CN112023019A - Medicine containing active polysaccharide with effect of reducing uric acid and preparation method thereof - Google Patents
Medicine containing active polysaccharide with effect of reducing uric acid and preparation method thereof Download PDFInfo
- Publication number
- CN112023019A CN112023019A CN202010970484.8A CN202010970484A CN112023019A CN 112023019 A CN112023019 A CN 112023019A CN 202010970484 A CN202010970484 A CN 202010970484A CN 112023019 A CN112023019 A CN 112023019A
- Authority
- CN
- China
- Prior art keywords
- parts
- powder
- vitamin
- active polysaccharide
- uric acid
- 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.)
- Pending
Links
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- 229920001282 polysaccharide Polymers 0.000 title claims abstract description 51
- 239000005017 polysaccharide Substances 0.000 title claims abstract description 51
- 239000003814 drug Substances 0.000 title claims abstract description 40
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 title claims abstract description 36
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 title claims abstract description 36
- 229940116269 uric acid Drugs 0.000 title claims abstract description 36
- 230000000694 effects Effects 0.000 title claims abstract description 28
- 230000001603 reducing effect Effects 0.000 title claims abstract description 24
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
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- URQMEZRQHLCJKR-UHFFFAOYSA-N 3-Methyl-5-propyl-2-cyclohexen-1-one Chemical compound CCCC1CC(C)=CC(=O)C1 URQMEZRQHLCJKR-UHFFFAOYSA-N 0.000 claims abstract description 15
- 235000003130 Arctium lappa Nutrition 0.000 claims abstract description 15
- 235000008078 Arctium minus Nutrition 0.000 claims abstract description 15
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- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 claims abstract description 3
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- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 6
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- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 4
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- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 3
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- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 claims description 2
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- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 claims description 2
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- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 2
- 229960001231 choline Drugs 0.000 claims description 2
- FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 claims description 2
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/01—Hydrolysed proteins; Derivatives thereof
- A61K38/012—Hydrolysed proteins; Derivatives thereof from animals
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L19/00—Products from fruits or vegetables; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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Abstract
The invention discloses an active polysaccharide-containing medicament with the effect of reducing uric acid and a preparation method thereof, wherein the active polysaccharide-containing medicament comprises the following components in parts by weight: 8-15 parts of marine fish oligopeptide powder, 5-12 parts of taxus chinensis polysaccharide, 7-15 parts of pawpaw, 6-11 parts of pit viper, 7-13 parts of coix seed, 11-20 parts of celery powder, 11-19 parts of burdock root powder, 1-15 parts of corn stigma powder, 3-16 parts of egg white chlorella powder, 6-19 parts of vitamin, 11-30 parts of edible auxiliary material and 5-15 parts of phellinus igniarius. The active polysaccharide-containing medicament has synergistic effect of the raw materials and obvious effect of reducing uric acid.
Description
Technical Field
The invention relates to the technical field of medicines, in particular to a medicine containing active polysaccharide and having the function of reducing uric acid and a preparation method thereof.
Background
Uric acid is a final product of purine metabolism in a human body, the daily production amount and the excretion amount of uric acid in the human body are approximately equal, but the uric acid content is increased when purine metabolism in the human body is disturbed, and because the solubility of uric acid is low, urinary calculus or gout can be formed when the uric acid is excessive in the human body. Hyperuricemia is a state of the body in which the uric acid concentration in blood is out of the normal range, and it is generally considered that hyperuricemia is considered when the uric acid concentration in blood of a male is more than 400. mu. mol/L and when the uric acid concentration in blood of a female is more than 360. mu. mol/L. Recent studies have shown that hyperuricemia is not only the most important biochemical basis of gout, but also an important factor causing hypertension, hyperlipidemia, atherosclerosis, obesity, insulin resistance, occurrence of cardiovascular diseases of metabolic syndrome and death, and has become one of the major metabolic diseases threatening human health.
The current clinical commonly used medicines comprise nonsteroidal anti-inflammatory drugs, colchicine, glucocorticoid, probenecid, benzydomone and allopurinol, and the treatment effect is obvious, but the medicines have toxic and side effects and adverse reactions of different degrees, damage the liver and the nervous system, cause skin allergy, life-threatening hypersensitivity and the like.
Disclosure of Invention
The invention aims to provide an active polysaccharide-containing medicament with the effect of reducing uric acid and a preparation method thereof aiming at the defects in the prior art.
In order to achieve the purpose, the invention adopts the technical scheme that:
the invention provides an active polysaccharide-containing medicament with the effect of reducing uric acid, which comprises the following components in parts by weight: 8-15 parts of marine fish oligopeptide powder, 5-12 parts of taxus chinensis polysaccharide, 7-15 parts of pawpaw, 6-11 parts of pit viper, 7-13 parts of coix seed, 11-20 parts of celery powder, 11-19 parts of burdock root powder, 1-15 parts of corn stigma powder, 3-16 parts of egg white chlorella powder, 6-19 parts of vitamin, 11-30 parts of edible auxiliary material and 5-15 parts of phellinus igniarius.
Preferably, the active polysaccharide-containing medicament comprises the following components in parts by weight: 10-13 parts of marine fish oligopeptide powder, 7-10 parts of taxus chinensis polysaccharide, 9-14 parts of pawpaw, 8-10 parts of pit viper, 8-11 parts of coix seed, 17-20 parts of celery powder, 16-18 parts of burdock root powder, 13-15 parts of corn stigma powder, 14-16 parts of chlorella pyrenoidosa powder, 10-15 parts of vitamin, 12-29 parts of edible auxiliary materials and 8-12 parts of phellinus igniarius.
Preferably, the vitamin is one or more of vitamin A, vitamin D, vitamin E, vitamin C, vitamin B1, vitamin B2, vitamin B6, vitamin B12, nicotinic acid, folic acid, pantothenic acid, choline and nicotinamide.
Preferably, the edible auxiliary materials are one or more of excipient, stabilizer, flavoring agent and color fixative.
The second aspect of the invention provides a preparation method of the active polysaccharide-containing medicament, which comprises the following steps:
s1, weighing the pawpaw and the pit viper according to the weight parts, adding 12-15 times of water, heating and extracting for several times, filtering, combining the filtrates, and concentrating the filtrate to a clear paste with the relative density of 1.2-1.4 measured at 65-75 ℃; weighing the coix seeds according to the parts by weight, crushing the coix seeds into fine powder, and sieving the fine powder by a sieve of 60-90 meshes;
s2, weighing the marine fish oligopeptide powder, the taxus chinensis polysaccharide, the celery powder, the burdock root powder, the corn stigma powder, the globulina powder, the vitamins, the edible auxiliary materials and the phellinus igniarius according to the parts by weight, adding the clear paste prepared in the step S1 and the coix seed powder, and uniformly mixing to prepare the active polysaccharide-containing pharmaceutical preparation.
Preferably, in S1, the heating is performed for 2-3 times, each for 2-3 hours.
Preferably, in S2, the active polysaccharide-containing pharmaceutical preparation is in the form of a tablet, capsule, powder, pill or granule.
The third aspect of the invention provides the application of the medicine containing active polysaccharide in preparing health products, foods or medicines with the effect of reducing uric acid.
By adopting the technical scheme, compared with the prior art, the invention has the following technical effects:
1. the Chinese yew polysaccharide has excellent effect of reducing uric acid and creatinine thereof, has a protection effect on kidney, and has an obvious uric acid reducing effect in clinical experiments when a medicament prepared by using the Chinese yew polysaccharide as an active ingredient. The ocean fish oligopeptide powder has the functions of reducing uric acid and relieving gout; the muscle exercise time is prolonged, and the muscle exercise intensity is increased; the inflammation phenomenon is reduced; reducing gastric ulcer symptoms and accelerating wound healing; relieving muscle aging weakness symptoms; enhancing the conduction velocity of the neural response; reduce myocardial ischemia and cerebral ischemia injury.
2. The pawpaw in the invention is a dry nearly mature fruit of chaenomeles speciosa belonging to the Rosaceae family, and has the functions of relaxing tendons, activating collaterals, harmonizing stomach and eliminating dampness; has obvious effect on treating symptoms such as damp arthralgia spasm, soreness and heaviness pain of waist and knee joints, spasm pain of rotating muscles, beriberi edema and the like. Agkistrodon Halys is dried whole body of Viperaceae animal with viscera removed, and has effects of dispelling pathogenic wind, relieving pain, removing toxic substance, strengthening body, and promoting lactation; it can be used for treating rheumatalgia, leprosy, lymph node, tuberculosis, skin ulcer, furuncle, asthenia, hyperhidrosis, and milk deficiency. Coicis semen is dried mature seed of Gramineae plant Coicis semen, and has effects of promoting diuresis, eliminating dampness, invigorating spleen, relieving diarrhea, eliminating arthralgia, promoting pus, removing toxic substance and resolving hard mass; can be used for treating edema, loempe, dysuresia, spleen deficiency, diarrhea, damp arthralgia, spasm, pulmonary abscess, intestinal abscess, wart, and cancer.
3. The celery powder, the burdock root powder, the corn stigma powder and the globulina powder are combined to be used as raw materials; wherein the celery powder is cool in nature, sweet and pungent in taste and nontoxic; entering liver, gallbladder and pericardium channel; mainly used for clearing heat, calming liver, relieving restlessness, dispelling wind, promoting diuresis and reducing edema. The bitter and cold burdock root powder is matched to dispel wind-heat and eliminate swelling and toxin; bitter and cold can purge and purge the pathogenic wind and dampness to calm the stomach-qi and purge the heat. The corn stigma powder is sweet and neutral, can induce diuresis and reduce edema, can purge heat and calm liver, and has excellent diuretic effect. The chlorella pyrenoidosa has the functions of clearing away heat and toxic materials, removing acid and descending turbidity, so that the arthralgia syndrome can achieve the effects of tonifying qi, invigorating spleen and promoting diuresis, dispelling wind and dissipating heat, and removing acid and descending turbidity from meridians to viscera. The 4 components have synergistic interaction, the effect of reducing the uric acid is obviously superior to the effect of reducing the uric acid by combining a single raw material or two or three raw materials, the effect of effectively reducing the uric acid is achieved, and no toxic or side effect is caused.
4. The invention adds a plurality of vitamins, and the addition of the vitamins interacts with other components, thereby quickening the dissolution speed of the active ingredients of the medicine and leading the medicine composition to have good performance.
Detailed Description
The present invention is further illustrated by the following examples, which are not to be construed as limiting the invention.
It should be noted that the embodiments and features of the embodiments may be combined with each other without conflict.
Example 1
An active polysaccharide-containing medicament with the effect of reducing uric acid comprises the following components in parts by weight: 8 parts of marine fish oligopeptide powder, 5 parts of taxus chinensis polysaccharide, 7 parts of pawpaw, 6 parts of pit viper, 7 parts of coix seed, 11 parts of celery powder, 11 parts of burdock root powder, 1 part of corn stigma powder, 3 parts of globulina powder, 6 parts of vitamin A, 11 parts of flavoring agent and 5 parts of phellinus igniarius.
The preparation method of the medicine containing active polysaccharide comprises the following steps:
s1, weighing the pawpaw and the pit viper according to the weight parts, adding 12 times of water, heating and extracting for 2 times, each time for 2 hours, filtering, combining the filtrates, and concentrating the filtrate to a clear paste with a relative density of 1.2 measured at 65 ℃; weighing the coix seeds according to the parts by weight, crushing the coix seeds into fine powder, and sieving the fine powder by a 60-mesh sieve;
s2, weighing the marine fish oligopeptide powder, the taxus chinensis polysaccharide, the celery powder, the burdock root powder, the corn stigma powder, the globulina powder, the vitamins, the edible auxiliary materials and the phellinus igniarius according to the parts by weight, adding the clear paste prepared in the step S1 and the coix seed powder, and uniformly mixing to prepare the active polysaccharide-containing medicine tablet.
Example 2
An active polysaccharide-containing medicament with the effect of reducing uric acid comprises the following components in parts by weight: 11 parts of marine fish oligopeptide powder, 8 parts of taxus chinensis polysaccharide, 12 parts of pawpaw, 9 parts of pit viper, 12 parts of coix seed, 18 parts of celery powder, 16 parts of burdock root powder, 7 parts of corn stigma powder, 10 parts of globulina powder, 111 parts of vitamin B, 25 parts of excipient and 9 parts of phellinus igniarius.
The preparation method of the medicine containing active polysaccharide comprises the following steps:
s1, weighing the pawpaw and the pit viper according to the weight parts, adding 13 times of water, heating and extracting for 3 times, each time for 2.5 hours, filtering, combining the filtrates, and concentrating the filtrate to a clear paste with a relative density of 1.3 measured at 70 ℃; weighing the coix seeds according to the parts by weight, crushing the coix seeds into fine powder, and sieving the fine powder by a sieve of 80 meshes;
s2, weighing the marine fish oligopeptide powder, the taxus chinensis polysaccharide, the celery powder, the burdock root powder, the corn stigma powder, the globulina powder, the vitamins, the edible auxiliary materials and the phellinus igniarius according to the parts by weight, adding the clear paste prepared in the step S1 and the coix seed powder, and uniformly mixing to prepare the active polysaccharide-containing medicine capsule.
Example 3
An active polysaccharide-containing medicament with the effect of reducing uric acid comprises the following components in parts by weight: 15 parts of marine fish oligopeptide powder, 12 parts of taxus chinensis polysaccharide, 15 parts of pawpaw, 11 parts of pit viper, 13 parts of coix seed, 20 parts of celery powder, 19 parts of burdock root powder, 15 parts of corn stigma powder, 16 parts of globulina powder, 19 parts of nicotinic acid, 30 parts of stabilizer and 15 parts of phellinus igniarius.
The preparation method of the medicine containing active polysaccharide comprises the following steps:
s1, weighing the pawpaw and the pit viper according to the weight parts, adding 15 times of water, heating and extracting for 3 times, each time for 3 hours, filtering, combining the filtrates, and concentrating the filtrate to a clear paste with a relative density of 1.4 measured at 75 ℃; weighing the coix seeds according to the parts by weight, crushing the coix seeds into fine powder, and sieving the fine powder by a sieve of 90 meshes;
s2, weighing the marine fish oligopeptide powder, the taxus chinensis polysaccharide, the celery powder, the burdock root powder, the corn stigma powder, the globulina powder, the vitamins, the edible auxiliary materials and the phellinus igniarius according to the parts by weight, adding the clear paste prepared in the step S1 and the coix seed powder, and uniformly mixing to prepare the active polysaccharide-containing medicinal granule.
Application example
Patient data: 150 patients, 100 males of which were aged between 35-75 years; 50 women, with the age distribution of 35-75 years.
Diagnostic criteria: the patient has arthralgia, attacks at night and is difficult to fall asleep; elevated blood uric acid levels, above 6.0mg/dL for men and 5.0mg/dL for women; has a tophus.
The taking method comprises the following steps: the preparation containing active polysaccharide is administered 3 times a day, 2 tablets or 2 tablets each time, one time in the morning, one time in the evening, and 7 weeks continuously.
Efficacy evaluation criteria: and (3) curing: the laboratory checks that the blood uric acid value is normal, the arthralgia symptom disappears, and the tophus is removed; improvement: the reduction of blood uric acid value, the resolution of joint swelling and pain and the obvious reduction of tophus are detected in a laboratory; and (4) invalidation: the blood uric acid value and symptoms are unchanged in laboratory examination, and the tophus is unchanged. The test results are shown in table 1:
TABLE 1
The data in table 1 show that the active polysaccharide-containing medicament provided by the invention is prepared by reasonably proportioning and scientifically matching the raw materials, the components play a synergistic effect, and edible auxiliary materials are reasonably matched, so that the active polysaccharide-containing medicament can be prepared into health care products, foods or medicaments such as tablets, capsules, powder, pills or granules with an obvious effect of reducing uric acid and no side effect, and the effective rate of reducing uric acid can reach more than 97.3% after a patient takes the active polysaccharide-containing medicament for 7 weeks.
While the invention has been described with reference to a preferred embodiment, it will be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention.
Claims (8)
1. The active polysaccharide-containing medicine with the effect of reducing the uric acid is characterized by comprising the following components in parts by weight: 8-15 parts of marine fish oligopeptide powder, 5-12 parts of taxus chinensis polysaccharide, 7-15 parts of pawpaw, 6-11 parts of pit viper, 7-13 parts of coix seed, 11-20 parts of celery powder, 11-19 parts of burdock root powder, 1-15 parts of corn stigma powder, 3-16 parts of egg white chlorella powder, 6-19 parts of vitamin, 11-30 parts of edible auxiliary material and 5-15 parts of phellinus igniarius.
2. The active polysaccharide containing drug with the effect of reducing uric acid according to claim 1, wherein the active polysaccharide containing drug comprises the following components in parts by weight: 10-13 parts of marine fish oligopeptide powder, 7-10 parts of taxus chinensis polysaccharide, 9-14 parts of pawpaw, 8-10 parts of pit viper, 8-11 parts of coix seed, 17-20 parts of celery powder, 16-18 parts of burdock root powder, 13-15 parts of corn stigma powder, 14-16 parts of chlorella pyrenoidosa powder, 10-15 parts of vitamin, 12-29 parts of edible auxiliary materials and 8-12 parts of phellinus igniarius.
3. The active polysaccharide medicine containing high uric acid lowering effect as claimed in claim 1, wherein the vitamin is one or more of vitamin A, vitamin D, vitamin E, vitamin C, vitamin B1, vitamin B2, vitamin B6, vitamin B12, nicotinic acid, folic acid, pantothenic acid, choline and nicotinamide.
4. The active polysaccharide-containing medicine with the effect of reducing uric acid according to claim 1, wherein the edible auxiliary materials are one or more of an excipient, a stabilizer, a flavoring agent and a color fixative.
5. The process for the preparation of a medicament containing an active polysaccharide according to any one of claims 1 to 4, comprising the steps of:
s1, weighing the pawpaw and the pit viper according to the weight parts, adding 12-15 times of water, heating and extracting for several times, filtering, combining the filtrates, and concentrating the filtrate to a clear paste with the relative density of 1.2-1.4 measured at 65-75 ℃; weighing the coix seeds according to the parts by weight, crushing the coix seeds into fine powder, and sieving the fine powder by a sieve of 60-90 meshes;
s2, weighing the marine fish oligopeptide powder, the taxus chinensis polysaccharide, the celery powder, the burdock root powder, the corn stigma powder, the globulina powder, the vitamins, the edible auxiliary materials and the phellinus igniarius according to the parts by weight, adding the clear paste prepared in the step S1 and the coix seed powder, and uniformly mixing to prepare the active polysaccharide-containing pharmaceutical preparation.
6. The process of claim 5, wherein the extraction under heating in S1 is performed 2-3 times for 2-3 hours each time.
7. The method for preparing a drug containing active polysaccharide according to claim 1, wherein in S2, the formulation of the drug containing active polysaccharide is tablet, capsule, powder, pill or granule.
8. Use of the active polysaccharide containing drug according to any one of claims 1-4 for the preparation of a uric acid lowering health product, food or medicament.
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CN114010755A (en) * | 2021-12-15 | 2022-02-08 | 本元大健康科技产业(广东)有限公司 | Preparation for controlling uric acid and preparation method thereof |
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