Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

35 results about "Phosphatidylethanol" patented technology

Phosphatidylethanols (PEth) are a group of phospholipids formed only in the presence of ethanol via the action of phospholipase D. Levels of phosphatidylethanols in blood are used as markers of previous alcohol consumption. For this purpose, PEth is more sensitive than carbohydrate deficient transferrin (CDT), urinary ethyl glucuronide (EtG) and ethyl sulfate (EtS).

Long-circulation irinotecan lipidosome composition and preparation method thereof

The invention belongs to the field of medicine preparations, which particularly relates to a long-circulation irinotecan lipidosome composition. The long-circulation irinotecan lipidosome composition is prepared from the following components in parts by weight: 1 part of irinotecan, 2 to 4 parts of hydrogenated soy phosphatidylcholine or distearoyl lecithin, 0.5 to 1.5 parts of cholesterol, 0.4 to 1.2 parts of phosphatidylethanolamine pegol and 0.0104 to 0.051 part of metal-chelator. The invention further discloses a preparation method of the long-circulation irinotecan lipidosome composition and an application of the long-circulation irinotecan lipidosome composition prepared into an irinotecan lipidosome composition injection. According to the irinotecan lipidosome composition and the preparation method thereof, the medicine loading ratio of the irinotecan is greatly improved and the encapsulation efficiency is greater than 99.5%, so that the toxic and side effect of the medicine which is not encapsulated can be obviously reduced; the content of relevant substances is lower than 0.5% and the limit of various toxic impurities is lower than 0.1%, so that the safety of the composition is obviously improved; and the composition is uniform in granularity distribution and good in stability.
Owner:JIANGSU AOSAIKANG PHARMA CO LTD

Method for quickly modifying avidin on interface based on lipidosome

The invention relates to a method for quickly modifying avidin on an interface based on lipidosome. The method comprises the steps of mixing phospholipid and biotinylated phosphatidyl ethanol, adding chloroform for ultrasonic stirring, drying under nitrogen, and vacuum drying; adding a neutral solution, matching films with different bore diameters for a squeezer, and squeezing for multiple times so as to form lipidosomes with different sizes; after cleaning a glass slide, soaking in a hydrofluoric acid solution with the concentration being 1 percent for dozens of seconds, then washing with pure water, and drying under the nitrogen; putting the glass slide into a clean utensil, dropwise adding a certain amount of synthetic lipidosome, incubating for several minutes at the temperature higher than the phase-transition temperature, and using super-pure water for cleaning excessive lipidosome; later, adding the avidin for incubating for several minutes, using the super-pure water or solution to clean excessive avidin, and obtaining a glass interface with the avidin modified on the surface. The method is simple, convenient and quick in modification steps, uniform in modification, and complete in sealing, and since silanization reagents are not introduced during a modification process, the background interference is less. The prepared interface can meet the requirement on single molecule enzymology research.
Owner:SHANGHAI NAT ENG RES CENT FORNANOTECH

A kind of spio traced pH-sensitive drug-loaded liposome and preparation method thereof

The invention discloses an SPIO labeled pH sensitive drug-carrying liposome which is prepared from the following components in parts by mass: 1-10 parts of bulk drugs, 1-50 parts of phosphatidyl ethanolamine, 1-30 parts of cholesterol, 1-30 parts of linoleic acid, 0-10 parts of carboxymethyl chitosan, and 0-10 parts of superparamagnetic iron oxide nanoparticles. The invention further discloses a preparation method of the SPIO labeled pH sensitive drug-carrying liposome. The preparation method comprises the following steps: S1, placing phosphatidyl ethanolamine, cholesterol and linoleic acid ina flask, adding chloroform for dissolving, adding a water soluble drug solution for ultrasonic treatment to form a W / O emulsion; S2, evaporating to a gel state under the pressure reduction condition;adding a buffering solution, and continuously evaporating to form an aqueous suspension; S3, adding the superparamagnetic iron oxide nanoparticles and performing freeze thawing on a liposome suspension for three times; and centrifugally removing the superparamagnetic iron oxide nanoparticles and the water soluble drug not in the aqueous suspension; and S4, adding a carboxymethyl chitosan solutionfor hydration.
Owner:重庆市人民医院

Oxygen-carrying phospholipid micro-capsule, preparation method thereof and application of oxygen-carrying phospholipid micro-capsule in preparation of anti-hypoxic drugs

The invention discloses an oxygen-carrying phospholipid microcapsule, a preparation method thereof and application of the oxygen-carrying phospholipid microcapsule in preparation of an anti-hypoxia drug, and the preparation method comprises the following steps: adding myristoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine, dipalmitoyl phosphatidylethanole-polyethylene glycol 2000-triphenyl phosphate and an organic solvent into a container, and carrying out ultrasonic treatment to obtain a clear solution; performing reduced pressure evaporation to remove the organic solvent, and adhering a layer of uniform and transparent faint yellow film on the inner wall of the container; carrying out vacuum drying, adding ultrapure water, hydrating in an ice bath to obtain phospholipid microcapsules, and putting the phospholipid microcapsules in the ice bath; adding perfluorohexane to obtain a mixed system, and performing ultrasonic dispersion until the mixed system is not layered to obtain an emulsion; and adding a freeze-drying protective agent, freeze-drying, storing at 4 DEG C, and redissolving and oxygenating before use to obtain the oxygen-carrying phospholipid microcapsule. The preparation method is simple and controllable, and raw materials and auxiliary materials are easy to obtain; the prepared oxygen-carrying phospholipid micro-capsule is uniform in particle size and good in stability and biocompatibility, oxygen can be supplemented to an organism in time, and the effect of treating diseases is achieved.
Owner:TIANJIN UNIV

A long-circulation irinotecan liposome composition and preparation method thereof

The invention belongs to the field of medicine preparations, which particularly relates to a long-circulation irinotecan lipidosome composition. The long-circulation irinotecan lipidosome composition is prepared from the following components in parts by weight: 1 part of irinotecan, 2 to 4 parts of hydrogenated soy phosphatidylcholine or distearoyl lecithin, 0.5 to 1.5 parts of cholesterol, 0.4 to 1.2 parts of phosphatidylethanolamine pegol and 0.0104 to 0.051 part of metal-chelator. The invention further discloses a preparation method of the long-circulation irinotecan lipidosome composition and an application of the long-circulation irinotecan lipidosome composition prepared into an irinotecan lipidosome composition injection. According to the irinotecan lipidosome composition and the preparation method thereof, the medicine loading ratio of the irinotecan is greatly improved and the encapsulation efficiency is greater than 99.5%, so that the toxic and side effect of the medicine which is not encapsulated can be obviously reduced; the content of relevant substances is lower than 0.5% and the limit of various toxic impurities is lower than 0.1%, so that the safety of the composition is obviously improved; and the composition is uniform in granularity distribution and good in stability.
Owner:JIANGSU AOSAIKANG PHARMA CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products