Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • A61K38/1767—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
• • A—HUMAN NECESSITIES
  • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
  • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
  • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
  • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
  • A23L33/17—Amino acids, peptides or proteins
  • A23L33/18—Peptides; Protein hydrolysates
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
  • A61K35/56—Materials from animals other than mammals
  • A61K35/618—Molluscs, e.g. fresh-water molluscs, oysters, clams, squids, octopus, cuttlefish, snails or slugs
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/02—Inorganic compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
  • A61K47/12—Carboxylic acids; Salts or anhydrides thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
  • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
  • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K47/38—Cellulose; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
  • A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0034—Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0043—Nose
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0046—Ear
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0048—Eye, e.g. artificial tears
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
  • A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/007—Pulmonary tract; Aromatherapy
  • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/20—Pills, tablets, discs, rods
  • A61K9/2004—Excipients; Inactive ingredients
  • A61K9/2013—Organic compounds, e.g. phospholipids, fats
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/20—Pills, tablets, discs, rods
  • A61K9/2004—Excipients; Inactive ingredients
  • A61K9/2022—Organic macromolecular compounds
  • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
  • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
  • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
  • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
  • A61L15/32—Proteins, polypeptides; Degradation products or derivatives thereof, e.g. albumin, collagen, fibrin, gelatin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
  • A61P11/02—Nasal agents, e.g. decongestants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2/00—Peptides of undefined number of amino acids; Derivatives 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
• • 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
  • A23V2200/00—Function of food ingredients
  • A23V2200/30—Foods, ingredients or supplements having a functional effect on health
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans

Definitions

• the present invention relates generally to the fields of pharmaceuticals, cosmetics, medical products, disinfecting products, health care products, foods, and daily chemical products, and more particularly to mussel mucin products and their use in inhibiting mucosal inflammation.
• the mucous membrane is the inner wall of various organs such as digestion, respiration, excretion, and reproduction in the body, and the surface of the mucus is kept moist by mucus, specifically including the moist lining of the oral cavity, the nasal cavity, the intestine, the vagina, the intestine, and the like.
• Inflammation is a defensive response of the body to stimuli, manifested as redness, swelling, heat, pain and dysfunction.
• the damage factor directly or indirectly causes destruction of tissues and cells, and on the other hand, through inflammation and hyperemia and exudation reactions, dilution, killing and surrounding damage factors.
• the damaged tissue is repaired and healed by the regeneration of parenchymal and interstitial cells. Therefore, it can be said that inflammation is a unified process of injury and damage resistance.
• Mussel adhesive protein also known as Mytilus edulis foot protein (Mefp)
• Mefp Mytilus edulis foot protein
• Mytilus coruscus A special protein secreted by Perna viridis. Mussels are usually attached in groups to the reefs on the coast or to the bottom of the ship, and have the ability to withstand wave impacts in the offshore. In fact, mussels can be attached extremely strongly to the substrate of any material, such as metal, wood, glass, and the like. The main reason for the above characteristics of mussels is that they can form and store this special mucin in the girth of the foot. The mussels release the mucin through the foot silk to a solid surface such as rock to form a water-resistant combination. Fix yourself.
• Mussel mucin has two structural features: (1) containing lysine, which has a high loading of positive charge; (2) containing 3,4 dihydroxyphenylalanine (DOPA, dopa). The cells and tissues of the human body are negatively charged.
• Mussel mucin through its own positive charge and static between the human body's cells and tissue negative charges Electrical interactions are tightly bound to cells and tissues to provide protection and treatment.
• dopa oxidation produces ortho-dioxins, which can be cross-linked with unoxidized dopa to form a membrane or a network scaffold, which promotes the protein to adhere more closely and firmly to the surface of the human body, thereby protecting.
• Mussel mucin is a macromolecular protein that is completely degraded in the human body for about 3-10 days. Its ability to attach to cell tissues is excellent, so that mussel mucin can be stabilized locally and continue to function.
• mussel mucin has the above characteristics, its current application field is very limited.
• Commercial mussel mucin products are Cell-Tak from BD Biosciences, MAP Trix from Kollodis, Korea, and Hydrogel from Biopolymer, Sweden. These products are either used directly in the mussel mucin solution state, or are stored as lyophilized powder formulations and dissolved prior to use. Their primary application is limited to microscopic cell adhesion and tissue adhesives. Mussel mucin has also been reported for use in the repair of fetal membranes, as a coating against seawater corrosion, and as a drug-loaded stent for the heart.
• Mussel mucin used herein refers to Mytilus edulis Linnaeus, Mytilus coruscus or Perna viridis from the Mytilidae bivalve mollusc. 11 subclasses of mussel mucin, currently known as purified from marine mussels: mefp1, mefp-2, mefp-3, mefp-4, mefp-5, mefp-6, collagen pre-COL- A mixture of one or more of P, pre-COL-D, pre-COL-NG, foot silk matrix proteins PTMP and DTMP.
• the mussel mucin used herein may have a pH of 1.0 to 7.0 in an aqueous solution, and particularly may be in the range of pH 3.0 to 6.5 to make the therapeutic effect better.
• the mussel mucin used herein can be obtained by the following preparation method, for example, a method for separating and purifying mussel mucin using mixed adsorption chromatography in Chinese Patent No. ZL200710179491.0, a kind of carboxy using Chinese Patent No. ZL200710179492.5 A method for purifying mussel mucin by methyl ion exchange chromatography, a method for separating and purifying mussel mucin using salting out and dialysis, Chinese Patent No. ZL200910087567.6.
• the mussel mucin used herein may be in the form of a solution or a lyophilized powder, in particular, the concentration of mussel mucin in the product may be 0.1-15.0 mg/ml, and when the concentration is too low, the effect of mussel mucin Not large, when the concentration is too high, it can cause cytotoxicity, skin irritation, etc., which is not conducive to the treatment of mucosal inflammation.
• the mussel mucin used herein can also be prepared as a liquid agent by combining it with an excipient.
• An exemplary mussel mucin liquid preparation is prepared by dissolving or diluting mussel mucin solution mother liquor or lyophilized powder to a certain concentration or pH, and the solution for dissolving or diluting may be water, physiological saline, phosphate solution, vinegar. Acid solution, borate solution, and the like.
• the pH of mussel mucin in the final product may be pH 1.0-7.0, and in particular, the therapeutic effect may be better in the range of pH 3.0-6.5.
• the mussel mucin used herein can also be prepared as a gelling agent in combination with an excipient.
• An exemplary mussel mucin gel is prepared by mixing a mussel mucin solution or a lyophilized powder with a gel matrix material, which may be selected from the group consisting of cellulose derivatives, carbomers, and seaweeds. Acid salt, tragacanth, gelatin, pectin, carrageenan, gellan gum, starch, xanthan gum, cationic guar gum, agar, non-cellulosic polysaccharide, ethylene polymer, acrylic resin, polyvinyl alcohol or poly One of carboxyvinyl or any combination thereof.
• the mussel mucin used herein can also be prepared as a foaming agent.
• An exemplary mussel mucin foaming agent is prepared by mixing a mussel mucin solution or a lyophilized powder with a foaming agent matrix, which may include hydroxypropylmethylcellulose, gelatin, and polyethylene.
• a foaming agent matrix which may include hydroxypropylmethylcellulose, gelatin, and polyethylene.
• the defoaming time of the foaming agent is long, and the action time is prolonged, so that the mussel mucin is more effective.
• the mussel mucin used herein can be used as a main raw material to prepare a medicine using a pharmaceutically acceptable carrier.
• the drug may be a liquid agent, a gel, or a foaming agent.
• the medicine can be administered orally, by sublingual (sublingual), perfusion (rectal administration), dripping (eye), spraying (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, ear, cervix) Etc., laparoscopic (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at low temperature or in a heated manner.
• the mussel mucin used herein can be used as a main raw material to prepare a medical device.
• the term medical device as used herein refers to materials that are used directly or indirectly to the human body and other similar or related items.
• the medical device may be a liquid agent, a gel, or a foaming agent.
• the medical device can pass through the mouth Oral, sublingual (sublingual), perfusion (rectal administration), instillation (eye), spray (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, ear, cervix, etc.), endoscope It is used in a manner of (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at a low temperature or in a heated manner.
• the mussel mucin used herein can be used as a main raw material to prepare a cosmetic using an auxiliary material which is acceptable in the field of cosmetics.
• the cosmetic may be a liquid, a gel, or a foaming agent.
• the cosmetic can be administered orally, by sublingual (sublingual), perfusion (rectal administration), dripping (eye), spraying (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, ear, cervix) Etc., laparoscopic (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at low temperature or in a heated manner.
• the mussel mucin used herein can be used as a main raw material to prepare a disinfecting product using an excipient which is acceptable in the field of disinfecting products.
• the term disinfecting product as used herein refers to a disinfectant, a disinfecting device, a sanitary article, and a disposable medical article that chemically, physically, or biologically kill or eliminate pathogenic microorganisms in the environment.
• the disinfecting product may be a liquid agent, a gelling agent, or a foaming agent.
• the disinfecting product can be administered orally, by sublingual (sublingual), perfusion (rectal administration), dripping (eye), spraying (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, ear, Cervical, etc., laparoscopic (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at low temperature or in a heated manner.
• the mussel mucin used herein can be used as a main raw material, and a health care product or food can be prepared by using an excipient which is acceptable in the field of health care or food.
• the health supplement or food may be a liquid, a gel, or a foam.
• the health care product or food can be administered orally, by sublingual (sublingual), perfusion (rectal administration), dripping (eye), spraying (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, Ear, cervix, etc.), laparoscopic (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at low temperature or heating.
• the mussel mucin used herein can be used as a main raw material to prepare a daily chemical product using an auxiliary material acceptable in the field of daily chemical products.
• the term daily chemical product as used herein refers to technical chemicals for daily use, including shampoos, shower gels, and the like.
• the daily chemical product may be a liquid agent, a gel agent, or a foaming agent.
• the daily chemical product can be administered orally, by sublingual (sublingual), perfusion (rectal administration), dripping (eye), spraying (mouth, nose), inhalation (mouth, nose), spraying (mouth, nose, ear) , cervix, etc.), laparoscopic (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration, and can be administered at low temperature or heating.
• Another object of the invention is to provide an application of a mussel mucin product to inhibit mucosal inflammation.
• mussel mucin can alleviate redness, edema, subcutaneous tissue fluid exudation, and mucosal damage caused by various mucosal inflammations.
• mucosal inflammations include oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis, enteritis, cervicitis, endometritis, and inflammation caused by inhalation injuries.
• Oral mucositis is a disease that occurs in the oral cavity or soft tissue.
• the clinical manifestation is oral mucosal disease refers to the damage of the oral mucosa.
• the specific symptoms are: mouth ulceration, dry tongue, hoarseness, dry mouth and bitterness, and then oral lichen planus.
• Oral diseases such as stomatitis, recurrent aphthous ulcers, cheilitis, etc., lead to eating difficulties, unbearable oral pain, uncomfortable, and once the disease is triggered, it will recur and be more serious than once.
• Oral mucositis can lead to a variety of complications in the body, directly affecting the patient's health and life. At present, clinically, the symptoms are often controlled by Western medicine, but it is difficult to cure. It has been listed as one of the major problems of oral diseases.
• Rhinitis a nasal inflammatory disease, is inflammation of the nasal mucosa caused by viruses, bacteria, allergens, various physical and chemical factors, and certain systemic diseases.
• the main pathological changes of rhinitis are nasal mucosal congestion, swelling, exudation, hyperplasia, atrophy or necrosis.
• Otitis media is an inflammatory reaction of the middle ear mucosa and is an inflammatory lesion involving all or part of the structure of the middle ear (including the eustachian tube, tympanic cavity, sinus sinus, and mastoid air chamber).
• Conjunctivitis is a general term for the inflammatory reaction of the conjunctival tissue under the influence of the outside and the body's own factors. Although conjunctivitis itself does not have a serious effect on vision, it can cause vision damage when its inflammation affects the cornea or causes complications. According to the condition and course of conjunctivitis, it can be divided into acute, subacute and chronic; according to the cause, it can be divided into bacterial, viral, chlamydia, fungal and allergic; according to the characteristics of conjunctival lesions, Divided into acute follicular conjunctivitis, chronic follicular conjunctivitis, membranous and pseudomembranous conjunctivitis. The clinical manifestations of conjunctivitis are conjunctival hyperemia and increased secretion.
• Pharyngitis is inflammation of the pharyngeal mucosa and its lymphoid tissue. Acute pharyngitis is often part of the upper respiratory tract infection and is often caused by viral infections. The lesion can be characterized by acute simple pharyngitis and acute suppurative pharyngitis. Chronic pharyngitis can be divided into chronic simple pharyngitis, chronic hypertrophic pharyngitis and chronic atrophic pharyngitis.
• Laryngitis is inflammation of the laryngeal mucosa and submucosal tissue. It is characterized by clinical cough and laryngeal swelling, warming and pain. According to the cause and clinical course, it can be divided into primary and secondary, acute and chronic laryngitis. Clinically, acute catarrhal laryngitis is common and often complicated by pharyngitis.
• Tracheitis is an inflammatory change of the trachea and bronchus caused by infection or non-infectious factors.
• the secretion of mucus is increased.
• the activity of respiratory enzymes in the epithelial villus of the trachea is reduced due to the lack of negative ions, which affects the secretion function of the alveoli and the ventilation and exchange of the lungs.
• Gas function Clinically, it is characterized by long-term cough, cough or wheezing.
• Esophagitis refers to inflammation caused by edema and congestion due to irritation or injury in the superficial or deep tissues of the esophageal mucosa.
• Chemical stimuli include stomach acid, bile, spirits, and strong acids, alkalis, drugs, etc.
• physical stimuli include hot foods, beverages, esophageal foreign bodies (fishbone, etc.) incarceration, long-term placement of nasogastric tubes.
• Tuberculosis, fungal (candida) or viral infection can also cause esophagitis due to localized damage to the esophagus due to chemotherapy or radiation therapy, or a decrease in the patient's own resistance.
• Gastritis is an acute and chronic inflammation of the gastric mucosa caused by a variety of different causes, often accompanied by epithelial damage, mucosal inflammatory response and epithelial regeneration.
• Acute simple gastritis refers to acute extensive or localized acute inflammation of the gastric mucosa caused by various extrinsic and intrinsic factors. Symptoms and signs of acute simple gastritis vary from disease to cause, and their causes are diverse, including acute stress, drugs, ischemia, bile reflux, and infection. Clinically, acute simple gastritis is divided into acute erosive gastritis, acute suppurative gastritis, and acute corrosive gastritis.
• Chronic gastritis refers to various chronic gastric mucosal inflammatory lesions caused by different causes, and its incidence rate ranks first among various stomach diseases. Common are chronic superficial gastritis, chronic erosive gastritis and chronic atrophic gastritis. Chronic gastritis mucosal intestinal metaplasia, often involving the cardia, accompanied by loss of G cells and decreased secretion of gastrin, may also involve the body, accompanied by loss of acid secretion glands, leading to a decrease in gastric acid, pepsin and endogenous factors .
• Enteritis is intestinal inflammation and colitis caused by bacteria, viruses, fungi, and parasites.
• Clinical manifestations include abdominal pain, diarrhea, septic flushing or mucus pus and blood. Some patients may have a feeling of fever, so it is also known as infectious diarrhea.
• Enteritis is divided into acute and chronic according to the length of the disease. Common clinical symptoms are chronic bacterial dysentery, chronic amoebic dysentery, schistosomiasis, non-specific ulcerative colitis and limited enteritis.
• Cervical mucositis or cervicitis lesions are confined to the cervical mucosa and submucosal tissue, the appearance of the cervix is very smooth, the cervix is blocked by purulent secretions, sometimes the cervical mucosa hyperplasia protrudes to the mouth, visible cervix Congestive redness. Cervical hypertrophy can be caused by hyperemia, edema, inflammatory cell infiltration and connective tissue hyperplasia of the cervical mucosa and submucosal tissue.
• Endometritis is an inflammatory change in the structure of the endometrium caused by various causes.
• the uterine cavity has good drainage conditions and periodic endometrial ablation, so that there is very little chance of inflammation staying in the endometrium for a long time, but Inflammatory treatment of the acute phase is not complete, or the source of infection is often present, and inflammation can be repeated.
• Endometritis can be divided into acute endometritis and chronic endometritis.
• Inflammation caused by inhalation injury refers to inhalation of high heat vapor, accidental drinking of boiling water, head and neck burns caused by inhalation of flame or dry hot air to cause mucosal burns.
• the initial appearance of the lesion is mucosal congestion, edema, erosion, cellulose exudation, and the formation of white membrane.
• Mucosal edema begins at 1-2 hours after injury and reaches a peak at 4-8 hours. After 2-3 days, the edema gradually subsides, and the leucorrhea falls off to form ulcers of varying depths. In severe cases, local tissue necrosis and even perforation of the esophagus or trachea.
• the mussel mucin of the present invention can be used for the treatment of oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis, enteritis, cervicitis, endometritis, inhalation Inflammation caused by injury, etc.
• the mussel mucin of the present invention can be used to inhibit oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis, enteritis, cervicitis, endometritis, etc.
• the mussel mucin application according to embodiment 1, wherein the mussel mucin concentration may be from 0.1 to 15.0 mg/ml.
• Mussel mucin application according to embodiment 1, wherein the mussel mucin in the final product may be in the range of pH 1.0-7.0, in particular in the range of pH 3.0-6.5.
• the mussel mucin application according to any one of embodiments 1 to 5, wherein the mucosal inflammation is selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagus Inflammation, gastritis, enteritis, cervicitis, endometritis, inflammation caused by inhalation injury, etc.
• the mucosal inflammation is selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagus Inflammation, gastritis, enteritis, cervicitis, endometritis, inflammation caused by inhalation injury, etc.
• the mussel mucin application according to any one of embodiments 1 to 5, wherein the mucosal inflammation is selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, endometrial cancer, etc. caused by gastritis, enteritis, cervicitis, endometritis, etc. .
• composition may be by oral administration, sublingual (sublingual), perfusion (rectal administration), instillation (eye), spray (mouth, nose), Inhalation (mouth, nose), spraying (mouth, nose, ear, cervix, etc.), endoscopy (uterine cavity, abdominal cavity, etc.), targeted local sustained release, targeted administration.
• a medicament for the treatment of mucosal inflammation comprising mussel mucin and a pharmaceutically acceptable carrier, wherein the mussel mucin is present in a concentration of from 0.1 to 15.0 mg/ml.
• a medical device for treating mucosal inflammation comprising a mussel mucin and a carrier acceptable for use in the field of medical devices, wherein the concentration of mussel mucin may be from 0.1 to 15.0 mg/ml.
• a cosmetic for treating mucosal inflammation comprising mussel mucin and a carrier acceptable for the cosmetic field, wherein the concentration of mussel mucin may be from 0.1 to 15.0 mg/ml.
• a disinfecting product for the treatment of mucosal inflammation comprising a mussel mucin and a carrier acceptable for the field of disinfecting products, wherein the concentration of mussel mucin may be from 0.1 to 15.0 mg/ml.
• a health care product/food for treating mucosal inflammation comprising mussel mucin and a health care/food-acceptable carrier, wherein the concentration of mussel mucin may be from 0.1 to 15.0 mg/ml.
• a daily chemical product for the treatment of mucosal inflammation comprising a mussel mucin and a carrier acceptable for use in the field of daily chemical products, wherein the mussel mucin concentration may be from 0.1 to 15.0 mg/ml.
• mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis , enteritis, cervicitis, endometritis, inflammation caused by inhalation injury.
• mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, intrauterine caused by esophagitis, gastritis, enteritis, cervicitis, endometritis Membrane cancer and the like.
• a medical device for treating mucosal inflammation wherein the mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, Gastritis, enteritis, cervicitis, endometritis, inflammation caused by inhalation injury, etc.
• a medical device for treating mucosal inflammation wherein the mucosal inflammation may be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, endometrial cancer, etc. caused by gastritis, enteritis, cervicitis, endometritis, etc. .
• mucosal inflammation may be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis , enteritis, cervicitis, endometritis, inflammation caused by inhalation injury.
• mussel mucin in a cosmetic for treating mucosal inflammation, wherein the mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, gastritis Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, endometrial cancer, etc. caused by enteritis, cervicitis and endometritis.
• mussel mucin in a disinfecting product for treating mucosal inflammation, wherein the mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, Gastritis, enteritis, cervicitis, endometritis, inflammation caused by inhalation injury, etc.
• a disinfecting product for treating mucosal inflammation wherein said mucosal inflammation may be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis, Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, endometrial cancer, etc. caused by gastritis, enteritis, cervicitis, endometritis, etc. .
• mucosal inflammation may be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagus Inflammation, gastritis, enteritis, cervicitis, endometritis, inflammation caused by inhalation injury Symptoms, etc.
• mucosal inflammation may be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagus Oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, gastric cancer, intestinal cancer, cervical cancer, endometrium caused by inflammation, gastritis, enteritis, cervicitis, endometritis Cancer, etc.
• mussel mucin in a daily chemical product for treating mucosal inflammation, wherein the mucosal inflammation can be selected from the group consisting of: oral mucositis, rhinitis, otitis media, conjunctivitis, pharyngitis, laryngitis, bronchitis, esophagitis Oral cancer, gastroenteritis, enteritis, cervicitis, endometritis, etc., oral cancer, nasopharyngeal cancer, middle ear cancer, conjunctival cancer, throat cancer, tracheal cancer, esophageal cancer, stomach cancer, intestinal cancer, cervical cancer, endometrial cancer Wait.
• Example 1 Application of mussel mucin liquid medical device in the treatment of compound aphthous ulcer.
• the selected patients were randomly divided into the control group and the experimental group, and the control group was treated with 0.1% citric acid solution.
• the test group was treated with the above mussel mucin medical device.
• the two groups were used 3 times a day, spraying the affected area after meals, spraying 2-3 times each time until the affected area was completely covered with 0.1% citric acid solution or mussel mucin water.
• Solution medical device coverage In the medical device group spraying mussel mucin aqueous solution, the pain of the affected area was significantly weakened within 5-15 minutes, and the visual analog VAS score decreased from 5.0-7.0 to 1.0-3.0 before treatment, and the analgesic time lasted for 2-7 hours. There was no change in the VAS score of the affected area before and after the control group. As the use time prolonged, the duration of analgesia was prolonged, and the interval of use was prolonged, showing no dependence.
• Example 2 Application of mussel mucin gel medical device in the treatment of compound aphthous ulcer.
• Twenty patients with light a compound aphthous ulcer diagnosed by experts in oral mucosa were enrolled in the study.
• the number of ulcers in the selected patients was greater than 5, and the ulcer site was not limited.
• the largest ulcer was selected as the target ulcer.
• the target ulcer diameter was less than 1 cm.
• the selected patients were randomly divided into the control group and the experimental group.
• the control group was treated with a blank gel matrix containing no mussel mucin
• the experimental group was treated with a mussel mucin gel medical device.
• the two groups were used three times a day. After the meal, the affected area was sprayed, and each time the spray was applied 2-3 times until the affected area was completely covered by a blank gel or mussel mucin gel medical device.
• the pain in the affected area was significantly weakened within 5-13 minutes, from the visual analog VAS score of 5.0-7.0 to 1.0-3.0 before treatment, and the analgesic time lasted for 2-9 hours. There was no change in the VAS score of the affected area before and after the control group. As the use time prolonged, the duration of analgesia was prolonged, and the interval of use was prolonged, showing no dependence.
• Example 3 Application of mussel mucin liquid daily chemical product in the treatment of rhinitis.
• a mussel mucin solution having a concentration of 0.5 mg/ml was taken and diluted 5 times with 0.001% acetic acid to a mussel mucin content of 0.1 mg/ml to obtain a mussel mucin liquid daily product.
• Example 4 Application of mussel mucin liquid medicine in the treatment of rhinitis.
• a mussel mucin solution having a concentration of 2.0 mg/ml was diluted 10 times with 0.05% citric acid to a mussel mucin content of 0.2 mg/ml to obtain a mussel mucin liquid medicine.
• Ten patients with rhinitis were enrolled and confirmed by otolaryngologists.
• the patient showed nasal congestion and salivation, and the salivation was sticky or sticky.
• the patient is administered by nebulized inhalation every day, and the mussel mucin liquid medicine is inhaled once a day.
• Ten patients had different degrees of nasal congestion relief after using mussel mucin liquid medicine for 3 days. After 7 days of use, the nasal congestion of all patients was alleviated, and all patients had no pus or mucous nasal discharge. It is proved that the mussel mucin liquid medicine of the present invention can be used for the treatment of rhinitis.
• Example 5 Application of mussel mucin gel disinfectant product in the treatment of otitis media.
• Example 6 Application of mussel mucin liquid medicine in the treatment of otitis media.
• a mussel mucin solution was prepared by taking a 5 mg/ml mussel mucin solution, adding an equal volume of 0.001% acetic acid to 2.5 mg/ml, and a solution pH of 3.0 to prepare a mussel mucin liquid medicine having a mussel mucin content of 2.5 mg/ml.
• Example 7 Application of mussel mucin liquid medical device in the treatment of conjunctivitis.
• the mussel mucin solution was taken, diluted with physiological saline, and the pH was adjusted to pH 6.0 with acetic acid to obtain a mussel mucin liquid medical device, wherein the mussel mucin concentration was 3 mg/ml.
• Example 8 Application of mussel mucin hydrogel health supplement in the treatment of pharyngitis.
• Example 9 Application of mussel mucin gel drug in the treatment of laryngitis.
• a mussel mucin solution Taking a mussel mucin solution, mixing the preparation with hydroxypropylmethylcellulose and glycerol at a mass ratio of 3:2:1, and adjusting the pH to pH 6.2 with citric acid to obtain a mussel mucin gel drug, wherein The mussel mucin concentration was 3 mg/ml.
• Example 10 Application of mussel mucin liquid health care product in the treatment of tracheitis.
• the mussel mucin solution was mixed with propylene glycol in a ratio of 2:1 by volume, and the pH was adjusted to pH 5.0 with acetic acid to obtain mussel mucin liquid health care product, wherein the mussel mucin concentration was 3.0 mg/ml.
• bronchitis Twelve patients with bronchitis were enrolled. The clinical manifestations were cough, cough, and asthma. The patient was diagnosed by a respiratory doctor before being admitted to the group. The patient was treated with aerosol inhalation for 30 minutes each time, once a day. After 3 days of use, the patient's cough was reduced and the amount of cough was reduced. After 7 days of use, all patients had no cough and one patient was still accompanied by a mild cough. It is proved that the mussel mucin liquid health care product of the present invention can be used for the treatment of bronchitis.
• Example 11 Application of mussel mucin liquid medicine in the treatment of esophagitis.
• the mussel mucin solution was taken and diluted with an aqueous borate solution to obtain a mussel mucin liquid agent having a pH of 5.5, wherein the mussel mucin concentration was 2.5 mg/ml.
• Example 12 Application of mussel mucin hydrogel drug in the treatment of gastritis.
• a mussel mucin solution was taken, and carboxymethylcellulose and glycerin were added in a volume ratio of 2:1:1 to obtain a mussel mucin hydrogel drug, wherein the mussel mucin concentration was 2.5 mg/ml.
• the mussel mucin hydrogel drug is further wrapped in a gastric-soluble coating material to form a gastric-soluble sustained-release administration preparation.
• Twenty patients with gastritis were enrolled in the study.
• the patients were enrolled in the gastroscope of the digestive department.
• the selected patients were orally administered a gastric-soluble sustained-release preparation containing a mussel mucin hydrogel drug once a day, one capsule at a time.
• gastroscopy showed that the ulcer surface of the subjects had different degrees of healing.
• gastroscopy was performed, and the ulcer surface of the subject was completely healed.
• Example 13 Application of mussel mucin liquid medicine in the treatment of acute enteritis.
• the mussel mucin freeze-dried powder was prepared, and a 1.0 mg/ml aqueous solution was prepared by using physiological saline, and the pH was adjusted to 5.8 with acetic acid to obtain a mussel mucin liquid medicine.
• the mussel mucin liquid medicine is further wrapped in an enteric coating material to form an enteric sustained-release preparation.
• Example 14 Application of mussel mucin gel disinfectant product in the treatment of cervicitis.
• the mussel mucin solution was taken, mixed with glycerol in a volume ratio of 1:1, and the pH was adjusted to 4.8 with acetic acid to obtain a mussel mucin gel disinfecting product.
• Example 15 Application of mussel mucin gel medical device in the treatment of cervicitis.
• the mussel mucin solution is mixed with gelatin and alginate at a mass ratio of 4:1:1, and the pH is adjusted to 4.8 with acetic acid to obtain a mussel mucin gel medical device, wherein mussel mucin concentration It is 5.0 mg/mL.
• Shellin products can be used in the treatment of cervicitis.
• Example 16 Application of mussel mucin foam medical device in the treatment of cervicitis.
• the mussel mucin solution was mixed with hydroxypropylmethylcellulose at a mass ratio of 4:1, and the pH was adjusted to 4.8 with acetic acid to obtain a mussel mucin foam medical device, wherein the mussel mucin concentration was 5 mg. /mL.
• Example 17 Application of mussel mucin liquid medicine in the treatment of endometritis.
• the mussel mucin solution was taken and diluted to 3 mg/ml with 0.1% citric acid, and the pH of the solution was 6.5 after dilution to obtain a mussel mucin liquid medicine.
• the catheter After the drug solution has entered the uterine cavity, the catheter is pulled out, and the supine or gluteal high bed is placed for 1-2 hours. 1 time a day. After 10 days of use, the pelvic region of the patient had no pain and the leucorrhea became normal, demonstrating that the mussel mucin drug of the present invention can be used for the treatment of endometritis.
• Example 18 Application of mussel mucin liquid medicine in the treatment of inhalation injury.
• a mussel mucin solution of 10.0 mg/ml was diluted 2 times with acetic acid to a mussel mucin concentration of 5.0 mg/ml, and the pH of the solution was 6.8, to obtain a mussel mucin liquid medicine.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical & Material Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Veterinary Medicine (AREA)
• Public Health (AREA)
• Animal Behavior & Ethology (AREA)
• Medicinal Chemistry (AREA)
• Pharmacology & Pharmacy (AREA)
• Epidemiology (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Molecular Biology (AREA)
• Inorganic Chemistry (AREA)
• Otolaryngology (AREA)
• Zoology (AREA)
• Biochemistry (AREA)
• Biophysics (AREA)
• Reproductive Health (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Pulmonology (AREA)
• Gastroenterology & Hepatology (AREA)
• Rheumatology (AREA)
• Pain & Pain Management (AREA)
• Genetics & Genomics (AREA)
• Nutrition Science (AREA)
• Hematology (AREA)
• Materials Engineering (AREA)
• Immunology (AREA)
• Marine Sciences & Fisheries (AREA)
• Ophthalmology & Optometry (AREA)
• Endocrinology (AREA)
• Gynecology & Obstetrics (AREA)
• Physiology (AREA)
• Urology & Nephrology (AREA)

Priority Applications (15)

Applications Claiming Priority (1)

Related Child Applications (2)

Publications (1)

Family

ID=58050454

Family Applications (2)

Family Applications After (1)

Country Status (12)

Cited By (3)

Families Citing this family (14)

Citations (3)

Family Cites Families (31)

• 2015
  • 2015-08-14 WO PCT/CN2015/087011 patent/WO2017028025A1/zh not_active Ceased
• 2016
  • 2016-08-15 WO PCT/CN2016/095364 patent/WO2017028777A1/zh not_active Ceased
  • 2016-08-15 KR KR1020187003844A patent/KR102708321B1/ko active Active
  • 2016-08-15 MX MX2018000654A patent/MX2018000654A/es unknown
  • 2016-08-15 AU AU2016309397A patent/AU2016309397B2/en active Active
  • 2016-08-15 US US15/751,551 patent/US10485848B2/en active Active
  • 2016-08-15 EP EP16836641.7A patent/EP3335739B1/en active Active
  • 2016-08-15 DK DK16836641.7T patent/DK3335739T3/da active
  • 2016-08-15 SG SG11201800578YA patent/SG11201800578YA/en unknown
  • 2016-08-15 CN CN201680041312.4A patent/CN108348636B/zh active Active
  • 2016-08-15 MA MA042629A patent/MA42629A/fr unknown
  • 2016-08-15 JP JP2018501271A patent/JP6816098B2/ja active Active
  • 2016-08-15 CA CA2995549A patent/CA2995549C/en active Active
• 2019
  • 2019-10-01 US US16/589,346 patent/US11458190B2/en active Active

Patent Citations (3)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events