1940 results about "Ionic polymerization" patented technology

Compositions, methods, and applications that increase the efficiency of nucleic acid transfection are provided. In one aspect, a pharmaceutical composition may include at least about 0.5 mg / ml concentration of a nucleic acid condensed with a cationic lipopolymer suspended in an isotonic solution, where the cationic lipopolymer includes a cationic polymer backbone having cholesterol and polyethylene glycol covalently attached thereto, and wherein the molar ratio of cholesterol to cationic polymer backbone is within a range of from about 0.1 to about 10, and the molar ratio of polyethylene glycol to cationic polymer backbone is within a range of from about 0.1 to about 10. The composition further may include a filler excipient.

An initiator is presented for anionically polymerizing monomers, to provide a functional head group on the polymer. A polymer having a functional head group derived from a sulfur containing anionic initiator, and optionally as additional functional group resulting from the use of a functional terminating reagent, coupling agent or linking agent is also provided. A method is presented for anionically polymerizing monomers comprising the step of polymerizing the monomers with a sulfur containing anionic initiator to provide a functional head group on the polymer. An elastomeric compound, comprising a functional polymer and filler is also described. Also provided is a tire having decreased rolling resistance resulting from a tire component containing a vulcanizable elastomeric compound.

Compositions, methods, and applications that increase the efficiency of nucleic acid transfection are provided. In one aspect, a pharmaceutical composition may include at least about 0.5 mg / ml concentration of a nucleic acid condensed with a cationic lipopolymer suspended in an isotonic solution, where the cationic lipopolymer includes a cationic polymer backbone having cholesterol and polyethylene glycol covalently attached thereto, and wherein the molar ratio of cholesterol to cationic polymer backbone is within a range of from about 0.1 to about 10, and the molar ratio of polyethylene glycol to cationic polymer backbone is within a range of from about 0.1 to about 10. The composition further may include a filler excipient.

A three dimensional object includes (a) a light polymerized first component; and (b) a second solidified component different from the first component. The object is preferably of a polymer blend formed from the first component and the second component, with the polymer blend as an interpenetrating polymer network, a semi-interpenetrating polymer network, or a sequential interpenetrating polymer network. In some preferred embodiments, the second component does not contain a cationic polymerization photoinitiator. In some preferred embodiments, the three dimensional object is produced by the process of continuous liquid interface production.

The present invention provides a unique non-viral carrier for nucleic acid delivery in vitro and in vivo, and methods of using thereof.

This invention relates to an ink-receptive composition, including: (a) a filler; (b) a binder having a Tg of less than 30° C.; and (c) a cationic polymer; wherein the composition, when coated on a substrate, forms an ink-receptive coating which accepts ink loading greater than about 300%. The coating compositions provide a printable surface receptive to high loading of ink-jet inks which do not crack at loading in excess of 300%, and in one embodiment, do not crack at loading up to about 400%. In addition, the print shows superior liquid resistance and the print quality of the inks is improved and a reduction in bleeding of colors occurs. Also, printed article have outdoor durability especially those with overlaminates.

The present invention provides a display device in which the adhesive for bonding the display panel and the substrate to each other is prevented from remaining as an uncured portion, and a method for production thereof. The present invention provides: a display device comprising a display panel, a substrate disposed on a display side, and an adhesive layer via which the display panel and the substrate are bonded to each other, wherein the adhesive layer contains a cationically polymerized resin; and the method for production thereof. The adhesive layer more preferably has a refractive index corresponding to that of a member adjacent to the adhesive layer.

The present invention relates to the discovery that biocompatible anionic polymers can effectively inhibit fibrosis, scar formation, and surgical adhesions. The invention is predicated on the discovery that anionic polymers effectively inhibit invasion of cells associated with detrimental healing processes, and in particular, that the effectiveness of an anionic polymer at inhibiting cell invasion correlates with the anionic charge density of the polymer. Thus the present invention provides a large number of materials for use in methods of inhibiting fibrosis and fibroblast invasion. Anionic polymers for use in the invention include but are not limited to natural proteoglycans, and the glycosaminoglycan moieties of proteoglycans. Additionally, anionic carbohydrates and other anionic polymers may be used. The anionic polymers dextran sulfate and pentosan polysulfate are preferred. In a more preferred embodiment, dextran sulfate, in which the sulfur content is greater than about 10% by weight, may be used. In a more preferred embodiment, the average molecular weight is about 40,000 to 500,000 Daltons. The present invention provides compositions and methods to inhibit fibrosis and scarring associated with surgery. The invention further provides compositions and methods to inhibit glial cell invasion, detrimental bone growth and neurite outgrowth. In a preferred embodiment, the inhibitory compositions further comprise an adhesive protein.

A cationically polymerizable pigmented composition comprising (A) a cationically polymerizable binder component containing at least one resin or compound selected from the group consisting of (A-1) a cationically polymerizable acrylic resin consisting of a copolymer of (a) a (meth) acrylic ester monomer having C6-31 aliphatic hydrocarbon group, (b) a polymerizable unsaturated monomer containing a polymerizable unsaturated group and at least one cationically polymerizable moiety selected from the group consisting of an epoxy group and an oxetane ring, and optionally (c) other polymerizable unsaturated monomer, and (A-2) a fatty acid-modified epoxy compound containing C6-32 aliphatic hydrocarbon group and epoxy group, (B) a cationic polymerization initiator initiating polymerization by irradiation or heating, and (C) a color pigment.

The present invention provides a polynucleotide delivery system including a cationic polymer to which a rabies virus glycoprotein (RVG) peptide is bound, wherein the cationic polymer includes a biodegradable bond, and a method of delivering polynucleotides to a target cell by using the delivery system.

A method of processing landfill leachate by use of a membrane separation process is disclosed. Specifically, the following steps are taken to process landfill leachate: collecting landfill leachate in a receptacle suitable to hold said landfill leachate; treating said landfill leachate with one or more water soluble polymers, wherein said water soluble polymers are selected from the group consisting of: amphoteric polymers; cationic polymers; zwitterionic polymers; and a combination thereof; optionally mixing said water soluble polymers with said landfill leachate; passing said treated landfill leachate through a membrane, wherein said membrane is an ultrafiltration membrane or a microfiltration membrane; and optionally back-flushing said membrane to remove solids from the membrane surface.

These objects and others may be accomplished with the present invention, the first embodiment of which provides an oil-in-water nanoemulsion, which includes:an oily phase dispersed in an aqueous phase;(i) at least one amphiphilic lipid selected from the group including nonionic amphiphilic lipids, anionic amphiphilic lipids, and combinations thereof; and(ii) at least one water-soluble nonionic polymer selected from the group including homopolymers and copolymers of ethylene oxide; polyvinyl alcohols; homopolymers and copolymers of vinylpyrrolidone; homopolymers and copolymers of vinylcaprolactam; homopolymers and copolymers of polyvinyl methyl ether; neutral acrylic homopolymers and copolymers; C1–C2 alkyl celluloses and their derivatives; C1–C3 alkyl guar; C1–C3 hydroxyalkyl guar; and combinations thereof;wherein a ratio of the weight of the oily phase to the weight of the amphiphilic lipid (i) ranges from 1.2 to 10;and wherein the oily phase includes oil globules having a number-average size of less than 100 nm. The nanoemulsion obtained is preferably transparent and stable on storage. It may form a composition for topical, preferably cosmetic or dermatological compositions, pharmaceutical compositions and ophthalmological compositions.

Methods comprising preparing an aqueous mixture of an anionic polymer, a charge screening surfactant, and a borate crosslinker, wherein the mixture has a conductivity less than 10 mS / cm, injecting the mixture down a wellbore, and gelling the mixture. An embodiment of the aqueous mixture can also include tetramethylammonium chloride as a clay stabilizer and a metal crosslinker such as a complex of zirconium and an amino acid ligand system. An embodiment can effectively provide borate crosslinking of an anionic polymer in a low-ionic-strength fluid system, without sacrificing ultimate gel strength or thermal persistence of the metal crosslinked polymer.

The present invention relates to a detergent auxiliary composition comprising: (i) a liquid or liquefiable active component; and (ii) a water-insoluble solid support component and (iii) a water-soluble and / or water dispersible encapsulating material; and (iv) optionally one or more adjunct components, characterised in that the composition further comprises (v) a surface deposition enhancing cationic polymer or oligomer having cationic groups such that fewer than 50% are de-activated when a 1% by weight solution of the polymer or oligomer (prepared in deionised water and then adjusted to pH 7.0 with sodium carbonate or citric acid) is stored at 25° C. for ten days (ten day storage test), wherein the surface deposition enhancing cationic polymer is adsorbed onto the water-insoluble solid support component, and wherein the water-soluble and / or water dispersible encapsulating material encapsulates the liquid or liquefiable active component, the water-insoluble solid support component and the surface deposition enhancing cationic polymer.

Multilayer articles, particularly multilayer articles having electrical or ionic conductivity, are made using an improved melt extrusion process. The process includes a combination step in which a macroscopically homogeneous mass is formed prior to introduction into an extruder. The multilayer article may include an electrode layer and a separator layer that are extruded onto a metal current collector. Such structures are particularly useful in lithium-ion batteries.

The invention provides a radiation-curable polymerizable composition of the invention having (a) a hindered amine compound having no nucleophilic moiety in a molecule, (b) a photo-acid generating agent and (c) a cationic polymerizable monomer. The invention further provides an ink composition formed of the radiation-curable polymerizable composition, a method for ink jet recording having: ejecting the ink composition onto a recording medium by using an ink jet recording apparatus and irradiating the ejected ink composition so as to cure the ink composition, and a printed material obtained thereby. The invention further provides a method for forming a planographic printing plate having: ejecting the ink composition onto a hydrophilic recording medium by using an ink jet recording apparatus; and irradiating the ejected ink composition so as to cure the ink composition for forming a hydrophobic region, and a planographic printing plate obtained thereby.

We claim a fragrance delivery system consisting of a mixture of various polymers oligomers and stabilizers capable of forming a surfactant complex gel dispersion when combined with a cleansing surfactant base and yielding high levels of fragrance deposition onto the skin, hair or other surface such as a textile, from a cleansing or softening consumer product comprising a micelle forming surfactant. The internal phase or dispersible phase of this surfactant complex gel dispersion (GLPPD) is made of a mixture of various immiscible polymers, oligomers and stabilizers forming a complex gel with the surfactant platform and whose ratio and composition are selected to dissolve preferentially a wide range of fragrance raw materials. The selection criteria are, first, that the fragrance should present a higher fragrance partitioning ratio into the surfactant complex gel phase than into the free micelles of the surfactant, second, that the surfactant complex gel should not be further solubilized by the free micelles, and third, that the polymer mixture selected should complex with the surfactant system. The external or dispersing phase of the GLPPD is made of a single cationic polymer or a mixture of cationic polymers that have been hydrated and associated with the surfactant to form a complex gel structure that cannot be further solubilized by the free micelles.

A photopolymerization initiator comprising (A) a photo acid-generating compound such as diaryliodonium salt (e.g., diphenyl iodonium, bis(p-chlorophenyl)iodonium, etc.), (B) a photo oxidation radical-generating compound such as diarylketone compound, alpha-diketone compound or ketocoumarin compound, and (C) a fused polycyclic aromatic compound such as 1,4-dimethylnaphthalene, 1-methylanthracene, 9-methylanthracene, 9,10-dimethylanthracene or 9,10-diethylanthracene. The photopolymerization initiator makes it possible to efficiently polymerize the cationically polymerizable monomer by the irradiation with visible light.