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299 results about "Hydrogel matrix" patented technology

Immobilized bioactive hydrogel matrices as surface coatings

InactiveUS7303814B2Improves tissue integrationImprove intimate contactSurgerySkeletal disorderHydrogel matrixMedical device
The present invention is directed to a stabilized bioactive hydrogel matrix coating for substrates, such as medical devices. The invention provides a coated substrate comprising a substrate having a surface, and a bioactive hydrogel matrix layer overlying the surface of the medical device, the hydrogel matrix comprising a first high molecular weight component and a second high molecular weight component, the first and second high molecular weight components each being selected from the group consisting of polyglycans and polypeptides, wherein at least one of the first and second high molecular weight components is immobilized (e.g., by covalent cross-linking) to the surface of the substrate.
Owner:PIONEER SURGICAL TECH INC

Bioactive wound dressings and implantable devices and methods of use

The present invention provides wound dressings, optionally surgically implantable, containing biodegradable, polymers and hydrogels having allogenic or autologous precursor cells, such as stem cells and progenitor cells dispersed within. Alternatively, the wound dressings can have conditioned medium obtained from the precursor cells dispersed within. The wound dressings promote tissue restoration processes at a site of application or implantation. Additional bioactive agents can also be dispersed within the polymer / hydrogel matrix, which can be formulated to biodegrade at a controlled rate by adjusting the composition. Methods are also provided for using such biodegradable wound dressings as a delivery device or carrier for the precursor cells, conditioned medium and bioactive agents, or as coatings on implantable medical devices, to promote tissue restoration at a lesion site.
Owner:MEDIVAS LLC

Methods and Compositions for Regenerating Connective Tissue

InactiveUS20090123547A1Halting progressionAntibacterial agentsBiocideProgenitorLigament structure
Connective tissue regenerative compositions and methods of repairing and regenerating connective tissue using such compositions are provided. The compositions generally comprise a bioactive hydrogel matrix comprising a polypeptide, such as gelatin, and a long chain carbohydrate, such as dextran. The hydrogel matrix may further include polar amino acids, as well as additional beneficial additives. Advantageously, the compositions include further components, such as osteoinductive or osteoconductive materials, medicaments, stem or progenitor cells, and three-dimensional structural frameworks. The compositions are useful for regenerating connective tissue, and can be administered to an area having injury to, or a loss of, connective tissue, such as bone, cartilage, tendon, and ligament.
Owner:PIONEER SURGICAL TECH INC

Cell Aggregation and Encapsulation Device and Method

The invention is a cell aggregation device comprising a hydrogel substrate having at least one, preferably a plurality, of cell-repellant compartments recessed into the uppermost surface. Each compartment is composed of an upper cell suspension seeding chamber having an open uppermost portion and a bottom portion, and one, or more than one, lower cell aggregation recess connected to the bottom portion of the upper cell suspension seeding chamber by a port. The diameter of the port may be fully contiguous with the walls of the chambers and walls of the recesses, or the diameter of the port may be more narrow than the walls of the chamber but fully contiguous with the walls of the recesses or more narrow than both the walls of the chamber and the walls of the recesses. The upper cell suspension seeding chambers are formed and positioned to funnel the cells into the lower cell aggregation recesses through gravitational force. The aggregation recesses are formed and positioned to promote cellular aggregation by coalescing cells into a finite region of minimum gravitational energy, increasing intercellular contact and minimizing or preventing cell adherence to the substrate. A device for encapsulating aggregates of live cells is provided. The device comprises (i) a biocompatible, bio-sustainable substrate having a cell-encapsulating face composed of one or more biocompatible, bio-sustainable, spaced-apart, cell-encapsulating compartments extending therefrom and (ii) a coating layer composed of a biocompatible, bio-sustainable polymer that completely surrounds the substrate and the cell-encapsulating compartments. A method for making the device is also provided.
Owner:BROWN UNIVERSITY

Composite comprising polysaccharide-functionalized nanoparticle and hydrogel matrix, a drug delivery system and a bone defect replacement matrix for sustained release comprising the same, and the preparation method thereof

The present invention relates to a nanoparticle-protein-hydrogel composite comprising (1) a polysaccharide-functionalized nanoparticle comprising a core composed of a biodegradable polymer, a hydrogel surface layer composed of a biocompatible polymer emulsifier, and a polysaccharide physically bound to the core and / or the hydrogel layer; (2) a protein forming a specific binding with the polysaccharide; and (3) a hydrogel matrix composed of a biocompatible polymer as a matrix for the nanoparticle. The present also relates to a drug delivery system and a bone defect replacement matrix comprising the composite for sustained release, and the preparation method thereof. Further, the present invention also provides a method for controlling the release rate of a protein drug by changing the content of the polysaccharide in a unit mass of the nanoparticle and / or by changing the content of the nanoparticle in a unit mass of the composite.
Owner:GWANGJU INST OF SCI & TECH

Medical cold compress plaster and preparation process thereof

The invention provides a medical cold compress plaster. The medical cold compress plaster is composed of a support layer, a gel layer and an isolating layer, and has the special shape according with the physiological curve of the applied part. An oil phase and a water phase forming the hydrophilic gel layer respectively comprise the following components in percentage by weight: the oil phase: 20-35% of a dispersing agent, 5-7% of macromolecule resin, 0.05-0.15% of dihydroxyaluminium aminoacetate, 0.01-0.15% of ethylene diamine tetraacetic acid, 0.15% of absolute ethyl alcohol, 0.04-0.1% of menthol, 0.1-1% of vitamin E, and 0.05-0.1% of triclosan; the water phase: 0.2-0.8% of tartaric acid, 1.2-2% of carbomer, 0.5-1% of sodium carboxymethylcellulose, 0.01-0.1% of vitamin C, the balance of medical purified water, and the total weight percentage is 100%. A preparation process comprises the following steps: dispersing all the components of the oil phase into the dispersing agent, and uniformly stirring the components; dissolving all the components of the water phase into water, and uniformly stirring the components; mixing the water phase and the oil phase, uniformly stirring the water phase and the oil phase in a vacuum mixing pot, thus obtaining the hydrophilic gel substrate of the medical cold compress plaster, coating the support layer with the hydrophilic gel substrate, meanwhile covering with the isolating layer, and carrying out cutting, solidifying and packaging to obtain the needed medical cold compress plaster product.
Owner:HANGZHOU JIERSI BIOTECH CO LTD
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