197results about How to "Quick effect" patented technology

The invention belongs to the technical field of veterinary preparations, and particularly relates to a tilmicosin premix and a preparation method thereof. The tilmicosin premix is prepared from the following raw materials: tilmicosin, a polylactic acid-glycolic acid copolymer, lecithin, modified hydroxypropyl methyl cellulose, grafted polyvinylpyrrolidone, polyethylene glycol and an antioxidant, a solid dispersion is formed through lecithin and grafted polyvinylpyrrolidone, the solubility and stability of tilmicosin are enhanced, polylactic acid-glycolic acid copolymer nano-microspheres are prepared through a double-emulsion solvent evaporation method, slow release of drugs is achieved, dodecyl modified hydroxypropyl methyl cellulose and polyethylene glycol are combined, and the sustained release effect is achieved. The solubility and the slow release characteristic are further enhanced. The activity of the granular premix is effectively preserved, and the granular premix is convenient to use and transport.

The invention relates to application of HGF mRNALNP in preparation of medicine for treating emphysema, and belongs to the field of biomedicine.The HGF mRNALNP is delivered to the lung through a lipid nanoparticle carrier LNP for the first time, experiments prove that the HGF mRNALNP is high in in-vivo expression efficiency, high in lung tissue targeting performance and capable of effectively promoting repair of lung tissue structures of mice with emphysema, and the HGF mRNALNP can be used for preparing medicine for treating emphysema. The method has the characteristics of minimally invasive property and high efficiency.

The invention relates to the field of food and health care products, and discloses a composition for dispelling effects of alcohol and protecting liver, which comprises 20-100 parts of ampelopsis grossedentata leaf extract; 50 to 200 parts of a radix puerariae extract; 10-50 parts of a semen hoveniae extract; 10-50 parts of a turmeric extract; 10 to 100 parts of a yeast extract; 5-50 parts of a licorice extract; and 5 to 20 parts of pyrroloquinoline quinone disodium salt. The ampelopsis grossedentata leaf extract, the kudzuvine root extract and the hovenia dulcis thunb extract are utilized, alcohol decomposition is promoted, the blood ethanol concentration is reduced, and drunkenness symptoms are relieved. Puerarin improves activity of liver metabolic enzymes, accelerates discharge of ethanol and acetaldehyde, and reduces liver damage. The anti-oxidation effects of dihydromyricetin and PQQ can eliminate alcohol metabolism free radicals and protect liver cells. The components such as puerarin, hovenia dulcis thunb, curcumin and glycyrrhizic acid jointly promote liver cell regeneration, inflammation and oxidative damage are reduced, the levels of ALT and AST in serum are reduced, and liver health is maintained.

The invention discloses a traditional Chinese medicine composition for treating acute exacerbation of chronic obstructive pulmonary disease, which is prepared from the following raw materials in parts by weight: 6-9 parts of honey-fried ephedra, 30-40 parts of gypsum, 6-9 parts of fried semen armeniacae amarae, 9-15 parts of fructus perillae, 9-15 parts of semen lepidii, 9-15 parts of radix asteris, 9-12 parts of radix peucedani, 9-12 parts of cynanchum glaucescens, 9-15 parts of thunberg fritillary bulb, 9-15 parts of honey-fried folium eriobotryae, 6-12 parts of rhodiola rosea and 6-9 parts of liquorice. Through scientific compatibility of the traditional Chinese medicine raw materials, clinical symptoms of patients in the acute exacerbation period of the chronic obstructive pulmonary disease can be effectively relieved, the acute exacerbation frequency and degree of the patients with the chronic obstructive pulmonary disease are reduced, and lung function decline is delayed. The traditional Chinese medicine composition is free of toxic and side effects and has the advantages of being good in curative effect, fast in effect taking, high in medicine effect, not prone to relapse and the like in the aspect of treating chronic obstructive pulmonary acute exacerbation.

The invention relates to the field of epilepsy, in particular to application of alprazolam gel particles in preparation of a medicine for treating the state of epilepsy. The invention provides application of alprazolam gel particles in preparation of a medicine for treating and / or preventing epileptic seizure of a subject, and is characterized in that the alprazolam gel particles are prepared by the following steps: S101, dropwise adding an alprazolam solution into a first solution to form an internal phase solution; s102, forming a preliminarily cured pre-crosslinked liquid drop; s103, forming cured particles; and S104, obtaining the alprazolam gel particles. The blood brain barrier transmittance of the alprazolam gel particles provided by the invention can reach 1.5-2 times that of the prior art, and the alprazolam gel particles are high in effect taking speed, have dual properties of quick release and continuous release, and are suitable for effective and timely treatment of epileptic seizure patients.

The invention provides a preparation composition of a glucagon-like peptide-1 receptor agonist for nasal mucosa administration, and particularly relates to the technical field of biological medicine materials. The preparation composition mainly comprises a glucagon-like peptide-1 receptor stimulant, alkyl glycoside and phospholipid, wherein the ratio of the glucagon-like peptide-1 receptor stimulant to the alkyl glycoside to the phospholipid is (0.25-17.5): (0.25-10): (0.1-10) by mass. The active pharmaceutical ingredients in the preparation composition provided by the invention are delivered through nasal mucosa, directly enter blood circulation from an absorption part, can take effect quickly, have higher bioavailability, and improve the compliance of patients.

The present invention relates to a pharmaceutical composition with joint repair efficacy, which is composed of collagen, chitosan and a pharmaceutically acceptable carrier, wherein the weight ratio of collagen to chitosan in the composition is 11:1-1:11, the average molecular weight of collagen is 3kDa-500kDa, and the weight average molecular weight of chitosan is 10000-200000. The pharmaceutical composition of the present invention is used to treat and relieve pain caused by joint cavity stenosis and bone wear, effectively prevent and treat traumatic or degenerative osteoarthritis, and has the advantages of good water solubility, good biocompatibility, fast onset, good repair effect, good stability, good re-dissolution stability, long effective period, easy storage, etc.

The invention discloses a python oil compound for treating skin burns, scalds and cuts and a preparation method thereof, and relates to the technical field of traditional Chinese medicine. The python oil compound formula is composed of python oil extract, aloe, borneol, jade square gold tablets, psoralea corylifolia, scutellaria baicalensis, rosmarinus officinalis, sophora flavescens extract, cnidium monnieri and glycerol. Appropriate raw materials are weighed in parts by weight, and the python oil compound is obtained through screening, crushing, boiling and cooling. The python oil compound for treating skin burns, scalds and cuts provided by the invention has a reasonable ratio of Chinese medicinal materials, has strong permeability, can promote blood circulation, has obvious analgesic effect, can repair damaged cells, is not easy to leave scars after healing, and has the advantages of simple preparation process and convenient product use.

The invention relates to the technical field of fishery breeding baits, and particularly discloses a fermentation inoculant for fermenting artemia, the fermented artemia and a preparation method of the fermented artemia. The fermentation inoculant for fermenting artemia at least comprises a compound of phaffia rhodozyma, lactobacillus johnsonii, lactobacillus rhamnosus and bifidobacterium lactis. The method has the advantage that artemia does not decay for a long time at normal temperature.

The invention provides a compound as shown in a formula I, or pharmaceutically acceptable salt or ester, prodrug, optical isomer, stereoisomer or solvate thereof. The compound disclosed by the invention can be used for preparing medicines for preventing or treating pain and related diseases thereof, so that a brand new material basis is laid for developing the pain and the related diseases thereof. # imgabs0 #

The invention discloses a preparation method of a hydroxyapatite pre-filling needle, which comprises the following steps: dispersing low-viscosity sodium carboxymethyl cellulose in water, adding a calcium salt solution, and uniformly mixing, so that part of sodium ions are replaced by calcium ions; adding a sodium carboxymethyl cellulose solution with medium viscosity; 3) adding a solution of phosphate or hydrophosphate or dihydric phosphate or a mixed salt of phosphate or hydrophosphate or dihydric phosphate, adjusting the pH value to 10-11, uniformly mixing, and standing for 1-7 days C, wherein the amount of phosphate ions is 40-60% of the amount of calcium ions; a calcium salt solution is added, the amount of calcium ions accounts for 60%-80% of the total amount of positive ions in the low-viscosity carboxymethyl cellulose and the medium-viscosity carboxymethyl cellulose, and the mixture is evenly mixed and aged for 1-7 days; and if necessary, filtering by using a nanofiltration membrane to remove small molecular substances. The pre-filling needle can achieve the unification of quick effect, high efficiency and slow release.

The invention belongs to the technical field of biological medicine, and provides an engineered extracellular vesicle, a preparation method, application and a drug for targeted repair of blood brain barrier in order to solve the technical problems that an existing repair tool takes effect slowly and is not enough in specificity, and the engineered extracellular vesicle is loaded with Wnt7a-K190A protein. After entering the brain, the engineered extracellular vesicle can be rapidly and specifically combined with a Gpr124 receptor to promote blood brain barrier repair, and in-vivo experiments verify that the engineered extracellular vesicle can promote blood brain repair, so that the engineered extracellular vesicle can be applied to preparation of targeted blood brain barrier repair drugs, becomes a supplement of existing tools, AAV, LNP and the like, and has a wide application prospect. Particularly, the high requirement on the treatment timeliness of central nervous system (injury irreversibility) diseases is met.

The invention discloses a traditional Chinese medicine composition for treating chronic obstructive pulmonary disease in a stable phase, which is prepared from the following raw materials in parts by weight: 6-9 parts of cordyceps sinensis, 15-30 parts of astragalus membranaceus, 12-15 parts of wine-processed rhizoma polygonati, 6-12 parts of rhodiola rosea, 3-6 parts of honey-fried ephedra, 6-9 parts of fried semen armeniacae amarae, 9-15 parts of semen lepidii, 9-12 parts of honey-fried radix asteris, 9-12 parts of fried fructus perillae, 6-9 parts of ginkgo kernel, 9-12 parts of earthworm and 6-9 parts of liquorice. Through scientific compatibility of the traditional Chinese medicine raw materials, clinical symptoms of chronic obstructive pulmonary disease patients in the stable phase can be effectively relieved, the acute exacerbation frequency of the chronic obstructive pulmonary disease patients is reduced, and lung function decline is delayed. The traditional Chinese medicine composition is free of toxic and side effects and has the advantages of being good in curative effect, fast in effect taking, high in medicine effect, not prone to relapse and the like in the aspect of treating chronic obstructive pulmonary disease.

The invention relates to the technical field of traditional Chinese medicines, in particular to a hangover-alleviating, liver-protecting and stomach-protecting agent and a preparation method thereof. The alcohol effect dispelling, liver protecting and stomach protecting agent is prepared from the following raw material components in parts by mass: 1-10 parts of peristrophe japonica, 1-10 parts of penthorum chinense pursh, 1-10 parts of flos puerariae, 1-10 parts of radix puerariae, 1-10 parts of lalang grass rhizome, 1-10 parts of hovenia dulcis thunb and 1-5 parts of taurine. The traditional Chinese medicine composition has better hangover-alleviating and liver-protecting effects, obviously shortens the hangover-alleviating and sobering time, is taken before drinking, takes effect faster, has the effects of alleviating hangover, inducing resuscitation, strengthening the spleen and stomach, calming the adverse-rising energy, arresting vomiting and protecting the liver, reduces AST and ALT in human serum, can enhance the activity of ethanol dehydrogenase and acetaldehyde dehydrogenase in the human liver, and promotes ethanol metabolism.

The tissue repair preparation at least comprises ECM, exosome and degradable glue, the ECM is an acellular matrix such as SIS, SIM and UBM, is granular and is injectable micro powder, and the content of the ECM is 10-50 mg / ml; the exosome is a healing-promoting cell, and is obtained by induction, polarization culture, centrifugation, supernatant collection and concentration and purification. The degradable glue is a polysaccharide with viscoelasticity; the advantages of a conventional filling agent are reserved, exosomes can be slowly released and internalized by various tissue cells, the activity of fibroblasts can be stimulated, the effect is lasting, and generation of new collagen is promoted; the defects of short effect and non-lasting effect of the existing filling agent are overcome; the product provided by the invention can achieve the effects of promoting rapid regeneration of collagen and maintaining for a long time; the functions of filling, face-lifting, tissue repairing and the like are achieved; the effect is remarkable, stable and lasting; the composition has multiple functions of quick effect, obvious effect and slow release and long-acting effect.

The invention discloses a semen ziziphi spinosae nerve soothing and sleep aiding liquid which is introduced into a micro-current application of a human body, and the semen ziziphi spinosae nerve soothing and sleep aiding liquid comprises 5-10 parts of semen ziziphi spinosae, 2-3 parts of poria cocos, 4-8 parts of tea leaf theanine, 3% of water-soluble azone and 2% of borneol. The micro-current application comprises a medical non-woven fabric layer, a printing primary battery layer, a composite microcapsule liquid medicine layer and a medical proof fabric layer which are sequentially connected in the direction facing the skin of the human body, the medical proof fabric layer is used for being pasted on the skin, and the composite microcapsule liquid medicine layer contains semen ziziphi spinosae nerve soothing and sleep aiding liquid. The invention solves the problems that the traditional semen ziziphi spinosae nerve-calming sleep-aiding liquid is sweet and bitter when being orally taken and decocted, is unwilling to take, takes effect slowly, is uncomfortable in digestive system and is large in dosage. The nerve-soothing and sleep-aiding liquid and the micro-current application prepared by adopting the iontophoresis technology are used together, so that the micro-current application has the advantages that the effect is quick, the micro-current application can permeate into a human body through the skin to bypass the digestive tract and the metabolic process, the stimulation and burden on the gastrointestinal tract are reduced, and the convenience and flexibility are realized.

The invention relates to a reinforced composite material, in particular to a fiber reinforced composite material which comprises unprocessed cellosilk raw materials and thermoplastic high-molecular polymer raw materials, cellosilk is one or more of carbon fibers, glass fibers, Kevlar fibers, UHMWPE fibers, basalt fibers, bamboo fibers, jute fibers and metal fibers, the thermoplastic high-molecular polymer raw materials are thermoplastic high-molecular polymer raw materials, the thermoplastic high-molecular polymer raw materials are thermoplastic high-molecular polymer raw materials, and the thermoplastic high-molecular polymer raw materials are thermoplastic high-molecular polymer raw materials. The thermoplastic high-molecular polymer comprises but is not limited to one or a mixture of more of polylactic acid (PLA), polyethylene glycol terephthalate (PET / PETG), polyethylene (PE), polypropylene (PP), acrylonitrile butadiene styrene (ABS), polycarbonate (PC), polyamide (PA), polyphenylene sulfide (PPS) and polyether-ether-ketone (PEEK). The compatilizer and other small materials are used for increasing the bonding property of the thermoplastic resin and the fiber to be impregnated, the quality of the fiber reinforced composite material is improved, and the continuous fiber reinforced thermoplastic resin impregnated wire rod used for the fused deposition process is obtained.

The invention relates to a solid orodispersible pharmaceutical dosing unit having a weight between 30 and 1000 mg, this dosing unit containing at least 100 µg of an estetrol component selected from estetrol, estetrol esters and combinations thereof; the solid dosing unit being obtainable by a process comprising the steps of: ⋅ providing an aqueous liquid comprising water, an estetrol component and optionally one or more other pharmaceutically acceptable ingredients; ⋅ mixing 1 part by weight of the aqueous liquid with 0.5 to 20 parts by weight of the carrier particles to produce wet particles; ⋅ removing water from the wet particles to produce charged particles; ⋅ optionally, mixing the charged particles with one or more tablet-making excipients;and to form the charged particles or mixture of charged particles and the tablet manufacturing excipient(s) in a solid dosing unit. The solid dosing unit is easy to manufacture and perfectly suited for sublingual, buccal or sublabial administration.

The present invention discloses an algae in-situ treatment device, including a cyanobacteria collection barrel, an inner shell, an electrode module, and an aeration module. The inner shell is arranged in the cyanobacteria collection barrel, and the inner shell includes an inner shell shell and a water outlet channel. The inner shell shell is fixedly connected to the inner wall of the cyanobacteria collection barrel through a connecting rod, and the water outlet channel is arranged at the top of the inner shell shell. The electrode module is arranged on the inner shell, and the electrode module includes an electrode plate and a gasket. A gasket is arranged between each electrode plate and the inner shell. The aeration module includes an air inlet pipe and an aeration pipe. The air inlet pipe runs through the cyanobacteria collection barrel, and the aeration pipe is arranged on the air inlet pipe in the cyanobacteria collection barrel. The device of the present invention can generate ions through electrolysis of the electrode module to form a flocculent gel, sweep and capture the algae in the water to form flocculation precipitation, and form bubbles in the water body through the airflow of the aeration pipe to disperse and escape, thereby improving the flocculation effect, and the device structure is relatively simple, easy to operate, and does not consume a lot of manpower and material resources.

The invention discloses a traditional Chinese medicine composition for reducing phlegm and dampness and dispersing nodules and a preparation process thereof, and relates to the technical field of traditional Chinese medicine preparation, and the preparation process comprises the following steps: cleaning medicinal materials, crushing and pretreating, extracting the treated medicinal materials by using an ultrasonic-assisted extraction technology, crushing the extracted effective components into superfine powder by using a superfine crushing technology, and preparing the traditional Chinese medicine composition for reducing phlegm and dampness and dispersing nodules. Mixing the ultrafine powder with a 3D printing material, and printing the medicine material into pills by using a photocuring 3D printer, the preparation method has the advantages that the pills with complex internal structures, such as a multilayer structure, a hollow structure and a porous structure, can be constructed through a 3D printing technology, and the special structures can realize accurate control of drug release, so that the preparation method is simple and easy to operate, and the application prospect is wide. The medicine is released according to the preset speed and time, a better treatment effect is achieved, the double-layer structure pill with the outer layer capable of rapidly releasing and the inner layer capable of slowly releasing is designed, the pill can rapidly take effect in a short time, and meanwhile the long-time medicine effect is maintained.

The present application belongs to the technical field of medicine, and particularly relates to a traditional Chinese medicine composition and application thereof in preparation of an oral care product. The traditional Chinese medicine composition is prepared from 12-18 parts of Qingdai, 7-12 parts of raw gypsum, 7-12 parts of Huangqi, 9-15 parts of Gushugu, 3-7 parts of Honghuajiao, 3-7 parts of Baizhi, 6-10 parts of Fangfeng, 1-5 parts of Bajie, 6-10 parts of Huanylencao, 1-5 parts of Wuji, and 4-8 parts of Baiji as raw medicinal materials. The components of the composition are reasonably matched, and can realize multiple effects of analgesia, antibiosis, anti-inflammation, repair, and tooth fixation and health. The present application is suitable for all kinds of toothache patients, has a wide application range, a safe use mode, and a wide market application prospect.

The invention discloses an isoxazoline substituted picolinamide compound as well as a preparation method and application thereof. The isoxazoline substituted picolinamide compound has broad-spectrum and efficient insecticidal activity, is safe to non-target organisms, and is more beneficial to crop protection and environmental safety.

The invention discloses a MaR1 nano-composite and a preparation method and application thereof, and belongs to the technical field of biological medicine, the MaR1 nano-composite comprises a liposome, a targeting peptide, and MaR1 or pharmaceutically acceptable salt thereof entrapped in the liposome. According to the invention, the effective drug MaR1 and the myocardial targeting peptide are connected by adopting lipidosome, and nano precipitation is carried out by using a microfluid mixing channel, so that the nano drug has high bioavailability and stability. The MaR1 nano-liposome drug prepared by the invention has the characteristics of high bioavailability, stable property, quick response, low side effect and the like, and has a remarkable protective effect on myocardial reperfusion injury.

The invention discloses a benidipine hydrochloride tablet. The benidipine hydrochloride tablet is a preparation formed by coating a tablet core with a coating solution, the tablet core is formed by mixing and pressing material particles with the following particle sizes in proportion: gt; 0.8%-8% of 20 meshes, 5%-20% of 20-40 meshes, 9%-21% of 40-60 meshes, 15%-48% of 60-80 meshes and 20%-51% of 80-100 meshes; 3-21% of 100 mesh; the material particles comprise the following raw and auxiliary materials in parts by weight: 2-5 parts of benidipine hydrochloride, 76-99 parts of a diluent, 1-2 parts of an adhesive and 0.5-1.5 parts of a lubricant. According to the invention, a specific process of stirring, cutting and atomizing is adopted, so that the raw and auxiliary materials in the tablet are uniformly mixed, material particles with specific granularity are easily prepared for tabletting, the preparation process is simple, and the obtained tablet has the advantages of low content of related substances, stable property, quick dissolution and quick effect, and has practical popularization and application values.

The invention belongs to the field of cosmetics, and relates to an acne-removing composition and application thereof, acne-removing essence containing the composition and a preparation method of the acne-removing essence, and the acne-removing composition is prepared from the following components in parts by weight: 5-10 parts of centella asiatica extract, 1-10 parts of PCA zinc, 1-10 parts of water-soluble salicylic acid, 1-10 parts of peony root and bark extract, 1-10 parts of folium artemisiae argyi extract and the balance of pure water. The composition is simple in medicine use and proper in compatibility, the problem of removing or relieving the acne on the skin is solved by solving two factors (oil control and bacteriostasis) which influence the generation of the acne, and meanwhile, the safety problems of skin irritation, sensitivity and the like which are left by conventional products are not caused.

The application discloses a kind of cosmetics suitable for sensitive skin and preparation method thereof, preparation raw materials include A phase, B phase, C phase and D phase;The preparation raw materials of A phase include emulsifier, emollient, thickening agent, antioxidant;The preparation raw materials of B phase include water, humectant, chelating agent, thickening agent B;The preparation raw materials of C phase include emulsifier C, humectant C, plant extract;The preparation raw materials of the D phase include preservative.The application does not contain synthetic pigment, plastic micro powder, mineral oil and other harmful ingredients of skin, nature is mild, no stimulation, no toxic side effect, the subject is continuously used the cosmetic prepared by the application 28 days, and the decrease rate of lactic acid stinging score compared with base value is 50.38%, and product effect is remarkable, and effect is fast.

The present invention provides a refrigeration unit that can achieve the wide range temperature requirements in the refrigerated compartment, including a normal refrigeration unit, an ultra-low temperature auxiliary refrigeration unit and a heat exchanger. The normal refrigeration unit and the ultra-low temperature auxiliary refrigeration unit are respectively equipped with evaporators. The refrigerant after heat release and refrigeration by the condenser in the normal refrigeration unit is output in two ways. The first way is delivered to the first evaporator through the first stop valve and the first thermal expansion valve, and the second way is delivered to the first heat exchange path of the heat exchanger through the second stop valve and the second thermal expansion valve. In the ultra-low temperature auxiliary refrigeration unit, the condenser is replaced by a heat exchanger, and the refrigerant in the ultra-low temperature auxiliary refrigeration unit flows through the second heat exchange path of the heat exchanger to release heat. The unit is equipped with an additional ultra-low temperature auxiliary refrigeration unit and relies on the refrigeration of the normal refrigeration unit for heat dissipation, thereby widening the temperature range of the refrigerated vehicle, playing the role of ultra-low temperature refrigeration under special circumstances, and improving the matching degree of the product to special needs.

The controlled release type ultrasonic rectal suppository comprises a specially-made suppository, an ultrasonic device, a regulation and control device, a power supply device and placing and taking-out accessories, and all the devices are modularly combined and can be detached and replaced. The controlled-release ultrasonic rectal suppository disclosed by the invention is suitable for children with faint of acupuncture, injection phobia, obesity and too low age, has no stimulation and pain sensation, is wide in applicable drug range, is particularly suitable for water-soluble macromolecular drugs, does not need to add a mucous membrane absorption enhancer, overcomes the defects of large difference of absorption individuals and slow effect of the conventional suppository administration, and is suitable for clinical application. The effect of promoting rapid absorption of the medicine is achieved.

The invention provides a traditional Chinese medicine composition for treating children atopic dermatitis and a preparation method thereof, and relates to the technical field of traditional Chinese medicine compositions. The traditional Chinese medicine composition comprises the following raw materials: 4-8 parts of rhizoma atractylodis, 6-10 parts of honeysuckle, 4-8 parts of cortex phellodendri, 4-8 parts of semen coicis, 4-8 parts of radix achyranthis bidentatae, 2-8 parts of radix sophorae flavescentis, 4-8 parts of cortex dictamni, 4-8 parts of fructus kochiae, 2-8 parts of cicada slough and The preparation method comprises the following steps: soaking the traditional Chinese medicinal materials in water, heating, refluxing, extracting, filtering and taking filtrate; concentrating the filtrate into clear paste, cooling, adding ethanol, standing, taking supernate, recovering ethanol, performing secondary concentration to obtain traditional Chinese medicine ointment, and granulating the traditional Chinese medicine ointment. The traditional Chinese medicine and modern pharmacological actions are combined to achieve the effects of clearing heat, eliminating dampness, tonifying spleen, excreting dampness, dispelling wind and arresting itching; in practical application, the traditional Chinese medicine composition has obvious improvement and cure conditions on children atopic dermatitis symptoms, and has the advantages of quick response, short curative effect, low side effect and no relapse after healing.

This invention discloses a traditional Chinese medicine composition for replenishing qi and nourishing blood, and its preparation method, belonging to the technical field of food-medicine homology traditional Chinese medicine health care preparations. The composition of this invention uses oyster peptide powder, compound amino acid powder, polygonatum powder, maca powder, eucommia male flower powder, ginseng powder, cordyceps powder, and earthworm protein peptide powder as core active ingredients, supplemented with deer antler powder, deer tendon powder, and deer blood peptide powder to enhance the effects of strengthening the body and nourishing blood. It is combined with xylitol, corn starch, maltodextrin, magnesium stearate, and caramel color as molding excipients. The dosage of each component is precisely controlled. Through a proprietary preparation process involving raw material pretreatment, segmented gradient mixing, and refined post-processing, a 1g / tablet formulation is prepared. The formulation of this invention is rigorously formulated, with clear distinctions between principal, assistant, and adjuvant ingredients, and each component synergistically enhances its effect. It can fundamentally improve problems such as qi and blood deficiency, insufficient vital energy, fatigue, and physical weakness. It has comprehensive efficacy, rapid onset of action, and wide applicability, possessing extremely high industrial promotion and health care application value.