CN103535801A - Health-care drink with physical fatigue relieving and anoxia endurance improving functions - Google Patents
Health-care drink with physical fatigue relieving and anoxia endurance improving functions Download PDFInfo
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- CN103535801A CN103535801A CN201210234925.3A CN201210234925A CN103535801A CN 103535801 A CN103535801 A CN 103535801A CN 201210234925 A CN201210234925 A CN 201210234925A CN 103535801 A CN103535801 A CN 103535801A
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- sodium
- potassium
- food
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 235000011496 sports drink Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/02—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation containing fruit or vegetable juices
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Mycology (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention relates to a health-care drink with physical fatigue relieving and anoxia endurance improving functions. The health-care drink is prepared from radix ophiopogonis, schisandra chinensis, American ginseng, rhodiola rosea, whey protein peptides and the like. The health-care drink has the effects of relieving physical fatigue and improving anoxia endurance, is suitable for fatigue and exhausted people, people like exercise and fitness and summer field trip, and people doing high-temperature operation and outdoor work.
Description
Technical field
[0001]the present invention relates to a kind of health drink that there is alleviating physical fatigue and improve anoxia endurance.
Background technology
The fast pace of the modern life, make people more by time consumption in the work of bustling about, people run every day in busy work and life, and often ignored most important health problem, health majority presents the state of a kind of " inferior health ", be body without organic disease, but have the state of some Functional changes.According to World Health Organization's update, there is 70% adult in the whole world in sub-health state, wherein, shows as accounting for more than 80% of battle-weary symptom.Luckily, along with the promotion of health care in recent years, people have slowed down busy step, and increasing general public joins the main forces of physical training in order to improve the health, because they know that a reason-health is only best capital, what carrys out happy life there is no healthy health.
People, in daily physical training, can discharge sweat.Somebody thinks can discharge the metabolic waste in body by sweat, has the effect of toxin expelling, so it is The more the better to feel to perspire.Sweat carrys out autoblood in fact, contains certain blood constituent in sweat, in sweat, except some metabolic wastes, also has many materials useful to body, as mineral matter, protein, amino acid, vitamin etc.Along with the loss of sweat, these nutriments have also been lost thereupon.For a small amount of perspiration, can take notice of very much, but for a large amount of perspirations, just should not regard as unimportant.Because a large amount of, perspire body fluid is reduced, if fluid infusion not in time can cause blood volume to decline, heart rate is accelerated, and perspire rate declines, and heat-sinking capability declines, hyperthermia, and body electrolyte disturbance and acid-base balance, cause dehydration.Dehydration causes some major organs physiological functions of body to be affected, as impaired in heart burden, kidney.Electrolytical a large amount of loss such as sodium, potassium can cause nerve-muscle systems obstacle, cause the symptoms such as muscle weakness, muscle cramp.Dehydration also can make locomitivity decline, and produces sense of fatigue, causes the discomfort of body.
Traditional Chinese medicine is thought, body fluid is body fluid, a large amount of perspirations easily cause body fluid consume, if long-term a large amount of perspiration also can cause the adverse consequences such as " profuse sweating impairment of yin ", " depletion of fluid involving qi desertion ", therefore exploitation has alleviating physical fatigue and improves the product of body anoxia endurance, make people both obtain supplementing of sufficient energy and body fluid, can make again muscle power be restored rapidly, there is significant realistic meaning.
The present invention is at a patent < < raw arteries and veins sports drink and preparation method thereof > > (number of patent application: the 201010524215.5) secondary innovation on basis.Its innovative point is: the present invention adds prescription by rhodiola root, has effectively strengthened the effect of prescription aspect raising body anoxia endurance and antifatigue.Research shows, rhodiola root can accelerate adrenal cortex and from depletion state, return to normal condition, improves the oxygen supply of body tissue organ, by suppressing the hemorheological sex change that anoxic causes, changes to realize its oxygen lack resistant function.Rhodiola root also can be accelerated blood circulation by the contraction of prevention capillary, improves the adaptability to low-oxygen environment.Rhodiola root body is more saved utilize glycogen and Adenosine triphosphate capable; for muscle activity provides energy more fully; diaphragmatic fatigue and diaphragmatic muscle damage are had to protective effect; the fatigue that can make a large amount of motions form improves; be a kind of good ancillary drug of endurance exercise and the motion of resistance to speed, also can be used as health treatment and improve Healthy People aerobic capacity and anti-fatigue ability.In addition, the present invention's American Ginseng prescription, American Ginseng is cool in nature, and long-term taking can boosting qi and nourishing yin, clearing heat and promoting fluid, the body fluid of body and the recovery of physical efficiency after suitable motion.Clinical research shows, the present invention not only can supplement rapidly the loss of protein and body fluid after motion, maintains body electrolyte balance, and can improve body anoxia endurance, makes the rapid fatigue-relieving of body.
Summary of the invention
The object of the present invention is to provide a kind of health drink that there is alleviating physical fatigue and improve anoxia endurance, the effect that has alleviating physical fatigue and improve anoxia endurance, the tired crowd of the tired god of the power that is applicable to, sport and body-building and summer tour in the field crowd, high-temperature operation and outwork crowd are edible.
Technical scheme of the present invention:
A kind of health drink that there is alleviating physical fatigue and improve anoxia endurance, it is characterized in that mainly containing following raw material composition and weight proportion is prepared from: 1～30 part of the tuber of dwarf lilyturf, 1～20 part, the fruit of Chinese magnoliavine, 1～20 part of dark plum, 1～20 part of American Ginseng, 1～20 part of rhodiola root, 1～20 part of whey protein peptide, 0.1～2 part of sodium salt, 0.05～0.5 part of sylvite, 0.1～120 part of sweetener, 0.1～8 part of acid.Preferred weight ratio range of the present invention is: 4～18 parts of the tubers of dwarf lilyturf, 2～12 parts, the fruit of Chinese magnoliavine, 2～12 parts of dark plums, 2～10 parts of American Ginsengs, 2～10 parts of rhodiola roots, 3～15 parts of whey protein peptides, 0.3～1.5 part of sodium salt, 0.1～0.35 part of sylvite, 0.2～90 part of sweetener, 0.5～4 part of acid.Optimum weight proportioning of the present invention is: 8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 6 parts of whey protein peptides, 0.6 part of sodium salt, 0.2 part of sylvite, 50 parts of sweeteners, 2.5 parts of acids.
As mentioned above, a kind of health drink that has alleviating physical fatigue and improve anoxia endurance, is characterized in that can changing effect into, curing mainly any one or more in similar ginseng, Radix Codonopsis, radix pseudostellariae or the Radix Astragali by being equal to substitutivity principle American Ginseng.
As mentioned above, a kind of health drink that has alleviating physical fatigue and improve anoxia endurance, is characterized in that can changing effect into the tuber of dwarf lilyturf, curing mainly any in close asparagus fern, the root of straight ladybell by being equal to substitutivity principle.
As mentioned above, a kind of health drink that there is alleviating physical fatigue and improve anoxia endurance, it is characterized in that sodium salt can be any or several in sodium chloride, sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate, preferably sodium chloride; Sylvite can be any or several in potassium chloride, saleratus, potassium acetate, potassium citrate, preferably potassium chloride.
As mentioned above, there is alleviating physical fatigue and improve the health drink of anoxia endurance, it is characterized in that whey protein peptide can use any or several replacements in lactalbumin, collagen, soybean protein, zein, soybean oligopeptide, collagen peptide, fish skin collagen peptide, turtle peptide, sea cucumber peptide.
As mentioned above, a health drink with alleviating physical fatigue and raising anoxia endurance, is characterized in that sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
As mentioned above, a kind of health drink that there is alleviating physical fatigue and improve anoxia endurance, it is characterized in that preparation method takes the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, American Ginseng, rhodiola root by recipe quantity, twice of boiling, add 10～15 times of amounts of water at every turn and decoct 1～3 hour, collecting decoction, is cooled to room temperature, centrifugal through supercentrifuge, supernatant is standby; By recipe quantity, take lactalbumin Gly-His-Lys, sodium chloride, potassium chloride, sweetener, acid again, add water and make in right amount abundant dissolving, merge with supernatant, add purified water and be settled to 1000mL, mix, filter, filling, sterilizing, obtains.
As mentioned above, a health drink with alleviating physical fatigue and raising anoxia endurance, is characterized in that finished dosage forms can be granule, tablet, capsule, soft capsule, pill, the pill that adopts pharmaceutically acceptable carrier or excipient to make.
As mentioned above, a kind of health drink that has alleviating physical fatigue and improve anoxia endurance, is characterized in that finished product can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
As mentioned above, a kind of health drink that has alleviating physical fatigue and improve anoxia endurance, is characterized in that preparing alleviating physical fatigue and improves the food of anoxia endurance or the application in health products.
The invention has the advantages that:
The sport beverage formula of selling is in the market single, most of carbohydrate (sucrose or glucose) that adopts adds electrolyte formula, the functional component that people's physical efficiency is utilized is more single, and can not meet such crowd for the demand of the anaerobic respiration of profuse sweating impairment of yin, depletion of fluid involving qi desertion, strenuous exercise's generation.We be take Traditional Chinese medical theory as guidance, science compatibility, and synergy, plays alleviating physical fatigue, improves anoxia endurance, regulates electrolyte balance and strengthens endurance and strength, and the albumen that improves muscle is synthetic, promotes the effect of glycogen deposit.We can be made into sugar-free formulation product, and applicable crowd is wider, and diabetic etc. also can long-term taking.
The invention provides a kind of health drink that there is alleviating physical fatigue and improve anoxia endurance, the effect of both there is enriching yin, tonifying Qi, promoting the production of body fluid, can supplement again because of motion or high temperature and perspire and to cause electrolytical loss, there is alleviating physical fatigue and improve the effect of anoxia endurance.Modern study shows: the blood lactic acid TG-AUC after this product can extend the mice burden swimming time, minimizing mouse is swum after blood Lactate, minimizing swimming, reduction mice serum urea nitrogen value, and point out we to there is the effect of alleviating physical fatigue; In addition, originally can extend mouse Hypoxia under normal pressure, poisoning rear mouse survival time of natrium nitrosum and Ischemia Injury in Brain hypoxia mice breathing time, prompting we have the effect that improves anoxia endurance.
1 alleviating physical fatigue test
1.1 materials: beverage of the present invention: be prepared from by American Ginseng, the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, rhodiola root, whey protein peptide, sodium chloride, potassium chloride etc.; Positive control: be prepared from according to prescription and preparation method in patent 201010524215.5 by ginseng, the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, whey protein peptide, sodium chloride, potassium chloride etc.; 120 male mice in kunming, body weight 18 Animal Experimental Study centers,～22g，You Hubei Province provide.
1.2 sample preparations: get the liquid that beverage of the present invention, positive control drug are 0.275g containing crude drug in being mixed with every milliliter after concentrated respectively, for beverage group of the present invention and positive controls mouse stomach, negative control group gavage gives physiological saline, and each experimental group is all by 0.20ml/10g body weight capacity gavage.
1.3 experimental techniques (1) Loaned swimming test: every group of 10 mouse, the continuous gavage of mouse 30 days, last to tested material after 30 min, mouse tail root 5% body weight of bearing a heavy burden, puts swimming trunk went swimming and observes mouse from swimming to the death time.(2) mensuration of Serum lactic acid content: every group of 10 mouse, the continuous gavage of mouse 30 days, last to tested material after 30 min, put into water went swimming 10 min of 30 ℃, before swimming, after swimming at once, swimming have a rest after 20 min get respectively blood (endocanthion is got blood) for three times and measure blood Lactate.(3) mensuration of serum urea nitrogen content: the continuous gavage of mouse 30 days, last to tested material after 30 min, put into water went swimming 90 min of 30 ℃, after water outlet, 60 min that have a rest, eyeball is got hematometry serum urea nitrogen content.
1.4 index detection method blood Lactates adopt Nanjing to build up the blood Lactic acid Kit mensuration that bio-engineering corporation produces.Kit lot number: 20110330; Determination of urea nitrogen adopts Hitachi's 7020 type automatic clinical chemistry analyzers to measure.Kit lot number: 101051.
1.5 result
1.5.1 the impact of beverage of the present invention on the mice burden swimming time
Beverage of the present invention can extend the mice burden swimming time, and with negative control group comparison, difference has significant difference (P<0.01), in Table 1.
1.5.2 the impact of beverage of the present invention on mouse swimming blood Lactate and blood lactic acid TG-AUC
Beverage of the present invention can reduce the blood Lactate after mouse swimming, relatively has significant difference (P<0.01), in Table 2 with negative control group.Meanwhile, beverage of the present invention can reduce the blood lactic acid TG-AUC of mouse swimming, relatively has significant difference (P<0.01), in Table 3 with negative control group.
1.5.3 the impact of beverage of the present invention on mice serum urea nitrogen
Beverage of the present invention can reduce mice serum urea nitrogen value, relatively has significant difference (P<0.01), in Table 4 with negative control group.
2 alleviating physical fatigue tests
2.1 materials: beverage of the present invention: be prepared from by American Ginseng, the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, rhodiola root, whey protein peptide, sodium chloride, potassium chloride etc.; Positive control: be prepared from according to prescription and preparation method in patent 201010524215.5 by ginseng, the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, whey protein peptide, sodium chloride, potassium chloride etc.; 144 male mice in kunming, body weight 18 Animal Experimental Study centers,～22g，You Hubei Province provide.
2.2 sample preparations: with 1.2.
2.3 experimental techniques: the resistance to anoxic experiment of (1) normal pressure: every group of 12 mouse, the continuous gavage of mouse 30 days, last gives 1h after tested material, each group mouse is put into respectively to the 250ml port grinding bottle (1 every bottle) that fills 5g soda lime, with vaseline, seal bottleneck, cover tightly, make it air tight, manual time-keeping immediately, take breath stopped as index, observes mouse because of the dead time of anoxic.(2) the poisoning survival experiment of natrium nitrosum: every group of 10 mouse, the continuous gavage of mouse 30 days, last gives 1h after tested material, and each treated animal is by 240mg/kgBW dosage lumbar injection natrium nitrosum (injection volume is 0.1ml/10gBW), manual time-keeping immediately, records the animals survived time.(3) Ischemia Injury in Brain anoxic experiment: the continuous gavage of mouse 30 days, last gives 1h after tested material, and each treated animal, records after mouse broken end to the dwell time of breathing of dehiscing by stopwatch by broken end only immediately from neck.
1.4 result
1.4.1 beverage of the present invention is on the impact of resistance to anoxic experiment time-to-live of mouse normal pressure
Beverage of the present invention can obviously extend the resistance to the survival time under hypoxic condition of mouse normal pressure, relatively has significant difference (P < 0.01), in Table 5 with negative control group.
1.4.2 beverage of the present invention is on the impact of poisoning survival experiment time-to-live of mouse natrium nitrosum
Beverage of the present invention can obviously extend the poisoning rear time-to-live of natrium nitrosum, relatively has significant difference (P < 0.01), in Table 6 with negative control group.
1.4.3 beverage of the present invention affecting beverage of the present invention and can obviously extend Ischemia Injury in Brain anoxic experiment mice breathing time the chmice acute cerebral ischemia anoxic experiment time-to-live, with negative control group comparison, there is significant difference (P < 0.01), see
Table 7.
2, conclusion
By above pharmacological tests, can be drawn, beverage of the present invention has alleviating physical fatigue and improves the health care of anoxia endurance.
four, the specific embodiment
With specific embodiment, the present invention is elaborated below:
Embodiment 1
Pressing column weight amount matches and gets raw material: 2 parts of the tubers of dwarf lilyturf, 1 part, the fruit of Chinese magnoliavine, 1.5 parts of dark plums, 2 parts of American Ginsengs, 3 parts of rhodiola roots, 3 parts of whey protein peptides, 0.13 part of sodium salt, 0.1 part of sylvite, 19 parts of sweeteners, 1.1 parts of acids.
Preparation method: the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, American Ginseng, rhodiola root are added to 13 times of decoctings and boil 2 hours, liquid filters, continues to add 10 times of amounts of water and decocts 1.5 hours, and merging filtrate, is cooled to room temperature, centrifugal, and supernatant is standby.Get lactalbumin Gly-His-Lys, sodium chloride, potassium chloride, sweetener, acid, add water and make in right amount abundant dissolving, merge with supernatant, add water to 1000ml stir, through 0.45 μ m diatomite micropore composite filter membrane filter, filling, sterilizing.
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 2
Pressing column weight amount matches and gets raw material: 28 parts of the tubers of dwarf lilyturf, 12 parts, the fruit of Chinese magnoliavine, 17 parts of dark plums, 15 parts of American Ginsengs, 18 parts of rhodiola roots, 18 parts of whey protein peptides, 0.2 part of sodium salt, 0.3 part of sylvite, 95 parts of sweeteners, 2.5 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 3
According to following proportioning, take raw material: 4 parts of the tubers of dwarf lilyturf, 2 parts, the fruit of Chinese magnoliavine, 2.5 parts of dark plums, 2.5 parts of American Ginsengs, 3 parts of rhodiola roots, 4 parts of whey protein peptides, 0.3 part of sodium salt, 0.15 part of sylvite, 22.5 parts of sweeteners, 1.9 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 4
According to following proportioning, take raw material: 17 parts of the tubers of dwarf lilyturf, 10 parts, the fruit of Chinese magnoliavine, 10.5 parts of dark plums, 9.5 parts of American Ginsengs, 10 parts of rhodiola roots, 14 parts of whey protein peptides, 0.8 part of sodium salt, 0.25 part of sylvite, 72.5 parts of sweeteners, 2.3 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 5
According to following proportioning, take raw material: 8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 6 parts of whey protein peptides, 0.6 part of sodium salt, 0.2 part of sylvite, 50 parts of sweeteners, 2.5 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 6
According to following proportioning, take raw material: 8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 7 parts of collagens, 0.6 part of sodium salt, 0.2 part of sylvite, 55 parts of sweeteners, 2.3 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 7
According to following proportioning, take raw material: 7.8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 7.5 parts of fish skin collagen peptides, 0.6 part of sodium salt, 0.2 part of sylvite, 58 parts of sweeteners, 2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 8
According to following proportioning, take raw material: 7.8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 6.5 parts of turtle peptides, 0.6 part of sodium salt, 0.2 part of sylvite, 48 parts of sweeteners, 1.7 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 9
According to following proportioning, take raw material: 7.8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 9.5 parts of sea cucumber peptides, 0.4 part of sodium salt, 0.18 part of sylvite, 48 parts of sweeteners, 2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 10
According to following proportioning, take raw material: 7.8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 9.5 parts of zeins, 0.4 part of sodium salt, 0.14 part of sylvite, 48 parts of sweeteners, 2.2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 11
According to following proportioning, take raw material: 8 parts of the tubers of dwarf lilyturf, 4.5 parts, the fruit of Chinese magnoliavine, 5 parts of dark plums, 3.8 parts of American Ginsengs, 4.3 parts of rhodiola roots, 9.5 parts of lactalbumins, 0.5 part of sodium salt, 0.15 part of sylvite, 50 parts of sweeteners, 1.2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 12
According to following proportioning, take raw material: 7 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4.5 parts of dark plums, 4 parts of American Ginsengs, 5 parts of rhodiola roots, 9 parts of soybean proteins, 0.45 part of sodium salt, 0.17 part of sylvite, 42 parts of sweeteners, 1.5 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 13
According to following proportioning, take raw material: 6 parts of the tubers of dwarf lilyturf, 2 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 6 parts of soybean oligopeptides, 0.55 part of sodium salt, 0.15 part of sylvite, 40 parts of sweeteners, 3 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 14
According to following proportioning, take raw material: 10 parts of the tubers of dwarf lilyturf, 3 parts, the fruit of Chinese magnoliavine, 6 parts of dark plums, 4 parts of American Ginsengs, 6 parts of rhodiola roots, 9 parts of collagen peptides, 0.4 part of sodium salt, 0.12 part of sylvite, 48 parts of sweeteners, 1.2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 15
According to following proportioning, take raw material: 7.8 parts of asparagus ferns, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of ginsengs, 3 parts of rhodiola roots, 9.5 parts of zeins, 0.4 part of sodium salt, 0.14 part of sylvite, 48 parts of sweeteners, 2.6 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 16
According to following proportioning, take raw material: 8 parts of the root of straight ladybell, 4.5 parts, the fruit of Chinese magnoliavine, 5 parts of dark plums, 3.8 parts of American Ginsengs, 4.3 parts of rhodiola roots, 9.5 parts of lactalbumins, 0.5 part of sodium salt, 0.15 part of sylvite, 50 parts of sweeteners, 2.2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 17
According to following proportioning, take raw material: 7 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4.5 parts of dark plums, 4 parts of ginsengs, 5 parts of rhodiola roots, 9 parts of soybean proteins, 0.45 part of sodium salt, 0.17 part of sylvite, 42 parts of sweeteners, 2.5 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 18
According to following proportioning, take raw material: 6 parts of the tubers of dwarf lilyturf, 2 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of Radix Codonopsis, 3 parts of rhodiola roots, 6 parts of soybean oligopeptides, 0.55 part of sodium salt, 0.15 part of sylvite, 40 parts of sweeteners, 1.9 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 19
According to following proportioning, take raw material: 8 parts of asparagus ferns, 3 parts, the fruit of Chinese magnoliavine, 5 parts of dark plums, 4 parts of radix pseudostellariaes, 5 parts of rhodiola roots, 9 parts of zeins, 0.4 part of sodium salt, 0.12 part of sylvite, 48 parts of sweeteners, 1.8 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 20
According to following proportioning, take raw material: 7 parts of asparagus ferns, 2.5 parts, the fruit of Chinese magnoliavine, 5 parts of dark plums, 4 parts of radix pseudostellariaes, 5 parts of rhodiola roots, 9 parts of sea cucumber peptides, 0.4 part of sodium salt, 0.12 part of sylvite, 60 parts of sweeteners, 2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Embodiment 21
According to following proportioning, take raw material: 7 parts of the tubers of dwarf lilyturf, 2.5 parts, the fruit of Chinese magnoliavine, 5 parts of dark plums, 4 parts of the Radixs Astragali, 5 parts of rhodiola roots, 3 parts of fish skin collagen peptides, 3 parts of lactalbumins, 0.4 part of sodium salt, 0.12 part of sylvite, 62 parts of sweeteners, 2 parts of acids.
Preparation method is with embodiment 1
Raw material as above, sodium chloride can be used any or several replacements in sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate; Potassium chloride can be used any or several replacements in saleratus, potassium acetate, potassium citrate; Sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
Preparation method as above, is characterized in that finished dosage forms can be the formulation that adopts pharmaceutically acceptable carrier or excipient to make, as granule, tablet, capsule, soft capsule, pill, pill.
Preparation method as above, is characterized in that finished dosage forms can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
Claims (12)
1. one kind has alleviating physical fatigue and the health drink that improves anoxia endurance, it is characterized in that mainly containing following raw material composition and weight proportion is prepared from: 1～30 part of the tuber of dwarf lilyturf, 1～20 part, the fruit of Chinese magnoliavine, 1～20 part of dark plum, 1～20 part of American Ginseng, 1～20 part of rhodiola root, 1～20 part of whey protein peptide, 0.1～2 part of sodium salt, 0.05～0.5 part of sylvite, 0.1～120 part of sweetener, 0.1～8 part of acid.
2. health drink as claimed in claim 1, wherein the weight proportion of each raw material is: 4～18 parts of the tubers of dwarf lilyturf, 2～12 parts, the fruit of Chinese magnoliavine, 2～12 parts of dark plums, 2～10 parts of American Ginsengs, 2～10 parts of rhodiola roots, 3～15 parts of whey protein peptides, 0.3～1.5 part of sodium salt, 0.1～0.35 part of sylvite, 0.2～90 part of sweetener, 0.5～4 part of acid.
3. health drink as claimed in claim 1 or 2, wherein the weight proportion of each raw material is: 8 parts of the tubers of dwarf lilyturf, 4 parts, the fruit of Chinese magnoliavine, 4 parts of dark plums, 3 parts of American Ginsengs, 3 parts of rhodiola roots, 6 parts of whey protein peptides, 0.6 part of sodium salt, 0.2 part of sylvite, 50 parts of sweeteners, 2.5 parts of acids.
4. the health drink as described in claim 1～3, any one or more that it is characterized in that American Ginseng can be in ginseng, Radix Codonopsis, radix pseudostellariae or the Radix Astragali substitutes.
5. the health drink as described in claim 1～3, is characterized in that can changing into any in asparagus fern, the root of straight ladybell the tuber of dwarf lilyturf.
6. the health drink as described in claim 1～3, it is characterized in that sodium salt can be any or several in sodium chloride, sodium acetate, gluconic acid sodium salt, sodium sulphate, sodium ethylene diamine tetracetate, sodium carbonate, natrium citricum, trisodium citrate, preferably sodium chloride; Sylvite can be any or several in potassium chloride, saleratus, potassium acetate, potassium citrate, preferably potassium chloride.
7. the health drink as described in claim 1～3, is characterized in that can using any or several replacements in lactalbumin, collagen, soybean protein, zein, soybean oligopeptide, collagen peptide, fish skin collagen peptide, turtle peptide, sea cucumber peptide by whey protein peptide.
8. the health drink as described in claim 1～3, is characterized in that sweetener can be any one or more in white granulated sugar, glucose, starch syrup, malt syrup, glucose syrup, maltitol, xylitol, antierythrite, oligoisomaltose, Sucralose, Aspartame, stevioside, acesulfame potassium or honey element; Acid can be any one or more in citric acid, malic acid, tartaric acid, lactic acid, phosphoric acid, glutamic acid, magnesium phosphate, C-aspartic acid, tricalcium phosphate, potassium glutamate.
9. the health drink as described in claim 1～3, it is characterized in that preparation method takes the tuber of dwarf lilyturf, the fruit of Chinese magnoliavine, dark plum, American Ginseng, rhodiola root by recipe quantity, twice of boiling, add 10～15 times of amounts of water decocts 1～3 hour at every turn, collecting decoction, be cooled to room temperature, centrifugal through supercentrifuge, supernatant is standby; By recipe quantity, take lactalbumin Gly-His-Lys, sodium chloride, potassium chloride, sweetener, acid again, add water and make in right amount abundant dissolving, merge with supernatant, add purified water and be settled to 1000mL, mix, filter, filling, sterilizing, obtains.
10. health drink as claimed in claim 9, is characterized in that finished dosage forms can also be granule, tablet, capsule, soft capsule, pill, the pill that adopts pharmaceutically acceptable carrier or excipient to make.
11. health drinks as claimed in claim 9, is characterized in that finished product can also be to adopt acceptable excipient or food additives on food, the food that food preparation technology makes routinely.
12. health drinks as described in claim 1～3, is characterized in that preparing alleviating physical fatigue and improve the food of anoxia endurance or the application in health products.
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| CN110559354A (en) * | 2019-09-02 | 2019-12-13 | 西南科技大学 | Compound rhodiola rosea composition and preparation method thereof |
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| CN115153032A (en) * | 2022-05-25 | 2022-10-11 | 北京东方红航天生物技术股份有限公司 | Composition for promoting health of sports people and preparation method thereof |
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| CN105029447A (en) * | 2015-08-11 | 2015-11-11 | 湖南科尔生物技术有限公司 | Sea-fish oligopeptide powder containing activated probiotics |
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| CN106333356A (en) * | 2016-04-14 | 2017-01-18 | 安徽华瑞医药技术开发有限公司 | Functional food for improving anoxia endurance of athletes |
| CN106343544A (en) * | 2016-06-08 | 2017-01-25 | 安徽华瑞医药技术开发有限公司 | Functional food capable of relieving chronic fatigue syndrome |
| CN107691952A (en) * | 2017-08-22 | 2018-02-16 | 北京同仁堂健康药业股份有限公司 | A kind of resisting kinetic fatigue, the composition for promoting postexercise recovery and preparation method thereof |
| CN107853622A (en) * | 2017-11-17 | 2018-03-30 | 荣成奥汛海洋生物科技有限公司 | One kind improves anoxia endurance and chews piece and preparation method thereof |
| WO2019191947A1 (en) * | 2018-04-04 | 2019-10-10 | 浙江泛亚生物医药股份有限公司 | Isaria cicadae miquel-hippophae fructus sports drinks and preparation method therefor |
| CN110559354A (en) * | 2019-09-02 | 2019-12-13 | 西南科技大学 | Compound rhodiola rosea composition and preparation method thereof |
| CN113397076A (en) * | 2021-06-25 | 2021-09-17 | 长春帮尔保健食品有限公司 | Traditional Chinese medicine beverage composition and preparation method thereof |
| CN115153032A (en) * | 2022-05-25 | 2022-10-11 | 北京东方红航天生物技术股份有限公司 | Composition for promoting health of sports people and preparation method thereof |
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Denomination of invention: A health drink that can alleviate physical fatigue and improve hypoxia tolerance Effective date of registration: 20231127 Granted publication date: 20160420 Pledgee: Jiangxi Guofang Asset Operation Co.,Ltd. Pledgor: Jiangzhong dietotherapy Technology Co.,Ltd. Registration number: Y2023980067616 |