic advancements are also examined. Finally, the future prospects of PNIPAM-HYDs remain promising, with ongoing research focused on enhancing their stability, responsiveness, and clinical applicability. Their continued development is expected to revolutionize biomedical technologies, paving the way for more efficient and targeted therapeutic solutions.

A. Schmalz, Holger Schmalz, Axel H. E. Müller

A series of smart hydrogels based on dual stimuli responsive star-block copolymers responding to pH and temperature were prepared via atom transfer radical polymerization (ATRP) employing the core-first method. They consist of poly(2-(dimethylamino)ethyl methacrylate) (PDMA) inner blocks and outer blocks comprised of poly(di(ethylene glycol) methyl ether methacrylate) (PDEGMA). The aggregation behavior of these block copolymer stars is analyzed by dependence on block length and arm number. The dual stimuli responsiveness of the stars is demonstrated by turbidity as well as dynamic light scattering on dilute aqueous solution, and the gelation behavior of concentrated aqueous solutions is studied by rheology. Above the transition temperature of the PDEGMA outer blocks the stars form flower-like aggregates in dilute solution or free-standing gels at higher concentrations. When the temperature is increased further above the transition temperature of the PDMA inner block, the aggregates start to contract and a weakening was observed for soft gels, whereas for strong gels no influence on the moduli was detected. The behavior is controlled by both concentration and pH value. In addition, we show that the minimum polymer concentration for gel formation can be lowered by quaternizing the inner block of the stars, but a second response to stimuli is lost during the procedure.

María Molina, Claudia R. Rivarola, César A. Barbero

A water soluble cationic metal complex (tris(2,2′-bipyridine)ruthenium(II)) can be loaded into hydrogels containing acrylamide and/or acrylic acid units. The cationic complex is retained in polymer containing acrylic acid units at high pH and released at low pH. This is likely due to electrostatic interactions of the cation with the carboxylate anions, present at high pH, which are converted into neutral carboxylic acid at low pH, releasing the metal complex. Since the gel contract at low pH, the water soluble cation is also released with the water expelled from the gel. However, a strong retention of the cation inside the gels is observed when acrylamide units are present. A possible explanation is a hydrophobic interaction of the large metal complex with the polyacrylamide network. Using the counteracting electrostatic and hydrophobic interactions of probe molecules with smart hydrogel matrixes it is possible to tune the pH of maximum release away from the pKa of the ionizable group.

Maria Bassil, Michael Ibrahim, Roland Habchi, J. Davenas · 6 authors

No abstract is available for this record.

Igor Galaev, Bo Mattiasson

Intelligent or smart polymers are biocompatible polymeric materials that can respond to the physiological or biological environment by expanding or contracting at different rates. This type of response can be used either to construct biomedical devices or to produce advanced responsive medical systems. In the pharmaceutical field, such systems have been used to develop new types of responsive or pulsatile delivery devices.