CN117018125A - Anti-fatigue pharmaceutical composition - Google Patents
Anti-fatigue pharmaceutical composition Download PDFInfo
- Publication number
- CN117018125A CN117018125A CN202311296744.8A CN202311296744A CN117018125A CN 117018125 A CN117018125 A CN 117018125A CN 202311296744 A CN202311296744 A CN 202311296744A CN 117018125 A CN117018125 A CN 117018125A
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- pharmaceutical composition
- fatigue
- northeast
- alpine
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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
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/896—Liliaceae (Lily family), e.g. daylily, plantain lily, Hyacinth or narcissus
- A61K36/8962—Allium, e.g. garden onion, leek, garlic or chives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/06—Fungi, e.g. yeasts
- A61K36/07—Basidiomycota, e.g. Cryptococcus
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K36/18—Magnoliophyta (angiosperms)
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- A61K36/73—Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
- A61K36/738—Rosa (rose)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/331—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation, decoction
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K2236/30—Extraction of the material
- A61K2236/39—Complex extraction schemes, e.g. fractionation or repeated extraction steps
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- A61K2236/50—Methods involving additional extraction steps
- A61K2236/53—Liquid-solid separation, e.g. centrifugation, sedimentation or crystallization
Abstract
The invention discloses a pharmaceutical composition for resisting fatigue, and relates to the technical field of traditional Chinese medicine compositions. The medicinal composition provided by the invention comprises the Changbai mountain shallot, northeast radix sileris, corn silk, polyporus, roxburgh rose and wild jujube seed, and has obvious anti-fatigue effect through reasonable compatibility, namely scientific proportion, natural and safe components and no toxic or side effect.
Description
Technical Field
The invention relates to the technical field of traditional Chinese medicine compositions, in particular to a medicine composition for resisting fatigue.
Background
Fatigue is a protective physiological phenomenon of organism for avoiding tissue damage caused by excessive movement and excessive fatigue, and the fatigue is often accompanied with extremely tired feeling, which reduces physiological performance of organism and causes physical and mental discomfort, so that people feel tired, weak and seriously influence metabolic efficiency, immunity and resistance of various organs of human body. Fatigue is an inevitable problem in daily life and work, however, excessive fatigue can have a series of negative effects on health, and therefore, reduction and prevention of fatigue are the research directions of interest.
At present, the body fatigue can be relieved by means of resting, nutrition supplementing, drug treatment and the like, and certain foods, health products, traditional Chinese medicine compositions and the like have certain anti-fatigue effects, and most of the anti-fatigue effects can relieve the body fatigue by promoting the metabolism and the immune function of a human body.
For example, chinese patent application CN200910312277.7 provides a pharmaceutical composition for anti-fatigue, which is prepared from the following raw materials in parts by weight: 5-15 parts of ginseng, 10-15 parts of curcuma zedoary, 5-15 parts of medlar, 5-15 parts of astragalus, 1-10 parts of polygonum multiflorum and 5-15 parts of ligusticum wallichii. Pharmacological experiments prove that the oral and external pharmaceutical composition has the anti-fatigue effect. Meanwhile, the pharmaceutical composition is prepared into an external preparation, and is applied to clinic in combination with massage, so that the fatigue syndrome caused by excessive mental labor, physical labor or long-term stress of the spirit can be improved, and the curative effects of symptoms such as insufficient energy, fatigue and sleepiness, listlessness, distraction, chest distress, palpitation, insomnia, amnesia and the like are remarkable.
For another example, chinese patent application CN201811318159.2 provides an anti-fatigue pharmaceutical composition, and a preparation method and use thereof, wherein the pharmaceutical composition comprises homoplantaginide and other anti-fatigue active ingredients, and preferably the other anti-fatigue active ingredients are selected from: rhodiola rosea glycoside, taurine, ginsenoside or gynostemma pentaphylla saponin. The pharmaceutical composition can obviously relieve the fatigue state of the body, can be widely applied to the prevention and treatment of sports fatigue, fatigue caused by sub-health, chronic fatigue and the like, and is safe without any toxic or side effect.
The herba Alii Fistulosi (Allium victorialis L.) is plant of Allium of Liliaceae, and is mainly distributed in natural protection region of Changbai mountain, and contains sulfur-containing compound, flavonoid compound, steroid, etc., and has hemostatic, analgesic, and fatigue relieving effects. Radix Ledebouriellae (Heracleum moellendorffii Hance) is an Umbelliferae plant, and its active ingredient angelicin has good artery dilating, i.e. blood circulation promoting, effects of dispelling pathogenic wind, eliminating dampness, detumescence, and relieving pain. Although the two raw materials have certain anti-fatigue effect, the anti-fatigue effect is not obvious in practical application, and the prior art does not optimize the composition containing the two components so as to obtain the anti-fatigue traditional Chinese medicine composition, so that the medicinal value of the composition cannot be fully utilized.
In view of the above, the invention has the advantages that the pharmacological actions of the chives and the radix sileris are fully exerted by screening the reasonable compatibility of the traditional Chinese medicine components, and the medicine composition with obvious anti-fatigue effect is obtained for people with easy fatigue.
Disclosure of Invention
The invention aims to provide a pharmaceutical composition with an anti-fatigue effect, which aims at people easy to fatigue, improves the anti-fatigue effect, and has natural and safe components and no toxic or side effect.
In order to achieve the above object, the present invention has the following technical scheme:
in one aspect, the invention provides an anti-fatigue pharmaceutical composition comprising a Changbai mountain shallot, northeast radix sileris, corn silk, polyporus, rosa roxburghii and semen Ziziphi Spinosae.
Preferably, the anti-fatigue pharmaceutical composition comprises, by weight, 10-20 parts of Changbai mountain shallot, 10-20 parts of northeast radix sileris, 1-5 parts of corn silk, 1-5 parts of Polyporus, 1-5 parts of Rosa roxburghii and 0.1-3 parts of wild jujube seed.
Further preferably, the anti-fatigue pharmaceutical composition comprises, by weight, 12-18 parts of Changbai mountain shallot, 12-18 parts of northeast radix sileris, 1-3 parts of corn silk, 2-4 parts of Polyporus, 3-5 parts of Rosa roxburghii and 0.5-2 parts of wild jujube seed.
Most preferably, the anti-fatigue pharmaceutical composition comprises, by weight, 16 parts of Changbai mountain shallot, 16 parts of northeast radix sileris, 2 parts of corn silk, 3 parts of Polyporus, 4 parts of Rosa roxburghii and 1 part of semen Ziziphi Spinosae.
Preferably, in the anti-fatigue pharmaceutical composition, the mass ratio of the Changbai mountain shallot to the northeast radix sileris is 1:0.5-2.
Further preferably, in the anti-fatigue pharmaceutical composition, the mass ratio of the alpine onion to the northeast radix sileris is 1:1.
In another aspect, the present invention provides a method for preparing the above pharmaceutical composition for anti-fatigue, comprising the steps of:
decocting herba Alii Fistulosi, radix Saposhnikoviae, stigma Maydis, polyporus, fructus Rosae Normalis and semen Ziziphi Spinosae in water, mixing decoctions, concentrating, and drying to obtain antifatigue pharmaceutical composition.
Wherein the water includes, but is not limited to, purified water, potable water, ultrapure water, distilled water.
Preferably, the number of times of the decoction is 2 to 4 times, more preferably 3 times.
Preferably, the time of the decoction is 0.5-2h, more preferably 1h.
The concentration method comprises, but is not limited to, reduced pressure distillation, centrifugation and other common concentration methods in the field.
Such drying means include, but are not limited to, drying means common in the art such as baking, spray drying, lyophilization, and the like.
In still another aspect, the invention provides a medicament, wherein the active ingredients of the medicament are the traditional Chinese medicine composition.
The medicine can be prepared into administration dosage forms such as pills, capsules, granules, oral liquid, powder, tablets, troches, lozenges and the like, and the proper medicine carriers in the field can be selected according to different dosage forms.
The pharmaceutical carrier used may be solid, liquid or gaseous. Examples of solid carriers include lactose, kaolin, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate and stearic acid. Examples of liquid carriers include syrup, peanut oil, olive oil, and water. Examples of the gas carrier include carbon dioxide and nitrogen.
In preparing the composition in oral dosage form, any convenient pharmaceutical medium may be used. For example, water, ethanol, oil, alcohols, flavoring agents, preservatives, coloring agents, and the like may be used to form oral liquid formulations, such as suspensions; and carriers such as starches, sugars, microcrystalline cellulose, diluents, granulating agents, emulsifying agents, lubricants, binders, disintegrating agents can be employed to form oral solid preparations such as powders, capsules and tablets.
Tablets containing the present invention may be prepared by compression or molding, optionally with the use of one or more auxiliary ingredients or adjuvants. Tableting may be prepared by tableting the active ingredient in free-flowing form (e.g. powder or granules) in a suitable machine, optionally in admixture with a binder, lubricant, inert diluent, surface active or dispersing agent. Molded tablets may be molded in a suitable machine, i.e. a mixture of the powdered compound moistened with an inert liquid diluent. Each tablet preferably contains from about 0.05mg to about 5g of active ingredient, and each pouch or capsule preferably contains from about 0.05mg to about 5g of active ingredient. For example, a formulation intended for oral administration to humans may contain about 0.5mg to about 5g of the active agent, mixed with an appropriate and convenient carrier material, which may constitute about 5% to 95% of the total composition. The unit dosage form will typically contain from about 1mg to about 2g of the active ingredient, typically 25mg, 50mg, 100mg, 200mg, 300mg, 400mg, 500mg, 600mg, 800mg or 1000mg.
Pharmaceutical compositions of the invention suitable for parenteral administration may be prepared as aqueous solutions or suspensions of the active compounds. Suitable surfactants may be included, such as hydroxypropyl cellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and oil mixtures thereof. In addition, preservatives may also be added to prevent detrimental growth of microorganisms.
The medicament of the invention may be in a form suitable for rectal administration wherein the carrier is a solid. The mixture is preferably formulated as a unit-dose suppository. Suitable carriers include cocoa butter and other materials commonly used in the art. Suppositories may be formed by first forming a mixture of the composition containing the softened or melted carrier, followed by cooling and shaping in a mold. In addition to the carrier ingredients, the pharmaceutical formulations may include one or more additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surfactants, thickeners, lubricants, preservatives (including antioxidants), and the like. In addition, other adjuvants such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, etc., colorants, flavoring agents, etc., can be added.
The beneficial effects of the invention are as follows:
(1) By selecting reasonable compatibility of traditional Chinese medicines, the anti-fatigue effect can be exerted more remarkably, and the compatibility effect of one or less components is better.
(2) The anti-fatigue effect is further improved through reasonable weight proportion.
(3) Animal experiments prove that the pharmaceutical composition provided by the invention can prolong the time of swimming in the absence of blood, improve the blood sugar and liver glycogen level of mice after swimming, reduce the generation of blood lactic acid and blood urea nitrogen, and has remarkable anti-fatigue effect.
(4) The formula of the invention is prepared by decocting natural traditional Chinese medicine components in water, is safe to use, has no toxic or side effect, and is applicable to a wider range of people.
Detailed Description
In order to make the technical means, the creation features, the achievement of the purpose and the effect of the present invention easy to understand, the present invention will be further elucidated with reference to the specific embodiments, but the following embodiments are only preferred embodiments of the present invention, not all of them. Based on the examples in the embodiments, those skilled in the art can obtain other examples without making any inventive effort, which fall within the scope of the invention.
In the following examples, unless otherwise specified, the methods of operation used were conventional, the equipment used was conventional, and the materials used in the examples were the same.
Example 1
A pharmaceutical composition for resisting fatigue comprises, by weight, 10 parts of Changbai mountain shallot, 20 parts of northeast radix sileris, 1 part of corn silk, 5 parts of Polyporus, 1 part of Rosa roxburghii and 3 parts of semen Ziziphi Spinosae.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decocting for 2 times, each time for 2 hours, combining the decoctions, centrifuging, concentrating, freeze-drying and drying to obtain the anti-fatigue pharmaceutical composition A1.
Example 2
A pharmaceutical composition for resisting fatigue comprises 12 parts of Changbai mountain cold shallot, 18 parts of northeast radix sileris, 1 part of corn silk, 4 parts of Polyporus, 3 parts of roxburgh rose and 2 parts of wild jujube seed according to parts by weight.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decoction for 3 times, each time for 1 hour, combining the decoction, centrifuging, concentrating and spray drying to obtain the anti-fatigue pharmaceutical composition A2.
Example 3
A pharmaceutical composition for resisting fatigue comprises, by weight, 16 parts of Changbai mountain shallot, 16 parts of northeast radix sileris, 2 parts of corn silk, 3 parts of Polyporus, 4 parts of Rosa roxburghii and 1 part of semen Ziziphi Spinosae.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decoction for 3 times, each time for 1 hour, combining the decoction, centrifuging, concentrating and spray drying to obtain the anti-fatigue pharmaceutical composition A3.
Example 4
A pharmaceutical composition for resisting fatigue comprises, by weight, 18 parts of Changbai mountain herba Alii Fistulosi, 12 parts of radix Ledebouriellae, 3 parts of stigma Maydis, 2 parts of Polyporus, 5 parts of fructus Rosae Normalis and 0.5 part of semen Ziziphi Spinosae.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decoction for 3 times, each time for 1 hour, combining the decoction, centrifuging, concentrating and spray drying to obtain the anti-fatigue pharmaceutical composition A4.
Example 5
A pharmaceutical composition for resisting fatigue comprises, by weight, 20 parts of Changbai mountain herba Alii Fistulosi, 10 parts of radix Ledebouriellae, 5 parts of stigma Maydis, 1 part of Polyporus, 5 parts of fructus Rosae Normalis and 0.1 part of semen Ziziphi Spinosae.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decocting for 4 times, each time for 0.5h, combining the decoctions, distilling under reduced pressure, and drying to obtain the anti-fatigue pharmaceutical composition A5.
Comparative example 1
A pharmaceutical composition for resisting fatigue comprises 8 parts of herba Alii Fistulosi in Changbai mountain, 22 parts of radix Ledebouriellae in northeast China, 0.5 part of stigma Maydis, 5.5 parts of Polyporus, 0.5 part of fructus Rosae Normalis and 3.5 parts of semen Ziziphi Spinosae in parts by weight.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decoction for 3 times, each time for 1 hour, combining the decoction, centrifuging, concentrating and spray drying to obtain the anti-fatigue pharmaceutical composition B1.
Comparative example 2
A pharmaceutical composition for resisting fatigue comprises 22 parts by weight of Changbai mountain shallot, 8 parts by weight of northeast radix sileris, 5.5 parts by weight of corn silk, 0.5 part by weight of Polyporus, 5.5 parts by weight of Rosa roxburghii and 0.05 part by weight of wild jujube seed.
The preparation method of the anti-fatigue pharmaceutical composition comprises the following steps:
taking the formula amount of the Changbai mountain shallot, the northeast cow divaricate saposhnikovia root, the corn silk, the grifola, the roxburgh rose and the wild jujube, adding purified water for decoction for 3 times, each time for 1 hour, combining the decoction, centrifuging, concentrating and spray drying to obtain the anti-fatigue pharmaceutical composition B2.
Comparative example 3
A pharmaceutical composition for anti-fatigue was different from example 3 in that it did not contain Changbaishan chives, and pharmaceutical composition B3 was prepared.
Comparative example 4
A pharmaceutical composition for anti-fatigue was different from example 3 in that it did not contain Ledebouriella sessilifolia, and pharmaceutical composition B4 was prepared.
Comparative example 5
A pharmaceutical composition for resisting fatigue is different from example 3 in that the mass ratio of the Changbai mountain shallot to the northeast radix sileris is 1:0.4, and the total mass of the Changbai mountain shallot and the northeast radix sileris is the same as that of example 3, so as to prepare a pharmaceutical composition B5.
Comparative example 6
A pharmaceutical composition for resisting fatigue is different from example 3 in that the mass ratio of the Changbai mountain shallot to the northeast radix sileris is 1:2.5, and the total mass of the Changbai mountain shallot and the northeast radix sileris is the same as that of example 3, so as to prepare a pharmaceutical composition B6.
Anti-fatigue animal experiment
1. Experimental drugs: the pharmaceutical compositions A1-A5 and B1-B6 obtained by the invention.
2. Experimental animals: SPF-grade Kunming male mice, weighing 18-22g.
3. Experimental method
3.1 pretreatment of animals: the mice were randomly divided into a normal control group, a swimming control group and a pharmaceutical composition group (low dose 1250mg/kg, medium dose 2500mg/kg, high dose 5000 mg/kg), 10 mice per group; the pharmaceutical composition group was filled with the pharmaceutical composition of the present invention 1 time per day for 2 weeks, and the normal control group and the swimming control group were filled with the same amount of distilled water.
3.2 swimming experiments:
before formal swimming, the mice were trained 5 times for swimming, and then subjected to an exhaustive swimming and 90min swimming experiment.
Exhaustive swimming: after one gastric lavage for 30min, the swimming control group and the pharmaceutical composition group are placed in a swimming device at 30 ℃ to begin to bear a load for 3%, and the time of swimming with exhaustion (the time when the mice are immersed in water for 30 s) is recorded.
Swimming for 90 min: the swimming control group and the pharmaceutical composition group are arranged in a swimming device at 30 ℃ for swimming for 90min after the last gastric lavage, and the normal control group does not swim; after swimming, immediately picking up the eyeballs of the mice to collect blood, centrifuging to collect serum, and measuring the blood sugar content, the lactic acid content, the blood urea nitrogen content and the liver glycogen content.
3.3 experimental results
Experimental data was analyzed by data analysis of variance using SPSS software and the results are shown in tables 1-2 below.
TABLE 1 time of exhaustive swimming
Note that: in comparison with the swimming control group,<0.05,/><0.01。
the results in table 1 show that the time to exhaustive swimming is significantly prolonged after the mice are given the pharmaceutical composition of the invention. Compared with the swimming control group, the low dose group has obvious difference (P is less than 0.05) of the time of the exhaustive swimming, and compared with the swimming control group, the medium dose group and the high dose group have obvious difference (P is less than 0.01) of the time of the exclusive swimming, which indicates that the pharmaceutical composition provided by the invention has obvious refreshing and anti-fatigue effects.
TABLE 2 blood sugar, blood lactic acid, blood urea nitrogen and liver glycogen content in mice
Note that: in comparison with the normal control group,<0.05,/>< 0.01; compared with swimming control group-><0.05,/><0.01。
The results in table 2 show that the pharmaceutical composition of the present invention has a significant effect on blood glucose, blood lactic acid, blood urea nitrogen and liver glycogen content after swimming in mice. Compared with the normal control group, the blood sugar and liver glycogen content of the mice in the swimming control group are reduced, the blood lactic acid and blood urea nitrogen content are increased, and the difference is very remarkable. Compared with the swimming control group, the blood sugar and liver sugar content of the drug composition mice are increased, the blood lactic acid and blood urea nitrogen content are reduced, and particularly, the differences of the drug compositions A1-A5 compared with the swimming control group are obvious. The pharmaceutical composition provided by the invention can improve the blood sugar and liver glycogen level of mice after swimming, reduce the generation of blood lactic acid and blood urea nitrogen, and has remarkable anti-fatigue effect. The contents of blood sugar, blood lactic acid, blood urea nitrogen and liver sugar of the mice after swimming of the pharmaceutical compositions B1-B5 are different from those of the pharmaceutical compositions A1-A5 to a certain extent, so that the invention can exert more remarkable anti-fatigue effect by selecting reasonable compatibility and scientific proportion of traditional Chinese medicines, and is superior to the compatibility effect of one or less components.
The foregoing description of the preferred embodiments of the invention is not intended to be limiting, but rather is intended to cover all modifications, equivalents, alternatives, and improvements that fall within the spirit and scope of the invention.
Claims (9)
1. A pharmaceutical composition for resisting fatigue is characterized by comprising herba Alii Fistulosi in Changbai mountain, radix Saposhnikoviae in northeast China, stigma Maydis, polyporus, fructus Rosae Normalis and semen Ziziphi Spinosae.
2. The pharmaceutical composition for anti-fatigue according to claim 1, wherein the pharmaceutical composition comprises, by weight, 10-20 parts of alpine onion, 10-20 parts of radix sileris, 1-5 parts of corn silk, 1-5 parts of grifola, 1-5 parts of rosa roxburghii and 0.1-3 parts of spina date seed.
3. The pharmaceutical composition for anti-fatigue according to claim 2, which comprises, by weight, 12-18 parts of alpine onion, 12-18 parts of northeast radix sileris, 1-3 parts of corn silk, 2-4 parts of grifola, 3-5 parts of rosa roxburghii and 0.5-2 parts of wild jujube seed.
4. The pharmaceutical composition for anti-fatigue according to claim 3, which comprises 16 parts of alpine onion, 16 parts of northeast radix sileris, 2 parts of corn silk, 3 parts of grifola, 4 parts of rosa roxburghii and 1 part of wild jujube seed according to parts by weight.
5. The pharmaceutical composition for anti-fatigue according to any one of claims 1 to 4, wherein the mass ratio of the alpine onion to the northeast radix sileris is 1:0.5-2.
6. The pharmaceutical composition for anti-fatigue according to claim 5, wherein the mass ratio of the alpine onion to the northeast radix sileris is 1:1.
7. A method for preparing the pharmaceutical composition for anti-fatigue according to any one of claims 1 to 6, comprising the steps of:
decocting herba Alii Fistulosi, radix Saposhnikoviae, stigma Maydis, polyporus, fructus Rosae Normalis and semen Ziziphi Spinosae in water, mixing decoctions, concentrating, and drying to obtain antifatigue pharmaceutical composition.
8. The preparation method according to claim 7, wherein the number of times of decoction is 2 to 4.
9. The method according to claim 7, wherein the time of the decoction is 0.5 to 2 hours.
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