Patent classifications
C08J2305/04
METHOD OF ADMINISTERING A SELF-FOAMING COMPOSITION
A method for managing and/or treating obesity and/or overweight and/or for inducing weight loss. The method includes orally administering to a patient a composition capable of being transformed into a hydrogel foam after its introduction into the patient stomach. The hydrogel foam occupies at least 20% of the volume of the patient stomach.
Polymer compositions
The invention relates to novel a high-volume swelling hydrogel which comprises a plurality of pores which are defined by an interpenetrating network, and/or a semi-interpenetrating network and/or simple cross-linked arrangement of a plurality of one or more species of hydrophilic polymers, optionally together with one or more biocompatible polymers and optionally together with one or more plasticising agents, characterised in that at least some of the pores are at least partially collapsed and/or flattened, and further characterised in that the interpenetrating network and/or semi-interpenetrating network and/or cross-linked arrangement which defines the collapsed and/or flattened pores is substantially unbroken. The invention also relates to a process for preparing such hydrogels, and to their use as an appetite suppressant.
ALGINATE HYDROGEL COMPOSITIONS
The present application provides a semi-permeable hydrogel composition comprising an alginate matrix that is covalently crosslinked in its periphery to a multi-armed water soluble polymer, along with related methods and uses thereof.
Process For Crosslinking Polysaccharides From Macroalgae to Form a Polymer Material
The present invention relates to a process for crosslinking polysaccharides from macroalgae to yield a polymer material in a processing chamber. The process includes the steps of producing a mixture comprising a solid containing polysaccharide from macroalgae and a water-containing liquid, with a ratio of liquid to solid of between 3:1 and 1:9, adjusting a pressure acting on the mixture to at least the vapour pressure of water at a first temperature, the first temperature being greater than/equal to 100° Celsius, and heating the mixture to the first temperature, wherein the solid comprises as polysaccharide at least one of alginate, alginic acid, agar and/or Carrageenan. The invention further relates to a process for producing a biopolymer product from such a polymer material in an apparatus comprising a processing chamber and a shaping apparatus. The invention also relates to a biopolymer product obtained by such a process.
Photocontrolled dynamic covalent linkers for polymer networks
Reversibly crosslinkable polymeric networks, including reversibly crosslinkable hydrogel networks are provided. Also provided are methods of making the polymeric networks and methods of using the hydrogel networks in tissue engineering applications. The reversibly crosslinkable polymeric networks are composed of polymer chains that are covalently crosslinked by azobenzene boronic ester bonds that can be reversibly formed and broken by exposing the polymeric networks to different wavelengths of light.
MULTI-LAYER DEVICE COMPRISING A REPAIR LAYER HAVING CONDUCTIVE A HYDROGEL FILM OR BEADS
A multi-layer device and its method of manufacture are disclosed. The multi-layer device comprises a first electrode layer, a first repair layer, a functional layer, and a second electrode layer. The first repair layer comprises a conductive hydrogel film or conductive hydrogel beads, the conductive hydrogel film or the conductive hydrogel beads comprising conductive filler particles dispersed in a cross-linked polymer. The repair layer protects the multi-layer device from electrical short circuits. A multi-layer device is also disclosed including a light-transmissive electrode layer comprising a porous mesh or porous spheres.
Dendritic Macroporous Hydrogels Prepared By Crystal Templating
The present invention includes a hydrogel and a method of making a porous hydrogel by preparing an aqueous mixture of an uncrosslinked polymer and a crystallizable molecule; casting the mixture into a vessel; allowing the cast mixture to dry to form an amorphous hydrogel film; seeding the cast mixture with a seed crystal of the crystallizable molecule; growing the crystallizable molecule into a crystal structure within the uncrosslinked polymer; crosslinking the polymer around the crystal structure under conditions in which the crystal structure within the crosslinked polymer is maintained; and dissolving the crystals within the crosslinked polymer to form the porous hydrogel.
METHODS FOR TREATING OR PREVENTING OBESITY AND BODY WEIGHT MANAGEMENT
This disclosure provides a method of administrating to a subject a two-portion solution system in a specific ingesting order to yield a water-insoluble cross-linked hydrogel mass in the stomach. The volume of the formed water-insoluble cross-linked hydrogel mass is at least 50% v/v of the total volume of the two-portion solution system. The method is useful for preventing and treating overweight and obesity.
Photocontrolled dynamic covalent linkers for polymer networks
Reversibly crosslinkable polymeric networks, including reversibly crosslinkable hydrogel networks are provided. Also provided are methods of making the polymeric networks and methods of using the hydrogel networks in tissue engineering applications. The reversibly crosslinkable polymeric networks are composed of polymer chains that are covalently crosslinked by azobenzene boronic ester bonds that can be reversibly formed and broken by exposing the polymeric networks to different wavelengths of light.
COMPOSITE PROTON CONDUCTIVE MEMBRANES
A composite proton conductive membrane, comprising an inorganic filler having covalently bonded acidic functional groups and a high surface area of at least 150 m.sup.2/g; and a water insoluble ionically conductive polymer. This membrane provides advantages over traditional polymeric proton conductive membranes for redox flow battery, fuel cell, and electrolysis applications include: 1) enhanced proton conductivity/permeance due to the formation of additional nanochannels for proton conducting; 2) improved proton/electrolyte selectivity for redox flow battery application; 3) reduced membrane swelling and gas or electrolyte crossover; 4) improved chemical stability; 5) increased cell operation time with stable performance, and 6) reduced membrane cost.