[go: up one dir, main page]

CN112138138A - A pharmaceutical composition for treating gout and preparation method thereof - Google Patents

A pharmaceutical composition for treating gout and preparation method thereof Download PDF

Info

Publication number
CN112138138A
CN112138138A CN202011300901.4A CN202011300901A CN112138138A CN 112138138 A CN112138138 A CN 112138138A CN 202011300901 A CN202011300901 A CN 202011300901A CN 112138138 A CN112138138 A CN 112138138A
Authority
CN
China
Prior art keywords
parts
pharmaceutical composition
alanine
methionine
arginine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN202011300901.4A
Other languages
Chinese (zh)
Other versions
CN112138138B (en
Inventor
徐庆阳
李志华
熊海波
张宁
杨柳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lekang Zhentai Tianjin Biotechnology Co ltd
Tianjin University of Science and Technology
Original Assignee
Lekang Zhentai Tianjin Biotechnology Co ltd
Tianjin University of Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lekang Zhentai Tianjin Biotechnology Co ltd, Tianjin University of Science and Technology filed Critical Lekang Zhentai Tianjin Biotechnology Co ltd
Priority to CN202011300901.4A priority Critical patent/CN112138138B/en
Publication of CN112138138A publication Critical patent/CN112138138A/en
Application granted granted Critical
Publication of CN112138138B publication Critical patent/CN112138138B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/716Glucans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/375Ascorbic acid, i.e. vitamin C; Salts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7008Compounds having an amino group directly attached to a carbon atom of the saccharide radical, e.g. D-galactosamine, ranimustine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/74Synthetic polymeric materials
    • A61K31/765Polymers containing oxygen
    • A61K31/78Polymers containing oxygen of acrylic acid or derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/01Hydrolysed proteins; Derivatives thereof
    • A61K38/012Hydrolysed proteins; Derivatives thereof from animals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Zoology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention provides a pharmaceutical composition for treating gout and a preparation method thereof, wherein the pharmaceutical composition comprises the following effective components, by weight, 18-30 parts of euglena beta-1, 3-glucan, 15-35 parts of compound active alkaloid, 3-15 parts of deep sea fish peptide, 2-5 parts of micromolecular potassium hyaluronate, 5-10 parts of D-glucosamine ketone glutarate, 3-5 parts of glutamine, 2-5 parts of L-alanine, 3-6 parts of L-arginine, 2-5 parts of L-methionine, 3-6 parts of L-lysine, 5-9 parts of L-leucine and 0.2-1 part of vitamin C, and can be prepared by a mixing mode, and the pharmaceutical composition can effectively improve and treat metabolic arthritis such as gout and the like, rheumatic arthritis, and the like, Chronic diseases such as rheumatoid arthritis and the like, joint repair, joint pain reduction, muscle synthesis increase and uric acid metabolism acceleration.

Description

一种用于治疗痛风的药物组合物及其制备方法A kind of pharmaceutical composition for treating gout and preparation method thereof

技术领域technical field

本发明涉及一种痛风治疗药物及其制备方法,尤其是涉及一种用于治疗痛风的药物组合物及其制备方法。The present invention relates to a medicine for treating gout and a preparation method thereof, in particular to a pharmaceutical composition for treating gout and a preparation method thereof.

背景技术Background technique

痛风是嘌呤代谢障碍所致的一组异质性慢性代谢性疾病, 其临床特点为高尿酸血症、反复发作的痛风性急性关节炎、间质性肾炎和痛风石形成;严重者伴关节畸形或尿酸性尿路结石。痛风临床特点为:高尿酸血症;痛风性急性关节炎反复发作;痛风石形成和沉积痛风石性漫性关节炎;关节畸形等。Gout is a heterogeneous group of chronic metabolic diseases caused by purine metabolism disorders. Its clinical characteristics are hyperuricemia, recurrent gouty acute arthritis, interstitial nephritis and tophi formation; severe cases are associated with joint deformities. or uric acid urolithiasis. The clinical characteristics of gout are: hyperuricemia; recurrent gouty acute arthritis; tophi formation and deposition of tophi diffuse arthritis; joint deformities.

通风形成过程主要是尿酸过度积累造成,尿酸的积聚主要原因有:过量食用高嘌呤的食物,体内嘌呤代谢出现问题,排泄量过少,尿酸无法正常排泄。根据尿酸产生的机理,要防治好痛风必需减少尿酸的产生,要减少尿酸的产生必需减少体内的嘌呤,减少体内的嘌呤必需减少核酸的氧化分解,和嘌呤的摄入,同时加强尿酸的排除。目前,市场上治疗痛风的药物较多,有秋水仙碱、葵花盘生物碱、别嘌呤醇、丙磺舒等药物,这些药物治标不治本,并造成造成肝肾功能严重伤害、溶血性贫血、过敏性休克等一系列副作用,一些植物碱可以中和尿酸,但患者出现疼痛加剧的现象。The formation process of ventilation is mainly caused by the excessive accumulation of uric acid. The main reasons for the accumulation of uric acid are: excessive consumption of high purine foods, problems in purine metabolism in the body, too little excretion, and uric acid cannot be excreted normally. According to the mechanism of uric acid production, to prevent gout, it is necessary to reduce the production of uric acid, to reduce the production of uric acid, it is necessary to reduce the purine in the body, to reduce the purine in the body, it is necessary to reduce the oxidative decomposition of nucleic acid, and the intake of purine, while strengthening the elimination of uric acid. At present, there are many drugs for the treatment of gout on the market, including colchicine, sunflower alkaloids, allopurinol, probenecid and other drugs. A series of side effects such as anaphylactic shock, some plant alkaloids can neutralize uric acid, but patients experience increased pain.

发明内容SUMMARY OF THE INVENTION

本发明所要解决的技术问题在于提供一种用于治疗痛风的药物组合物。The technical problem to be solved by the present invention is to provide a pharmaceutical composition for treating gout.

本发明所要解决的另一技术问题在于提供上述用于治疗痛风的药物组合物的制备方法。Another technical problem to be solved by the present invention is to provide a preparation method of the above-mentioned pharmaceutical composition for treating gout.

本发明采用的技术方案是:The technical scheme adopted in the present invention is:

一种用于治疗痛风的药物组合物,功效成分由裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C组成,按其重量份数计裸藻β-1,3-葡聚糖18-30份、复合活性生物碱15-35份、深海鱼肽3-15份、小分子透明质酸钾(分子量小于3000)2-5份、D-氨基葡萄糖酮戊二酸盐 5-10份、谷氨酰胺3-5份、L-丙氨酸2-5份、L-精氨酸3-6份、L-蛋氨酸2-5份、L-赖氨酸3-6份、L-亮氨酸5-9份、维生素C 0.2-1份。A pharmaceutical composition for treating gout, the functional components are composed of Euglena β-1,3-glucan, complex active alkaloids, deep-sea fish peptides, small molecule potassium hyaluronate (molecular weight less than 3000), D-amino Glucose ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, in parts by weight Algae β-1,3-glucan 18-30 parts, compound active alkaloids 15-35 parts, deep-sea fish peptides 3-15 parts, small molecule potassium hyaluronate (molecular weight less than 3000) 2-5 parts, D- Glucosamine Ketoglutarate 5-10 parts, Glutamine 3-5 parts, L-Alanine 2-5 parts, L-Arginine 3-6 parts, L-Methionine 2-5 parts, L- 3-6 parts of lysine, 5-9 parts of L-leucine, 0.2-1 part of vitamin C.

优选的,上述用于治疗痛风的药物组合物,按其重量份数计裸藻β-1,3-葡聚糖26.5份、复合活性生物碱29.4份、深海鱼肽7.2份、小分子透明质酸钾3.5份、D-氨基葡萄糖酮戊二酸盐 8.6份、谷氨酰胺4.1份、L-丙氨酸3.0份、L-精氨酸4.2份、L-蛋氨酸3.5份、L-赖氨酸3.5份、L-亮氨酸6.0份、维生素C 0.5份。Preferably, the above-mentioned pharmaceutical composition for treating gout contains 26.5 parts by weight of Euglena β-1,3-glucan, 29.4 parts of complex active alkaloids, 7.2 parts of deep-sea fish peptides, and small molecular hyaluronic acid. Potassium acid 3.5 parts, D-glucosamine ketoglutarate 8.6 parts, glutamine 4.1 parts, L-alanine 3.0 parts, L-arginine 4.2 parts, L-methionine 3.5 parts, L-lysine 3.5 parts, L-leucine 6.0 parts, vitamin C 0.5 parts.

上述用于治疗痛风的药物组合物可以制作为散剂、胶囊剂或颗粒剂。The above-mentioned pharmaceutical composition for treating gout can be made into powder, capsule or granule.

上述用于治疗痛风的药物组合物的制备方法,具体步骤如下:The above-mentioned preparation method of the pharmaceutical composition for the treatment of gout, the concrete steps are as follows:

(1)按重量份数称取裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C;(1) Weigh Euglena β-1,3-glucan, compound active alkaloid, deep-sea fish peptide, small molecule potassium hyaluronate (molecular weight less than 3000), D-glucosamine ketoglutarate by weight parts Salt, Glutamine, L-Alanine, L-Arginine, L-Methionine, L-Lysine, L-Leucine and Vitamin C;

(2)将步骤(1)中各组分混合均匀即得。(2) Mix the components in step (1) evenly to obtain.

本发明的有益效果是:The beneficial effects of the present invention are:

所述用于治疗痛风的药物组合物,可有效改善和治疗痛风等代谢性关节炎、风湿性关节炎、类风湿性关节炎等慢性疾病,修复关节,减少关节疼痛,增加肌肉合成,加快尿酸代谢。The pharmaceutical composition for treating gout can effectively improve and treat chronic diseases such as metabolic arthritis such as gout, rheumatoid arthritis, rheumatoid arthritis, etc., repair joints, reduce joint pain, increase muscle synthesis, and accelerate uric acid. metabolism.

具体实施方式Detailed ways

为进一步说明本发明,结合以下实施例具体说明:In order to further illustrate the present invention, it is specified in conjunction with the following examples:

实施例1Example 1

一种用于治疗痛风的药物组合物,功效成分由裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C组成,其中,裸藻β-1,3-葡聚糖26.5%、复合活性生物碱29.4%、深海鱼肽7.2%、小分子透明质酸钾3.5%、D-氨基葡萄糖酮戊二酸盐 8.6%、谷氨酰胺4.1%、L-丙氨酸3.0%、L-精氨酸4.2%、L-蛋氨酸3.5%、L-赖氨酸3.5%、L-亮氨酸6.0%、维生素C 0.5%。A pharmaceutical composition for treating gout, the functional components are composed of Euglena β-1,3-glucan, complex active alkaloids, deep-sea fish peptides, small molecule potassium hyaluronate (molecular weight less than 3000), D-amino Glucose ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, among which, Euglena β-1 ,3-glucan 26.5%, compound active alkaloid 29.4%, deep-sea fish peptide 7.2%, small molecule potassium hyaluronate 3.5%, D-glucosamine ketoglutarate 8.6%, glutamine 4.1%, L -Alanine 3.0%, L-Arginine 4.2%, L-Methionine 3.5%, L-Lysine 3.5%, L-Leucine 6.0%, Vitamin C 0.5%.

上述用于治疗痛风的药物组合物制作为散剂(5g/袋),制备方法具体步骤如下:The above-mentioned pharmaceutical composition for the treatment of gout is made into powder (5g/bag), and the specific steps of the preparation method are as follows:

(1)按重量份数称取裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C;(1) Weigh Euglena β-1,3-glucan, compound active alkaloid, deep-sea fish peptide, small molecule potassium hyaluronate (molecular weight less than 3000), D-glucosamine ketoglutarate by weight parts Salt, Glutamine, L-Alanine, L-Arginine, L-Methionine, L-Lysine, L-Leucine and Vitamin C;

(2)将步骤(1)中各组分混合均匀即得。(2) Mix the components in step (1) evenly to obtain.

实施例2Example 2

一种用于治疗痛风的药物组合物,功效成分由裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C组成,其中,裸藻β-1,3-葡聚糖30%、复合活性生物碱15%、深海鱼肽15%、小分子透明质酸钾(分子量小于3000)5%、D-氨基葡萄糖酮戊二酸盐 5%、谷氨酰胺5%、L-丙氨酸5%、L-精氨酸3%、L-蛋氨酸2%、L-赖氨酸3%、L-亮氨酸9%、维生素C 1%。A pharmaceutical composition for treating gout, the functional components are composed of Euglena β-1,3-glucan, complex active alkaloids, deep-sea fish peptides, small molecule potassium hyaluronate (molecular weight less than 3000), D-amino Glucose ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, among which, Euglena β-1 ,30% 3-glucan, 15% compound active alkaloid, 15% deep-sea fish peptide, 5% small molecule potassium hyaluronate (molecular weight less than 3000), 5% D-glucosamine ketoglutarate, glutamate Amide 5%, L-Alanine 5%, L-Arginine 3%, L-Methionine 2%, L-Lysine 3%, L-Leucine 9%, Vitamin C 1%.

制备方法参照实施例1。For the preparation method, refer to Example 1.

实施例3Example 3

一种用于治疗痛风的药物组合物,功效成分由裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C组成,其中,裸藻β-1,3-葡聚糖18%、复合活性生物碱35%、深海鱼肽3%、小分子透明质酸钾(分子量小于3000)2%、D-氨基葡萄糖酮戊二酸盐10%、谷氨酰胺3%、L-丙氨酸2%、L-精氨酸6%、L-蛋氨酸5%、L-赖氨酸6%、L-亮氨酸5%、维生素C 0.2%。A pharmaceutical composition for treating gout, the functional components are composed of Euglena β-1,3-glucan, complex active alkaloids, deep-sea fish peptides, small molecule potassium hyaluronate (molecular weight less than 3000), D-amino Glucose ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, among which, Euglena β-1 ,3-glucan 18%, compound active alkaloid 35%, deep-sea fish peptide 3%, small molecule potassium hyaluronate (molecular weight less than 3000) 2%, D-glucosamine ketoglutarate 10%, glutamate Amide 3%, L-Alanine 2%, L-Arginine 6%, L-Methionine 5%, L-Lysine 6%, L-Leucine 5%, Vitamin C 0.2%.

制备方法参照实施例1。For the preparation method, refer to Example 1.

实施例4Example 4

一种用于治疗痛风的药物组合物,功效成分由裸藻β-1,3-葡聚糖、复合活性生物碱、深海鱼肽、小分子透明质酸钾(分子量小于3000)、D-氨基葡萄糖酮戊二酸盐、谷氨酰胺、L-丙氨酸、L-精氨酸、L-蛋氨酸、L-赖氨酸、L-亮氨酸和维生素C组成,其中,裸藻β-1,3-葡聚糖23%、复合活性生物碱27%、深海鱼肽10%、小分子透明质酸钾(分子量小于3000)4%、D-氨基葡萄糖酮戊二酸盐8%、谷氨酰胺4%、L-丙氨酸3%、L-精氨酸5%、L-蛋氨酸4%、L-赖氨酸4%、L-亮氨酸7%、维生素C 0.6%。A pharmaceutical composition for treating gout, the functional components are composed of Euglena β-1,3-glucan, complex active alkaloids, deep-sea fish peptides, small molecule potassium hyaluronate (molecular weight less than 3000), D-amino Glucose ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, among which, Euglena β-1 ,3-glucan 23%, compound active alkaloid 27%, deep-sea fish peptide 10%, small molecule potassium hyaluronate (molecular weight less than 3000) 4%, D-glucosamine ketoglutarate 8%, glutamate Amide 4%, L-Alanine 3%, L-Arginine 5%, L-Methionine 4%, L-Lysine 4%, L-Leucine 7%, Vitamin C 0.6%.

制备方法参照实施例1。For the preparation method, refer to Example 1.

组方分析:Group analysis:

(1)治标治本,裸藻葡聚糖可降低尿酸、降低胆固醇、增强抵抗力,复合活性生物碱直接中和尿酸,谷氨酰胺、丙氨酸、精氨酸(扩张血管)、VC具有协同护肝养肾的作用;从养肝养肾的根本上治疗通风;(1) Treat the symptoms and cure the root cause. Paraglucan can reduce uric acid, lower cholesterol, and enhance resistance. The complex active alkaloids directly neutralize uric acid. Glutamine, alanine, arginine (blood vessels), and VC have synergistic effects. The function of protecting the liver and nourishing the kidney; Treating ventilation from the root of nourishing the liver and nourishing the kidney;

(2)小分子纳米物质,快速吸收,无毒副作用,没有任何激素,没有依赖性;(2) Small molecule nano-materials, fast absorption, no toxic side effects, no hormones, no dependence;

(3)赖氨酸、丙氨酸具有协同利尿的作用,有利于尿酸的排出,与蛋氨酸协同抑制重症高血压病(一般通风伴有高血压);(3) Lysine and alanine have a synergistic diuretic effect, which is beneficial to the excretion of uric acid, and cooperates with methionine to inhibit severe hypertension (general ventilation is accompanied by hypertension);

(4)小分子透明质酸钾和D-氨基葡萄糖酮戊二酸盐具有协同保护关节、软化关节、软化血管等作用,减少关节疼痛,修复关节;(4) Small molecule potassium hyaluronate and D-glucosamine ketoglutarate can synergistically protect joints, soften joints, soften blood vessels, reduce joint pain and repair joints;

(5)维生素C,消炎止痛,修复肾脏,减少体内尿素含量,促进其它四种成分的吸收。(5) Vitamin C, anti-inflammatory and analgesic, repair the kidneys, reduce the urea content in the body, and promote the absorption of the other four components.

各组分协同作用,治疗痛风效果显著。Each component acts synergistically and has a remarkable effect on the treatment of gout.

实验例1Experimental example 1

应用实施例1所述药物组合物(5g/袋),服用方法为每天4次,每6小时服用一次,每次饮水500-700ML纯净水。服用30天后为一个疗程。试验痛风患者50例,其中中青年30例,青年患者年龄为20-45岁,平均年龄35.5岁,中老年患者为46-76岁,平均年龄为57.2岁。患者均为男性,所有患者均符合痛风的诊断标准。青年患者尿酸水平平均为523±71.2μmol / L,中老年患者尿酸水平平均为 565±62.3μmol / L。临床发作次数青年患者平均3.5±0.6次/年,中老年患者平均3.8±0.4次/年。The pharmaceutical composition (5g/bag) described in Application Example 1 is used, and the method of administration is 4 times a day, once every 6 hours, and drinking 500-700ML of purified water each time. After 30 days of taking, it is a course of treatment. There were 50 gout patients in the trial, including 30 young and middle-aged patients. The young patients were 20-45 years old with an average age of 35.5 years old, and the middle-aged and elderly patients were 46-76 years old with an average age of 57.2 years old. All patients were male, and all patients met the diagnostic criteria for gout. The average uric acid level in young patients was 523±71.2 μmol/L, and the average uric acid level in middle-aged and elderly patients was 565±62.3 μmol/L. The average number of clinical attacks was 3.5±0.6 times/year in young patients and 3.8±0.4 times/year in middle-aged and elderly patients.

本组收治的痛风患者50例患者,主要病变,单一关节炎23例,多关节炎34 例,主要受累关节为第一趾关节46例,踝关节16例,其它趾跖关节11例,膝关节9例。经实施例1药物治疗42例完全缓解, 7例好转,临床有效率达98.0%。50 patients with gout were treated in this group. The main lesions were monoarthritis in 23 cases and polyarthritis in 34 cases. The main involved joints were the first toe joint in 46 cases, ankle joint in 16 cases, other toe-metatarsal joints in 11 cases, and knee joints in 11 cases. 9 cases. After the drug treatment of Example 1, 42 cases were completely relieved, 7 cases were improved, and the clinical effective rate was 98.0%.

实验例2Experimental example 2

选取一组8位患者,患者年龄在43-61岁,全部为男性,进行跟踪测试,8位患者静脉血测得尿酸值均大于550umol/L,服用应用实施例1所述药物组合物(5g/袋)、4次/天,每6小时服用一次,每次饮水500-700ML纯净水。通过观察,在第5天检测尿酸含量下降较快,在30天检测时6位患者恢复正常值,通过60天治疗,全部恢复正常。Select a group of 8 patients, the age of the patients is 43-61 years old, all of them are male, and the follow-up test is carried out. The uric acid values measured in the venous blood of the 8 patients are all greater than 550umol/L. / bag), 4 times / day, take once every 6 hours, drink 500-700ML pure water each time. Through observation, the uric acid content decreased rapidly on the 5th day, and 6 patients returned to normal values on the 30th day, and all returned to normal after 60 days of treatment.

Figure DEST_PATH_IMAGE001
Figure DEST_PATH_IMAGE001

以上所述实施例仅仅是对本发明的优选实施方式进行描述,并非对本发明的范围进行限定,在不脱离本发明设计精神的前提下,本领域普通工程技术人员对本发明的技术方案作出的各种变形和改进,均应落入本发明的权利要求书确定的保护范围内。The above-mentioned embodiments are only to describe the preferred embodiments of the present invention, and do not limit the scope of the present invention. Variations and improvements should fall within the protection scope determined by the claims of the present invention.

Claims (4)

1. A pharmaceutical composition for treating gout, comprising: the functional components comprise beta-1, 3-glucan of euglena, compound active alkaloid, deep sea fish peptide, micromolecule potassium hyaluronate with the molecular weight less than 3000, D-glucosamine ketoglutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C, wherein the euglena beta-1, 3-glucan is 18-30 parts, the compound active alkaloid is 15-35 parts, the deep sea fish peptide is 3-15 parts, the micromolecule potassium hyaluronate is 2-5 parts, the D-glucosamine ketoglutarate is 5-10 parts, the glutamine is 3-5 parts, the L-alanine is 2-5 parts, the L-arginine is 3-6 parts, the L-methionine is 2-5 parts, 3-6 parts of L-lysine, 5-9 parts of L-leucine and 0.2-1 part of vitamin C.
2. The pharmaceutical composition for the treatment of gout according to claim 1, wherein: 26.5 parts of euglena beta-1, 3-glucan, 29.4 parts of compound active alkaloid, 7.2 parts of deep sea fish peptide, 3.5 parts of micromolecular potassium hyaluronate, 8.6 parts of D-glucosamine ketoglutarate, 4.1 parts of glutamine, 3.0 parts of L-alanine, 4.2 parts of L-arginine, 3.5 parts of L-methionine, 3.5 parts of L-lysine, 6.0 parts of L-leucine and 0.5 part of vitamin C.
3. The pharmaceutical composition for the treatment of gout according to claim 1, wherein: the medicine composition is powder, capsule or granule.
4. The process for preparing a pharmaceutical composition for treating gout according to claim 1, wherein: the method comprises the following specific steps:
(1) weighing euglena beta-1, 3-glucan, composite active alkaloid, deep sea fish peptide, micromolecular potassium hyaluronate (the molecular weight is less than 3000), D-aminoglucosone glutarate, glutamine, L-alanine, L-arginine, L-methionine, L-lysine, L-leucine and vitamin C according to the parts by weight;
(2) and (2) uniformly mixing the components in the step (1).
CN202011300901.4A 2020-11-19 2020-11-19 Pharmaceutical composition for treating gout and preparation method thereof Active CN112138138B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011300901.4A CN112138138B (en) 2020-11-19 2020-11-19 Pharmaceutical composition for treating gout and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011300901.4A CN112138138B (en) 2020-11-19 2020-11-19 Pharmaceutical composition for treating gout and preparation method thereof

Publications (2)

Publication Number Publication Date
CN112138138A true CN112138138A (en) 2020-12-29
CN112138138B CN112138138B (en) 2023-05-23

Family

ID=73887447

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011300901.4A Active CN112138138B (en) 2020-11-19 2020-11-19 Pharmaceutical composition for treating gout and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112138138B (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020068718A1 (en) * 2000-10-03 2002-06-06 Pierce Scott W. Chondroprotective/restorative compositions and methods of use thereof
CN103920135A (en) * 2014-04-23 2014-07-16 青岛昆布生物工程有限公司 Kelp-amino composite tablet for lowering content of uric acid and preparation method thereof
CN104621432A (en) * 2013-11-12 2015-05-20 江苏艾兰得营养品有限公司 Glucosamine composite tablets and preparation method thereof
CN104645332A (en) * 2015-03-06 2015-05-27 江苏正大清江制药有限公司 Pharmaceutical composition for relieving and preventing arthritis
CN105709207A (en) * 2016-01-29 2016-06-29 徐宝贞 Medicine for treating gout
WO2017203529A1 (en) * 2016-05-24 2017-11-30 Bol Pharma Ltd. Compositions comprising cannabidiol and hyaluronic acid for treating inflammatory joint diseases
CN107660795A (en) * 2017-09-01 2018-02-06 武汉龙族药号生物医药科技有限公司 One kind prevention gout plaster taste and preparation method thereof
CN110946874A (en) * 2019-12-27 2020-04-03 华熙生物科技股份有限公司 Hyaluronic acid composition for relieving osteoarthritis
CN111513325A (en) * 2020-04-29 2020-08-11 私诺(北京)健康科技有限公司 Food for reducing uric acid
CN111732675A (en) * 2020-08-18 2020-10-02 山东华熙海御生物医药有限公司 Hyaluronic acid-glucosamine graft copolymer, preparation method and application thereof

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020068718A1 (en) * 2000-10-03 2002-06-06 Pierce Scott W. Chondroprotective/restorative compositions and methods of use thereof
CN104621432A (en) * 2013-11-12 2015-05-20 江苏艾兰得营养品有限公司 Glucosamine composite tablets and preparation method thereof
CN103920135A (en) * 2014-04-23 2014-07-16 青岛昆布生物工程有限公司 Kelp-amino composite tablet for lowering content of uric acid and preparation method thereof
CN104645332A (en) * 2015-03-06 2015-05-27 江苏正大清江制药有限公司 Pharmaceutical composition for relieving and preventing arthritis
CN105709207A (en) * 2016-01-29 2016-06-29 徐宝贞 Medicine for treating gout
WO2017203529A1 (en) * 2016-05-24 2017-11-30 Bol Pharma Ltd. Compositions comprising cannabidiol and hyaluronic acid for treating inflammatory joint diseases
CN107660795A (en) * 2017-09-01 2018-02-06 武汉龙族药号生物医药科技有限公司 One kind prevention gout plaster taste and preparation method thereof
CN110946874A (en) * 2019-12-27 2020-04-03 华熙生物科技股份有限公司 Hyaluronic acid composition for relieving osteoarthritis
CN111513325A (en) * 2020-04-29 2020-08-11 私诺(北京)健康科技有限公司 Food for reducing uric acid
CN111732675A (en) * 2020-08-18 2020-10-02 山东华熙海御生物医药有限公司 Hyaluronic acid-glucosamine graft copolymer, preparation method and application thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
李楠等: "《有机化学第2版》", 31 July 2017, 北京:中国农业大学出版社 *

Also Published As

Publication number Publication date
CN112138138B (en) 2023-05-23

Similar Documents

Publication Publication Date Title
RU2491062C2 (en) Compositions of protectors against acute and chronic hepatic encephalopathies and method of treating acute and chronic hepatic encephalopathies
JPH06510760A (en) Metabolic disorders and metabolic treatments
WO2008122190A1 (en) The composition comprising l-carnitine or derivatives thereof and its use
WO2023005265A1 (en) Application of nucleotide mixture in preparation of formulations for preventing or alleviating senile sarcopaenia
CN113413461A (en) Medicine for resisting senile dementia and its preparing method
CN112546052A (en) Composition containing marine oligosaccharide for preventing and treating gout
US20050282772A1 (en) New dietary supplement composition for obesity and inflammation
Kaur et al. A review on pharmacological activities of betaine
US9526793B1 (en) Salts of phenylethylamines and inorganic acids and methods of use thereof
CN112057605A (en) Marine collagen oligopeptide and preparation method thereof
CN112138138B (en) Pharmaceutical composition for treating gout and preparation method thereof
Kim et al. Synergistic antiinflammatory effects of pinitol and glucosamine in rats
CN111939179A (en) Application of cobra venom or extract thereof in preparation of medicine for reducing uric acid and/or resisting gouty arthritis
CN103893226A (en) Application of nutmeg extract
WO2023000263A1 (en) Use of brown algae oligosaccharide
CN108379455B (en) Uric acid reducing composition
CN110917209A (en) Application of selenium-containing compound or selenium nano-grade in preparation of injection or microneedle of arthritis treatment drug
WO2017088177A1 (en) Mussel adhesive protein product, and use thereof in preventing and suppressing neuronal inflammation
CN114832004B (en) Pharmaceutical composition for treating metabolic abnormality and preparation method thereof
JP2020100601A (en) Nitric oxide synthase activator
CN1111064C (en) Hepatitis treating medicine and its production process
US20080095865A1 (en) Composition and method for increasing lean muscle mass, decreasing muscle loss, increasing muscle strength and improving athletic performance
CN1739556A (en) Dietotherapeutic nutrient for preventing and treating secondary gout and its prepn process
EP3981423B1 (en) Composition for preventing or treating uric acid-related disease
CN100551357C (en) Application of Yunzhi mycelium in preparation of anti-fatigue medicine

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant