93results about How to "Play an anti-inflammatory role" patented technology

The invention provides mouth wash for oral hygiene and health care. The mouth wash for oral hygiene and health care comprises the following components in percentage by weight: 0.2-2% of small molecular active peptide, 5-15% of glycerinum, 0.5-2% of hydrogenated castor oil, 0.05-0.5% of chlorhexidine gluconate, 2.5-10% of xylitol, 0.1-0.3% of potassium sorbate, 0.01-0.03% of sucralose, 0.025-0.1% of menthol, 0.025-0.1% of sweet orange essence, 1-15% of ethanol and the balance of distilled water. The mouth wash provided by the invention has the bacteriostatic and cleaning effect on human oral cavities; in addition, the small molecular active peptide is uses together with chlorhexidine gluconate, so that the mouth wash has the effects of resisting inflammations, accelerating repair of oral mucosa, treating dental ulcer and the like.

The invention relates to the technical field of traditional Chinese patent medicine, in particular to an itch relieving and detoxifying liquid for mosquito and insect biting. The itch relieving and detoxifying liquid for mosquito and insect biting comprises the following raw materials in parts by weight: 0.1-8 parts of camphor, 0.5-20 parts of menthol, 0.01-2 parts of borneol and 75-99 parts of medical alcohol. The camphor has the functions of dispelling the pollution, killing insects, relieving itch, eliminating swelling and stopping pain; the menthol is used as an excitant and is acted on the skin or musosa and has the efficacies of cooling and relieving itch; the borneol has the functions of inhibiting bacteria and resisting inflammation; and the medical alcohol has the efficacies of disinfecting and sterilizing. The raw materials of the itch relieving and detoxifying liquid are selected from the common and easily-obtained raw materials in daily life, have low cost and unique curative effects for red and swelling and intense itching formed by the mosquito and insect biting and can be directly coated or sprayed on wounds formed by the mosquito and insect biting; and after a moment, the itch relieving and detoxifying liquid can eliminate the inflammation and remove the detoxified liquid and has the advantages of favorable curative effect, quick response, convenience for use, has no paint and adverse reaction on human body and damage to the skin as well as no toxic or side effects.

The invention relates to a scalp care solution. The scalp care solution comprises, by weight, 1-2% of salicylic acid, 5-10% of a slow-release dispersant, 1-3.5% of a sebum conditioner, 0.5-2% of a repairing agent, 1% of a plant extract and the balance water; preferably, a suitable quantity of a cooling agent such as menthol can be added. The scalp care solution does not contain an alcohol reagent,reduces scalp stimulation and further repairs the skin barrier; by proportioning the content of the components, a synergistic effect of the components is fully exerted, a patient feels comfortable during use and has no stimulation and adverse reactions, and the clinical curative effect is good.

The invention provides an additive having a function of regulating intestines and stomach of a pet as well as preparation method and application thereof, and belongs to the technical field of animal feed. The additive having the function of regulating the intestines and the stomach of the pet is prepared from the following components in parts by weight: 2 to 10 parts of lactobacillus acidophilus powder, 1 to 5 parts of fructus crataegi, 2 to 10 parts of rhizoma dioscoreae, 2 to 10 parts of poria cocos, 1 to 5 parts of liquorice root and 1 to 5 parts of pericarpium citri reticulatae, wherein the viable bacteria concentration of the lactobacillus acidophilus powder is 0.5*10<10> to 1.5*10<10> CFU (Colony Forming Unit) / g. The additive provided by the invention is capable of obviously increasing anti-stress capability of puppies in a weaning stage and regulating the gastrointestinal function, an experiment shows that compared with a control group, the prevalence rate, the appetite, the skin and hair glossiness, the activity, the daily gain and the intestinal flora composition of an experimental group are all remarkably improved, and compared with a rhizoma dioscoreae and poria cocos taste-lack group, the prevalence rate, the appetite, the skin and hair glossiness, the activity and the daily gain of the experimental group have remarkable difference.

The invention discloses a method for preparing a bee venom injection, which comprises the following steps of: (a) weighing bee venom, water for injection and octanol in a mass-to-volume ratio of 1:(20-30):(5-7); (b) dissolving the bee venom in the water for injection and then adding the octanol for extraction; separating extract liquor by using a sephadex column; and (c) freezing the bee venom for 1-2h at the temperature ranging from -10 DEG C to -15 DEG C; diluting the frozen bee venom solution to an specific amount with a prepared buffer solution; carrying out ultrafiltration by using ultrafiltration equipment, adding 0.05-0.1% of glycine, stirring, carrying out rough filtration and fine filtration and finally packaging. The bee venom injection prepared by the method has the advantage of stable quantity and high percent of pass.

The invention discloses Bacillus subtilis M406 and an application thereof to preparation of bacteriocin and cellulase. The Bacillus subtilis M406 strain is preserved with the number of CCTCC NO:M 2018234. One probiotic strain, namely, the Bacillus subtilis M406 is screened out on the basis of the thought of taking one character as main and various characters as auxiliaries, and use value of probiotic is increased. Antibacterial active substances which can be produced by the Bacillus subtilis M406 can inhibit various harmful bacteria including S. typhimurium, Salmonella enteritidis, S.aureus, E.coli and Listeria monocytogenes in animal intestines. The probiotic can ferment multiple saccharides for acid production, and pH of intestinal juice is reduced. The Bacillus subtilis M406 produces cellulase, so that structural carbohydrates in coarse fodder can be degraded effectively, part of NSP can be transformed into soluble saccharides, fats, proteins and amino acids, and nutritional value of the coarse fodder is increased.

The invention discloses a wet tissue for relieving hemorrhoid symptoms. The wet tissue consists of a conditioning liquid and non-woven fabric bearing the conditioning liquid, wherein the conditioning liquid is prepared from components in parts by weight as follows: 30-60 parts of a witch hazel extracting solution, 0.05-0.1 parts of glucose chlorhexidine, 0.01-0.05 parts of borneol, 2-5 parts of dealdehyding alcohol, 2-8 parts of propylene glycol, 0.3-1 part of a preservative, 0.05-0.3 parts of a pH regulator and 26-66 parts of deionized water. The wet tissue can effectively relieve the hemorrhoid symptoms, perform sterilization, disinfection and detumescence, reduce exudation and promote wound healing, is mild and safe, has no side or toxic effects and is convenient to use. The invention further discloses a preparation method of the wet tissue for relieving the hemorrhoid symptoms. The preparation method adopts a simple process and is convenient to operate, high in security coefficient, operability and efficiency and low in cost.

The invention discloses an acne-removal cosmetic composition containing a purslane herb extract and a preparation method thereof. The acne-removal cosmetic composition is prepared from the following raw materials of purslane herb extract, mulberry leaf extract, pine needle essential oil, betaine, liquorice root extract, loquat leaf extract, a moisturizer, an emulsifier, a pH (potential of hydrogen) regulator, a thickener and water. The acne-removal cosmetic composition has the advantages that under the cooperation function of the purslane herb extract, the mulberry leaf extract, the liquoriceroot extract, the loquat leaf extract and the pine needle essential oil, the high-efficiency and safe antibacterial effect is realized, and the propionibacterium acnes, mites and other skin parasiticbacteria colonies can be quickly killed; the inflammation and acne forming due to invasion by bacterial promoters can be prevented, and the function of diminishing inflammation is realized; the function of controlling oil is realized, the excretion of grease is inhibited, the hair follicle is dredged, the metabolism of keratinocytes is accelerated, the death cells at the skin surface are stripped,the acne scar is removed, the injured skin is repaired, and the unevenness at the surface of the lesion is eliminated.

The invention discloses a temperature sensitive injectable drug-loading controlled release system, which comprises a star-shaped poly-lactic-co-glycolic acid-methoxy polyethylene glycol segmented copolymer and a simulated body fluid, and the content of the copolymer accounts for 15-40 weight by percent. The drug-loading controlled release system exists in a state of liquid which can freely flow in or below room temperature, is rapidly changed into oyster white physical crosslinking hydrogel which cannot flow at a human body temperature, and expresses a reversible sol- gel conversion behavior; the drug-loading controlled release system can uniformly disperse a loaded drug, and exists in a state of liquid which can freely flow in or below room temperature and gel which cannot freely flow at the body temperature; as a vagina drug-loading controlled release system, the temperature sensitive injectable drug-loading controlled release system has the characteristics that contraceptive compound estrogen, progestogen and an anti-inflammation drug are loaded into a copolymer hydrogel carrier by adopting a solution blending method, and the prepared drug-loading system serves as a birth control spraying agent; the drug-loading system is sprayed into vagina after women menses, and is shaped into mesh gel and attached into a wall, and the drug is slowly and controllably released and have an effect of birth control.

The invention discloses a preparation method and application of a dexamethasone sodium phosphate-sodium alga acid composite slow-release coating. A high polymer material is soaked in a sulfuric acid solution of potassium permanganate to conduct acidizing; then the high polymer material is placed in a polymine solution to obtain an amination embellished surface; and oxidation treatment is carried out on the sodium alga acid by using periodic acid or sodium periodate to enable aldehyde groups to be exposed at the tail end of an alginic acid segment to obtain multi-aldehyde group oxidation sodium alga acid, the dexamethasone sodium phosphate solution is soluble in deionized water, and finally materials of the amination embellished surface is placed in a reaction liquid to obtain the composite coating. The technical scheme is that the dexamethasone sodium phosphate and the sodium alga acid can be fixed on the surface of an extracorporeal circulation pipeline in a surface coating mode and has anti-freezing and anti-inflammatory double activity, external medicines are durable and stable in slow-release performance, the dexamethasone sodium phosphate-sodium alga acid composite slow-release coating can replace vein heparinization in a short period, systemic inflammatory response can be lightened through slow release, and short-period operation requirements in department of cardiac surgery can be met.

The near-infrared therapeutic cupping structure is shown in figure 1, which includes a tank body 1 with elastic rubber, a small barrel 2 arranged in the tank body, two small holes 3 arranged at the bottom of the small barrel, a high-power LED near-infrared emitting diode 4 and two leading-out power lines of the near-infrared emitting diode, infuser mixed with resin glue and mineral powder for fixing the near-infrared emitting diode. The power supply device is shown in figure 2. The AC 220v / 110v power supply, a K power switch, a BX safety tube and an L indicator light are connected. The cuppingalso includes a controllable voltage-regulating device 7 and a power supply transformer B. Because the near infrared rays in the tank can penetrate the subcutaneous of the human body for about 5cm, the nitric oxide in the blood vessel can be released, the blood can be softened and the blood flow can be promoted, the nerves can be nourished, and the treatment effect of the traditional cupping canbe greatly improved.

The invention discloses a urinary catheter having anti-clogging and anti-inflammatory functions. The urinary catheter is mainly composed of a urinary catheter body, an air supply tube and a urinary catheterization head; a support frame is arranged inside the part, close to the urinary catheterization head, of the urinary catheter body, so as to prevent the urinary catheter body from getting clogged; a drug accommodating hole, in which drugs made from a photo-biotin composite medical material or other anti-inflammatory drugs are accommodated, is formed in the urinary catheterization head; a drug hole formed in the urinary catheterization head is communicated with the drug accommodating hole to enable urine to make contact with the drugs; and urine conveys the drugs to the inner wall of bladder and urethra, so that the drugs can be directly applied to focuses to achieve an anti-inflammatory effect.

The invention discloses a mouth rinsing salt solution for effectively relieving throat inflammation. The mouth rinsing salt solution is prepared from the following ingredients through combination: table salt, traditional Chinese herbal medicine extracts, fresheners, sweetening agents, edible preservatives, stabilizing agents and pure water. The mouth rinsing salt solution has the advantages that the main ingredients are all pure natural green edible ingredients; the optimized traditional Chinese herbal medicine substances are used; the special effects of clearing away heat, cooling blood, diminishing swelling, eliminating toxin, stopping pain, removing stasis, moisturizing throat and reducing phlegm are achieved; the table salt is used as a main sterilization agent; the oral bacterium breeding can be effectively inhibited on the premise of no toxic and side effects; the daily oral cavity environment is maintained; the mouth rinsing salt solution is an edible mouth rinsing salt solutionand has certain prevention and treatment effects on oral cavity diseases such as stomatitis, dental ulcer and pharyngitis.

The invention discloses a veterinary doxycycline hydrochloride freeze-dried preparation and a preparation method thereof, the veterinary doxycycline hydrochloride freeze-dried preparation consists of an active component of doxycycline hydrochloride and medical excipients, the medical excipients comprise lysine, sodium sulfite and polyvinyl pyrrolidone, the weight ratio of doxycycline hydrochloride to lysine is 1:0.8-1:1, the weight ratio of doxycycline hydrochloride to sodium sulfite is 1:0.01-1:0.05 and the weight ratio of doxycycline hydrochloride to polyvinyl pyrrolidone is 1:0.05-1:0.1. The preparation method comprises the steps of adding lysine, sodium sulfite and polyvinyl pyrrolidone in doxycycline hydrochloride according to the weight ratio, placing solution after the filtration in a tube antibiotics glass vial after sub-packaging treatment, carrying out semi-tamponade and vacuum freeze-drying, thereby obtaining the veterinary doxycycline hydrochloride freeze-dried preparation. The preparation can lead the pH value to achieve 8-8.33 after re-dissolution, thereby thoroughly solving the problem of lower pH value of the doxycycline hydrochloride veterinary drug; and the prepration is non-toxic and has the advantages of easy transportation, long storage time, no degeneration, good stability, very small intramuscular injection stimulation, low manufacturing cost and the like.

The invention provides moisturizing lotion and a preparation method thereof. The lotion takes and combines active polysaccharide as a long-acting humectant for locking skin for skin; and various special greases and various grease proportions are adopted, so that the moisturizing effect is achieved, and inflammation resistance and itching relieving further can be achieved; and the prepared productis excellent in skin feeling, is good in ductility, is liable to coat, selects a natural preservative, and is safe and free of stimulus on skin.

The invention provides new medical application of thiazolopyranone analogues, in particular relates to application of the thiazolopyranone analogues in preparation of anti-inflammatory medicines. Theinflammation is aseptic inflammation. A general structural formula of the thiazolopyranone analogues is described in the description; the thiazolopyranone analogues are free from significant cytotoxicity and can effectively inhibit the release of nitric oxide from macrophage RAW264.7 induced by LPS; an experiment for detecting nitric oxide (NO) release by using a Griess method, an ELISA assay of PGE2, a Western Blot experiment and Xylene-induced mouse ear swelling experiments prove that the thiazolopyranone analogues can inhibit the production of NO and PGE2, and reduces the expression of iNOSand COX-2 by inhibiting MAPK (ERK, JNK and p38) signaling pathways. Therefore, the thiazolopyranone compounds can be used as active substances for the preparation of the anti-inflammatory medicines.

The invention belongs to the technical field of cosmetics, and particularly relates to a high-permeability moisturizing mask and a preparation method thereof. The mask liquid contains hyaluronic acid,hydrolyzed oat protein, sodium polyglutamate, acetyl hexapeptide-1, palmitoyl pentapeptide-4, acetyl hexapeptide-8, chondrus crispus extract, a bifida yeast fermentation product lysate alcohol, phytosphingosine and other nourishing components, can effectively reach dermal tissues, quickly improve the phenomena of dryness and darkness, repair cells with damaged skin barrier function and lack of nutrients, prevent skin moisture loss, achieve the effect of continuous long-acting moisturizing, and does not generate the phenomenon of essence dripping in the use process.

The invention relates to the technical field of daily chemical products, and discloses a bath gel mainly composed of radix sophorae flavescentis extract. The body wash gel of the invention comprises an active component and a base component, and the active component is a root extract of radix sophorae flavescentis, a root extract of radix glycyrrhizae inflata and a root extract of scutellaria baicalensis. The bath gel of the invention has no irritation to skin and can make skin tender, sterilize, inhibit bacteria, reduce inflammation and relieve itching, and the preparation process of the bathgel of the invention is simple and the cost is low.

The invention relates to the field of medical correction instruments, in particular to an ingrowing nail correction device.The ingrowing nail correction device is characterized by comprising a groove-shaped hook and a bandage, the groove-shaped hook is composed of an upper curved surface and a lower curved surface, the bandage is arranged at an opening end of the upper curved surface of the groove-shaped hook, and a plurality of penetrating holes are formed in the bandage.The ingrowing nail correction device is reasonable in design, simple in structure, low in cost and comfortable to wear, has good correction effect, can be adjusted according to width of nails (toenails) of different patients and is suitable for treatment of one-side and double-side ingrowing nails.

The invention relates to the technical field of biomedicine, and particularly discloses an oligopeptide and an active peptide composition and application of the oligopeptide and the active peptide composition in preparation of a product with an anti-inflammatory effect. The oligopeptide has a structure as shown in a formula I which is described in the specification. The active peptide composition comprises the oligopeptide with the structure as shown in the formula I and active cyclic peptide with the structure as shown in a formula II; and experiments show that both the oligopeptide bifidobacterium oligopeptide-alpha and the active peptide saccharomyces cerevisiae cyclic peptide-beta can inhibit HaCaT cell inflammatory injury and apoptosis caused by LPS exposure. Therefore, the bifidobacterium oligopeptide-alpha, the saccharomyces cerevisiae cyclopeptide-beta and the composition of the bifidobacterium oligopeptide-alpha and the saccharomyces cerevisiae cyclopeptide-beta can be used as active substances in cosmetics, skin care products, foods, health care products or medicines to play an anti-inflammatory role.

The invention belongs to the technical field of plastic and cosmetic surgery, and particularly relates to a biomimetic chitosan filling agent for preventing capsule contracture and a preparation method thereof, wherein the biomimetic chitosan filling agent for preventing the capsule contracture comprises a chitosan gel, cross-linked sodium hyaluronate, a surfactant, an isotonicity adjusting agent,autologous fat stem cells, a pH adjuster, and water, and the pH adjuster is added according to an adding amount that allows the pH of the biomimetic chitosan filling agent to be 6.5 to 7.5. The biomimetic chitosan filling agent prepared by the method can reduce inflammation caused by postoperative silicone exudation and prevent the occurrence and development of the capsule contracture.

The invention discloses a compound eucommia ulmoides concentrated solution for improving the resistance of cows in the perinatal period. The solution comprises 30-35 parts of rumen bypass glucose, 10-15 parts of calcium gluconate, 8-12 parts of potassium gluconate, 25-35 parts of magnesium dipropionate, 15-20 parts of iodised salt iodized salt, 25-30 parts of soda powder, 6-8 parts of vitamin A, 5-8 parts of vitamin D, 10-15 parts of vitamin E, 10-15 parts of selenium, 1-5 parts of vitamin B12 and 1-2 parts of the eucommia ulmoides concentrated solution. The compound eucommia ulmoides concentrated solution is high in safety, easy to prepare and low in preparation cost, the raw materials are easily obtained, the nutrient, microelements and mineral elements required by the cows after delivery can be supplemented in time, the mastitis, low calcemia and other diseases caused by energy metabolic diseases and immunosuppression of the cows in the perinatal period can be well prevented and treated, the milk quality can also be improved, the milk yield is increased, the breeding cost can be lowered, and the solution has high economic benefit.

The invention discloses an anti-bacterial pants-type sanitary towel comprising a pants body. An elastic band is arranged at the position of a waist opening of the pants body, elastic fastening strips are arranged at positions of leg openings of the pants body, a moisture-absorbing core layer is further arranged at the bottom of the pants body, and anti-bacterial gel is arranged inside the moisture-absorbing core layer. The anti-bacterial pants-type sanitary towel can achieve anti-bacterial and anti-inflammation effect, and can effectively and completely eradicate lateral leakage, back leakage and the like as being of a pants-type structure.

The invention relates to application of lactobacillus plantarum DP189 in preparation of medicine for preventing and / or treating Alzheimer's disease, and belongs to the field of biology, the lactobacillus plantarum DP189 is deposited in China Center for Type Culture Collection on March 25, 2019, and has a deposit number of CCTCC NO: M2019199. The lactobacillus plantarum DP189 is prepared into bacterial suspension with number of viable bacteria greater than or equal to 1 * 10 < 9 > CFU / ml. The lactobacillus plantarum DP189 can improve learning and memory ability, improve cognitive impairment, relieve damage degree of hippocampal neurons, reduce a level of malonaldehyde in serum, improve a level of superoxide dismutase in serum and improve levels of glutathione and glutathione peroxidase in serum; reduces levels of interleukin-1beta and tumor necrosis factor-alpha in serum, increases a level of interleukin-6 in serum, increases a level of dopamine in serum, and increases a level of 5-hydroxytryptamine in serum.

The invention provides a gene editing microneedle for treating inflammatory skin diseases and application thereof. The gene editing microneedle comprises a needle tip part and a base part, wherein the needle tip part comprises two nano compounds and a needle tip matrix, and the base part is a base matrix. The gene editing microneedle can improve the gene editing efficiency, deliver the retention of glucocorticoid drugs and gene editing ribonucleoprotein compounds in the skin, and synergistically improve the skin inflammation environment. The microneedle has the skin barrier function of repairing skin lesion tissues, thereby achieving the inflammatory process of relieving psoriasis and atopic dermatitis. The invention also provides the application of the gene editing microneedle in the preparation of drugs for treating inflammatory skin diseases.

The present invention relates to the technical field of feed additives and particularly relates to a feed additive for relieving immune stress of piglets, a preparation method thereof and an application thereof. The feed additive for relieving the immune stress of the piglets comprises 3.0 parts of compound Chinese herbal medicines, 2.0 parts of glutamine and 1.0 part of tea polyphenol; and the compound Chinese herbal medicines are composed of the following traditional Chinese medicinal materials: 20 parts of rhizoma anemarrhenae, 12 parts of hierochloe odorata, 12 parts of borneol, 18 parts of red paeony roots, 14 parts of fossilia ossis mastodi, 18 parts of dried rehamnnia root, 25 parts of honeysuckles, 8 parts of felwort, 20 parts of heartleaf houttuynia herb, 12 parts of common andrographis herb, 12 parts of acanthopanax roots, 10 parts of szechuan lovage rhizome, 8 parts of pilose asiabell root, 15 parts of platycodon grandiflorum and 8 parts of pseudo-ginseng. The additive can alleviate the immune stress of the piglets caused by normal vaccine immunization, improves daily feed intake and daily weight gain of the piglets during the immune stress, and reduces a feed-to-meat ratio.

The invention discloses liquid antibacterial mask and belongs to the technical field of daily chemicals. The liquid antibacterial mask disclosed by the invention is prepared by the following steps: heating, stirring and reflowing potato sprouts and absolute ethyl alcohol according to the mass ratio ranging from (1 to 30) to (1 to 50); filtering, decompressing and distilling to obtain a concentrated solution; stirring and mixing the concentrated solution and sulfuric acid according to the mass ratio ranging from (1 to 30) to (1 to 50), and filtering; after regulating the pH (Potential of Hydrogen), centrifuging and separating; washing to obtain potato sprout extract; putting a dopamine solution, gelatin powder, a chitosan solution, the potato sprout extract, hyaluronic acid, aloe juice, pearl powder, a cactus extracting solution, a traditional Chinese medicine extracting solution, plant essential oil and water into a No. 3 beaker; putting the No.3 beaker into a digital display speed measurement constant-temperature magnetic stirrer and heating, stirring and mixing for 30 to 50min under the conditions that the temperature is 60 to 80 DEG C and the rotary speed is 300 to 500r / min. Theliquid antibacterial mask provided by the invention has an excellent disinfection effect.

The invention belongs to the technical field of pharmaceutical preparations and nanomedicine, and relates to a bionic nano-drug for preventing and treating aortic dissection, in particular to a mononuclear / macrophage membrane bionic modified multidrug co-loaded anti-inflammatory liposome and a preparation method thereof. The liposome is composed of cationic phospholipid and neutral phospholipid, co-loading of multiple anti-inflammatory drugs can be achieved in the liposome, anti-inflammatory cell-penetrating peptide is covalently modified on the surface of the liposome, and then mononuclear / macrophage membrane protein is used for bionic modification. According to the bionic anti-inflammatory liposome, multiple receptors and adhesion molecular ligands mediated and chemotactic on the surface of a mononuclear / macrophage membrane are utilized to realize a natural targeting effect on an inflammatory site, and non-specific clearance of a reticuloendothelial system (RES) to the liposome is reduced by virtue of modification of leukocyte self-recognition molecules. The bionic anti-inflammatory lipidosome can effectively cross a vascular endothelial barrier, gather and release anti-inflammatory drugs at the early lesion part of the aortic dissection in a targeted manner, play a synergistic anti-inflammatory role, inhibit inflammation-related cells from chemotaxis and infiltration into the lesion part, and further prevent and treat the occurrence and development of the aortic dissection.

The invention discloses a preparation method of a compound deodorant capable of reducing odor of livestock manure. On one hand, catechin and other ingredients contained in tea polyphenol of tea residues have a strong chemical adsorption function on polar gas molecules such as ammonia gas, hydrogen sulfide and the like, and tea polyphenol has an inhibition function on growth and propagation of harmful bacteria; on the other hand, fiber of the tea residues has a physical adsorption function on odor substances and an adjustment function on microecological balance of the intestinal tract, essential oil extracted after pine needles, mint leaves and radix glycyrrhizae are mixed is mixed with montmorillonite, the mixture is effectively adsorbed on montmorillonite and mixed with a water extract and the tea residues, the functions of killing bacteria and eliminating inflammation are effectively realized, the compound deodorant has high odor decomposition and absorption functions, and the breeding working environment is improved. The preparation method has a good odor removal effect and is low in cost, the production efficiency is improved while the piggery environment is improved, and the breeding benefits can be improved.