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85 results about "Polycarbonate membrane" patented technology

Copper alloy, copper alloy plate, and process for producing the same

ActiveCN101171349AImprove featuresImprove stress relaxation resistanceElectrolysisFiltration
This invention provides a copper alloy having excellent stress relaxation resistance, comprising Ni: 0.1 to 3.0% (% by mass; the same shall apply hereinafter), Sn: 0.01 to 3.0%, and P: 0.01 to 0.3% with the balance consisting of copper and unavoidable impurities, characterized in that the content of Ni in an extraction residue after extraction separation on a filter having an opening size of 0.1 [mu]m by an extraction residue method is not more than 40% in terms of the proportion to the content of Ni in the copper alloy. In the extraction residue method, 10 g of the copper alloy is immersed in 300 ml of a methanol solution having an ammonium acetate concentration of 10% by mass. This copper alloy is used as an anode. On the other hand, platinum is used as a cathode. Galvanostatic electrolysis is carried out at a current density of 10 mA / cm<2>. A solution containing this copper alloy dissolved therein is subjected to suction filtration by a polycarbonate membrane filter having an opening size of 0.1 [mu]m, and the insolubles as the residue are separated and extracted on the filter. The content of Ni in the extraction residue is determined by dissolving the insolubles as the residue on the filter in a solution composed of a mixture of aqua regia and water at a ratio of 1 : 1, and then analyzing the solution by ICP emission spectrometry.
Owner:KOBE STEEL LTD

Copper alloy, copper alloy plate, and process for producing the same

InactiveUS20090116996A1High stress relaxation resistanceImprove bending performanceElectrolysisFiltration
A copper alloy with an excellent stress relaxation resistance including Ni: 0.1 through 3.0 mass %, Sn: 0.01 through 3.0 mass %, P: 0.01 through 0.3 mass % and remainder copper and inevitable impurities, and the Ni content in extracted residues separated and left on a filter having filter mesh size of 0.1 μm by using an extracted residues method accounting for 40 mass % or less of the Ni content in the copper alloy, wherein the extracted residues method requires that 10 g of the copper alloy is immersed in 300 ml of a methanol solution which contains 10 mass % of ammonium acetate, and using the copper alloy as the anode and platinum as the cathode, constant-current electrolysis is performed at the current density of 10 mA / cm2, and the solution in which the copper alloy is thus dissolved is subjected to suction filtration using a membrane filter of polycarbonate whose filter mesh size is 0.1 μm, thereby separating and extracting undissolved residues on said filter, and the Ni content in the extracted residues is identified through analysis by ICP after dissolving said undissolved residues separated and left on said filter into a solution prepared by mixing aqua regia and water at the ratio of 1:1.
Owner:KOBE STEEL LTD

One-dimensional rod-like mesoporous material and preparation method thereof and application thereof

The invention discloses a one-dimensional rod-like mesoporous material and a preparation method thereof and an application thereof, and belongs to the field of mesoporous materials. The preparation method comprises four steps including precursor preparation, filtration preparation of composite mesoporous membrane, elution of surfactant in membrane and dissolving of organic porous membrane, namely, mainly using filtration method to assemble inorganic mesoporous material in the holes of polycarbonate membrane to prepare composite membrane, then using extraction and elution to remove the surfactant in the composite membrane so as to obtain organic-inorganic composite mesoporous membrane, and soaking the organic-inorganic composite mesoporous membrane in dichloromethane solution, and obtaining the one-dimensional rod-like mesoporous material after completely dissolving the organic porous membrane. The rod-like material is a one-dimensional mesoporous silicon dioxide rod with a diameter of 200nm, a length of 10 mu m and a sequential hexagonal mesoporous structure belonging to MCM-41 type with an aperture of 3nm or belonging to SBA-41 type with an aperture of 8nm. The obtained one-dimensional rod-like mesoporous material is applied in the fields of biological macromolecule and catalyst adsorption and the like.
Owner:SHANGHAI INST OF TECH

Gold nano-channel membrane for detecting atrazine and application thereof

The invention provides a chloride modified gold nano-channel membrane for detecting atrazine and a method for detecting the atrazine by using the gold nano-channel membrane. In the invention, polycarbonate membrane is taken as basilar membrane, Au nano-channel membrane with the diameter of 20-50 nm is prepared by using a chemical precipitation method, and chloride ions self-assembles to the pore wall of the gold nano-channel through a gold-chloride covalent bond. The detection method comprises the following steps of: placing the chloride modified gold nano-channel membrane between a sample injection pool and a transmission pool; adding a buffer solution containing atrazine antibody into the sample injection pool; adding a buffer solution into the transmission pool; maintaining a parallel liquid level of the two pools; applying voltage on the two pools and measuring basement currents; adding a buffer solution containing a sample to be tested into the sample injection pool and carrying out a current signal test through a electrochemical workstation, wherein if current undershoot occurs, the sample to be tested contains the atrazine. The invention has the advantages of high detectionefficiency, strong specificity, capability of measuring the atrazine with the concentration lower limit of 1.7*10-10 M, and better application prospect.
Owner:SHANGHAI NORMAL UNIVERSITY

Method for controlled release of active small molecules based on liposomes and application thereof

The invention discloses a method for controlled release of active small molecules based on liposomes and an application thereof. The liposomes wrapped with the active small molecules are prepared by afilm dispersion method, and the method includes the following steps: (1) dissolving the active small molecules and lipids in a mixture of methanol and chloroform (1:1, v / v); (2) removing methanol andchloroform by a rotary vacuum evaporation instrument, and then hydrating a lipid membrane with a hydrating liquid; carrying out water bath ultrasonic treatment to obtain liposomes wrapped with the active small molecules, and extruding by a porous polycarbonate membrane; and dialyzing overnight; (3) adding a dopamine solution to a biomaterial, and gently shaking overnight evenly; and carrying outultrasonic cleaning in sterile distilled water; and (4) adding the liposomes loaded with the active small molecules, and carrying out static reaction; and then washing with a sterile phosphate buffersolution, and thus obtaining the surface of a culture plate modified by the liposomes with the small active molecules. In the method, the active small molecule liposomes are covalently grafted on thesurface of polystyrene, and the liposomes are used as a drug delivery carrier to realize controlled release of drugs.
Owner:PEKING UNIV SCHOOL OF STOMATOLOGY

Method for preparing organic-inorganic compound mesoporous film and application thereof

The invention discloses a method for preparing an organic-inorganic compound mesoporous film and application thereof, and belongs to the field of film materials. The preparation method comprises three steps of preparing precursor liquid, synthesizing a compound mesoporous film by using microwaves and eluting an surface active agent in the film, wherein the inorganic meso-porous material is assembled in pores in the polycarbonate film by the microwave synthesis to prepare the compound film, and the surface active agent in the compound film is removed by an extraction elution method, so that one or more organic-inorganic compound mesoporous films are obtained. The pore diameter of the mesoporous materials in the film is 3.0nm or 6.0nm. Compared with a hydrothermal synthesis method and a pulping filtration method, the microwave synthesis method has the advantages of higher synthetic rate, less time consumption, lower energy consumption, higher efficiency and complete structure of formed film materials. In addition, because of the orderliness of the mesoporous structure and the nanometer size effect of the pore diameter, the organic-inorganic compound mesoporous film can be applied inthe fields of embedment of biological molecules, biological sensors and the like.
Owner:SHANGHAI INST OF TECH

Preparation method of polymeric micelle nanofiltration membrane and application thereof

The invention discloses a preparation method of a polymeric micelle nanofiltration membrane and application thereof, which belongs to the field of porous material separation membranes. The polymer membrane is mainly attached to a macroporous substrate, and a polycarbonate membrane is chosen as the substrate layer. The preparation method of the micelle membrane comprises the following steps: a polymer with an appropriate block proportion and molecular weight is chosen to be dissolved in selective solvent, so that a micelle solution with a specific morphology is formed; the micelle solution is uniformly dispersed, spread onto the macroporous substrate by the vacuum filtration technology and naturally dried, and thereby the block copolymer separation membrane prepared by the dilute micelle solution is obtained. The voids formed between the piled micelles serve as part of membrane pores, thus playing the role of selective separation, while the macroporous substrate of the lower layer helpsincrease the separation efficiency of the membrane. Most of the current methods for preparing polymer membranes are complex and consume a great deal of energy. The membrane production method is universal and simple, the needed cost is low, and moreover, the produced membrane has high separation efficiency, and can be applied to the separation of different sizes of gold nanoparticles.
Owner:NANJING UNIV OF TECH

Multicellular co-culture dish and application method thereof

The invention provides a multicellular co-culture dish and an application method thereof. The co-culture dish comprises a casing, clamping grooves and baffles, wherein the casing is divided into a specific cell cavity and more than 3 peripheral cavities by the baffles and the clamping grooves; the peripheral cavities surround the periphery of the specific cell cavity; the baffles on the periphery of the specific cell cavity are detachable baffles; and the baffles among the peripheral cavities are fixed baffles. Membranes are arranged beside the baffles and are made of polycarbonate membranes, and the baffles are made of plastic or glass. The multicellular co-culture dish has a unique model, can be used for researching the single action and synergistic action of a plurality of cells to certain specific target cell, can be applied among a plurality of cells to research the interrelation among the cells, can be used for researching the single action of drugs in Chinese herbal compound and the compatibility action of assistant and guide, can be used for the research and development of new medicine, and can also be used for monitoring the interaction of drugs, so as to reduce toxic and side effects.
Owner:唐培培 +2

Method for constructing tissue engineering epidermis for detecting irritation of cosmetics on polycarbonate film

The invention relates to a method for constructing a tissue engineering epidermis for detecting the irritation of cosmetics on a polycarbonate film. The method is characterized by comprising the following steps: (1) carrying out separated culture on epidermization cells; (2) preparing a lipid mixture solution; and (3) constructing the tissue engineering epidermis on the polycarbonate film. The method has the advantages that the operation is easy and convenient and the cost is low; the method is good for synthesis and large-scale production of a product and the product has a basal layer, a spinous layer, a granular layer, a transparent layer and the cuticle tissue engineering epidermises which are in completely differentiated shapes, and the irritation of the cosmetics can be conveniently detected.
Owner:PROYA COSMETICS

Novel composite nano preparation based on sonodynamic/immune combined therapy and preparation method and application thereof

The invention discloses a novel composite nano preparation based on sonodynamic / immune combined therapy and a preparation method and application thereof, the novel composite nano preparation comprises a sound-sensitive agent, an immune activator, an active oxygen enhancing drug and liposome, the sound-sensitive agent and the active oxygen enhancing drug are entrapped in a liposome phospholipid bimolecular layer, and the immune activator is embedded on the lipidosome phospholipid bimolecular layer. The method comprises the following steps: (1) preparing a sound-sensitive agent, a cinnamyl aldehyde derivative, MPLA, a lecithin and DSPE-PEG5k into a solution; (2) evaporating out the solvent in the solution obtained in the step (1), and dispersing the drug-loaded lipid film in a buffer solution to obtain a drug-loaded liposome suspension; and (3) enabling the solution obtained in the step (2) to pass through a polycarbonate film to obtain the composite nano-liposome. The preparation can induce anti-tumor reaction, not only can prevent the development of in-situ solid tumors, but also can prevent the tumors from metastasis to far-end tissues. The composition is especially suitable for a combined treatment preparation of sonodynamic therapy and immunotherapy.
Owner:DALIAN UNIV OF TECH

In-vitro cell contact type co-culture device and culture operation method thereof

ActiveCN104164365AConvenient and easy to change liquidRealize contact co-cultivationArtificial cell constructsSkeletal/connective tissue cellsPaleontologyBarrel Shaped
The invention discloses an in-vitro cell contact type co-culture device and a culture operation method thereof. According to the device, a box bottom is arranged at the bottom end of a culture box body; a box cover is arranged at the upper end of the box body; a cell culture tank is arranged in the culture box body; the culture box body is in the shape of a conical gyro, and the diameter at the upper end of the culture box body is larger than the diameter of the bottom of the culture box body; the cell culture tank is barrel-shaped; the upper and lower diameters of the barrel are the same as the diameter of the box bottom of the culture box body; an isolating membrane is fixedly arranged in the middle of the culture tank, and divides the culture tank into an upper culture tank and a lower culture tank. The culture tank is ingeniously divided into the upper culture tank and the lower culture tank by using the polycarbonate membrane and is respectively inoculated on the upper and lower sides, and the culture tank is arranged in the cell culture box after being overturned, so that substantive cell contact type co-culture is realized, and influence of metabolites of one kinds of cells on another kinds of cells and an intercellular effect caused by direct contact are conveniently researched.
Owner:广州陈运贤生命科技有限公司

Method for preparing polypyrole-polycarbonate composite membrane fixed and carried cibacron blue

Disclosed is a preparation method of the poly pyrrole-polycarbonate composite membrane of the supported Cibacron Blue, which relates to the preparation technique of the affinity membrane used for the separation and purification of the protein, the invention provides the preparation method of the poly pyrrole-polycarbonate composite membrane of the supported Cibacron Blue having good hydrophilic property and excellent biocompatibility. The invention takes the polycarbonate membrane as the basement membrane, the basement membrane is fixed in the middle of the diffusion pool containing double pools after the pretreatment in the Cibacron Blue solution; the oxidant and pyrrole monomer solution are respectively added into each pool of the diffusion pool that contains two pools; the active ligand Cibacron Blue is added into any pool of the diffusion pool with the reaction temperature being controlled between 0-40 DEG C and the reaction time is 0.5-8h; finally the poly pyrrole-polycarbonate composite membrane of the supported active ligand Cibacron Blue can be obtained after the cleaning treatment of the basement membrane when the reaction finishes. The prepared affinity membrane has great chemical durability, hydrophilic property and excellent biocompatibility. The composite membrane can be used for separation and purification of protein.
Owner:XIAMEN UNIV

Circulating tumor cell detection device based on hollow nano needle tube electroporation system and detection method thereof

The invention belongs to the technical field of circulating tumor cell detection. The invention particularly discloses a circulating tumor cell detection device based on a hollow nano needle tube electroporation system. The cell detection device comprises a cell culture tank, wherein the cell culture tank comprises a polydimethylsiloxane lump and a polycarbonate membrane, the polydimethylsiloxanelump is provided with a central hole, the polycarbonate membrane corresponds to the bottom of the central hole and is provided with a hollow nano needle tube array, and a cavity formed by the centralhole and the polycarbonate membrane is used for storing cell suspension; the micro-flow channel is used for delivering a drug solution and comprises a PDMS film with a channel and ITO glass, and the PDMS film is adhered to the conductive surface of the ITO glass; and the cell culture tank and the micro-flow channel take uncured PDMS as an adhesion substance, and are integrated and packaged with each other. The cell detection device can well complete in-situ drug regulation and control in a device after CTC recognition, has excellent biocompatibility, and effectively solves the problem of bloodcell background interference in CTC recognition.
Owner:SUN YAT SEN UNIV

Cytomembrane nano-vesicles and production method thereof

The invention discloses cytomembrane nano-vesicles and a production method thereof. The cytomembrane nano-vesicles are composed of bi-molecule-layer lipid membranes and contents wrapped by the bi-molecule-layer membranes, wherein the membranes and the contents of the cytomembrane nano-vesicles all come from metrocytes used for production. The production method of the cytomembrane nano-vesicles comprises the following step: sequentially and repeatedly extruding a single-cell suspension to pass through polycarbonate membranes, with different pore diameters, of an extruder to obtain a clear solution, and conducting gradient centrifugation, separation and purification on the clear solution to obtain the cytomembrane nano-vesicles. The production method of the cytomembrane nano-vesicles is highin yield, the nano-vesicles are stable in property, the product uniformity is good, operation is simple and convenient, the quality is controllable, and the repeatability is high, so that large-scaleproduction is facilitated, and the cytomembrane nano-vesicles can be applied to treatment of Parkinson's disease.
Owner:FIRST AFFILIATED HOSPITAL OF DALIAN MEDICAL UNIV

Preparation method and application of endothelial vesicles of Escherichia coli with endogenous high expression of microRNA in anti-tumor drug preparation

The invention discloses a preparation method of endothelial vesicles of Escherichia coli for anti-tumor drugs with endogenous high expression of nucleic acids. According to the preparation method of the endothelial vesicles of Escherichia coli, a 'tRNA scaffolding means' is adopted so as to stably insert microRNA into a vector; the vector is transformed into Escherichia coli, thereby allowing highendogenous expression of microRNA with cancer-cell-killing effects; epicellular and periplasmic components of the Escherichia coli are removed by using lysozyme, thereby obtaining protoplast of Escherichia coli; the protoplast is filtered by using polycarbonate membrane, thereby having the protoplast broken; and then, purification is carried out by adopting a ultracentrifugation means so as to have endothelial vesicles of the protoplast separated, thereby obtaining the endothelial vesicles of Escherichia coli with high expression of miRNA and low toxicity. The preparation method provided by the invention is easy to operate, low in production cost, feasible for large-scale fermentation and preparation, low in toxicity, and highly efficient. As a novel pharmaceutical carrier, being appliedin anti-tumor drug preparation, the endothelial vesicles of Escherichia coli are capable of significantly inhibiting development of non-small cell lung cancer; and thus, the endothelial vesicles of Escherichia coli have broad application prospects in the field of pharmaceutical carriers.
Owner:ZHENGZHOU UNIV

Preparation method of ergosterol combined gefitinib lipidosome

The invention relates to a preparation method of an ergosterol and gefitinib combined liposome. According to the method, GEF is entrapped by an ammonium sulfate gradient method to prepare the ERG combined GEF compound lipidosome; the specific preparation method comprises the following steps: fully dissolving SPC, Chole and ERG with chloroform, performing spin-drying on a rotary evaporator, and carrying out vacuum drying to be odorless; adding pure water, and hydrating the material on a horizontal shaking table for 20-50 minutes to obtain an intermediate product; putting the intermediate product in an ice bath, and carrying out ultrasonic treatment; and finally, filtering the material by adopting a multi-stage microfiltration membrane in sequence, and finally, carrying out high-pressure extrusion by adopting a polycarbonate membrane with a thickness of 0.1 mu m. The GEF encapsulation efficiency is taken as an index, the preparation process of the ERG/GEF-LIP is optimized through singlefactor and response surface design, the form, particle size distribution, Zeta potential, in-vitro cumulative release degree and peroxide value of the ERG/GEF-LIP are preliminarily investigated, and in-vitro lung cancer resistance preliminary research is carried out on drug-resistant cells PC-9/GR.
Owner:ZHEJIANG CHINESE MEDICAL UNIVERSITY

Preparation method and application of nano material with synovial immunoregulation function

The invention discloses a preparation method and application of a nano material with a synovial immunoregulation function, and belongs to the technical field of biologication.The key point of the technical scheme is that the preparation method comprises the following steps that S1, constructing shRNA-LeptinR: specifically, inserting a synthesized shRNA-LeptinR fragment into a plasmid vector to obtain a recombinant plasmid vector, then, transforming the recombinant plasmid vector into escherichia coli, and extracting the shRNA-LeptinR plasmid; S2, preparing a macrophage membrane; S3, preparing gene-loaded nanoparticle M2H@RPK: preparing the nanoparticle M2H@RPK by adopting an electrostatic adsorption method; and wrapping the nanoparticle H@RPK with the M2 macrophage membrane extracted in the step S2, and repeatedly passing through a polycarbonate membrane by using a micro extruder to obtain the nanoparticle M2H@RPK. The invention is mainly used for inhibiting synovial immune response and relieving inflammatory cascade reaction in the OA process.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Lanthanide fluoride two-dimensional nanosheet membrane and preparation method and application thereof

The invention provides a lanthanide fluoride two-dimensional nanosheet membrane as well as a preparation method and application thereof, and belongs to the technical field of membrane separation. The preparation method comprises the following steps: mixing water-soluble lanthanide metal salts with a sodium acetate aqueous solution in inert gas to obtain a mixed solution; mixing the mixed solution with a fluorine-containing salt aqueous solution, and carrying out precipitation reaction to obtain a lanthanide fluoride two-dimensional nanosheet suspension; depositing the lanthanide fluoride two-dimensional nanosheet suspensionon a porous substrate, carrying out drying to obtain the lanthanide fluoride two-dimensional nanosheet membrane, wherein the porous substrate is a polyethersulfone membrane, a nylon membrane, a polyvinylidene fluoride membrane, a polycarbonate membrane, a ceramic membrane, a metal membrane or an anodic aluminum oxide membrane. The lanthanide fluoride two-dimensional nanosheet membrane prepared by the invention has the characteristics of high permeability, high separation precision and good stability, and the preparation method is simple; and when the porous substrate is an inorganic membrane, the prepared lanthanide fluoride two-dimensional nanosheet membrane has high solvent resistance and separation performance.
Owner:TIANJIN POLYTECHNIC UNIV

Modified zein nano-drug delivery system wrapped by outer membrane vesicles of bacteria as well as preparation method and application of modified zein nano-drug delivery system

The invention discloses a modified zein nano drug delivery system wrapped by bacterial outer membrane vesicles as well as a preparation method and application of the modified zein nano drug delivery system. The medicine is dissolved in absolute ethyl alcohol, deionized water is added after ultrasonic dissolution, zein is added, and ultrasonic treatment is carried out; quickly adding a sodium caseinate solution into the obtained mixed solution while stirring, and stirring to obtain a modified zein drug-loaded nanoparticle solution; the preparation method comprises the following steps: uniformly mixing bacterial outer membrane vesicles with a modified zein drug-loaded nanoparticle solution, extruding the mixed solution for 2-8 times by using high-pressure nitrogen as an extrusion pressure source through a 200nm polycarbonate film, centrifuging the obtained product, and collecting the precipitate, thereby obtaining the bacterial outer membrane vesicle wrapped modified zein drug-loaded nanoparticle system. The nano drug-loading system provided by the invention is narrow in particle size distribution range and good in stability, and can load hydrophobic drugs which can be dissolved in ethanol, so that the solubility of the hydrophobic drugs in water is enhanced, and the stability and bioavailability of the drugs are improved.
Owner:LIAONING UNIVERSITY

Extracellular vesicle active medicine loading method

ActiveCN111529712AChange membrane permeabilityPromotes membrane fusionOrganic active ingredientsPharmaceutical non-active ingredientsExtracellular vesiclePharmaceutical drug
The invention relates to an extracellular vesicle active medicine loading method. The extracellular vesicle active medicine loading method comprises the following steps of performing resuspension on extracellular vesicles with an ammonium sulfate solution, performing ultrasonic treatment with a low-frequency probe, and performing incubation at 4 DEG C for 1h; repeatedly extruding the incubated extracellular vesicles through a polycarbonate membrane, performing PBS dialysis for overnight, and establishing an ammonium sulfate gradient; and performing incubation on the extracellular vesicles after dialysis for overnight and medicines, so as to obtain medicine loading dialysis extracellular vesicles. According to the method disclosed by the embodiment of the invention, the extracellular vesicle active medicine loading method based on ultrasonic treatment through the low-frequency probe and extrusion through the polycarbonate membrane can effectively improve the medicine loading rate of theextracellular vesicles and the medicine stability, is broad in application range.
Owner:JIMEI UNIV

Preparation method and application of nano material with synovitis inhibition function

PendingCN113797355AAlleviate the inflammatory cascadeSuppress severityAntipyreticAnalgesicsEscherichia coliCell membrane
The invention discloses a preparation method and application of a nano material with a synovitis inhibition function, and belongs to the technical field of biology. According to the key point of the technical scheme, the preparation method comprises the following steps that S1, shRNA-LeptinR is constructed, specifically, a synthesized shRNA-LeptinR fragment is inserted into a plasmid vector to obtain a recombinant plasmid vector, then, the recombinant plasmid vector is transformed into escherichia coli, and the shRNA-LeptinR plasmid is obtained through extraction; S2, a macrophage membrane is prepared; and S3, gene-loaded nanoparticles M2H@RPK is prepared, specifically, the nanoparticles M2H@RPK is prepared by adopting an electrostatic adsorption method, the nanoparticles H@RPK is wrapped with the M2 macrophage membrane extracted in the step S2, and a polycarbonate membrane repeatedly passes through by using a micro extruder to obtain the nanoparticles M2H@RPK. The preparation method is mainly used for relieving the inflammatory cascade reaction in the OA process, and the nano-system targets the cartilage matrix and can effectively relieve joint injury and inhibit the severity of overall arthritis.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Preparation method of mitochondria-targeted tocopherol-oleanolic acid double-drug nanoparticle

PendingCN111920957ATo achieve the effect of targeted drug deliveryOrganic active ingredientsPowder deliveryCholesterolOrganosolv
The invention relates to a preparation method of mitochondria-targeted tocopherol-oleanolic acid double-drug nanoparticles. The bioavailability and the targeting property of the medicine can be effectively improved. The technical scheme is as follows: the preparation method comprises the following steps of: respectively dissolving an anti-cancer drug, a targeting carrier, lecithin and cholesterolin an organic solvent until the materials are totally dissolved, mixing the dissolved solutions together, carrying out rotary evaporation to remove the organic solvent to obtain a film formed on the wall, drying the film in a vacuum drying oven, thoroughly removing the organic solvent, adding a hydration solvent, magnetically stirring the hydrated product, carrying out ultrasonic treatment, sequentially passing through polycarbonate films with different pore diameters, and carrying out extrusion crushing to obtain the mitochondria-targeted tocopherol-oleanolic acid double-drug nanoparticles. According to the nanoparticle, triphenylphosphine connected to tocopherol is utilized, positive charges carried by triphenylphosphine are easily enriched in mitochondria, so that the effect of mitochondria targeted drug delivery is achieved, and the nanoparticle is an innovation on mitochondria targeted preparations of nanoparticles.
Owner:HENAN UNIV OF CHINESE MEDICINE

Method for manufacturing polycarbonate resin, polycarbonate resin, polycarbonate-resin film, and methods for manufacturing polycarbonate-resin pellets and polycarbonate-resin films

InactiveCN103459112AEfficient and stable manufacturingHigh mechanical strengthFlat articlesForeign matterThermal stability
The present invention relates to a polycarbonate-resin manufacturing method whereby polycarbonate-resin pellets or polycarbonate-resin films that contain little foreign material and exhibit excellent optical properties, thermal stability, hue, and mechanical strength are manufactured efficiently and stably.
Owner:MITSUBISHI CHEM CORP

Preparation method of delivery system of treatment medicine capable of crossing blood brain barrier and specifically targeting brain glioma

The invention discloses a preparation method of a delivery system of a treatment medicine capable of crossing a blood brain barrier and specifically targeting brain glioma. The preparation method comprises the following steps: step 1) preparing an NK cell membrane: adding NK cells into a cell lysis buffer solution containing a protease inhibitor, and performing ultrasonic centrifugal treatment to obtain the NK cell membrane; step 2) adding 1, 2-distearoyl-sn-glyceryl-3-phosphoethanolamine-N-[amino (polyethylene glycol) 2000] (ammonium salt) and a medicine into pure water, and performing ultrasonic treatment, so as to obtain liposome nano-particles; and step 3) co-extruding the NK cell membrane and the liposome nano-particles through a polycarbonate membrane with a pore size of 220nm to form an NK cell bionic nano-carrier. The NK cell bionic nano-carrier prepared by the preparation method disclosed by the invention is the delivery system of the treatment medicine which crosses the blood brain barrier and specifically targets the brain glioma.
Owner:SHENZHEN INST OF ADVANCED TECH

Application and preparation method of erythrocyte bionic nanomaterial of PCM polypeptide combined with KALA polypeptide

The invention discloses an application of an erythrocyte bionic nanomaterial of PCM polypeptide combined with KALA polypeptide in treatment of cardiovascular diseases, and also discloses a preparation method of the erythrocyte bionic nanomaterial. The method comprises the following steps: obtaining a proper quantity of PCM, performing combining with KALA, and performing fusing into a fusion peptide; enabling the fusion peptide to be subjected to amino acid protection operation treatment, so as to obtain PCM / KALA polypeptide; enabling the PCM / KALA polypeptide to be combined on the surface of an erythrocyte membrane (RBCM); and enabling the PCM / KALA polypeptide combined with the erythrocyte membrane to pass through a polycarbonate membrane with the pore diameter of 400nm by utilizing an Extrusion method, so as to construct the RBCM-PCM / KALA erythrocyte bionic nanoparticles. The erythrocyte bionic nanomaterial prepared by the method can be efficiently and rapidly introduced into cells without depending on concentration, and compared with the prior art, the erythrocyte bionic nanomaterial also has a heart enrichment function.
Owner:THE SECOND HOSPITAL AFFILIATED TO WENZHOU MEDICAL COLLEGE

Liposome adjuvant, temperature-sensitive gel and temperature-sensitive gel preparation

The invention specifically discloses a liposome adjuvant, a temperature-sensitive gel and a temperature-sensitive gel preparation. The liposome adjuvant is prepared from the following components in parts by weight: 1 to 4 parts of DOTAP, 280 to 320 parts of soybean lecithin and 40 to 60 parts of cholesterol. The preparation method comprises the following steps: S1, dissolving DOTAP, soybean lecithin and cholesterol in a solvent; rotating and evaporating the solvent to dryness to obtain a film; s2, adding PBS (Phosphate Buffer Solution) into the film obtained in S1, stirring at 45-55 DEG C for 0.5-1.5 hours, and dissolving the film to obtain a liposome stock solution; s3, enabling the liposome stock solution to pass through a polycarbonate film, and extruding for 20-80 times to obtain the liposome adjuvant. The temperature-sensitive gel is prepared from poloxamer gel and a liposome adjuvant; the temperature-sensitive gel can be used for preparing a temperature-sensitive gel adjuvant. The liposome adjuvant has the advantages that the phase change temperature and viscosity of the temperature-sensitive gel can be adjusted, and the administration efficiency of the temperature-sensitive gel preparation can be improved.
Owner:LIAONING CHENGDA BIOTECH

Toner and method for producing toner

A toner comprising a toner particle that contains a binder resin and fine particles A at the surface of the toner particle, wherein the fine particles A are organosilicon polymer fine particles, the organosilicon polymer fine particles have a number-average primary particle diameter of 30 nm to 500 nm, the organosilicon polymer fine particles have an attachment index for a polycarbonate film of not more than 3.5, the organosilicon polymer fine particles penetrate into the toner particle in a penetration depth b (nm), and protrude from the toner particle in a protrusion height c (nm), and b and c satisfy 0.05≤b / (b+c)≤0.40.
Owner:CANON KK

Preparation method of alpha-glucosyl hesperidin modified xanthophyll liposome

The invention discloses a preparation method of alpha-glucosyl hesperidin modified xanthophyll liposome. The xanthophyll liposome provided by the invention is obtained by modification with alpha-glucosyl hesperidin, and the specific method is as follows: (1) dissolving xanthophyll and a lipid material to obtain a xanthophyll lipid solution; (2) hydrating a lipid membrane, and then performing ultrasonic treatment to obtain a dispersion solution; (3) dropwise adding an alpha-glucosyl hesperidin solution into the dispersion solution, and performing stirring at room temperature overnight; and (4)squeezing the dispersion solution through a polycarbonate membrane to obtain the xanthophyll liposome. The xanthophyll liposome modified by alpha-glucosyl hesperidin has high stability and long-term circulation performance, and significantly improves the absorption of xanthophyll in the eye.
Owner:JIANGSU ACADEMY OF AGRICULTURAL SCIENCES
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