CN101953857A - Compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder) composite medicine - Google Patents
Compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder) composite medicine Download PDFInfo
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Abstract
The invention discloses weight ratio of material components of a compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) A composite medicine and, weight ratio of material components of a compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) B composite medicine, weight ratio of material components of a compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) C composite medicine, a preparation method and steps of the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) A composite medicine, a preparation method and steps of the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) B composite medicine, a preparation method and steps of the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) C composite medicine, as well as the application of the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) A composite medicine, the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) B composite medicine and the compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder ) C composite medicine for anti-aging, antifatigue, anti-hypoxia, immunity enhanced, sedative, antishock and anti irradiation.
Description
Technical field
Technical characterictic of the present invention is compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) composition of medicine prescription, preparation method, purposes.
Background technology
Current war in the world, natural disaster, survival and development pressure make people's physical and mental health enjoy challenge.This challenge endangers the human body psychosoma not second to traditional disease, must open up this emerging medical treatment field.China is a country that natural disaster takes place frequently, and earthquake, great drought, flood, freezing, typhoon, mud-rock flow belong in the world that the condition of a disaster takes place frequently and one of serious country; In the national economic development process, international financial crisis, trade dispute are frequent, even the prestige of war association; Peaceful development also has major disease not radical cure and disease transmission, the aging of population challenge period, especially will improve veteran revolutionaries, veteran cadre, old expert, all old man's life cycle, quality of life.In order to tackle the challenge of all these natural and man-made calamities, if invention has the medicine that improves China the army and the people body immunity, enhancing resisting fatigue energy, excites defying age vitality, the calm psychology of adjusting, make China the army and the people more effectively tackle above-mentioned human survival and development significant challenge, improve national power, have strategic economic benefit and social benefit.
Cordyceps is called for short Cordyceps, is the human over the past thousands of years famous and precious natural drug that is handed down, ill curing the disease, and no treating diseases and making health-care, and also suitable all people take, and do not have insulting side effect and untoward reaction.But its resource-constrained, Jiangxi Traditional Chinese Medicine Factory utilizes a large amount of suitability for industrialized production of natural living Chinese caterpillar bacterium artificial fermentation, for production famous medicine fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is supplied raw materials, this product content is a peacilomyce hepiahi Cs-4 mycopowder, perhaps be called fermented Cordyceps powder again, be commonly called as the Cordyceps powder, Cordyceps powder, Cordyceps extract, ferment cordyceps sinensis powder etc.The peacilomyce hepiahi bacterium powder is separating obtained Cordyceps from fresh Cordyceps fungus (cordyceps sinensis (Berk) sacc)---peacilomyce hepiahi (Paecilomyces hepiali Chen ﹠amp; Dai) product of making through liquid submerged fermentation cultivation, filtration, drying, pulverizing, the Cordyceps powder that the present invention comes out this fermenting and producing is defined as fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder), has another name called Cordyceps powder.Cordyceps is the traditional famous and precious medicated nourishing product of China, and the flat sweet in the mouth of its property has the function that tonifying the lung kidney, cough-relieving are coughed, benefit is deficient, support vital essence.According to clinical research, Cordyceps has ten big functions: 1. antibiotic, and 2. immunomodulating, 3. anticancer, 4. antiinflammatory, 6. 5. nourishing kidney improves adrenal cortex alcohol content, 7. arrhythmia, 8. resisting fatigue, 9. eliminating phlegm and relieving asthma, 10. tranquilizing soporific.Utilizing the big industrial fermentation of modern biological project to produce fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is that the historical contribution and the historical productivity are progressive, but the reach a small amount of heavy metal ion and high price iron ion and assorted bacterium that are mingled with in the production process just make excellent drug also have blemish in an otherwise perfect thing, and slight stomach upset sense is arranged after minute quantity people takes.Remove the above-mentioned slight side effect and the slight untoward reaction of the fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of artificial fermentation production, adding increases its physiological function, can produce new compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) preparation.
Alprostadil, the former name prostaglandin E
1, it is historical less than research in 30 years to become drug use, separates from the human seminal fluid the earliest, so be called prostaglandin E
1, in fact it is present in human body and all histiocytes of mammal and the body fluid, for fear of with correct to misread, country changes its Alprostadil by name, it also is the material of the natural extensive physiological function character of tool.Its discovery has caused a sensation the world, and nineteen eighty-two has three scientists to obtain Nobel Prize simultaneously.Its physiological function has almost contained human all great physiological functions.The application of prostaglandin has been deep into the every field (Li En, prostaglandin and modern medicine, the 1st edition, Beijing: People's Health Publisher, 1985, synopsis) of medical science, that is to say that it relates to each sick treatment and prevention of planting.Its ultimate principle is: the edible oil that we eat every day, under the serial enzymes effect, generate gamma-Linolenic acid earlier in vivo, and generate dihomo-gamma-linolenic acid then, generate Alprostadil at last.When human body physiological function needed, it produced in various histiocytes of human body and body fluid immediately, regulated the various physiological functions of human body, and circulated in organ major parts such as lung, liver, kidney through blood and be inactivated and excrete.The inventor passes through nearly 30 years research theories and facts have proved, especially modern medical theory and facts have proved: lack edible oil at human body, or it is worn with age, the endocrine disturbance, chemical substance is polluted, rule of life is upset, tired anxiety or the like lose in the body must enzymatic activity or the interior Alprostadil that must enzyme quantity all has influence on inadequately of body secrete in vivo and make human body produce all diseases, if replenish a certain amount of Alprostadil in body, ill people can reach a cure, there is not the people of disease can anti-disease, defying age, resisting fatigue, anxiety, anti-insomnia, keep persistent strong, full of vitality, thinking is clear, improve quality of life, be called life source material again.Alprostadil preparation becomes sales volume first medicine in the cardiovascular medicament at home.But by separating the Alprostadil resource-constrained with histiocyte from the mammal seminal fluid, so USA and Europe, Japanese chemosynthesis prepare Alprostadil, China Norman Bethune Medical University, Jilin Province Medicine Research Institute have been opened up one and have been utilized the specialties of the Northeast Radix Oenotherae erythrosepalae oil to make raw material, from sheep spermary, extract compound enzyme catalysis, the semi-synthetic path of preparing Alprostadil of synthetic Alprostadil has solved raw material sources restriction bottleneck.The inventor improves white medical university again and the Jilin medicine grinds semi-synthetic route, and invention gas, liquid, solid three's co-absorbed and compound enzyme immobilization carrier and suitability for industrialized production Alprostadil biochemical reactor (China such as inventor is patent of invention formerly, patent name: Alprostadil production of raw medicine technology, the patent No.: 961211350).Realize the suitability for industrialized production Alprostadil, realize that process cycle is external 1/7th, cost is external 1/10th, and quality is the standard substance that are better than external famous expert.Jilin medicine inspecting institute and national drug biological products assay institute substitute foreign standard product (380000 yuans/gram of valency) with your standard substance (7000 yuans/gram of valency) of preceding sharp ground that the inventor provides.The Alprostadil crude drug of inventor preparation and preparation have overcome injection pain, refrigerator accumulating, the content three big world difficult problems that fall progressively.Serial China of the present invention formerly patent of invention solved that the big suitability for industrialized production of alprostadil liposome preparation is energy-conservation, de-carbon, zero emission technology, equipment, solved fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) fermentation tail gas dedusting, degerming, removed phage, eliminated the unusual smell, the increment of de-carbon oxygen enrichment and recycled Processes and apparatus.Make the former and material preparation big suitability for industrialized production of Alprostadil even fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) enter international most advanced level and have the independent intellectual property right protection at technology, equipment, quality, scale, cost, consumption, energy-conservation, reduction of discharging, de-carbon.Substantially possessed the comprehensive intellectual property protection of the medicine system that exploitation improves national power, raising army fighting capacity, improves the people's life quality.
Summary of the invention
One. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) composition of medicine and preparation thereof:
(1). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine and preparation process and method:
1, each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.30-0.70
Taurine 0.45-0.90
Vitamin C 0.10-0.20
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Illustrate: here taurine or or baicalin, its molecular formula is C
21H
18O
11, molecular weight is 446.35, its weight fraction in prescription is 0.0500-0.1000.
2. compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine preparation process and method are:
2.1 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
2.2 taurine or baicalin, vitamin C are dissolved in the water for injection, and making proportion is the 1.0-1.1 aqueous solution, is that 8% analytical pure hydrochloric acid solution adjust pH is 4.0-6.0 with mass percent, again solution is crossed degerming through 0.22 μ m membrane filtration;
2.3 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.1 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, the proportion that 2.2 steps were made is that the 1.0-1.1 aqueous solution is by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
2.4 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine.
(2). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine and preparation process and method:
1. each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000-0.7000
Taurine 0.4500-0.9000
Beta-schardinger dextrin-0.0050-0.0100
Alprostadil 0.0001-0.0003
Reduced glutathion 0.0050-0.0100
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0050-0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, it is that Araliaceae Radix Ginseng or Radix Notoginseng extraction separation obtain monomer, molecular formula is C
42H
72O
14, molecular weight is 830.03, weight ratio is 0.0500-0.1000 in prescription.
2. the preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are:
2.1 with anhydrous alcohol solution Alprostadil or ginsenoside Rg
1To just dissolving is complete, make Alprostadil or ginsenoside Rg
1Nearly saturated ethanol solution;
2.2 beta-schardinger dextrin-is dissolved in the part water for injection, fully make near saturated solution to dissolving just, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent;
2.3 Alprostadil or ginsenoside Rg with the preparation of 2.1 steps
1Ethanol solution under 60-100 rev/min of stirring, room temperature drops in the beta-schardinger dextrin-near saturated solution of 2.2 step preparations, to Alprostadil dissolving or ginsenoside Rg
1Fully, make Alprostadil or ginsenoside beta-schardinger dextrin-comprise solution;
2.4 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
2.5 taurine, reduced glutathion under 60-80 rev/min of stirring, are dissolved in the remaining water for injection, and making proportion is the 1.0-1.2 aqueous solution, again Alprostadil or the ginsenoside Rg that 2.3 steps were prepared
1The solution that comprises of beta-schardinger dextrin-add, stir, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent then, at last solution is crossed degerming through 0.22 μ m membrane filtration;
2.6 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.4 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, 2.5 sterile liquid medicines made of step by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
2.7 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) group B composition of medicine.
(3). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine and preparation process method thereof:
1. each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000-0.7000
Danshensu 0.2000-0.5000
Gamma-Linolenic acid 0.0010-0.0050
Beta-schardinger dextrin-0.0060-0.0150
Dehydrated alcohol (volatilization during drying) 0.0100-0.0500
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Illustrate: danshensu or curcumin here, the curcumin molecular formula is C
21H
20O
6,, molecular weight is 368.37, its weight ratio is 0.1000-0.3000 in prescription.
Danshensu is that danshensu is the water solubility extract of medicinal plants Radix Salviae Miltiorrhizae, is the main component of FUFANG DANSHEN DIWAN, chemistry β by name-(3, the 4-dihydroxy phenyl) lactic acid.
Gamma-Linolenic acid claims vitaminF again, and the initiation material of its preparation is a Radix Oenotherae erythrosepalae oil.
2. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine preparation process and method are:
2.1 with the anhydrous alcohol solution gamma-Linolenic acid, make the gamma-Linolenic acid ethanol solution, or gamma-Linolenic acid and curcumin be dissolved in the dehydrated alcohol jointly, even make the solution that gamma-Linolenic acid and curcumin are dissolved in dehydrated alcohol jointly;
2.2 beta-schardinger dextrin-is dissolved in the part water for injection, fully make near saturated solution to dissolving just, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent;
2.3 go on foot the ethanol solution of preparation under 60-100 rev/min of stirring with 2.1, room temperature drops in the beta-schardinger dextrin-near saturated solution of 2.2 steps preparation, till gamma-Linolenic acid dissolving fully, or till gamma-Linolenic acid and curcumin all dissolve fully, make the beta-cyclodextrin inclusion compound solution of gamma-Linolenic acid, or the solution that comprised by beta-schardinger dextrin-jointly of gamma-Linolenic acid and curcumin;
2.4 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
2.5 with danshensu under 60-80 rev/min of stirring, be dissolved in the comprising in the solution of beta-schardinger dextrin-of the gamma-Linolenic acid of 2.3 step preparations, and with remaining water for injection under the prerequisite that stirs, adjusting solution proportion is 1.0-1,1, the reuse mass percent is that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5, at last solution is crossed degerming through 0.22 μ m membrane filtration; Or curcumin is when substituting danshensu, it is 1.0-1.1 with remaining water for injection adjustment solution proportion that the gamma-Linolenic acid of 2.3 step preparations and curcumin are comprised solution by beta-schardinger dextrin-jointly, the reuse mass percent is that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5, at last solution is crossed degerming through 0.22 μ m membrane filtration;
2.6 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.4 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, the 2.5 danshensu sterile liquid medicines made of step or curcumin sterile liquid medicine (when replacing danshensu) by curcumin by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
2.7 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine.
Two. the advantage of medicine of the present invention:
(1). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine advantage:
1. compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A has increased taurine on fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) basis; main disease curing range is controlled the kidney effect except keeping fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) to control lung; expand to and control hypertension, hyperglycemia, cardiovascular and cerebrovascular disease, resisting fatigue, defying age, shock, radioprotective.
2. taurine also is inherent biological active substances in the animal body, and its function has:
2.1 antiinflammatory, antiallergic;
2.2 immunologic enhancement;
2.3 ischemic myocardial cell, hypoxic pulmonary arterial endothelial cell, anoxia cerebral arteries endotheliocyte are all had protective effect;
2.4 the increase myocardial contraction, arrhythmia, shock, defying age, resisting fatigue, radioprotective;
2.5 blood pressure lowering, blood sugar lowering;
2.6 arteriosclerosis;
2.7; Improve one's memory the treatment dysthymia;
2.8 anti-intestinal endotoxin shifts, treatment viral myocarditis, treatment upper respiratory tract infection.
Baicalin also has above-mentioned functions, the ginsenoside Rg for the plant scutellariae,radix extracts monomer
1The taurine above-mentioned functions is also arranged.
3. compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A has also increased the antioxidant vitamin C, the present invention also uses taurine and vitamin C that fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is carried out coating, avoid fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) in manufacturing, accumulating, use in vitro and in vivo oxidation, peroxidating and the side effect that produces and bad should; It also is used for: vitamin C deficiency prevention and treatment, acute and chronic infectious disease or convalescent period, wound healing phase are replenished the cardiogenic shock treatment after being ill, hepatic injury and the treatment of chronic poisoning hepatic injury, be used for anemia, anaphylaxis dermatosis treatment, promote wound healing, to flu, cancer, hyperlipidemia treatment.
4. the present invention produces compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A under 100 grades of aseptic environment purifications, than injection production rank also high (injection is the local laminar flow environment purification under ten thousand grades), also have the medicinal liquid Entkeimung to reach except that high price precipitation of iron ions thing, remove insoluble particle, favourable raising product quality avoids assorted bacterium and oxidant to make product rotten.This is a unique production process of the present invention;
(2). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine advantage:
1. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B goes up on compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A prescription basis increases Alprostadil, except keeping compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A treatment and pre-diseases prevention kind, because of Alprostadil has antibody mediated immunity complex exceptional function in the human body of removing, make antigen not reach morbidity concentration in vivo, antigen is entered in the body in time please be removed, both made morbidity, disease is very light.Suppress tumor cell in addition, the differentiation tumor cell develops to normal cell.Emphasis increases antitypy unknown virus infectious disease, the biochemical reagents viral disease and the infectious disease known, unknown retrovirus of control hostile nations.Also emphasis increases prevention and treats sick kind such as tumor, acquired immune deficiency syndrome (AIDS), serious symptom hepatitis, viral hepatitis.Therefore compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B can reach wartime, extraordinary serious natural calamities period, peaceful development basically and improves the needs that the army and the people's muscle power, psychology are deposited stressed, vitality, national power and answering pressure period.
2. the present invention replaces vitamin C among compound fermented aweto mycopowder (the peacilomyce hepiahi Cs-4 mycopowder) A with the antioxidant reduced glutathion, and reduced glutathion also is the important physiologically substance that exists in the human body.Participate in interior tricarboxylic acid cycle of body and carbohydrate metabolism, promotion fat, protein metabolism, make human body obtain high-energy; Detoxifcation; Lonizing radiation, chemical substance, damage there is protective effect; Antiallergic; Protect the liver eye protection; Symptom palliates a disease.
3. medicine of the present invention all is that intrinsic or natural drug is made raw material with human body, finds a swollen seat of local government ill medicine in quality, curative effect, safety three aspect quality higher but deliver at newspaper than nearest U.S. a company on the net.The multiple sick developing direction of a kind of medical treatment of exploitation is arranged in the world, and to save resource, energy-saving and emission-reduction make things convenient for medication.Medicine of the present invention is more advanced than them, and unique distinction is more arranged.
4. compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B carries out coating with taurine and reduced glutathion to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder), and coating effect among compound fermented aweto mycopowder (the peacilomyce hepiahi Cs-4 mycopowder) A is also arranged.
5. preparation compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B method also has the advantage of preparation compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A.
(3). compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine advantage:
1. medicine of the present invention is fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) and the combination of natural product danshensu.Radix Salviae Miltiorrhizae have defying age, coronary artery dilator, inhibition platelet T XA
2Synthetic, anticoagulation, microcirculation improvement, arteriosclerosis, anti-oxidative damage, blood fat reducing, inhibition endogenous cholesterol synthetic, to liver protection and anti-fibrosis effect, sedation, antitumor action.Curcumin is that zingiberaceous plant HUANGJIANG rhizome extracts monomer, and the above-mentioned effect of danshensu is also arranged.
2. medicine of the present invention is with gamma-Linolenic acid, and promptly vitaminF is an antioxidant, and strong reducing property is arranged, and it derives from Radix Oenotherae erythrosepalae oil.VitaminF is an intrinsic material in the human body.The physiological function of vitaminF has: defying age, arteriosclerosis, guarantor's kidney and control renal insufficiency, blood pressure lowering, blood sugar lowering, blood fat reducing, fat-reducing, skin whitening, anti-gastric-ulcer, antiinflammatory, control women's premenstrual syndrome, control carbuncle of breast.
3. medicine of the present invention comprises vitaminF with cyclodextrin, and vitaminF that comprises with cyclodextrin and curcumin are to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating again.Prevent fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) oxidation in vivo and in vitro and peroxidating.
4. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine also is to prepare under the aseptic purification condition of strictness, preparation compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is also arranged and prepare attached side's fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine advantage.
The specific embodiment:
Embodiment 1:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.30
Taurine 0.45
Vitamin C 0.10
Water for injection (evaporating into clean during drying) fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20
Here taurine or baicalin, the baicalin components by weight is 0.05.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine are described with the front.
Embodiment 2:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.70
Baicalin 0.90
Vitamin C 0.20
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Here baicalin or taurine.The taurine components by weight is 0.10.
The preparation method and the step of multiple compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine of the present invention are described with the front.
Embodiment 3:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.30
Taurine 0.90
Vitamin C 0.10
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Here taurine or baicalin, the baicalin components by weight is 0.10.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine are described with the front.
Embodiment 4:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.70
Taurine 0.45
Vitamin C 0.20
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Here taurine or baicalin, the baicalin components by weight is 0.05
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine are described with the front.
Embodiment 5:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.39
Taurine 0.58
Vitamin C 0.17
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Here taurine or baicalin, the baicalin components by weight is 0.08.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine are described with the front.
Embodiment 6:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000
The ginsenoside Rg
10.0500
Beta-schardinger dextrin-0.0050
Alprostadil 0.0001
Reduced glutathion 0.0050
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0050
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here ginsenoside Rg
1Or taurine, the taurine components by weight is 0.4500.
The preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are described with the front.
Embodiment 7:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.7000
Taurine 0.9000
Beta-schardinger dextrin-0.0100
Alprostadil 0.0003
Reduced glutathion 0.0100
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, ginsenoside's components by weight is 0.1000.
The preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are described with the front.
Embodiment 8:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000
Taurine 0.9000
Beta-schardinger dextrin-0.0050
Alprostadil 0.0003
Reduced glutathion 0.0050
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, ginsenoside's components by weight is 0.1000.
The preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are described with the front.
Embodiment 9:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.7000
Taurine 0.4500
Beta-schardinger dextrin-0.0100
Alprostadil 0.0001
Reduced glutathion 0.0100
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0050
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, ginsenoside's components by weight is 0.0500.
The preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are described with the front.
Embodiment 10:
Each raw material components weight ratio of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.5600
Taurine 0.5900
Beta-schardinger dextrin-0.0080
Alprostadil 0.0002
Reduced glutathion 0.0090
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0070
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, ginsenoside's components by weight is 0.0760.
The preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are described with the front.
Embodiment 11:
Each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000
Danshensu 0.2000
Gamma-Linolenic acid 0.0010
Beta-schardinger dextrin-0.0060
Dehydrated alcohol (volatilization during drying) 0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Here danshensu or curcumin, the curcumin components by weight is 0.1000.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine are described with the front.
Embodiment 12:
Each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.7000
Danshensu 0.5000
Dihomo-gamma-linolenic acid 0.0050
Beta-schardinger dextrin-0.0150
Dehydrated alcohol (volatilization during drying) 0.0500
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Here danshensu or be curcumin, the curcumin components by weight is 0.3000.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine are described with the front.
Embodiment 13:
Each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000
Danshensu 0.5000
Gamma-Linolenic acid 0.0020
Beta-schardinger dextrin-0.0150
Dehydrated alcohol (volatilization during drying) 0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Here danshensu or be curcumin, the curcumin components by weight is 0.3000.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine are described with the front.
Embodiment 14:
Each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.7000
Danshensu 0.2000
Dihomo-gamma-linolenic acid 0.0050
Beta-schardinger dextrin-0.0060
Dehydrated alcohol (volatilization during drying) 0.0500
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Here danshensu or be curcumin, the curcumin components by weight is 0.1000.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine are described with the front.
Embodiment 15:
Each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.5600
Curcumin 0.1900
Gamma-Linolenic acid 0.0042
Beta-schardinger dextrin-0.0096
Dehydrated alcohol (volatilization during drying) 0.040
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Here curcumin or be danshensu, the danshensu components by weight is 0.37.
The preparation method and the step of compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine are described with the front.
The pharmacodynamics demonstration test: following test all is to entrust the test of the Experimental Animal Center well-established law of specialty.
1. defying age test:
1.1 spontaneously hypertensive rat model with 4 monthly ages.Be divided into food and contain Oleum Helianthi 2.4%, contain the treatment group that oleum lini core oil 7.9% matched group and food contain the feedstuff of medicine 3% of the present invention, its crapulous syncope contains 15 groups of the medicines that medication therapy groups of the present invention is divided the preparation of embodiment 1-15 example again, totally 17 groups.Every group 12, experiment is to getting hematometry triglyceride meansigma methods and highdensity lipoprotein-cholesterol meansigma methods 16 weeks.Result of the test sees Table:
| Project | Oil three ester value mmol/L | Highdensity lipoprotein-cholesterol value mmol/L |
| Food Oleum Helianthi feedstuff group | 0.380? | 0.460? |
| Food oleum lini feedstuff group | 0.235? | 0.435? |
| Food embodiment 1 pharmaceutical feed group | 0.156? | 0.655? |
| Food embodiment 2 pharmaceutical feed groups | 0.160? | 0.650? |
| Food embodiment 3 pharmaceutical feed groups | 0.162? | 0.643? |
| Food embodiment 4 pharmaceutical feed groups | 0.153? | 0.649? |
| Food embodiment 5 pharmaceutical feed groups | 0.150? | 0.689? |
| Food embodiment 6 pharmaceutical feed groups | 0.151? | 0.673? |
| Food embodiment 7 pharmaceutical feed groups | 0.148? | 0.681? |
| Food embodiment 8 pharmaceutical feed groups | 0.156? | 0.670? |
| Food embodiment 9 pharmaceutical feed groups | 0.140? | 0.679? |
| Food embodiment 10 pharmaceutical feed groups | 0.154? | 0.685? |
| Food embodiment 11 pharmaceutical feed groups | 0.167? | 0.665? |
| Food embodiment 12 pharmaceutical feed groups | 0.160? | 0.658? |
| Food embodiment 13 pharmaceutical feed groups | 0.170? | 0.670? |
| Food embodiment 14 pharmaceutical feed groups | 0.175? | 0.653? |
| Food embodiment 15 pharmaceutical feed groups | 0.165? | 0.675? |
1.2 get the healthy mice model, every 18-20g, 10 every group.Matched group was irritated stomach 10 with oleum lini 4ml/kg, and treatment is organized 15 groups, irritated stomach with the each 200mg/kg of the medicine of the present invention of embodiment 1-15 respectively, every day twice, irritated stomach 10.Blood sampling in 1 hour after the last administration is with H
2O
2Be substrate, survey the trap value at ultraviolet spectrophotometer 230nm place, to irritate H in the oleum lini mice blood
2O
2It is 100% that meansigma methods is made as the resistive to hydrogen peroxide enzyme activity.With H in the medicine group mice blood of the present invention
2O
2Reduce meansigma methods divided by irritating H in Caulis et Folium Lini line of oils mice blood
2O
2Meansigma methods is a resistive to hydrogen peroxide enzyme activity improvement value.Result of the test is as follows:
2. resisting fatigue, hypoxia endurance test:
Healthy mice, body weight 18-22g, random packet.Two groups of matched groups, 10 every group, every caudal vein injecting normal saline 0.3ml organizes and tail vein injection protocatechualdehyde 300mg/kg (being dissolved in the 0.5ml normal saline) group; Treatment group tail vein injection medicine 300mg/kg of the present invention water extract concentrates in the water for injection of 0.5ml volume, every group of 10 mices.After the medication 5 minutes, place in the wide mouthed bottle of airtight normal pressure 1000ml.Calculating is respectively organized mice and is survived average time.Result of the test is as follows:
| Project | Min of following time-to-live of anoxia | Remarks |
| The injecting normal saline group | ?19.8? | ? |
| Injection protocatechualdehyde group | ?20.7? | ? |
| Injection embodiment 1 medicine water extract group | ?29.5? | ? |
| Injection embodiment 2 medicine water extract groups | ?30.2? | ? |
| Injection embodiment 3 medicine water extract groups | 28.7? | ? |
| Injection embodiment 4 medicine water extract groups | 32.3? | ? |
| Injection embodiment 5 medicine water extract groups | 27.2? | ? |
| Injection embodiment 6 medicine water extract groups | 32.1? | ? |
| Injection embodiment 7 medicine water extract groups | 29.8? | ? |
| Injection embodiment 8 medicine water extract groups | 31.5? | ? |
| Injection embodiment 9 medicine water extract groups | 33.1? | ? |
| Injection embodiment 10 medicine water extract groups | 30.6? | ? |
| Injection embodiment 11 medicine water extract groups | 28.5? | ? |
| Injection embodiment 12 medicine water extract groups | 27.6? | ? |
| Injection embodiment 13 medicine water extract groups | 26.8? | ? |
| Injection embodiment 14 medicine water extract groups | 29.1? | ? |
| Injection embodiment 15 medicine water extract groups | 25.3? | ? |
3. raising immunity:
3.1 nonspecific immunity: healthy mice, body weight 18-20g.15 of matched groups, every day, normal saline 0.5ml irritated stomach 2 times.Medicine of the present invention is irritated 15 groups of stomach groups, 15 every group, irritates stomach, every day 2 times with 500mg/kg medicine of the present invention at every turn.Put to death after 10 days, measure blood rosettes vigor by measuring thymosin rosettes vigor method (national drug standards have been stipulated algoscopy).With a normal saline matched group blood piece rare colored vigor is 100%.Calculate relative vigor, vigor is high more relatively, and immunity is strong more.Result of the test is as follows:
| Project | The relative vigor % of blood rosettes | Remarks |
| Normal saline is irritated the stomach group | 100? | ? |
| Embodiment 1 medicine is irritated the stomach group | 121? | ? |
| Embodiment 2 medicines are irritated the stomach group | 118? | ? |
| Embodiment 3 medicines are irritated the stomach group | 115? | ? |
| Embodiment 4 medicines are irritated the stomach group | 122? | ? |
| Embodiment 5 medicines are irritated the stomach group | 114? | ? |
| Embodiment 6 medicines are irritated the stomach group | 126? | ? |
| Embodiment 7 medicines are irritated the stomach group | 120? | ? |
| Embodiment 8 medicines are irritated the stomach group | 129? | ? |
| Embodiment 9 medicines are irritated the stomach group | 123? | ? |
| Embodiment 10 medicines are irritated the stomach group | 125? | ? |
| Embodiment 11 medicines are irritated the stomach group | 117? | ? |
| Embodiment 12 medicines are irritated the stomach group | 120? | ? |
| Embodiment 13 medicines are irritated the stomach group | 114? | ? |
| Embodiment 14 medicines are irritated the stomach group | 123? | ? |
| Embodiment 15 medicines are irritated the stomach group | 118? | ? |
3.2 specific immunity: healthy mice, body weight 18-20g.15 of matched groups, every day, normal saline 0.5ml irritated stomach 2 times.Medicine of the present invention is irritated 15 groups of stomach groups, 15 every group, irritates stomach, every day 2 times with 500mg/kg medicine of the present invention at every turn.Put to death after 15 days, measure the anti-sheep red blood cell (SRBC) antibody titer meansigma methods that anti-sheep red blood cell (SRBC) antibody test in the blood serum (entrusting the Experimental Animal Center test) obtains.And to irritate with normal saline that the stomach group tires be 100%, and calculating each group, to resist sheep red blood cell (SRBC) antibody relative potency mutually high more, and immunity is strong more.Result of the test is as follows:
| Project | Anti-sheep red blood cell (SRBC) antibody relative potency % | Remarks |
| Normal saline is irritated stomach group regulation 100 | 100? | ? |
| Embodiment 1 medicine is irritated the stomach group | 116? | ? |
| Embodiment 2 medicines are irritated the stomach group | 121? | ? |
| Embodiment 3 medicines are irritated the stomach group | 117? | ? |
| Embodiment 4 medicines are irritated the stomach group | 119? | ? |
| Embodiment 5 medicines are irritated the stomach group | 123? | ? |
| Embodiment 6 medicines are irritated the stomach group | 126? | ? |
| Embodiment 7 medicines are irritated the stomach group | 129? | ? |
| Embodiment 8 medicines are irritated the stomach group | 132? | ? |
| Embodiment 9 medicines are irritated the stomach group | 134? | ? |
| Embodiment 10 medicines are irritated the stomach group | 127? | ? |
| Embodiment 11 medicines are irritated the stomach group | 123? | ? |
| Embodiment 12 medicines are irritated the stomach group | 118? | ? |
| Embodiment 13 medicines are irritated the stomach group | 127? | ? |
| Embodiment 14 medicines are irritated the stomach group | 120? | ? |
| Embodiment 15 medicines are irritated the stomach group | 125? | ? |
4. sedation: matched group: injection 0.1ml water for injection in 1 tricorn of clear-headed dog, test group: regain consciousness dog side injection of brain water for injection after 48 hours at matched group, the aqueous extract 0.2ml that contains medicine 2mg of the present invention again at the side injection of brain, from injection embodiment 1 medicine, under injection in 48 hours-individual embodiment medicine aqueous extract.Inject to begin to measure the generation of brain wave slow wave in back 10 minutes and observe dog and have or not sedation.Result of the test is as follows:
| Injection embodiment 5 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 6 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 7 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 8 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 9 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 10 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 11 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 12 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 13 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 14 medicine aqueous extracts | Have | Be | ? |
| Injection embodiment 15 medicine aqueous extracts | Have | Be | ? |
5. shock: healthy mice, body weight 18-20g.20 of endotoxin groups, lumbar injection endotoxin 300mg/kg (being dissolved in the 0.5ml normal saline); Test group: get 10 of injection endotoxin mices at random, lumbar injection medicine 300mg/kg of the present invention aqueous extract (being dissolved in the 0.5ml water for injection) is immediately observed and is given mice existence digit rate in the medicine of the present invention 6 hours.Put to death mice after 6 hours, core, liver, kidney, brain, measure malonaldehyde in these tissues (MDA) amount and endotoxin respectively.With endotoxin group MDA content is 100%, calculates the relative MDA% of test group.Result of the test is as follows:
| Embodiment 9 medicine groups | 0? | 77％? | 42％? | 68％? | 77％? |
| Embodiment 10 medicine groups | 10? | 73％? | 43％? | 71％? | 72％? |
| Embodiment 11 medicine groups | 20? | 79％? | 58％? | 75％? | 78％? |
| Embodiment 12 medicine groups | 10? | 76％? | 54％? | 79％? | 75％? |
| Embodiment 13 medicine groups | 10? | 80％? | 51％? | 73％? | 71％? |
| Embodiment 14 medicine groups | 20? | 74％? | 59％? | 78％? | 79％? |
| Embodiment 15 medicine groups | 10? | 77％? | 51％? | 74％? | 80％? |
6. anti-light radiation: healthy mice, body weight 18-20g.10 of matched groups are fed water for injection 1.0ml, every day 2 times at every turn; Test group is fed medicine 300mg/kg of the present invention, every day 2 times at every turn.Shine after 30 minutes at medicine feed after 5 days
60C
o9.0GY1 it is inferior.Medicine feed is 7 days again, and the existence mice is put to death end product malonaldehyde (MDA) amount of surveying lipid peroxidation in blood, the heart, liver, kidney, the brain and feeds the contrast of water for injection group.With matched group MDA content is 100%, the relative MDA% of experiment with computing group.Result of the test is as follows:
Above pharmacodynamics demonstration test as seen, medicine of the present invention, improve the army and the people's fighting capacity, viability needs in the time of can satisfying war, burst natural disaster fully, in peacetime, can satisfy the army and the people fully improves work energy, prolongs the worker and organize age, height old people's life-span, improve old people's self-care ability and vitality needs, in a word, medicine tool of the present invention improves national power substantial economics and great social benefit.
Claims (7)
1. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) composition of medicine is characterized in that, each raw material components weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.30-0.70
Taurine 0.45-0.90
Vitamin C 0.10-0.20
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into clean during drying)
Illustrate: here taurine or or baicalin, its molecular formula is C
21H
18O
11, molecular weight is 446.35, its weight fraction in prescription is 0.0500-0.1000.
2. according to the described compound fermented aweto mycopowder of claim 1 (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine, it is characterized in that compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine preparation process and method are:
2.1 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
2.2 taurine or baicalin, vitamin C are dissolved in the water for injection, and making proportion is the 1.0-1.1 aqueous solution, is that 8% analytical pure hydrochloric acid solution adjust pH is 4.0-6.0 with mass percent, again solution is crossed degerming through 0.22 μ m membrane filtration;
2.3 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.1 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, the proportion that 2.2 steps were made is that the 1.0-1.1 aqueous solution is by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
2.4 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine.
3. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) composition of medicine is characterized in that, each raw material components weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000-0.7000
Taurine 0.4500-0.9000
Beta-schardinger dextrin-0.0050-0.0100
Alprostadil 0.0001-0.0003
Reduced glutathion 0.0050-0.0100
Dehydrated alcohol (evaporating into to the greatest extent during drying) 0.0050-0.0100
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (evaporating into to the greatest extent during drying)
Here taurine or ginsenoside Rg
1, it is that Araliaceae Radix Ginseng or Radix Notoginseng extraction separation obtain monomer, molecular formula is C
42H
72O
14, molecular weight is 830.03, weight ratio is 0.0500-0.1000 in prescription.
4. according to the described compound fermented aweto mycopowder of claim 3 (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine, it is characterized in that the preparation process and the method for compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine are:
4.1 with anhydrous alcohol solution Alprostadil or ginsenoside Rg
1To just dissolving is complete, make Alprostadil or ginsenoside Rg
1Nearly saturated ethanol solution;
4.2 beta-schardinger dextrin-is dissolved in the part water for injection, fully make near saturated solution to dissolving just, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent;
4.3 Alprostadil or ginsenoside Rg with the preparation of 2.1 steps
1Ethanol solution under 60-100 rev/min of stirring, room temperature drops in the beta-schardinger dextrin-near saturated solution of 2.2 step preparations, to Alprostadil dissolving or ginsenoside Rg
1Fully, make Alprostadil or ginsenoside beta-schardinger dextrin-comprise solution;
4.4 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
4.5 taurine, reduced glutathion under 60-80 rev/min of stirring, are dissolved in the remaining water for injection, and making proportion is the 1.0-1.2 aqueous solution, again Alprostadil or the ginsenoside Rg that 2.3 steps were prepared
1The solution that comprises of beta-schardinger dextrin-add, stir, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent then, at last solution is crossed degerming through 0.22 μ m membrane filtration;
4.6 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.4 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, 2.5 sterile liquid medicines made of step by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
4.7 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) group B composition of medicine.
5. compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) composition of medicine is characterized in that, each component raw material weight ratio of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine is:
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) 0.3000-0.7000
Danshensu 0.2000-0.5000
Gamma-Linolenic acid 0.0010-0.0050
Beta-schardinger dextrin-0.0060-0.0150
Dehydrated alcohol (volatilization during drying) 0.0100-0.0500
Fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) weight 15-20 doubly for water for injection (volatilization during drying)
Illustrate: danshensu or curcumin here, the curcumin molecular formula is C
21H
20O
6,, molecular weight is 368.37, its weight ratio is 0.1000-0.3000 in prescription.
Danshensu is that danshensu is the water solubility extract of medicinal plants Radix Salviae Miltiorrhizae, is the main component of FUFANG DANSHEN DIWAN, chemistry β by name-(3, the 4-dihydroxy phenyl) lactic acid.
Gamma-Linolenic acid claims vitaminF again, and the initiation material of its preparation is a Radix Oenotherae erythrosepalae oil.
6. according to the described fermented Cordyceps powder of claim 5 (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine, it is characterized in that compound fermented aweto mycopowder of the present invention (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine preparation process and method are:
6.1 with the anhydrous alcohol solution gamma-Linolenic acid, make the gamma-Linolenic acid ethanol solution, or gamma-Linolenic acid and curcumin be dissolved in the dehydrated alcohol jointly, even make the solution that gamma-Linolenic acid and curcumin are dissolved in dehydrated alcohol jointly;
6.2 beta-schardinger dextrin-is dissolved in the part water for injection, fully make near saturated solution to dissolving just, be that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5 with mass percent;
6.3 go on foot the ethanol solution of preparation under 60-100 rev/min of stirring with 2.1, room temperature drops in the beta-schardinger dextrin-near saturated solution of 2.2 steps preparation, till gamma-Linolenic acid dissolving fully, or till gamma-Linolenic acid and curcumin all dissolve fully, make the beta-cyclodextrin inclusion compound solution of gamma-Linolenic acid, or the solution that comprised by beta-schardinger dextrin-jointly of gamma-Linolenic acid and curcumin;
6.4 exsiccant fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) is pulverized, is made 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder);
6.5 with danshensu under 60-80 rev/min of stirring, be dissolved in the comprising in the solution of beta-schardinger dextrin-of the gamma-Linolenic acid of 2.3 step preparations, and with remaining water for injection under the prerequisite that stirs, adjusting solution proportion is 1.0-1,1, the reuse mass percent is that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5, at last solution is crossed degerming through 0.22 μ m membrane filtration; Or curcumin is when substituting danshensu, it is 1.0-1.1 with remaining water for injection adjustment solution proportion that the gamma-Linolenic acid of 2.3 step preparations and curcumin are comprised solution by beta-schardinger dextrin-jointly, the reuse mass percent is that 8% analytical pure hydrochloric acid solution adjust pH is 5.0-5.5, at last solution is crossed degerming through 0.22 μ m membrane filtration;
6.6 under 100 grades of aseptic environment purifications, the 120-150 order fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) of 2.4 steps preparation is put into boiling coating-boiling drier, press the well-established law operation, the filtrated air negative pressure is introduced in control makes fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) boiling highly be 400mm-500mm, under 40-50 ℃ of temperature, the 2.5 danshensu sterile liquid medicines made of step or curcumin sterile liquid medicine (when replacing danshensu) by curcumin by vaporific ebullient fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) the intensive place of particle that is sprayed in the nozzle, to fermented Cordyceps powder (peacilomyce hepiahi Cs-4 mycopowder) coating, be controlled at that coating finishes in 30-60 minute; This temperature range airpillow-dry 20-30 minute, make dry solids moisture again less than 1%;
6.7 press the dosage that pharmaceutics allows, under 100 grades of aseptic environment purifications, well-established law is made capsule, granule, the tablet of compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine.
7. described compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) A composition of medicine, compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) B composition of medicine, compound fermented aweto mycopowder (peacilomyce hepiahi Cs-4 mycopowder) C composition of medicine, it is characterized in that, be used for defying age, resisting fatigue, shock, anti-light radiation, calmness, anoxia enduring, raising immunity purposes.
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| CN 201010278624 CN101953857A (en) | 2010-09-13 | 2010-09-13 | Compound fermented cordyceps sinensis bacterium powder (paecilomyces hepiali Cs-4 bacterium powder) composite medicine |
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| CN 201110177620 Division CN102430110B (en) | 2010-09-13 | 2010-09-13 | CAlprostadil composite medicament of compound fermented cordyceps sinensis powder and alprostadil composite drug |
| CN 201110177658 Division CN102600211B (en) | 2010-09-13 | 2010-09-13 | Complex fermented cordycepic fungal powder curcumin combined medicine |
| CN201110177656.7A Division CN102727863B (en) | 2010-09-13 | 2010-09-13 | Combined drug of compound fermented Cordyceps sinensis powder and ginsenoside Rg1 |
| CN 201110177618 Division CN102429929B (en) | 2010-09-13 | 2010-09-13 | Compound fermented cordyceps fungus powder and taurine combined drug |
| CN 201110177643 Division CN102429931B (en) | 2010-09-13 | 2010-09-13 | Compound fermented cordyceps fungus powder salvianic acid combined drug |
| CN 201110177641 Division CN102429930B (en) | 2010-09-13 | 2010-09-13 | Compound fermented cordyceps fungus powder and baicalin combined drug, |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN103816529A (en) * | 2014-03-20 | 2014-05-28 | 蔡欣 | Pharmaceutical composition for treating various serious diseases and preparation and use thereof |
| CN104397499A (en) * | 2014-12-24 | 2015-03-11 | 武汉华扬动物药业有限责任公司 | Feed additive for preventing or easing toxin infection of piglets at weaning period, and preparation method of feed additive |
| CN115804813A (en) * | 2022-12-20 | 2023-03-17 | 江西九华药业有限公司 | Fermented cordyceps sinensis powder microsphere composite liquid and preparation method and application thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN1903227A (en) * | 2006-07-06 | 2007-01-31 | 复旦大学 | Water soluble active component of fermented cordyceps and its application |
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| CN1903227A (en) * | 2006-07-06 | 2007-01-31 | 复旦大学 | Water soluble active component of fermented cordyceps and its application |
Non-Patent Citations (1)
| Title |
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| 《中国药学杂志》 19940430 沙静姝,等 金水宝胶囊(发酵虫草菌粉) 第245-246页 权利要求1-7 第29卷, 第4期 2 * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103816529A (en) * | 2014-03-20 | 2014-05-28 | 蔡欣 | Pharmaceutical composition for treating various serious diseases and preparation and use thereof |
| CN104397499A (en) * | 2014-12-24 | 2015-03-11 | 武汉华扬动物药业有限责任公司 | Feed additive for preventing or easing toxin infection of piglets at weaning period, and preparation method of feed additive |
| CN115804813A (en) * | 2022-12-20 | 2023-03-17 | 江西九华药业有限公司 | Fermented cordyceps sinensis powder microsphere composite liquid and preparation method and application thereof |
| CN115804813B (en) * | 2022-12-20 | 2024-02-06 | 江西九华药业有限公司 | Fermented cordyceps sinensis powder microsphere composite liquid and preparation method and application thereof |
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