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56results about How to "No physiological toxicity" patented technology

Asymmetrical polyurethane/nano TiO2 thin film wound dressing and preparation method thereof

The invention discloses an asymmetrical polyurethane / nano TiO2 thin film wound dressing, which is characterized by being composed of a dense surface layer and a porous support layer, wherein the dense surface layer is integrally shaped with the porous support layer, the dense surface layer has the thickness of 7-15 mu m, the porous support layer has the total pore volume of 4.80-5.24 cm<3> / g, and in-situ generated nano TiO2 particles are uniformly dispersed in an entire polyurethane thin film and have the particle size of 30-150 nm. The invention also discloses a preparation method of the asymmetrical polyurethane / nano TiO2 thin film wound dressing. In the technical scheme disclosed by the invention, a solvent evaporation film-forming method, a wet process phase inversion film-forming method and a nano particle in-situ generation technique are felicitously organically combined, the structure of the polyurethane thin film wound dressing is reconstructed, the defects of the existing performance of the polyurethane thin film wound dressing are compensated, the comprehensive and clinical application value of the product is greatly improved, and a new method is provided for preparation of the asymmetrical polyurethane / nano TiO2 thin film wound dressing.
Owner:SICHUAN UNIV

Polyurethane drug release controlling body with thermoswitch and preparation method thereof

The invention discloses a polyurethane drug release controlling body with a thermoswitch, which is prepared by compounding thermosensitive polyurethane with drug micromolecules. The free volume of the thermosensitive polyurethane is subjected to reversible contraction-expansion mutation at a certain temperature from 39 to 45 DEG C so as to have an on-off effect, thus the drug micromolecules loaded in the thermosensitive polyurethane have the characteristic of releasing in response to the temperature, wherein below the on-off temperature, the releasing rate of the drug micromolecules is extremely low; and when the temperature rises to above the on-off temperature, the releasing rate of the drug micromolecules rises dramatically. The invention also discloses the preparation method of the polyurethane drug release controlling body. The polyurethane drug release controlling body can conveniently control the response release of the drug micromolecules through temperature change and is highin response speed and free of physiological toxicity, the repeatability of the release switch is good, and the drug release amount can be adjusted freely, thus the polyurethane drug release controlling body has wide application prospect in treatment on postoperation pain, organ infection, local tumor and other diseases; and the preparation method is simple and mature and is easy to grasp.
Owner:SICHUAN UNIV

Capsule polyurethane drug controlled release body with temperature control switch, and preparation method thereof

The invention discloses a capsule polyurethane drug controlled release body with a temperature control switch. The capsule polyurethane drug controlled release body is prepared by loading the drug by a temperature-sensitive polyurethane capsule pipe. In the application of the capsule polyurethane drug controlled release body, a drug release characteristic with temperature response is expressed; and an 'open-close' effect is present. The capsule wall polyurethane molecules are in a rigid crystalline state below the switch temperature, so that diffusion and release of the drug in the controlled release body are blocked; when the temperature rises to higher than the switch temperature, the polyurethane molecules are in a molten state, so that the drug in the body migrates to the capsule wall and the capsule wall drug release outward continuously, with the concentration as a mass ladder force. Besides, the special design of the capsule wall can realize ideal drug diffusion capacity. The invention also discloses a preparation method of the capsule polyurethane drug controlled release body. The temperature-sensitive polyurethane capsule pipe of the drug controlled release body and unsymmetrical structure of the capsule wall design makes the drug controlled release body have fast temperature response speed, good repeatability of the drug release switch, freely adjustable drug release amount, capacity of uniform drug release, no physiological toxicity, so that the drug controlled release body has wide application prospects in clinic local drug treatment.
Owner:SICHUAN UNIV

Power relay equipment for insulating building

The invention discloses power relay equipment for an insulating building. The power relay equipment comprises a base, a coil, an armature, a restoring spring, a push rod, contacts, a lower plate spring, a middle ratchet wheel and an upper plate spring, wherein an insulating shell is arranged above the base; an iron core is arranged in the insulating shell through a bracket; the coil is arranged on the iron core; the bracket is connected with the restoring spring. The power relay equipment for the insulating building, disclosed by the invention, is simple in structure and convenient to operate; the armature attracts the iron core under the action of electromagnetic attraction to drive the push rod to rotate the middle ratchet wheel anticlockwise; the plate springs move, so that a contact state of upper and lower layers of the contacts is changed; when driving electric pulse disappears, the armature returns to an initial state under the action of the restoring spring, a ratchet abuts against a tooth surface on a seedling wheel and the ratchet wheel does not rotate, so that the contacts can keep the state unchanged; only if the quantity of teeth and tooth shapes of upper and lower layers of ratchet wheels are changed, 2 to 4 steps form one cycle of 1 to 2 contacts, and different control functions are realized.
Owner:芜湖浩权建筑工程有限公司

Doxorubicin hydrochloride self-assembled polymer nanoparticle and preparation method thereof

The invention discloses a doxorubicin hydrochloride self-assembled polymer nanoparticle which is prepared from doxorubicin hydrochloride and an amphipathic high-molecular polymer PLGA (Polylactic-co-Glycolic Acid), wherein the PLGA is formed by two monomers, namely lactic acid (LA) and glycolic acid (GA). The preparation method comprises the following steps: 1) dissolving a drug doxorubicin hydrochloride into a polar organic solvent A so as to obtain a doxorubicin hydrochloride solution; 2) dissolving the PLGA into a polar organic solvent B so as to obtain a PLGA solution; 3) uniformly mixing the doxorubicin hydrochloride solution with the PLGA solution so as to obtain an eutectic solution, dripping the eutectic solution into an aqueous phase under the stirring condition, continuously stirring, and volatilizing the organic solvent; and 4) centrifuging the completely volatilized solution at a high speed by using a centrifugal machine, and collecting the precipitate, thereby obtaining the doxorubicin hydrochloride self-assembled polymer nanoparticle. The prepared product can achieve the effects of reducing the drug toxicity, reducing the administration frequency, improving the drug stability, delaying in-vivo release time of the drug, reducing adverse reactions of the drug, improving the bioavailability and efficacy of the drug and achieving excellent treatment effects.
Owner:LIAONING UNIVERSITY

Preparation method of moisture-proof traditional Chinese medicine coated film

The invention discloses a preparation method of a moisture-proof traditional Chinese medicine coated film, which relates to a coating technology of the traditional Chinese medicine and belongs to the medicinal preparation field. The moisture-proof traditional Chinese medicine coated film comprises the following components: 30-40 parts of hydroxypropyl methyl cellulose, 5-8 parts of triethyl citrate, 6-10 parts of xylitol, 4-8 parts of castor oil, 4-8 parts of tween-80, 14-18 parts of dextrin, 6-10 parts of aerosol, 6-10 parts of zein, 5-10 parts of 1% of artificial food coloring solution, 350-420 parts of distilled water (40-50 DEG C) and balance of ethanol with 95% of concentration; wherein weight unit of solid is gram, and volume unit of liquid is milliliter. The moisture-proof traditional Chinese medicine coated film has the beneficial effect of stable chemical property of a film forming substance, inertia to an enzyme system, no physiological toxicity and no usage of cane sugar; the coated film has the advantages of moisture resistance, heat resistance, cold resistance and abrasion resistance which are better than that of the sugar coated tablets, so that the stability of the coated film is increased, and storage period is prolonged.
Owner:刘桐言

Method for preparing calcium lysine chelate with shell of Argopecten irradias as calcium source

ActiveCN106631848AConsiderable yieldAppreciable calcium contentMetabolism disorderOrganic compound preparationAlcoholCentrifugation
The invention discloses a method for preparing a calcium lysine chelate with the shell of Argopecten irradias as a calcium source. The method comprises the following steps: treatment of the shell of Argopecten irradias: successively subjecting the shell of Argopecten irradias to conventional cleaning, air drying, crushing, charing and ashing; ash content treatment: treating the ash content of the shell with a slightly excess HCl solution so as to obtain a CaCl2 solution; mixing reaction: heating and mixing the CaCl2 solution and lysine under stirring so as to realize chelating; centrifugation: carrying out centrifugation and retaining a supernatant; evaporative concentration: subjecting a reaction solution to slow heating for evaporative concentration; alcohol precipitation: purifying a calcium lysine chelate obtained in the previous step by using absolute ethyl alcohol; and drying: collecting a gel precipitate, repeatedly washing the gel precipitate with absolute ethyl alcohol and then carrying out drying at a constant temperature of 60 to 80 DEG C so as to obtain the calcium lysine chelate. The preparation method for the calcium lysine chelate in the invention uses processing waste of Argopecten irradias, i.e., the shell, and the essential amino acid lysine as raw materials and prepares the calcium lysine chelate through water-phase synthesis; and the method is low in cost, good in chelation yield and suitable for large-scale batch production.
Owner:HEBEI AGRICULTURAL UNIV.
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