38 results about "Phosphoglyceride" patented technology

The invention relates to a compound feed for Macrobrachium rosenbergii, which comprises the following compositions: 46 percent CP bean meal, imported steam fish meal, peanut meal, squid paste, yeast extract, rapeseed meal, beer yeast, monocalcium phosphate, 60 percent CP corn protein powder, Tanimoto powder, special powder, shrimp multi-vitamin, shrimp multi-mineral, phosphoglyceride, imported fish oil, zeolite powder and mildewcide. The compound feed for Macrobrachium rosenbergii has the following advantages that: (1) a scientific formula and comprehensive nutrition: the superior beam meal, rapeseed meal, peanut meal, corn protein powder, special powder and other main materials are adopted and scientifically matched with shrimp multi-vitamin, mineral and other added compositions, besides the abundant energy compositions, the feed also contains abundant protein, amino acid and various nutritional compositions and can meet the nutritional and growing requirements of Macrobrachium rosenbergii, and the feed can also allow Macrobrachium rosenbergii to rapidly grow and have strong disease resistance; and (2) low cost: the bean meal, the rapeseed meal, the peanut meal and the like are used as main materials and greatly reduce the product cost.

The invention relates to an enteric-coated oral vaccine for fishing, belonging to the field of oral vaccines for fishing. The enteric-coated oral vaccine for fishing comprises particles or pellets sprayed with a vaccine layer and sequentially coated with an isolating layer and an enteric-coated layer outside the vaccine layer. A dry powder composition A for spraying vaccine and coating the isolating layer comprises the following components (by weight parts) one or more film-forming agents selected from hydroxypropyl methylcellulose, polyvinyl alcohol and polyvinyl pyrrolidone 40-60 parts, one or more plasticizing agents selected from phosphoglyceride, triethyl citrate and polyethylene glycol 3-10 parts, one or more antisticking agents selected from silicon dioxide, magnesium stearate, talcum powder and titanium oxide 30-50 parts, and surfactant selected from lecithin and Tween-80 0-5 parts. The vaccine can be directionally released in intestinal tract.

The invention provides a lipid-modified substance of chlorogenic acid and a derivative thereof, and a preparation and purification method of the lipid-modified substance, wherein the lipid-modified substance includes the chlorogenic acid or the derivative thereof and phosphoglyceride. A preparation process includes steps of performing constant-temperature magnetic stirring reflux for a certain time to the chlorogenic acid or the derivative thereof and the phosphoglyceride with an aprotic solvent and drying an obtained reaction liquid to obtain a crude product. A purification process includes the steps of re-dissolving the crude product with filtration to obtain a filtrate and then drying the filtrate. The lipid-modified substance of the chlorogenic acid and the derivative thereof is high in composition rate and can significantly improve the fat-solubility of the chlorogenic acid and the derivative thereof, so that a subsequent preparation is convenient to process and shape. The lipid-modified substance can be used as an intermediate for preparing a lipidosome, nano particles, polymer micelles or a dendritic polymer and the like nano drug-delivery systems and micro emulsion, self-micro emulsion and the like micron drug-delivery systems, thereby enhancing in-vivo absorption of the chlorogenic acid and the derivative thereof and further increasing the bioavailability of the medicines in a preparation.

The invention relates to a composition for enhancing the water solubility of curcumin and a preparation method of the composition and belongs to the technical field of foods and health-care products.The composition provided by the invention comprises the following components in parts by weight: 0.1 to 35.0 parts of the curcumin or a derivative thereof, 0.03 to 560.0 parts of phospholipid containing glycerol phosphate or the glycerol phosphate and 0.2 to 70.0 part of resistant dextrin. In the composition provided by the invention, the dissolution rate and the releasing rate of the composition,and the in-vivo transportation efficiency and the bioavailability of the curcumin are cooperatively enhanced through the glycerol phosphate and the resistant dextrin, and the intestinal absorption condition of the lipid-soluble curcumin is improved; and the types and forms, and a functional application range of a curcumin solid preparation are expanded under the condition that original propertiesand anti-oxidization performance of the curcumin are not influenced.

The invention relates to a leather softening agent which is prepared from the following raw materials in parts by weight: 6-14 parts of acrylate, 3-11 parts of lauryl sodium sulfate, 4-10 parts of ammonium persulfate, 3-9 parts of ethanol, 4.5-10 parts of phosphoglyceride, 6-13 parts of ethylene-vinyl acetate copolymer, 2-8 parts of sulfonated grease, 2-7 parts of solvent, 2-6 parts of emulsifier, 3.5-10 parts of fatty alcohol polyethenoxy ether, 4-10 parts of mildew preventive, 3-10 parts of jojoba wax and 3-8 parts of ethyl methyl p-hydroxybenzoate. The leather softening agent can well enhance the softness and hand feeling of the leather, improves the air permeability of the leather and prolongs the service life.

The invention discloses a preparation method of waterproof anti-crack environment-friendly coating. The preparation method comprises the following steps: mixing 35 to 55 parts of attapulgite, 12 to 16 parts of sericite, and 10 to 17 parts of titanium dioxide to obtain a mixture I, putting the mixture I into a grinding machine for grinding, so as to obtain a substance A; adding the substance A, 20 to 30 parts of a styrene-acrylic emulsion and 11 to 18 parts of polyethylene glycol into a stirring device, and carrying out stirring at 60 to 80 DEG C for reaction, so as to obtain a substance B; adding 8 to 15 parts of betulin, 12 to 16 parts of hydroxypropyl methyl cellulose, and 7 to 13 parts of phosphoglyceride into the substance B in sequence under the condition that stirring is carried out continuously, and carrying out a primary reaction at 80 to 100 DEG C; adding 2 to 8 parts of silver oxide, 3 to 7 parts of zinc sulfate, and 2 to 7 parts of carbohydrazide, and carrying out a secondary reaction for 40 to 60 minutes; carrying out cooling and drying to obtain the waterproof anti-crack environment-friendly coating. The waterproof anti-crack environment-friendly coating prepared according to the preparation method not only has application properties of common coating, but also is environment-friendly, generates no pollution to human bodies and the ambient environment, and is excellent in water resistance and anti-crack property, and wide in application prospect.

Methods for hydrolyzing solid ungranulated lysophosphatidylcholine with phospholipase A₂ are provided. Also disclosed are methods for making a lipid matrix of lysophosphatidylcholine, monoglyceride and fatty acid, and lipid matrices of particular structure.

The invention discloses a leather softening agent which is prepared from the following raw materials in parts by weight: 15-35 parts of polyether-modified hydrophilic silicon oil, 10-22 parts of phosphoglyceride, 8-25 parts of sodium dodecyl sulfonate, 40-60 parts of alcohol, 5-15 parts of peregal, 30-50 parts of water and 0-3 parts of lemon essential oil. Active ingredients in the leather softening agent disclosed by the invention can enter the leather very well to form hydrogen bond binding with hydrophilic groups on fibers inside the leather, so that the interwoven or hardened fibers are separated or re-formed into sequenced arrangement, the elastic force of the leather is recovered by increasing gaps among the fibers, and the good gas permeability of the leather is supplemented; the active ingredients are bridged inside the leather, so that the fibers inside the leather and grease are firmly connected and the grease inside the leather is not prone to volatilize, and the service life of the leather is prolonged. The leather treated by the leather softening agent disclosed by the invention has characteristics of good air permeability, softness, rebound resilience and a smooth hand feeling.

A liposomal drug formulation for treating a disease in a patient characterized by overexpression of HIF-1α and/or HIF-2α includes a plurality of liposomes in a pharmaceutically acceptable carrier. The liposomes encapsulate echinomycin and are made from a peglyated phospholipid, a neutral phosphoglyceride, and a sterol. The PEGylated liposomes may be used to treat proliferative diseases, leukemia, cancer, autoimmune diseases and graft-versus-host disease.

The invention discloses a cholinesterase inhibitor preparation method, and belongs to the technical field of separation and purification of natural medicines. The preparation method comprises: soakinga macroporous cation exchange resin by using an acid solution, completely removing the acid liquid, rinsing with water, soaking with an alkali liquid, rinsing with water, soaking with an acid liquid,rinsing with deionized water, and replacing with lower alcohol; adding glycerol phosphate to the lower alcohol, adding an alkali, carrying out a reaction, carrying out suction filtration, washing with lower alcohol, adjusting the pH value to a weakly alkaline state, carrying out pressure reducing concentrating, cooling, transferring into a separatory funnel, standing, and separating to obtain a lower layer lower alcohol phase; loading glycerol phosphate and a phenol formaldehyde resin onto a column, loading the alcoholysis mixing liquid onto the column, adsorbing, washing the resin with loweralcohol to remove impurities, and eluting the resin with pure water; and decolorizing with a decolorizing agent, and carrying out pressure reducing concentrating to obtain the finished product. According to the present invention, the process steps are short, the requirements of industrial production are met, the resources are saved, the cost is reduced, the total yield of the finished products is65.47-86.08%, the external standard content is over 99%, and the optical purity is 99%.

The invention relates to a gray sparkle silver printing ink, and belongs to the technical field of printing ink. The gray sparkle silver printing ink comprises 8.5-8.8 wt% of black pigment, 0.53-0.55 wt% of transparent yellow pigment, 0.61-0.65 wt% of transparent blue pigment, 18.0-32.0 wt% of gloss oil, 0.80-1.0 wt% of aluminum powders, 2.2-2.5 wt% of phosphoglyceride compound, 1.2-1.5 wt% of glycerol carbonate allyl ether and residual fine-workmanship T-926 diluent. The gray sparkle silver printing has no stimulation on skin and is green and environmental-friendly, and a good storage stability and good film-forming property are achieved. The gray sparkle silver printing ink applies to printing on PET, PMMA and the surface of glass substrate, a good adhesiveness and abrasive resistance are archived when the printing ink is dried totally, and bleeding phenomenon does not occur basically.

The invention relates to the technical field of rabbit skin treatment and breeding, and in particular relates to a high-quality, high-efficiency and environment-friendly rabbit skin tanning technologywhich comprises the following steps: S1, skin selection and water immersion: selecting rabbit skin without skin and hair damage and hair removal; S2, preparing a softener: weighing an amino acid typesurfactant, polyether modified hydrophilic silicone oil, phosphoglyceride, a preservative, lauryl sodium sulfate, a mildew preventive and the like in parts by weight in proportion, and blending withwater; S3, softening: soaking the rabbit skin in the S1 in the softener until the rabbit skin is completely soaked in the softener; s4, tanning the rabbit skin: adding a tanning agent and water according to the concentration of 5-15g/L, mixing, and soaking the rabbit skin in the mixture; and S5, drying: fishing out the rabbit skin obtained in the step S4, and putting the rabbit skin on a drying rack for drying treatment until the rabbit skin is completely dried, thereby obtaining a finished rabbit skin product. The rabbit skin prepared by the method is softer and softer, and then the rabbit skin is tanned, so that the tanned rabbit skin is natural in color and luster and lighter in texture.

This invention relates to a process for removing sterols and phosphorous compounds from naturally occurring lipid mixtures. The process involves hydrolyzing a naturally occurring lipid mixture containing phospholipids, triglycerides, and sterols to form a two-phase product containing a fatty acid phase comprised of free fatty acids and sterols, and an aqueous phase comprised of water, glycerol, and glycerol phosphoric acid esters. The aqueous phase is separated from the fatty acid phase and the crude fatty acid phase is heated to convert the free sterols to fatty acid sterol esters. The free fatty acids are distilled from the fatty acid sterol esters to yield purified fatty acids which are free of cholesterol and other sterols, and phosphorous compounds.

The present invention addresses the problem of providing a method for the efficient phosphorylation of glycerol. The problem is solved by reacting glycerol with either a kinase that includes the active center expressed by sequence (1) and exhibits a catalytic activity with respect to the phosphorylation of glycerol, or a kinase that includes the amino acid sequence represented by SEQ ID NO: 2 and exhibits a catalytic activity with respect to the phosphorylation of glycerol, in the presence of a phosphate group donor.

The invention belongs to the technical field of vaccines and particularly relates to a freeze-drying protective agent used for a viral vaccine host and a preparation method thereof. The freeze-drying protective agent used for the viral vaccine host includes chitosan, beta-cyclodextrine, sodium alginate, raffinose, lactic acid, inositol phosphoglyceride and butyl hydroxy anisd. The freeze-drying protective agent used for the viral vaccine host is designed for the host, and reasonable synergistic combination is conducted by researching and exploring matter having a protective function on cells. Host cell preservation conditions are optimized by means of the freeze-drying protective agent, and a foundation is laid for better virus preservation.

The invention provides a preparation method of an anti-respiratory-system-virosis fiber. According to the fiber, polyethylene terephthalate (PET) is used as a substrate, exogenous pulmonary surfactantis used, by surface modifying long-chain phospholipid molecules, and glycerol phosphate, acidic phospholipids and a pulmonary surfactant antiviral drug composed of specific proteins are further adsorbed. The protection and treatment of respiratory system virosis are realized. The fiber can be used to prepare products such as protective masks, wherein exogenous pulmonary surfactant are loaded on the surface of the fiber by means of adsorption and can enter a body through breathing to play an antiviral effect. The preparation method is simple in preparation procss, the reaction is easy to control, the stability is good, and the preparation method can be industrialized and has a broad promotion prospect.

The invention relates to a preparation method of grey flash silver ink and belongs to the technical field of printing ink. The grey flash silver ink comprises black pigment, transparent yellow pigment, transparent blue pigment, gloss oil, silver powder, phosphoglyceride compound, glycerol carbonate allyl ether and the balance of Seiko T-926 diluent. The preparation method includes mixing and grinding. The preparation method has the advantages that the prepared grey flash silver ink is free of stimulation to the skin, environmental friendly, good in storage stability, good in film forming property and applicable to the printing of the surfaces of PET, PMMA and glass base material, and the ink is good in attaching performance, good in wear resistance and basically free of exudation after being completely dried.

The invention discloses a preparation technology of DNA (DesoxyriboNucleic Acid) for treating pneumonia and belongs to the technical field of separation purification of natural drugs. The preparationtechnology comprises the following steps: soaking macroporous cation exchange resin with acid fluid, completely draining the acid fluid and flushing with water; then soaking with lye and flushing withthe water; then soaking the macroporous cation exchange resin with the acid fluid again, flushing with deionized water and replacing with low carbon alcohol; adding phosphoglyceride into the low carbon alcohol, adding alkali for reacting, carrying out suction filtration, washing with the low carbon alcohol, and adjusting the pH to weak basicity, carrying out vacuum concentration, cooling, transferring to a separating funnel, standing and separating out a lower low carbon alcohol phase; loading the phosphoglyceride and phenolic resin on a column, carrying out column adsorption on alcoholysis mixed liquid, washing the resin with the low carbon alcohol, purifying and eluting the resin with pure water; decolorating by using a decoloring agent and carrying out vacuum concentration to obtain afinished product. The preparation technology has the advantages that technological steps are short and the requirements of industrial production are met; resources are saved and the cost is reduced; the total yield of a finished product reaches 65.47 to 86.08 percent, the external standard content reaches 99 percent or above and the optical purity reaches 99 percent.

The invention provides a biological regulator for fracturing, and a preparation method and application thereof. The biological regulator comprises the following substances in percentage by weight: 8-15% of sodium citrate dihydrate, 3-6% of iron ion stabilizer, 21-32% of p-toluenesulfonic acid, 3-7% of phosphoglyceride, 2-12% of ethanol and the balance of water. The biological regulator can effectively shield high-valence (bivalent and trivalent) ions in fluid preparation water or a flow-back fluid, can reduce the influence on the performance of a prepared fracturing fluid, and can improve thetemperature tolerance of the fracturing fluid; the sodium citrate dihydrate in the regulator can regulate the pH value; and the regulator is biodegradable, nontoxic and harmless, and ensures the greenenvironment-friendly production and sustainable development of oilfields.

The present invention discloses a toilet cleaning agent, which comprises the following raw materials by weight: 20-26% of sodium dodecylbenzenesulfonate, 12-20% of phosphoglyceride, 3-9% of phosphoamide, 1-4% of glycerol, 0.4-0.8% of sodium hydroxide, 0.1-0.5% of melamine, 0.04-0.08% of pigment, and the balance of water.

The invention discloses a novel glycerol phosphatidylcholine preparation method, and belongs to the technical field of separation and purification of natural medicines. The preparation method comprises: soaking a macroporous cation exchange resin by using an acid solution, completely removing the acid liquid, rinsing with water, soaking with an alkali liquid, rinsing with water, soaking with an acid liquid, rinsing with deionized water, and replacing with lower alcohol; adding glycerol phosphate to the lower alcohol, adding an alkali, carrying out a reaction, carrying out suction filtration, washing with lower alcohol, adjusting the pH value to a weakly alkaline state, carrying out pressure reducing concentrating, cooling, transferring into a separatory funnel, standing, and separating toobtain a lower layer lower alcohol phase; loading glycerol phosphate and a phenol formaldehyde resin onto a column, loading the alcoholysis mixing liquid onto the column, adsorbing, washing the resinwith lower alcohol to remove impurities, and eluting the resin with pure water; and decolorizing with a decolorizing agent, and carrying out pressure reducing concentrating to obtain the finished product. According to the present invention, the process steps are short, the requirements of industrial production are met, the resources are saved, the cost is reduced, the total yield of the finished products is 65.47-86.08%, the external standard content is over 99%, and the optical purity is 99%.