80 results about "Diammonium Glycyrrhizinate" patented technology

The invention provides a combination medicament of ilaprazole sodium. The medicament is characterized by comprising the following raw materials in percentage by weight: 5-10 percent of ilaprazole sodium, 25-35 percent of reduction composition containing glutathione and tiopronin with a weight ratio of 1:10 and 45-55 percent of diammonium glycyrrhizinate. The invention also provides a preparation process of the medicament. According to a pharmaceutically acceptable dosage of the ilaprazole sodium, the combination medicament can be respectively prepared into medical preparations of the dosage forms of injections of the combination medicament of the ilaprazole sodium, freeze-drying injections of combination medicament of the ilaprazole sodium, coated tablets of the combination medicament of the ilaprazole sodium, enteric capsules, sprays, and the like and is used for treating gastric ulcer.

The invention relates to a preparation method of ammonium 18alpha,beta-H-glycyrrhetate and a hydrate thereof. The method selecting 75% crude glycyrrhizic acid as a raw material comprises the following steps: purifying the crude glycyrrhizic acid to obtain purified glycyrrhizic acid with the content of above 98%, converting 18alpha,beta-H-glycyrrhizic acid into 18alpha-H-glycyrrhizic acid, and controlling different pH values of the 18alpha-H-glycyrrhizic acid to generate the following different salts: diammonium 18alpha-H-glycyrrhetate, triammonium 18alpha-H-glycyrrhetate and hydrate thereof, and converting 18beta-H-glycyrrhizic acid to generate monoammonium 18beta-H-glycyrrhetate and hydrate thereof. The method has the advantages of simple operation, mild reaction condition, easy control of the quality, high conversion rate, and suitableness for large scale preparation.

The invention relates to a preparation method of a diammonium glycyrrhizinate salt capable of accurately controlling ammonium radical content, which is characterized by comprising the following steps of: using a mono-ammonium glycyrrhizinate salt as an initiative raw material; dissolving by adding a protic solvent; regulating a pH value as 4.5-9.0 by adding ammonia; drying by using a suitable method; and monitoring the ammonium radical content by adopting indophenol blue colorimetry to consequently prepare the diammonium glycyrrhizinate salt with correct ammonium radical content. A preparation technology and a monitoring method of the invention solve the problem of wrong ammonium radical content of the diammonium glycyrrhizinate salt prepared by the prior art in a breakthrough mode, reduce crystallizing steps at the same time, greatly increase the diammonium salt yield and are suitable for industrialized production. The prepared diammonium glycyrrhizinate salt also has definite18alpha and 18beta configurational compositions.

The invention discloses a diammonium glycyrrhizinate salt preparation method. According to the method, according to the special physical and chemical properties of glycyrrhizic acid, the diammonium glycyrrhizinate salt with characteristics of good color, good character, high content and meeting of the industry standard is produced by using an ammonium glycyrrhizinate salt as a raw material. Compared to the method in the prior art, the method of the present invention has significant advantages of novel process, simple operation, energy saving, environmental protection, strong practicality, mild reaction condition, high conversion rate, easy quality control, reduction of the use of other solvents, reduction of impurity introduction, good product color, simple operation process, low equipment and material cost, high treatment capacity, good product chrominance, good product yield, high content, excellent product color, uniform crystal and good quality, and is suitable for industrial production.

The present invention relates to a compound medicine formed from diammonium glycyrrhizinate and one or several kinds of halfcystine, glycine, methionine and vitamin B1. Its therapeutic action is extensive, and side effect is low. Said compound medicine can be used for curing the liver diseases of acuter, chronic and virus hepatitises, cirrhosis and fatty liver, etc. and can be used for improving function of liver and cholestasis in the liver. Besides, it also can be used for auxiliary therapy of alcoholism and barbitones and sulfonamides drug poisoning.

The present invention relates to medicine technology. The diammonium glycyrrhizinate freeze drying powder for injection includes the following components: diammonium glycyrrhizinate 10-100 wt%, solabilizer 0-90 wt% and excipient 0-80 wt%. Its preparation process includes dissolving the above said components, regulating pH value, filtering, packing and freeze drying. The medicine is used clinically in intravenous dripping for treating chronic organizing hepatitis accompanied with raised glutamic pyruvic transaminase and chronic mobile hepatitis. It has stable quality, long storage period and fast dissolution in water, and may be matched with glucose injection and/or sodium chloride injection clinically.

The invention relates to a preparation method for trans-glycyrrhizic acid. Diammonium glycyrrhizinate is directly placed in carbinol, a proper amount of protonic acid is added for catalysis, and under room temperature conditions, trans-glycyrrhizic acid methyl ester is selectively combined in automatic coherent type multicomponent reactive mode so as to change physical and chemical properties of a glycyrrhizic acid stereoisomer mixture, enable trans-glycyrrhizic acid methyl ester with weak polarity to be dissolved out from reaction liquid and filtered and obtain trans-glycyrrhizic acid methyl ester to be separated from cis-glycyrrhizic acid. Then, single-component trans-glycyrrhizic acid is prepared through saponification, acid neutralization and the like, and cis-glycyrrhizic acid is recycled. The preparation method resolves the technical problem that the glycyrrhizic acid stereoisomer mixture cannot be separated and has the advantages of being simple, low in energy consumption and high in yield and improving utilization ratio of natural glycyrrhizic acid.

The invention provides a rabeprazole sodium combined medicament and a preparation process thereof. The rabeprazole sodium combined medicament is characterized by comprising the following raw materials as components in proportion by weight: 5-10 of ilaprazole sodium, 20-30 of composition of reduced glutathione and hepatocyte growth-promoting factors in proportion by weight of 1:10, and 50-60 of diammonium glycyrrhizinate. According to a pharmaceutically allowable dose of rabeprazole sodium, pharmaceutical preparations in dosage forms of injection, lyophilized powder injection, enteric coated tablets, enteric coated capsules, spray and the like of the rabeprazole sodium combined medicament are respectively prepared for treating gastric ulcer.

The invention relates to the technical field of medicines and in particular relates to a diammonium glycyrrhizinate enteric-coated pellet as well as a preparation method and preparation thereof. The diammonium glycyrrhizinate enteric-coated pellet comprises diammonium glycyintestinal tractrrhizinate, excipient, adhesive and coating material in a mass ratio of 1:(0.30-8):(0.02-0.1):(0.2-3.2). The diammonium glycyrrhizinate enteric-coated pellet is table in gastric juice and good in dissolution rate in intestinal tract. The damages of the gastric juice to the diammonium glycyrrhizinate are avoided, so that the stability of the diammonium glycyrrhizinate is ensured, and the biological utilization rate is improved.

A freeze dried powder injection of diammonium glycyrrhetate is prepared from diammonium glycyrrhetate and mannitol or sodium chloride or glucose in ratio of 1:(0.5-2) through dissolving the diammonium glycyrrhetate in water, adding mannitol, stirring for dissolving, regulating pH value, adding carbon for injection, heating to 80 deg.C and holding the temp for 30 min, cooling to 45 deg.C, decarbonizing, adding the water for injection, fine filter, pouring in bottles, and freeze drying. Its advantage is high curative effect.

The invention relates to a pharmaceutical composition, in particular to a pharmaceutical composition of acetaminophen and glycyrrhizic acid or medicinal salt thereof or medicinal derivative thereof. The weight ratio of acetaminophen to glycyrrhizic acid or medicinal salt thereof or medicinal derivative thereof is (40:1)-(1:1). Glycyrrhizic acid medicinal salt or glycyrrhizic acid medicinal derivative is selected from mono-ammonium glycyrrhizinate, diammonium glycyrrhizinate, monopotassium glycyrrhizinate, dipotassium glycyrrhizinate, disodium glycyrrhizate, trisodium glycyrrhetate, magnesium isoglycyrrhizinate, glycyrrhetinic acid or glycyrrhizin. The invention further relates to an oral drug prepared from the pharmaceutical composition, and the oral drug can be tablets, capsules or particles. By the adoption of the pharmaceutical composition, liver injury caused by acetaminophen can be reduced to a certain extent, using convenience is ensured, and therefore a solution is provided for safer and more efficient use of acetaminophen.

A composite medicine for treating hepatism is prepared from scutelloside (60-2000 Wt portions) and glycyrrhizic acid or its pharmacologically acceptable salt (10-800). Its preparing process is also disclosed.

The invention discloses a cefoxitin sodium drug combination, which consists of the following effective ingredients in part by weight: 1000 to 2000 parts of cefoxitin sodium, 100 to 200 parts of lidocaine, 50 to 120 parts of reduced glutathione and 80 to 120 parts of diammonium glycyrrhizinate. The drug combination cannot cause adverse reactions, and has a high curative effect, and moreover, the preparation method is simple and environment-friendly.

The invention discloses a method for removing solvent residues of a diammonium glycyrrhizinate bulk drug. The method comprises the following steps: using a mixing solvent for performing decolorizing re-crystallization on a synthetic crude product of diammonium glycyrrhizinate; centrifugally filtering; drying under reduced pressure; absorbing water and moisture, and then performing suction filtration, and continuing to dry under reduced pressure, thereby acquiring the diammonium glycyrrhizinate bulk drug. Through detection, the residual solvent ethyl alcohol of the acquired diammonium glycyrrhizinate bulk drug is less than or equal to 2000ppm and is far lower than the quality standard (less than or equal to 5000ppm) for residual solvent of diammonium glycyrrhizinate bulk drug in Chinese pharmacopoeia. The diammonium glycyrrhizinate bulk drug is a white granular crystal in larger crystal size and is high in purity and stability.

The invention discloses a preparation method of 18 alpha type diammonium glycyrrhizinate. Under a certain alkali concentration, 18 beta type diammonium glycyrrhizinate is converted into 18 alpha type diammonium glycyrrhizinate. The end point is judged according to a principle that under a certain chromatographic condition, the retention time of 18 beta type diammonium glycyrrhizinate and the retention time of 18 alpha type diammonium glycyrrhizinate are different, and high performance liquid chromatography (HPLC) is used to judge the end point. The obtained 18 alpha type diammonium glycyrrhizinate is added into stronger ammonia water, and after refinement, qualified diammonium salt can be obtained. Compared with the conventional technology, the reaction temperature is reduced by about 10 DEG C, the time is also shortened, thus the energy loss of industrial production can be largely reduced; at the same time, the service life of equipment is prolonged, and the cost is reduced. Furthermore, the high temperature of conventional technology will deepen the product color, and the post treatment becomes difficult. The prepared 18 alpha type diammonium glycyrrhizinate has the advantages of good color, high yield and high content. The preparation method is suitable for industrial massive production, the product color is good, the crystals are uniform, and the quality is good.

The invention discloses a novel application of diammonium glycyrrhizinate, and relates to the technical field of biological medicines. The invention relates to a novel application of diammonium glycyrrhizinate, in particular to a novel application of diammonium glycyrrhizinate in preparation of medicines for treating novel coronavirus pneumonia 2019-nCoV or chronic obstructive pulmonary disease, and meanwhile, diammonium glycyrrhizinate can also be used in combination with an immunopotentiator or a medicinal antioxidant. The diammonium glycyrrhizinate can replace hormones to resist inflammatory factors to protect the lung, but has no immunosuppressive effect and osteoporosis effect of the hormones.

The invention discloses a preparation method and an application of a Sarsasapogenin (SAR) monoclonal antibody. On the basis of Sarsasapogenin artificial antigen preparation, the anti-Sarsasapogenin monoclonal antibody is prepared by using a hybridomas technology, the cross reaction rate of the monoclonal antibody with liriope muscari baily saponins C, diosgenin and ruscogenin are respectively detected as 29%, 5.7% and 33%, no obvious cross reaction is generated by monoclonal antibody with diammonium glycyrrhizinate, pseudo-ginseng saponins R1 and oleanolic acid. The invention establishes an ELISA analysis method based on the Sarsasapogenin monoclonal antibody, the correlation of the ELISA analysis method and the HPLC method detection result is good, compared with the HPLC method, the ELISA analysis method has characteristic of rapid microscale detection. The Sarsasapogenin monoclonal antibody is suitable for Sarsasapogenin microscale detection in Sarsasapogenin-containing traditional Chinese medicinal materials and biology samples like blood plasma, and can be used for medicine quality control of active components-containing medicines and pharmacokinetics research.

The invention discloses diammonium glycyrrhizinate microemulsion and a preparation process thereof, providing a microemulsion preparation for patients with viral hepatitis. The diammonium glycyrrhizinate microemulsion is prepared from a medical raw material and three auxiliary materials; and the preparation method of diammonium glycyrrhizinate microemulsion comprises a step of preparing auxiliary material solution, a step of preparing raw material solution and a step of preparing microemulsion. The preparation method of diammonium glycyrrhizinate microemulsion is scientific and novel; the preparation process is simple and convenient; the diammonium glycyrrhizinate microemulsion has more functions of non-specific anti-inflammatory, anti-allergy, stable effect on lysosome membrane and immunoregulation in clinical application; in addition, the diammonium glycyrrhizinate microemulsion improves the thermodynamic activity, prevents the first-pass effect of liver and is easier to work. Compared with the other diammonium glycyrrhizinate oral liquid preparations, the diammonium glycyrrhizinate microemulsion has higher bioavailability and more remarkable efficiency of antiviral therapy and is more convenient for patients, who have difficulty to swallow solid medicine.

The invention relates to a Diammonium Glycyrrhizinate freeze-drying preparation and process for preparing it, wherein the preparation is prepared from Diammonium Glycyrrhizinate, mannitol, sorbitol, sodium chloride, glucose, cane sugar, lactose, sulfo-aminolactic acid, or pharmacologically accepted expanding material of other amino acids through freeze drying.

The invention discloses a mengjin-1 lonicera japonica yield-increasing planting method and relates to the technical field of lonicera japonica planting. The method is characterized in that 15% paclobutrazol wettable powder, diammonium glycyrrhizinate, boric acid zinc oxide and 800 times netropsin solution are evenly sprayed onto branches and leaves of lonicera japonica between March and April every spring in the lonicera japonica twig production and vigorous growing period before floral bud emergence, wherein paclobutrazol wettable powder, diammonium glycyrrhizinate, boric acid zinc oxide and netropsin are added according to the ratio of 5:4:1:0.5. By the adoption of the method, plant growth is delayed, stem lengthening is inhibited, plant tillering is promoted, plant adverse resistance is improved, the number and size of flower buds are increased, and flower buds do not fall off easily.

The invention discloses a compound preparation for treating cholestatic jaundice and a preparing method thereof. The compound preparation is prepared from ademetionine 1,4-butanedisulfonate, diammonium glycyrrhizinate, dihydroxydibutylether, baicalin, methionine, anethol trithione, potassium magnesium aspartate, crocetin dimethyl ester, glucurolactone, cholestyramlne, hydroxymethylnicotinamide, trimethoprim lactate, bumetanide, piperazine citrate and azathioprine. The compound preparation has the effects of resisting bacteria and diminishing inflammations, clearing dampness and heat, soothing the liver and benefiting the gallbladder, removing the toxicity and eliminating jaundice and strengthening the spleen and the stomach, can reduce stasis of bile in liver cells, promote bile excretion, improve the liver functions and the tissue cell respiration function, reduce accumulation of fat in the liver and promote jaundice elimination and liver function recovery and is significant in treatment effect, safe and few in side effect when the compound preparation is used for treating the cholestatic jaundice and complications thereof.