C08J9/26

Porous microparticles of biodegradable polymer, and polymer filler comprising same

The present invention relates to porous microparticles of a biodegradable polymer, and a polymer filler comprising the same.

POLYIMIDE PRECURSOR SOLUTION, METHOD FOR PRODUCING POLYIMIDE PRECURSOR SOLUTION, METHOD FOR PRODUCING POLYIMIDE FILM, AND METHOD FOR PRODUCING POROUS POLYIMIDE FILM

A polyimide precursor solution contains a polyimide precursor having a weight average molecular weight of 40,000 or more, and an aqueous solvent containing a tertiary amine compound and water, in which a viscosity of the polyimide precursor solution after a storage at 25° C. for 14 days is 50% or more and 200% or less with respect to a viscosity of the polyimide precursor solution before the storage.

POLYIMIDE PRECURSOR SOLUTION, METHOD FOR PRODUCING POLYIMIDE PRECURSOR SOLUTION, METHOD FOR PRODUCING POLYIMIDE FILM, AND METHOD FOR PRODUCING POROUS POLYIMIDE FILM

A polyimide precursor solution contains a polyimide precursor having a weight average molecular weight of 40,000 or more, and an aqueous solvent containing a tertiary amine compound and water, in which a viscosity of the polyimide precursor solution after a storage at 25° C. for 14 days is 50% or more and 200% or less with respect to a viscosity of the polyimide precursor solution before the storage.

Photo-responsive spiropyran-based N-isopropylacrylamide (NIPAM) gels

The present teaching relates to photo-responsive hydrogels comprising a copolymer comprising N-isopropylacrylamide (NIPAM), a polymerisable derivative of benzospiropyran, a cross-linking agent and an acid, the acid having a pKa of less than 6, wherein the hydrogel is operably responsive to exposure to water so as to undergo spontaneous protonation and swelling. The photo-responsive hydrogels described can be used in the field of microfluidic platforms.

Photo-responsive spiropyran-based N-isopropylacrylamide (NIPAM) gels

The present teaching relates to photo-responsive hydrogels comprising a copolymer comprising N-isopropylacrylamide (NIPAM), a polymerisable derivative of benzospiropyran, a cross-linking agent and an acid, the acid having a pKa of less than 6, wherein the hydrogel is operably responsive to exposure to water so as to undergo spontaneous protonation and swelling. The photo-responsive hydrogels described can be used in the field of microfluidic platforms.

IMMUNE CELL TRAPPING DEVICES AND METHODS FOR MAKING AND USING THE SAME

Embodiments herein described provide devices for identifying and collecting rare cells or cells which occur at low frequency in the body of a subject, such as, antigen-specific cells or disease-specific cells. More specifically, the devices are useful for trapping immune cells and the devices contain a physiologically-compatible porous polymer scaffold, a plurality of antigens, and an immune cell-recruiting agent, wherein the plurality of antigens and the immune cell recruiting agent attract and trap the immune cell in the device. Also provided are pharmaceutical compositions, kits, and packages containing such devices. Additional embodiments relate to methods for making the devices, compositions, and kits/packages. Further embodiments relate to methods for using the devices, compositions, and/or kits in the diagnosis or therapy of diseases such as autoimmune diseases or cancers.

IMMUNE CELL TRAPPING DEVICES AND METHODS FOR MAKING AND USING THE SAME

Embodiments herein described provide devices for identifying and collecting rare cells or cells which occur at low frequency in the body of a subject, such as, antigen-specific cells or disease-specific cells. More specifically, the devices are useful for trapping immune cells and the devices contain a physiologically-compatible porous polymer scaffold, a plurality of antigens, and an immune cell-recruiting agent, wherein the plurality of antigens and the immune cell recruiting agent attract and trap the immune cell in the device. Also provided are pharmaceutical compositions, kits, and packages containing such devices. Additional embodiments relate to methods for making the devices, compositions, and kits/packages. Further embodiments relate to methods for using the devices, compositions, and/or kits in the diagnosis or therapy of diseases such as autoimmune diseases or cancers.

Porous devices and processes for producing same

Devices and methods for making a polymer with a porous layer from a solid piece of polymer are disclosed. In various embodiments, the method includes heating a surface of a solid piece of polymer to a processing temperature and holding the processing temperature while displacing a porogen layer through the surface of the polymer to create a matrix layer of the solid polymer body comprising the polymer and the porogen layer. In at least one embodiment, the method also includes removing at least a portion of the layer of porogen from the matrix layer to create a porous layer of the solid piece of polymer.

Porous devices and processes for producing same

Devices and methods for making a polymer with a porous layer from a solid piece of polymer are disclosed. In various embodiments, the method includes heating a surface of a solid piece of polymer to a processing temperature and holding the processing temperature while displacing a porogen layer through the surface of the polymer to create a matrix layer of the solid polymer body comprising the polymer and the porogen layer. In at least one embodiment, the method also includes removing at least a portion of the layer of porogen from the matrix layer to create a porous layer of the solid piece of polymer.

INSTRINSICALLY ANTIMICROBIAL POROSIC MATRIX COMPOSITES AND METHOD OF MANUFACTURE THEREOF
20220079145 · 2022-03-17 ·

A method of manufacturing a flexible intrinsically antimicrobial absorbent porosic composite controlling for an effective pore size using removable pore-forming substances and physically incorporated, non-leaching antimicrobials. A flexible intrinsically antimicrobial absorbent porosic composite controlled for an effective pore size composited physically incorporated, high-surface area, non-leaching antimicrobials, optionally in which the physically incorporated non-leaching antimicrobial exposes nanopillars on its surface to enhance antimicrobial activity. A kit that enhances the effectiveness of the intrinsically antimicrobial absorbent porosic composite by storing the composite within an antimicrobial container.