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31 results about "Destructive agent" patented technology

Enhanced transport using membrane disruptive agents

InactiveUS7737108B1Prevent uptakePrevent clearanceBiocidePeptide/protein ingredientsMetaboliteCell layer
Compositions and methods for transport or release of therapeutic and diagnostic agents or metabolites or other analytes from cells, compartments within cells, or through cell layers or barriers are described. The compositions include a membrane barrier transport enhancing agent and are usually administered in combination with an enhancer and/or exposure to stimuli to effect disruption or altered permeability, transport or release. In a preferred embodiment, the compositions include compounds which disrupt endosomal membranes in response to the low pH in the endosomes but which are relatively inactive toward cell membranes (at physiologic pH, but can become active toward cell membranes if the environment is acidified below ca. pH 6.8), coupled directly or indirectly to a therapeutic or diagnostic agent. Other disruptive agents can also be used, responsive to stimuli and/or enhancers other than pH, such as light, electrical stimuli, electromagnetic stimuli, ultrasound, temperature, or combinations thereof. The compounds can be coupled by ionic, covalent or H bonds to an agent to be delivered or to a ligand which forms a complex with the agent to be delivered. Agents to be delivered can be therapeutic and/or diagnostic agents. Treatments which enhance delivery such as ultrasound, iontopheresis, and/or electrophereis can also be used with the disrupting agents.
Owner:UNIV OF WASHINGTON

Systems and methods for reducing unintended use of active ingredients in dermal delivery devices

The present invention is drawn to systems and methods for reducing unintended use of an active ingredient, such as residual active ingredients present in spent dermal patches and peels. The system can include a dermal patch including an active ingredient and a destructive agent configured to chemically react with the active ingredient. The destructive agent can be present in a container or an absorber. In one embodiment, the absorber can be used within the container. The container can be configured to receive the dermal patch such that the active ingredient contacts the destructive agent within the container. The absorber can be configured to contact the dermal patch such that the active ingredient contacts the destructive agent of the absorber. Additionally, systems and methods for impeding the unintended use of an active ingredient, such as those present in dermal patches or peels, are also provided. The system includes a dermal patch having a first side configured to deliver an active ingredient to a skin or mucosal surface, wherein the first side also includes a dermal adhesive. The system also includes an adhesive-coated device. The adhesive-coated surface of the device can be configured to adhere to the first side, wherein upon use of the dermal patch followed by contacting the adhesive-coated surface with the first side, residual active ingredient is rendered substantially inaccessible.
Owner:ZARS INC

Apparatus for target compound treatment

An apparatus adapted to treat at least one target compound comprising a housing through which fluid may pass; a receiving zone defined within the housing; disposed after the receiving zone within the housing, a destruction zone in which an aqueous solution containing at least one target compound is exposed to a destruction agent, the destruction agent adapted to convert the target compound into destruction byproducts; disposed after the destruction zone, a filtration zone containing a filtration agent adapted to remove the destruction byproducts from the solution; liquid disposal means for receiving solution from the filtration zone; and solid disposal means for receiving solids from the filtration zone, whereby, the target compound is first converted to byproducts, then the byproducts are filtered out of the solution, preventing target compounds from entering wastewater systems and ultimately re-entering the water supply. Physical embodiments of the invention include an in-line version for mounting under a sink; a version mounted near a sink and in communication with plumbing, but not in-line; a version that is transportable within a cart; and a toilet-mounted version for removing target compound from urine. Docking stations may be provided for collection of target compounds, which stations then releasably communicate with the apparatus to transfer collected target compounds from the station to the apparatus. Various agents and processes are disclosed for destroying target compounds and for filtering byproducts.
Owner:CLEAR RIVER ENVIRO

Method for preparing fracturing fluid thickener with self-destruction effect

The invention discloses a fracturing fluid thickener with a self-destruction effect. The fracturing fluid thickener comprises, by weight, 5-80% of monomer aqueous phase, 12-70% of oil-based solvents and 8-25% of emulsifiers. The usage of reducing agent solution in oxidation-reduction initiators accounts for 0.1-0.5% of the mass of emulsion. A method for preparing the fracturing fluid thickener mainly includes dissolving the emulsifiers in the oil-based solvents; adding the monomer aqueous phase with excessive oxidizing destruction agents into the oil-based solvents; carrying out stirring and deoxidizing, adding the reducing agent solution at the temperatures of 10-40 DEG C and initiating reaction for 0.5-4 hours to obtain inverse emulsion with the oxidizing destruction agents partially coated by micro-spheres; directly diluting the emulsion by the aid of water to prepare the fracturing fluid thickener with the self-destruction effect, or separating out the micro-spheres by sedimentation and then preparing the fracturing fluid thickener with the self-destruction effect. The fracturing fluid thickener and the method have the advantages that the fracturing fluid thickener and destruction agents can be produced by the aid of the method in an integrated manner, the destruction agents can be uniformly placed and can be released in a delayed manner, and accordingly the problems of difficulty in controlling the destruction time of directly mixed destruction agents for use in conventional processes or high cost and uneven destruction of capsule destruction agents can be solved.
Owner:YANSHAN UNIV

Preparation method for chlorinated polypropylene resin

ActiveCN103275251AMeet the use requirementsUniform chlorinationButyl acetateKetone solvents
The invention discloses a preparation method for chlorinated polypropylene resin. The preparation method comprises the following steps of: (1) fully swelling polypropylene in a solvent, adding a lattice destructive agent, uniformly dispersing the lattice destructive agent in the solvent, adding an initiator to initiate reaction, adding the mixture of an emulsifier and water, fully mixing and dispersing to form emulsion, and filtering, washing the emulsion with water and drying the emulsion to obtain polypropylene powder; and (2) dissolving the polypropylene powder into a mixed solvent formed by trichloroethane and water, fully mixing and dispersing, heating, adding the initiator, introducing a chlorine gas to react after mixing and dispersing the initiator uniformly, removing the residual chlorine gas from the liquid after the chlorination degree reaches a set value, and obtaining the chlorinated polypropylene resin by performing two-phase separation, washing with water, neutralizing, drying and crushing. The chlorinated polypropylene produced by the invention is chlorinated uniformly, and can be fully dissolved in the solvents such as dimethylbenzene, methylbenzene, ketone solvents and environment-friendly butyl acetate solvents. In addition, through the preparation method disclosed by the invention, the product with controllable chlorination degree can be prepared.
Owner:广州合成材料研究院有限公司

Enhanced transport using membrane disruptive agents

InactiveUS20100160216A1Prevent uptakePrevent clearanceBiocidePeptide/protein ingredientsMetaboliteCell layer
Compositions and methods for transport or release of therapeutic and diagnostic agents or metabolites or other analytes from cells, compartments within cells, or through cell layers or barriers are described. The compositions include a membrane barrier transport enhancing agent and are usually administered in combination with an enhancer and / or exposure to stimuli to effect disruption or altered permeability, transport or release. In a preferred embodiment, the compositions include compounds which disrupt endosomal membranes in response to the low pH in the endosomes but which are relatively inactive toward cell membranes (at physiologic pH, but can become active toward cell membranes if the environment is acidified below ca. pH 6.8), coupled directly or indirectly to a therapeutic or diagnostic agent. Other disruptive agents can also be used, responsive to stimuli and / or enhancers other than pH, such as light, electrical stimuli, electromagnetic stimuli, ultrasound, temperature, or combinations thereof. The compounds can be coupled by ionic, covalent or H bonds to an agent to be delivered or to a ligand which forms a complex with the agent to be delivered. Agents to be delivered can be therapeutic and / or diagnostic agents. Treatments which enhance delivery such as ultrasound, iontopheresis, and / or electrophereis can also be used with the disrupting agents.
Owner:UNIV OF WASHINGTON

Nano liquid destroying agent for fracturing fluid and preparation method thereof

The invention discloses a nano liquid destroying agent for fracturing fluid and a preparation method thereof. The nano liquid destroying agent for the fracturing fluid is prepared from, by weight, 5.2-16.4% of peroxide, 2.3-10% of a gemini surfactant, 8.4-16.0% of a nonionic emulsifier, 1.9-4.4% of an auxiliary additive and 62.5-78.5% of a solvent; the structure of the nano liquid destroying agentfor the fracturing fluid is that the nonionic emulsifier and the gemini surfactant form a mixed micelle or vesicle having a closed double layer structure, and the peroxide and the inner layer structure constitute an ion pair and are wrapped inside the micelle or vesicle; the mixed micelle or vesicle size of the nano liquid destroying agent is nanometer-scale and specifically is between 15 and 100nanometre. The agent can meet the gel breaking requirements of the polymer fracturing fluid and the silicone fracturing fluid, and has the advantages of good storage stability at room temperature, weak corrosiveness, long storage period and good delayed gel breaking effect.
Owner:CHENGDU LEARN PRACTICES TECH CO LTD

Preparation method for chlorinated polypropylene resin

ActiveCN103275251BMeet the use requirementsUniform chlorinationButyl acetateKetone solvents
The invention discloses a preparation method for chlorinated polypropylene resin. The preparation method comprises the following steps of: (1) fully swelling polypropylene in a solvent, adding a lattice destructive agent, uniformly dispersing the lattice destructive agent in the solvent, adding an initiator to initiate reaction, adding the mixture of an emulsifier and water, fully mixing and dispersing to form emulsion, and filtering, washing the emulsion with water and drying the emulsion to obtain polypropylene powder; and (2) dissolving the polypropylene powder into a mixed solvent formed by trichloroethane and water, fully mixing and dispersing, heating, adding the initiator, introducing a chlorine gas to react after mixing and dispersing the initiator uniformly, removing the residual chlorine gas from the liquid after the chlorination degree reaches a set value, and obtaining the chlorinated polypropylene resin by performing two-phase separation, washing with water, neutralizing, drying and crushing. The chlorinated polypropylene produced by the invention is chlorinated uniformly, and can be fully dissolved in the solvents such as dimethylbenzene, methylbenzene, ketone solvents and environment-friendly butyl acetate solvents. In addition, through the preparation method disclosed by the invention, the product with controllable chlorination degree can be prepared.
Owner:广州合成材料研究院有限公司
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