Abstract:
A method of creating a layer of a single use processing substrate includes the steps of extruding a polymeric sheet with a particulate substance dispersed therein, cooling the polymeric sheet with the particulate substance therein, removing the particulate substance from the polymeric sheet to form holes in the polymeric sheet, and attaching the polymeric sheet to an absorbent sheet.
Abstract:
Microporous structures characterized by having a three-dimensional interconnecting network skeleton, which are obtained by comprising mixing a thermoplastic resin, a water-soluble organic compound and a water-soluble polymer material and then eliminating said water-soluble organic compound and said water-soluble polymer material by extracting with water. A process for producing microporous structures comprising mixing a thermoplastic resin with water-soluble components which contain a water-soluble organic compound and a water-soluble polymer material, at a specific volume ratio, thus forming a mixture having a three-dimensional interconnecting network skeleton made of said thermoplastic resin wherein said water-soluble components are maintained, bringing said mixture into contact with water and thus extracting and eliminating said water-soluble components from said mixture, wherein a volume ratio of the water-soluble organic compound to the water-soluble polymer material ranges from 35 to 95/65 to 5.
Abstract:
PARTICULATE CROSSLINKED ORGANOILICO MATERIALS ARE PREPARED BY REACTING IN SUSPENSION IN AN ENERT LIQUID OF AN ORGANOPOLYSILOXANE CONTAINING SILICON-BONDED OLEFINICALLY UNSATURATED GROUPS WITH HYDROGEN SUBSTITURED ORGANOPOLYSILOXANE. SUCH MATERIALS HAVING A MICROPOROUS STRUCTURE ARE SUITABLE AS A PACKING MATEIAL IN THE COLOUMS OF GAS CHROMATOGRAPHS.
Abstract:
The present disclosure is directed to methods of forming polyimide gels. The methods generally include forming a polyamic acid and dehydrating the polyamic acid with a dehydrating agent in the presence of water. The resulting polyimide gels may be converted to polyimide or carbon xerogels or aerogels. The methods are advantageous in providing rapid or even instantaneous gelation, which may be particularly useful in formation of beads comprising the polyimide gels. Polyimide or carbon gel materials prepared according to the disclosed method are suitable for use in environments containing electrochemical reactions, for example as an electrode material within a lithium-ion battery.
Abstract:
The present disclosure is directed to methods of forming polyimide gels. The methods generally include forming a polyamic acid and dehydrating the polyamic acid with a dehydrating agent in the presence of water. The resulting polyimide gels may be converted to polyimide or carbon xerogels or aerogels. The methods are advantageous in providing rapid or even instantaneous gelation, which may be particularly useful in formation of beads comprising the polyimide gels. Polyimide or carbon gel materials prepared according to the disclosed method are suitable for use in environments containing electrochemical reactions, for example as an electrode material within a lithium-ion battery.
Abstract:
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.
Abstract:
A polymeric composite coating includes a drug release retardant polymer matrix, and pH-responsive nanoparticulate pore former. The pH-responsive pore formers function to modulate the permeability of the coating in response to pH changes which can compensate any changes in drug solubility with negligible leaching of the pore formers. The pH-responsive nanoparticulate pore formers may also function as alcohol-resistant component to the overall composite coating to resist increased solubility and permeability in presence of alcohol at 40% ethanol concentration in aqueous media. In one embodiment, the drug release retardant polymer is made of cellulose derivatives.
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:
Molecularly imprinted polymers (MIPs) are materials exhibiting molecular recognition of a target molecule. MIPs are synthesized in the presence of an aflatoxin template, a mimic to the targeted molecule, used as an imprint that is further washed away with suitable solvent after completion of the polymerization process, leaving a cavity in the polymer of the same stereochemistry, functionality and morphology to the template. When the MIP encounters an aflatoxin, the molecule is bound in the cavity with a receptor-like affinity.