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30 results about "Palmitoylphosphatidyl choline" patented technology

Gas-filled microbubbles and systems for gas delivery

InactiveUS20140010848A1Eliminate side effectsLow viscosityBiocideBreathing masksDipalmitoylphosphatidylcholinePhosphorylcholine
Compressible and concentrated suspensions containing gas-filled microbubbles, uses thereof for delivering gas into a subject in need thereof, and systems for delivering the compressible suspensions. The gas-filled microbubbles each comprise a gas core surrounded by a lipid membrane, which includes (a) one or more lipids, such as 1,2-disteroyl-sn-glycero-3-phosphocholine (DSPC) or dipalmitoylphosphatidylcholine (DPPC), and (b) one or more stabilizing detergents, such as poloxamer 188, Pluronic F108, Pluronic F127, polyoxyethylene (100) stearyl ether, cholesterol, gelatin, polyvinylpyrrolidone (PVP), and sodium deoxycholate (NaDoc).
Owner:CHILDRENS MEDICAL CENT CORP

Preparing method and application of ginsenoside-multi-component jointly-loading targeting nanometer system

The invention discloses a preparing method of a ginsenoside-multi-component jointly-loading targeting nanometer system.The preparing method includes the steps that after egg yolk lecithin, cholesterol and polyethylene glycol-dipalmitoyl phosphatidyl choline are dissolved, warm water is slowly and dropwise added for stirring, and a lipid water solution is obtained; the multi-component active ingredients containing ginsenoside Rg3, ginsenoside Rh2 and ginsenoside Rb1 and a copolymer of polylactic acid-hydroxyacetic acid are dissolved to be slowly and dropwise added into the lipid water solution to be stirred to be even, a solvent is removed, and lipidosome nanometer particles are obtained; aptamer is dissolved to be modified to the surfaces of the lipidosome nanometer particles, and an even and opalescence-flooding nanometer system solution is obtained by filtering and sterilizing.According to the preparing method, the anti-tumor effect of medicine is improved with the nanocrystallization technology, joint transmission of a multi-component tumor tissue can be achieved in the mode that the three ginsenoside ingredients are jointly loaded to the nanometer system, and therefore the problems that the metabolic behaviors and the tumor-cell entering capacity of different ingredients are different are solved.
Owner:CHENGDU UNIV

Preparation method of targeted temperature-controlled water-loading silibinin temperature-sensitive lipidosome-microbubble complex drug delivery system

The invention provides a preparation method of a targeted temperature-controlled water-loading silibinin temperature-sensitive lipidosome-microbubble complex drug delivery system. The preparation method comprises the following steps of with single-palmitoyl phosphatidyl choline, dipalmitoyl phosphatidyl choline, distearoyl phosphatidyl ethanolamine-polyethylene glycol-amino and silibinin as raw materials, preparing water-loading silibinin temperature-sensitive lipidosome by virtue of a membrane rotary evaporation method; and coupling the water-loading silibinin temperature-sensitive lipidosome with an ultrasonic contrast agent, namely SonoVue microbubble, so as to prepare the targeted temperature-controlled water-loading silibinin temperature-sensitive lipidosome-microbubble complex drug delivery system. According to the preparation method, a new drug delivery system is established by combining the temperature-sensitive lipidosome with the microbubble; the efficient release of local tissues of a drug at a sub-high temperature field are achieved by virtue of the targeted explosion of the microbubble and the local temperature control effect of the temperature-sensitive lipidosome, so that the bioavailability of the drug is improved, and furthermore, residual tumors during thermal ablation treatment are reduced.
Owner:FOURTH MILITARY MEDICAL UNIVERSITY

Percutaneous-absorption-promoting propranolol composite phospholipid transfersome, and prepartion method and application thereof

The invention provides a composite phospholipid transfersome which promotes propranolol percutaneous absorption, and a preparation method thereof. According to the invention, two phospholipid materials with different phase-change temperatures, which are dipalmitoyl phosphatidyl choline and soybean lecithin, are adopted as a composite phospholipid material. Compared with a transfersome with a single phospholipid material in prior art, the propranolol composite phospholipid transfersome prepared with the phospholipid material provided by the invention has substantially improved encapsulation efficiency, reduced leakage, improved stability in rat plasma, and substantially improved bioavailability after percutaneous administration. The propranolol composite phospholipid transfersome provided by the invention is especially suitable to be used for treating infantile hemangioma. With the transfersome, propranolol percutaneous administration can be realized, and propranolol can directly act upon a hemangioma affected part. The treatment effect is improved, toxic and side effects are reduced, and children medication compliance can be improved. Also, the invention provides a preparation method of the propranolol composite phospholipid transfersome.
Owner:NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE

Preparing technique of nano magnetic gene-loaded liposome of temperature-controlled release

InactiveCN101744766AGood external magnetic induction heating capacityGood dispersionGenetic material ingredientsMacromolecular non-active ingredientsFreeze thawingPhosphate
A preparing technique of a nano magnetic gene-loaded liposome of temperature-controlled release relates to a medicament for treating cancers. Manganese sulfate, zinc sulphate and ferrous sulphate are crushed into power according to a certain ratio and dissolved by sodium hydroxide, and nano magnetic particles of manganese, zinc and ferrum are obtained after the steps of agitation, drying, baking, etc. The nano magnetic particles of manganese, zinc and ferrum are decorated with a proper amount of polyethyleneimine, and then combined with expression plasmids of green florescent protein, so the nano magnetic gene-loaded particles of manganese, zinc and ferrum are obtained. A proper amount of dipalmitoyl phosphatidyl choline and cholesterol is added to an eggplant-shaped flask and dissolved by chloroform absolute ether. The eggplant-shaped flask is subsequently put in a rotating evaporator for evaporation, and a uniform film is formed on the bottom of the flask as a result. Then, phosphate buffer containing the nano magnetic gene-loaded particles of manganese, zinc and ferrum is added and electrically agitated until the film falls off. Glycerol is added for repeated freeze-thaw, and the nano magnetic gene-loaded liposome of temperature-controlled release is obtained.
Owner:SOUTHEAST UNIV

Preparation method and application of liposome composite material for light-controlled release of tungsten sulfide quantum dots and vancomycin

The invention belongs to the field of antibacterial drugs, and discloses a preparation method and application of a liposome composite material for light-controlled release of tungsten sulfide quantumdots and vancomycin. The material is called WS2QDs-Van@lipo for short, wherein WS2QDs are the tungsten sulfide quantum dots, Van is the vancomycin, and lipo is liposome. The preparation method comprises the following steps of firstly, dissolving dipalmitoyl phosphatidylcholine, cholesterol and distearoyl phosphatidylethanolamine-polyethylene glycol-hydroxyl in trichloromethane, and carrying out vacuum drying to generate a lipid film; then, adding the lipid film into PBS containing the WS2QDs and the Van, and performing hydrating to form a thin film; and finally, carrying out ultrasonic treatment after vortex oscillation, and carrying out centrifugal purification to obtain the WS2QDs-Van@lipo composite material. The material can be used as an antibacterial reagent, and can be accurately released at a target part through light control, so that the use amount of antibiotics and the systemic toxicity of organisms are reduced; and the material has a relatively good inhibition effect on theactivity of escherichia coli and vancomycin-resistant staphylococcus aureus, and can provide a safe and effective solution for treatment of refractory drug-resistant bacteria.
Owner:THE FIRST AFFILIATED HOSPITAL OF ANHUI MEDICAL UNIV

Ultrasound-sensitive liposome and application thereof

The invention relates to an ultrasound-sensitive liposome and application thereof, and aims to effectively solve the problems of large toxic and side effects, poor curative effect, low treatment efficiency and high immune toxicity in chemotherapy. According to the technical scheme, the ultrasound-sensitive liposome is prepared by the following steps: weighing 2 to 10mg of cholesterol, 2 to 20mg of 1,2-dipalmitoyl phosphatidylglycerole (DPPG), 5 to 30mg of dipalmitoyl phosphatidylcholine (DPPC) and 0 to 20mg of dioleoyl phosphatidyl ethanolamine (DOPE); dissolving the weighed materials in 5 to 30m of solvent; performing ultrasonic treatment for 5 to 60 minutes till the materials are fully dissolved; performing rotary evaporation at the temperature of 50 DEG C to remove the solvent; performing rotary evaporation under the vacuum condition for 4 hours to remove residual solvent; adding 1 to 10mg of medicinal mannitol containing solution, wherein the mannitol concentration is 0.2 to 1M; quickly blowing the bottom of a bottle with hot air to accelerate hydration; performing ultrasonic treatment for 5 to 10 minutes till the solution becomes uniform and transparent; freezing and unfreezing for 3 to 6 times to obtain the ultrasound-sensitive liposome. Medicaments wrapped in the liposome are released at a fixed point, so that the toxic and side effects of chemical medicaments are lowered, and the curative effect is enhanced; the ultrasound-sensitive liposome can be used as an ultrasonic imaging diagnostic agent, and is an innovation on chemotherapeutic medicaments.
Owner:ZHENGZHOU UNIV

Pulmonary Surfactant Formulations

Synthetic pulmonary surfactant compositions comprising dipalmitoyl phosphatidylcholine, phosphatidylglycerol, and essentially neutral lipid, and having essentially no 1-palmitoyl 2-oleoyl phosphatidylglycerol and essentially no palmitic acid are provided. Methods for treating respiratory disease are also provided comprising administering a therapeutically effective amount of a synthetic pulmonary surfactant comprising dipalmitoyl phosphatidylcholine, phosphatidylglycerol, and essentially neutral lipid, and having essentially no 1-palmitoyl 2-oleoyl phosphatidylglycerol and essentially no palmitic acid.
Owner:DISCOVERY LABORATORIES INC

Vitamin D2 and calcium levulinate injection composition and preparation method thereof

The invention discloses a vitamin D2 and calcium levulinate injection composition and a preparation method thereof. The vitamin D2 and calcium levulinate injection composition comprises vitamin D2, calcium levulinate, dipalmitoyl phosphatidylcholine, cholesterol, distearoyl phosphatidylcholine, polyethylene glycol and water for injection. The preparation method comprises the following steps: (1) weighing the materials for later use according to weight ratio; (2) respectively communicating a three-way selector valve in a constant temperature water supply system with a reaction kettle and a homogenizer; (3) putting the calcium levulinate into the water for injection to dissolve so that a calcium levulinate solution for use is obtained; (4) putting the dipalmitoyl phosphatidylcholine, the distearoyl phosphatidylcholine, the cholesterol and the polyethylene glycol into the reaction kettle to react; (5) putting the materials obtained after the reaction of the step (4) into the homogenizer, and putting the vitamin D2 and the homogenizer into the homogenizer to obtain a semifinished product of the vitamin D2 and a calcium levulinate injection; (6) filtering the semifinished product and potting to obtain the vitamin D2 and calcium levulinate injection. The invention solves the disadvantages of the prior art.
Owner:JIANGXI GANNAN HAIXIN PHARMA

Contrast medium and preparation method thereof

The invention provides a contrast medium and a preparation method thereof and relates to the technical field of medical treatment. The contrast medium is mainly prepared from, by weight, 2-4 parts of diphenyl azidophosphate, 8-12 parts of dipalmitoyl phosphatidyl choline, 3-5 parts of phospholipid, 2.5-3.5 parts of cholesterol, 1.5-2.5 parts of melanin and 8-15 parts of perfluoropropane, wherein the phospholipid refers to PEGylated phospholipid. The contrast medium has the advantages of good biocompatibility, no toxic or side effect and good contrast effect. The preparation method of the contrast medium is simple in steps and convenient to operate.
Owner:CHILDRENS HOSPITAL OF CHONGQING MEDICAL UNIV

Preparation of lipidosome containing MAP30 protein and entrapping method

The invention provides preparation of lipidosome containing MAP30 protein and an entrapping method. A thin film hydration method is used for preparing. The preparation specifically comprises the following steps of dissolving 10mg of DPPC (dipalmitoyl phosphatidyl choline), 1mg of cholesterol, 1mg of n-(carbonyl-methoxypolyethyleneglycol 2000)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine (SDPE-mPEG2000) into chloroform, performing pressure relief and rotary evaporation to form a uniform thin film, thoroughly volatizing the remained chloroform overnight under the vacuum condition, adding 1ml of 2mg ml<-1> PBS (poly(butylene succinate)) solution containing protein, performing ultrasonic treatment for 20min in an ice bath, and enabling the lipidosome film to fall down; oscillating for 5min on an oscillator, fully hydrolyzing, and forming turbid liquid; transferring the turbid liquid into an EP (electrochemical polishing) tube, using a probe to perform ultrasonic treatment for 30min at the power equal to 15% of 135W ultrasonic power, so as to obtain a transparent and uniform blue lipidosome suspension. The preparation has the advantages that the technology is simple, the conditions are mild, the repeatability is high, the structure of the lipidosome is stable, the protein adsorbing capacity is large, the particle sizes of the lipidosome are more uniform, and the encapsulating rate is 78%.
Owner:XUZHOU CENT HOSPITAL

Composition for regulating and controlling epidermal micro-ecological balance and application thereof

The invention relates to the technical field of skin care products, in particular to a composition for regulating and controlling epidermal micro-ecological balance and application of the composition.The composition is prepared from the following raw materials in parts by weight: 20 parts of pogostemon cablin leaf extract, 20 parts of plankton extract, 35 parts of inulin / alpha-glucan oligosaccharide, 35 parts of butanediol and 10 parts of dipalmitoyl phosphatidylcholine. The composition provided by the invention can be used for effectively regulating and controlling a microbial ecological barrier on the skin surface; tree ages of probiotics and harmful bacteria on epidermis are effectively controlled, and the skin problems of excessive skin grease, coarse pores, a large amount of acnes, skin inflammation and the like caused by mass propagation of harmful bacteria on epidermis, change of epidermis micro-ecology and promotion of sebaceous gland to secrete a large amount of grease are avoided. And the skin problem of volunteers with a large amount of grease secreting vigorously is effectively improved. In addition, the composition provided by the invention also has excellent heat-resistant stability and cold-resistant stability, and can be stored and used for a long time in a harsh environment.
Owner:上海科颜生物科技有限公司

Preparation technology of oral vaccine for resisting salmonella

The invention discloses a preparation technology of an oral vaccine for resisting salmonella. The preparation technology comprises the following steps of constructing escherichia coli for expressing antigens of salmonella SEF14 and SEF21 fimbriaes, carrying out fimbrial antigen purification by a protein purification technology, dissolving dipalmitoyl phosphatidyl choline, dipalmitoyl phosphatidylserine and cholesterol in an organic solvent, fully mixing, drying mixed lipid, adding a certain amount of the antigens of SEF14 and SEF21 into a mixed lipid membrane, fully mixing, and carrying out lipid membrane vortex-type dispersion to obtain the oral vaccine. The preparation technology greatly improves the purity of salmonella antigens, and realizes stable, simple and controllable production having a high yield and high purity. The oral vaccine obtained by the preparation technology has effects of effectively resisting an acid environment and a damage caused by a body enzyme system. Through the preparation technology, SEF14 and SEF21 fimbriae protein antigens can be applied by an oral method. The preparation technology realizes complete detoxification and high immunogenicity and does not produce environmental pollution.
Owner:DALIAN UNIV

A preparation method of targeted temperature-controlled silibinin-loaded thermosensitive liposome-microbubble complex drug delivery system

The invention provides a preparation method of a targeted temperature-controlled water-loading silibinin temperature-sensitive lipidosome-microbubble complex drug delivery system. The preparation method comprises the following steps of with single-palmitoyl phosphatidyl choline, dipalmitoyl phosphatidyl choline, distearoyl phosphatidyl ethanolamine-polyethylene glycol-amino and silibinin as raw materials, preparing water-loading silibinin temperature-sensitive lipidosome by virtue of a membrane rotary evaporation method; and coupling the water-loading silibinin temperature-sensitive lipidosome with an ultrasonic contrast agent, namely SonoVue microbubble, so as to prepare the targeted temperature-controlled water-loading silibinin temperature-sensitive lipidosome-microbubble complex drug delivery system. According to the preparation method, a new drug delivery system is established by combining the temperature-sensitive lipidosome with the microbubble; the efficient release of local tissues of a drug at a sub-high temperature field are achieved by virtue of the targeted explosion of the microbubble and the local temperature control effect of the temperature-sensitive lipidosome, so that the bioavailability of the drug is improved, and furthermore, residual tumors during thermal ablation treatment are reduced.
Owner:FOURTH MILITARY MEDICAL UNIVERSITY

A kind of doxorubicin and gene drug co-delivery nano drug loading system and preparation method

ActiveCN107811972BTo achieve co-loadingInhibition of effluxOrganic active ingredientsGenetic material ingredientsCholesterolPhospholipid
The invention provides an adriamycin and gene medicine co-transporting nano medicine carrying system and a preparation method. The co-transporting nano medicine carrying system is TPGS modified cationic liposome for co-carrying adriamycin and gene medicine, wherein a membrane material of the cationic liposome is prepared from 1,2-dioleoyl-3-trimethylammonio-propane or chlorate of the 1,2-dioleoyl-3-trimethylammonio-propane, dipalmitoyl phosphatidylcholine, TPGS and cholesterol. The prepared co-transporting nano medicine carrying system disclosed by the invention has a higher adriamycin encapsulating efficiency, stability of the co-transporting nano liposome is improved; meanwhile, complete inhibition on a tumor cell efflux pump can be achieved by only adjusting a formula, the purposes of two drug resistance mechanisms of inhibiting tumor medicine efflux and resisting apopotosis are achieved at the same time, and tumor multidrug resistance can be more completely and more effectively reversed.
Owner:HUAZHONG UNIV OF SCI & TECH

Podophyllotoxin ethosomes and preparation methods thereof

The invention discloses podophyllotoxin ethosomes. Podophyllotoxin is encapsulated in ethosomes, and a medicine carrying lipid material is phosphatidylcholine, phosphatidylethanolamine or dipalmitoylphosphatidylcholine, wherein the grain diameter of the lipid material is between 50 and 300 nanometers. The podophyllotoxin ethosomes can be prepared into external preparations such as patches, gel and the like, and can reduce medicinal dose, and fulfill the aims of increasing curative effect and reducing relapse and toxic and side effects. The invention also discloses two preparation methods for the podophyllotoxin ethosomes.
Owner:SHANGHAI UNIV OF T C M

Methods and compositions for reducing adipocyte numbers

A method for reducing a subcutaneous fat deposit or a visceral fat deposit in vivo by contacting the fat deposit with a composition of latanoprost encapsulated in a liposome formed solely of egg phosphatidylcholine (EggPC) or palmitoyloleoyl phosphatidylcholine (POPC). Also disclosed are methods for treating steatoblepharon, proptosis, and obstructive sleep apnea associated with excess upper airway fat by injecting into the eyelid, intraconal space, and upper airway fat deposit, respectively, the composition of latanoprost encapsulated in an EggPC or POPC liposome.
Owner:佩雷格林眼科私人有限公司

Preparation method of airway mucus model

InactiveCN111763335AConducive to medical research analysisExtended use timeCelluloseHuman airway
The invention belongs to the field of airway mucus models, and relates to a preparation method of an airway mucus model. The airway mucus model is prepared from the following raw materials: hydroxyethyl cellulose; dipalmitoyl phosphatidylcholine, serum egg, mucoprotein, benzalkonium bromide and a phosphate buffer solution; the mucoprotein is secretory mucoprotein Mucin5AC, Mucin2 or Mucin5B of anairway. The airway mucus model is prepared by a plurality of steps of preparation of model materials, preparation of the phosphate buffer solution, preparation of the model, disinfection treatment, characteristics endowment of the model and the shaping of the model. According to the preparation method of the airway mucus model, the most important mucoprotein element such as human airway mucus is added in the preparation of the airway mucus model; and benzalkonium bromide disinfection and hydroxyethyl cellulose shaping are carried out, so that the prepared airway mucus model is more suitable for the real human airway mucus, is durable and can facilitate subsequent medical research.
Owner:深圳市龙华区中心医院

The preparation method of albendazole thermosensitive liposome

InactiveCN105078892BHigh encapsulation efficiencyHigh ABZ drug loadingOrganic active ingredientsPharmaceutical non-active ingredientsDipalmitoylphosphatidylcholineSolubility
The invention discloses an albendazole thermosensitive liposome, which consists of dipalmitoylphosphatidylcholine, monopalmitoylphosphatidylcholine, distearoylphosphatidylglycerol and albendazole. The preparation process is as follows: first put the above four raw materials into a round-bottomed flask in proportion, then add the chloroform-methanol mixed solution, remove the chloroform-methanol mixed solution on a rotary evaporator after dissolving; continue to add phosphate buffer solution, and hydrate to obtain Milky white liquid; then transfer the milky white liquid to a centrifuge tube, and use an ultrasonic cell disruptor to process it for 150 seconds; finally filter, and freeze-dry the filtrate to obtain a finished product. The remarkable effect of the present invention is that ABZ is encapsulated in the heat-sensitive liposome carrier to improve the solubility of the drug, slow down the release of the drug, enhance the liver targeting, and finally achieve the purpose of improving bioavailability; in addition, the present invention The obtained albendazole thermosensitive liposome (TSL‑ABZ) has a high significant encapsulation efficiency and ABZ drug loading.
Owner:CHONGQING MEDICAL UNIVERSITY

Protein free surfactant composition for pulmonary diseases and a process for preparing the same

A protein free surfactant composition comprising dipalmitoylphosphatidyl choline (DPPC) and eugenol having a ratio in the range of 10:5 to 4:2 with >99% airway patency in the presence of albumin, for treating acid lung injury, adult respiratory distress syndrome and meconium aspiration syndrome.
Owner:INDIAN INSTITUTE OF TECHNOLOGY BOMBAY

Intelligent gas-phase anti-oxidation film containing rosemary temperature-sensitive lipidosome and preparation method thereof

The invention provides an intelligent gas-phase anti-oxidation film containing rosemary temperature-sensitive lipidosome and a preparation method thereof, and can solve the technical problem that the practical application effect is poor due to the fact that an existing anti-oxidation active packaging film cannot have the characteristics of long-acting effect and temperature sensitivity at the same time. The intelligent gas-phase antioxidant film containing rosemary temperature-sensitive lipidosome is characterized in that the film contains a rosemary temperature-sensitive lipidosome, the rosemary temperature-sensitive lipidosome is prepared from the following raw materials: dipalmitoyl phosphatidylcholine, cholesterol and rosemary essential oil, and the mass ratio of the dipalmitoyl phosphatidylcholine to the cholesterol to the rosemary essential oil is 10: 2: 1. The intelligent gas-phase antioxidant film has an obvious slow release effect, the DPPH free radical scavenging rate reaches 47.3% within 720 h, meanwhile, the film has an obvious temperature sensitive characteristic, and two obvious endothermic peaks exist at the temperatures of about 38.5 DEG C and 41.8 DEG C.
Owner:JIANGNAN UNIV

Preparation and application of a targeted thermosensitive liposome modified by e-selectin peptide ligand

The present invention relates to a preparation method and application of tumor targeting liposome modified by E-selectin polypeptide ligand, and the targeting liposome is composed of phosphatidylethanolamine-polyethylene glycol-maleimide-E The selectin peptide-ligand conjugate, dipalmitoyl phosphatidylcholine, cultured phosphatidylethanolamine and myristoyl lysolecithin are prepared. The conjugate DSPE-PEG-Mal-8CR involved is chemically coupled and synthesized by E-selectin peptide ligand 8-CR and phosphatidylethanolamine-polyethylene glycol-maleimide, and the tumor prepared by the present invention Targeting long-circulating thermosensitive liposomes, loaded with different anti-tumor drugs, can actively target tumor angiogenesis and inhibit the migration of tumor cells, which is of great significance for the treatment of tumor metastasis and recurrence.
Owner:TIANJIN UNIV OF SCI & TECH

Method for preparing nano particles for adsorption of heavy metal ions

The invention provides a method for preparing nano particles for adsorption of heavy metal ions. The method includes steps: (1) adding a certain amount of acetic acid into water, stirring to obtain an acetic acid solution in a certain concentration, weighing a certain amount of chitosan powder to add into the acetic acid solution, and stirring for a certain time to obtain a well dissolved chitosan-acetic acid solution; (2) weighing a certain amount of dipalmitoyl phosphatidyl choline, cholesterol and phospholipid, adding an appropriate amount of ethyl alcohol and stirring to obtain a completely dissolved solution; (3) adding the dipalmitoyl phosphatidyl choline-ethyl alcohol solution into the chitosan-acetic acid solution, and constantly stirring at a certain temperature to obtain chitosan nano particles. The nano particles for adsorption of the heavy metal ions have the advantages of high efficiency, low cost, adsorption of a great variety of ions and the like.
Owner:SHANGHAI NAT ENG RES CENT FORNANOTECH

Breviscapinum long-circulating nanoliposome and its preparation method

The invention discloses a breviscapinum long-circulating nanoliposome and its preparation method, wherein the constituents include breviscapine, phosphatide, polyethylene glycol derived phosphatide (PEG2000-DSPE) and cholestrin by a molar ratio of 55:25-55:3-7:2.2-18.3, the dose type of the medicinal preparation includes injections, freeze-dried powder injections and sprays. The phospholipids canbe soya bean lecithin, yolk phosphatidy icholine, hydrogenated soya bean lecithin, hydrogenated yolk lecithin, di-palmityl phosphatidyl choline or DPOG.
Owner:TSINGHUA UNIV

Liposome skin repair preparation and preparation method thereof

The invention provides a liposome skin repair preparation and a preparation method thereof, the liposome skin repair preparation is used for scalp repair, the preparation comprises an active component and a drug carrying component, the active component comprises one or more of a white willow bark extract, minoxidil, phytosterol and ceramide; the medicine carrying component comprises phospholipid, cholesterol and hyaluronic acid, and the phospholipid is any one of soybean phospholipid, hydrogenated lecithin, egg yolk lecithin, dipalmitoyl phosphatidylcholine or dipalmitoyl phosphatidyl ethanolamine. The preparation has the functions of repairing head skin, eliminating skin, diminishing inflammation and preventing and treating alopecia, and has a good treatment effect; the preparation method is simple, easy to operate and stable and reliable in preparation performance.
Owner:成都科建生物医药有限公司

Vaccine composition based on sticholysin encapsulated into liposomes

The present invention relates to the field of biotechnology applied to human health. The invention describes a vaccine vehicle which toxins from eukaryotic organisms are encapsulated in liposomes with multiple lipid layers, obtained by means of the process of dehydration / rehydration, the lipid composition of which is dipalmitoylphosphatidylcholine:cholesterol in a molar ration of 1:1, which are designed for subcutaneous or intramuscular administration. These compositions do not require the use of other adjuvants. The compositions described allow modulation of the specific CTL immune response to one or more antigens co-encapsulated in the liposomes that containing the toxin. The vaccine vehicle of the present invention presents advantages as compared with others described in the prior art owning to the robust and functional nature of the immune response induced and also the immunomodulating properties thereof.
Owner:CENT DE INMUNOLOGIA MOLECULAR CENT DE INMUNOLO

Protein free surfactant composition for pulmonary diseases and a process for preparing the same

A protein free surfactant composition comprising dipalmitoylphosphatidyl choline (DPPC) and eugenol having a ratio in the range of 10:5 to 4:2 with >99% airway patency in the presence of albumin, for treating acid lung injury, adult respiratory distress syndrome and meconium aspiration syndrome.
Owner:INDIAN INSTITUTE OF TECHNOLOGY BOMBAY

Lipopolysaccharide/indocyanine green/oxaliplatin nanoparticles and preparation method thereof

The lipopolysaccharide / indocyanine green / oxaliplatin nanoparticle is characterized in that a PLGA inner core is loaded with oxygen-carrying perfluoropentane, indocyanine green and oxaliplatin molecules, and the outer part of the PLGA inner core is tightly coated with a layer of a material consisting of dipalmitoyl phosphatidylcholine, 1, 2-dipalmitoyl phosphatidylcholine and oxaliplatin. The lipid membrane is composed of 1, 2-palmitoyl phosphatidyl glycerol, distearoyl phosphatidyl ethanolamine-polyethylene glycol 2000 and cholesterol, and lipopolysaccharide is loaded on the surface of the lipid membrane. The preparation method is simple. The oxygen-carrying lipopolysaccharide / indocyanine green / oxaliplatin nanoparticles have good particle size potential, dispersibility, encapsulation efficiency, drug loading capacity and optical properties, have no obvious toxic effect on organisms, and have great popularization and application values in improvement of tumor immune microenvironment and anti-tumor immunotherapy.
Owner:THE SECOND AFFILIATED HOSPITAL OF CHONGQING MEDICAL UNIV
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