Abstract:
Polymerní kompozice s ko-kontinuální strukturou je tvorena vzájemne propojenou kontinuální strukturou nosného skeletu a kontinuální strukturou biresorbovatelné výplne, pricemz nosný skelet je na bázi alespon jednoho bioinertního polymeru a bioresorbovatelná výpln je na bázi alespon jednoho polymeru hydrolyticky anebo enzymaticky rozlozitelného v prostredí zivých organismu, a zároven hmotnostní pomer nosného skeletu a bioresorbovatelné výplne je 20:80 az 80:20. Polymerní kompozice má s výhodou nosný skelet vytvoren na bázi polyolefinu, polyuretanu, polyesteru, vinylových polymeru, polymethylmethakrylátu a/nebo jejich kopolymeru. Bioresorbovatelná výpln pak je s výhodou tvorena materiálem na bázi polylaktidu a/nebo jeho kopolymeru, polyanhydridu, skrobu a/nebo jeho derivátu a ve vode rozpustných polymeru - polyethylenglykolu, polypropylenglykolu, polyvinylalkoholu a/nebo polyvinyl-pyrrolidonu.
Abstract:
Biochemical carriers are provided. Each of the biochemical carriers includes: biochemical molecules having a sequence into which digital data information is encoded; a carrier particle composed of a polymer matrix and in which the biochemical molecules are connected to the surface or inside of the polymer matrix; and an index code introduced into the carrier particle. Also provided is a method for fabricating biochemical carriers. The fabrication method includes: encoding digital data into a sequence of biochemical molecules; synthesizing the biochemical molecules based on the encoded sequence; mixing the biochemical molecules with a photocurable material; curing the mixture to obtain carrier particles including a polymer matrix; and introducing an index code into the carrier particles simultaneously with or separately from the curing. Also provided is a method for restoring digital data from the biochemical carrier. The restoration method includes: analyzing the index code of the biochemical carrier; reacquiring the biochemical molecules from the biochemical carrier based on the analytical results of the index code; sequencing the biochemical molecules; and decoding the sequencing results to restore digital data.
Abstract:
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.
Abstract:
A nanoporous material is disclosed having a plurality of lamellae. Through each lamella is an array of penetrating pores. Adjacent lamellae are spaced apart by an intervening spacing layer. The spacing layer comprises an array of spacing elements integrally formed with and extending between the adjacent lamellae. The spacing layer has interconnected porosity extending within the spacing layer. Such a nanoporous material can be manufactured using block copolymer materials. First, a morphology is formed comprising a three dimensional array of isolated islands in a continuous matrix. The islands are formed of at least one island component of the block copolymer and the matrix is formed of at least one matrix component of the block copolymer. Next, channels are formed in the matrix between at least some of the islands. The island component is then selectively removed to leave the matrix with an array of interconnected pores.
Abstract:
A porous film which is produced using a resin composition containing an ultra-high-molecular-weight polyolefin and a polyolefin wax having a weight average molecular weight of 3000 or less, in which the number of branches per 1000 carbon atoms that constitute the main chain of the polyolefin wax is 15 or less; a porous film which is produced using a resin composition containing an ultra-high-molecular-weight polyolefin and a polyolefin wax having a weight average molecular weight of 3000 or less, and which does not substantially contain a component that melts at a temperature of 60° C. or lower; a laminated porous film which comprises one of the porous films and a heat-resistance porous layer laminated on at least one surface of the porous film; and a separator for batteries, which comprises the porous film or the laminated porous film.
Abstract:
The present invention relates to a polymeric porous material characterized in that: the porous material has a bimodal pore size distribution attributable to macropores having a pore size of at least 50 nm and mesopores having a pore size of from 2 nm to less than 50 nm, the proportion of the specific surface area of the macropores to the specific surface area of all pores of the porous material is at least 10%, and the porous material is produced by (1) polymerizing a monomer in the presence of a polymerization initiator using as a porogen a solution obtained by dissolving a polymer having a weight-average molecular weight of at least 100,000 and a molecular weight distribution Mw/Mn of not more than 1.5 in a good solvent for the monomer, and (2) removing the porogen from the resultant product.
Abstract:
The present invention relates to a method of manufacture of an interconnected porous non-biodegradable polymer implant suitable for implantation into a mammal for the treatment, repair or replacement of defects or injury in musculoskeletal tissue, wherein the mechanical properties of the implant can be controlled by varying the concentration of the non-biodegradable polymer and/or varying the duration and number of freeze-thaw cycles and the interconnected porous non-biodegradable polymer implant has sufficient percent porosity and pore diameter to facilitate integration of cells and attachment within the mammal via ingrowth of surrounding tissue. The present invention also relates to an implant manufactured by the method.
Abstract:
Porous infusible polymer (IP) parts are made by incorporating 0.2 to 10 volume percent organic fibers, preferably with short lengths, into the particulate IP, consolidating the mixture under pressure and optionally heating, and then “burning off” the fibers. After the fibers are burned off the resulting part has porosity in which the pores are elongated, usually retaining the shape of the organic fibers. When these parts are exposed to moisture (which they usually absorb) and then suddenly heated they tend not to blister from vaporization of the water. This makes them useful as parts for aircraft (jet) and other engines and other applications where sudden temperature increase may occur.