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42results about How to "Low organic residue" patented technology

Method for purifying chenodeoxycholic acid

The invention discloses a method for purifying chenodeoxycholic acid. The method comprises the following steps: pretreatments such as degreasing, decoloration and impurity removal are carried out on commercially available crude bile paste or crude bile powder, so as to obtain a component to undergo chromatographic separation; the component to undergo chromatographic separation undergoes purification and separation by the use of a chromatographic column with a hydrophilic resin filler as a stationary phase; and separation products undergo concentration, acidification, washing and drying, so as to obtain chenodeoxycholic acid. In comparison with the prior art, the invention has the following beneficial effects: 1, content of the main component is high; 2, reappearance is high and operability is good; 3, short cycle: it only takes two days to prepare the high-purity chenodeoxycholic acid product from processing of the bile paste raw material; and 4, low content of organic residues: as processes such as solvent extraction, column chromatography on silica gel and the like in the traditional techniques are abandoned, an industrial chromatographic process with low dosage of an organic solvent is adopted and the final product undergoes drying process, the content of the residual organic solvent in the final product is especially low.
Owner:SHANGHAI FENPU NEW MATERIAL TECH CO LTD

Temozolomide lyophilized powder preparation and preparation method thereof

The invention belongs to the technical field of pharmaceutical preparations and specifically relates to a temozolomide lyophilized powder preparation. The temozolomide lyophilized powder preparation comprises an active ingredient of temozolomide or a pharmaceutically acceptable salt thereof, and a solution before lyophilization further contains an excipient, a wetting agent, a buffer agent, an osmotic pressure regulating agent, a pH regulating agent, water for injection and an organic solvent, wherein the organic solvent is selected from one or any combination of ethanol, acetone, isopropanol, n-propanol, butanone, sec-butyl alcohol and methanol, and is preferably ethanol. The temozolomide lyophilized powder preparation provided by the invention has the advantages of stable quality, high re-dissolution speed and a small residual amount of the organic solvent. The invention further provides a method for preparing the preparation. The process provided by the invention is simple and convenient in preparation process and easy to control production links, the organic solvent accounts for a relatively small part of total volume of material liquid, the pollution to production equipment and environment caused by the organic solvent is reduced, and thus the method is suitable for large-scale production.
Owner:QILU PHARMA HAINAN

Extraction process of high-purity phloridzin

The invention discloses an extraction process of high-purity phloridzin. The process includes the steps of: (1) stock solution extraction: adding water that is 8 times the amount of a phloridzin-containing mashed raw material into the same, conducting soaking for 3h, performing heating to boiling, maintaining slight boiling for 2h to obtain an extracted solution; adding purified water that is 6 times the amount of residue into the same and performing heating to boiling, maintaining slight boiling for 2h to obtain a secondary extracted solution; merging the extracted solutions, carrying out cooling and filtering, and collecting the filtrate; (2) preliminary extraction of a finished product: subjecting the filtrate to adsorption by macroporous resin D101, controlling the column pass flow at 80L/H, using 20-50degree ethanol to conduct gradient elution, performing fractional collection on the outflow solution, carrying out vacuum concentration, standing and cooling, conducting crystal precipitation at 0-4DEG C, and carrying out high-speed centrifugal dehydration; and (3) finished product extraction: conducting pure water redissolution, vacuum concentration, recrystallization, high-speed centrifugal dehydration and drying, thus obtaining a finished product. The extraction process of high-purity phloridzin provided by the invention has easily available raw materials, not only solves the environmental problem, but also improves the product yield, and greatly reduces the cost, and has the advantages of simple reaction process, convenient operation and no pollution.
Owner:TIANJIN UNIQUE FRUITS & VEGETABLES FOOD CO LTD

A treatment process for resource utilization of medical waste salt by medium-temperature pyrolysis

The present invention relates to the field of environmental protection, and specifically relates to a treatment process for resource utilization of medical waste salt at medium temperature pyrolysis; the present invention provides a process for resource utilization of waste medical salt at medium temperature pyrolysis. The principle is to use lower temperature to fully oxidize and decompose organic pollutants from the waste salt that has removed volatile substances, so as to achieve the purpose of harmless treatment of waste salt and then resource utilization; the invention adds an inorganic salt anti-caking agent, It can effectively prevent the waste salt from agglomerating in the fluidized bed reactor and ensure the sufficient oxidation and decomposition of organic pollutants, which is the key to the process; the waste salt obtained by the treatment method of medical waste salt of the present invention has extremely low organic residues and no agglomeration phenomenon. The organic matter is fully oxidized, and the energy saving is significantly reduced. The effective treatment of medical waste salt can not only protect the environment, but also reuse the main component sodium chloride salt to make up for the market gap, which has high economic value.
Owner:浙江红狮环保股份有限公司

Preparation method of silver powder

According to the scheme, a liquid phase reduction method is firstly adopted, silver nitrate and a reducing agent are adopted according to the main principle, and a certain amount of water-based dispersing agent or oil-based dispersing agent is added, so that the silver powder with certain dispersing performance is obtained, and in order to guarantee that the silver powder with high dispersity and uniform particle size can be obtained, the preparation method is simple, and the cost is low. The water-based dispersing agent is selected, meanwhile, the reducing agent is any one or more of ascorbic acid, formaldehyde, hydrazine hydrate and hydrogen peroxide, after the reduction reaction is finished, alkali liquor continues to be added, the pH of the suspension C is adjusted to be 8-14, hydroxyl ions are contained in the system in the process, the structure of the dispersing agent can be destroyed through strong alkalinity, and therefore the dispersing effect is improved. Therefore, the dissociation effect is achieved; the method can be applied to any preparation method of the silver powder using the water-based dispersing agent, complete sedimentation of the silver powder can be achieved, organic residues on the surface of the obtained silver powder are lower than those of the silver powder not using the method by 0.3% or above, and high practicability is achieved.
Owner:南通领跑者新材料科技有限公司 +1

Method for preparing hydrophilic drug microsphere through spray drying process

The invention relates to the technical field of preparation of hydrophilic drug microspheres, in particular discloses a method for preparing a hydrophilic drug microsphere through a spray drying process. The method comprises preparation steps of: uniformly dispersing hydrophilic drug powder into an isolation oil phase to form an S / O1 type suspension, and then slowly adding into a spray solution (O2) which contains a macromolecular carrier, an anti-sticking agent and a plasticizing agent, homogeneously emulsifying to form an S / O1 / O2 type spray emulsion, decompressing and drying at 60 DEG C or less through a spray drying technology after collecting the microspheres in a cyclone separator, and screening with a sieve of 80 meshes so as to prepare the hydrophilic drug twice-embedded sustained-release microsphere. The microsphere prepared by spray drying have the advantages of round shape, smooth surface, good mobility, uniform grain size distribution, high encapsulating rate, capability ofeffectively controlling burst release, and accordance with the characteristics of a long-acting preparation; and the method has the advantages of reducing consumption of a great quantity of oil substances and volatile organic solvents , greatly shortening drying time and being remarkable in effect, and is applicable to industrial production.
Owner:武汉回盛生物科技股份有限公司

A kind of temozolomide freeze-dried powder preparation and preparation method thereof

The invention belongs to the technical field of pharmaceutical preparations and specifically relates to a temozolomide lyophilized powder preparation. The temozolomide lyophilized powder preparation comprises an active ingredient of temozolomide or a pharmaceutically acceptable salt thereof, and a solution before lyophilization further contains an excipient, a wetting agent, a buffer agent, an osmotic pressure regulating agent, a pH regulating agent, water for injection and an organic solvent, wherein the organic solvent is selected from one or any combination of ethanol, acetone, isopropanol, n-propanol, butanone, sec-butyl alcohol and methanol, and is preferably ethanol. The temozolomide lyophilized powder preparation provided by the invention has the advantages of stable quality, high re-dissolution speed and a small residual amount of the organic solvent. The invention further provides a method for preparing the preparation. The process provided by the invention is simple and convenient in preparation process and easy to control production links, the organic solvent accounts for a relatively small part of total volume of material liquid, the pollution to production equipment and environment caused by the organic solvent is reduced, and thus the method is suitable for large-scale production.
Owner:QILU PHARMA HAINAN
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