WO2015152444A1 - Oral composition for inhibiting halitosis - Google Patents

Oral composition for inhibiting halitosis Download PDF

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Publication number
WO2015152444A1
WO2015152444A1 PCT/KR2014/002866 KR2014002866W WO2015152444A1 WO 2015152444 A1 WO2015152444 A1 WO 2015152444A1 KR 2014002866 W KR2014002866 W KR 2014002866W WO 2015152444 A1 WO2015152444 A1 WO 2015152444A1
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extract
oral composition
bad breath
weight
inhibiting
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PCT/KR2014/002866
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French (fr)
Korean (ko)
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장선오
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장선오
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Priority to CN201480077603.XA priority Critical patent/CN106163497A/en
Publication of WO2015152444A1 publication Critical patent/WO2015152444A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365Hydroxycarboxylic acids; Ketocarboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67Vitamins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67Vitamins
    • A61K8/678Tocopherol, i.e. vitamin E
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/965Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of inanimate origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/592Mixtures of compounds complementing their respective functions
    • A61K2800/5922At least two compounds being classified in the same subclass of A61K8/18
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof

Definitions

  • the present invention relates to an oral composition for inhibiting bad breath, and in particular, it comprises a golden extract and a mold extract, and in addition to the natural medicinal extract including a duct extract, gold silver extract, gilyeong extract, etc.
  • the present invention relates to an oral composition excellent in inhibiting bad breath, inhibiting dental caries and inhibiting periodontal disease, further including tocopherol acetate and malic acid.
  • Tooth decay is a disease in which carbohydrates in food are metabolized by microorganisms in the gingival and subgingival bacterial membranes, and the hard tissues of teeth are destroyed by the action of locally produced organic acids.
  • Tooth decay does not have a direct relationship to human life, but the chewing function of food deteriorates, so it directly or indirectly affects diseases of the digestive system.
  • the prevalence of tooth decay is especially high in children, with 85% of children aged 5 or older experiencing or experiencing pain from tooth decay. This tooth decay is caused by Streptococcs mutans ( S. mutans ), among the microorganisms in the oral cavity.
  • S. mutans Streptococcs mutans
  • Streptococcus mutans is a Gram-positive anaerobic bacterium that resides in the dental plaque in the oral cavity. To destroy enamel of teeth (Kim Jong-bae et al., Public Oral Health Science, Advisor, pp. 68-84, 1991).
  • VSC Volatile sulfur compounds
  • VSCs are mainly caused by the decay activity of anaerobic bacteria in the oral cavity using gingival fissure, saliva, proteins in food residues (particularly those containing cysteine and methionine), peptides and amino acids as substrates. Is generated.
  • Representative Gram-negative anaerobic bacteria include Porphyromonas gingivalis , Prevotella intermedia , Fusobacterium nucleatum , and large amounts of hydrogen sulfide and methylmercaptan. Is being reported. As a result, it has been reported that periodontal disease bacteria play an important role in inducing bad breath. Many studies have shown that volatile sulfur compounds have a detrimental effect on periodontal tissues.
  • VSC's action on tissues increases mucosal permeability, collagen breakdown, changes in gingival fibroblasts and periodontal ligament cells, and wounds.
  • the effects of delayed healing have been experimentally demonstrated (Kwon Jin-hee et al., The Korean Periodontological Society 2000).
  • MMP3 an intracellular matrix protein, is considered to be an important protease involved in tissue destruction and tissue reorganization in various diseases such as chronic inflammatory disease, rheumatoid arthritis, skin disease, and cancer, and polymorphonuclear leukocytes and fibroblasts associated with periodontal disease It is expressed in macrophages, epithelial cells, etc. and is known as the causative enzyme of periodontitis (Cho Jong-Hee et al 1999).
  • Periodontitis is an inflammatory disease that results in the destruction of tooth-supporting tissues such as gingiva, periodontal ligament, chalky and alveolar bone. Periodontitis is strongly associated with the presence of cytokines such as interleukin-1 ⁇ (IL-1 ⁇ ). Physiologically, the activation of cyclooxygenases (COX) is closely related to periodontitis. In particular, COX-2 is induced by the production of cytokines and bacteria before inflammation (Kim, Sun-Woo et al. 2007).
  • IL-1 ⁇ interleukin-1 ⁇
  • COX-2 cyclooxygenases
  • the present invention has been conducted in order to solve the problems of the prior art, as a result, it is essential to include a golden extract and a mold extract, and, in addition to the natural medicinal extracts including yeongyo extract, gold silver extract and Gilyeong extract, etc.
  • tocopherol acetate and malic acid were further included, and it was confirmed that it can provide the oral composition which is excellent in the bad breath suppression, the dental caries suppression, and the periodontal disease suppression effect, and came to complete this invention.
  • an oral composition having a composition such that the pH is preferably maintained at 6 to 8, more preferably neutral such as saliva.
  • Oral composition for inhibiting bad breath according to the present invention, 0.1 to 5.0% by weight of the mixture of natural medicinal extracts, including golden extract and mold extract, 0.01 to 1.0% by weight of tocopherol acetate, 0.01 to 1.0% by weight of malic acid.
  • the natural medicinal herb extract may further comprise 0.1 to 5.0% by weight of an extract selected from the group consisting of duct bridge extract, gilding extract, gilyeong extract and a mixture of two or more thereof.
  • the oral composition for inhibiting bad breath may have a pH within the range of 6 to 8, more preferably may be neutral.
  • the oral composition for inhibiting bad breath may be a paste, and in particular, may be formulated with a toothpaste, mouthwash or mouthwash.
  • the oral composition for inhibiting bad breath preferably, may be filled in a double container having a septum.
  • essential extracts include golden extracts and mold extracts, and in addition, natural herbal extracts, including duct extracts, gold and silver extracts, and gil dynasty extracts, and the like, and further include tocopherol acetate and malic acid. Therefore, there is an effect of providing an oral composition excellent in inhibiting bad breath, inhibiting dental caries and periodontal disease.
  • FIG. 1 is a graph showing the interleukin 1 ⁇ gene expression inhibitory effect of the oral composition according to the present invention in comparison with the control and comparative examples.
  • Figure 2 is a graph showing the cyclooxygenase-2 (COX-2) gene expression inhibitory effect of the oral composition according to the present invention in comparison with the control and comparative examples.
  • Oral composition for inhibiting bad breath characterized in that it comprises 0.1 to 5.0% by weight of the mixture of natural medicinal extracts, including golden extract and mold extract, 0.01 to 1.0% by weight of tocopherol acetate, 0.01 to 1.0% by weight of malic acid do.
  • the sterling silver extract, duct bridge extract, mold extract, gilyeong extracts used in the present invention may be extracted by conventional extraction methods well known in the art, preferably hot water extraction method or extracted by mixing ethanol or water and ethane Can be used.
  • the golden extract of the natural medicinal extract is an extract of the root of golden ( Scutellaria baicalensis GEORGE ), which is a perennial herbaceous plant belonging to the Lamiaceae.
  • Gold is a herbaceous plant cultivated in various places and is widely used for medicinal, the active ingredient is known as Baikalein (Baicalein), Baikalin (Baicalin), wogonin (Wogonin), wogonoside (Wogonoside) and the like.
  • the taste is bitter and weak.
  • Efficacy is a fact that lowers ( ⁇ ⁇ ), so the body has a lot of fever and hunger and thirst severely, if you improve the symptoms of conscious confusion. It is known that antipyretic effect is high from high fever due to cold to high fever of general infectious disease.
  • the hyunggae extract is an extract of the annual herb belonging to the family Lamiaceae called hyeonggae, hyeonggae is called purple, so the shape and color is similar to a purple tea, it is mainly used for medicinal rather than edible.
  • Hyeonggae's outpost and the flowered ear are used as medicine for Hyeonggaesu.
  • Dongbobom Herb “The quality is warm, the taste is very bitter, and it is poisonous.
  • Bad winds, red winds, lack of sensation all over the body, upper head hurts, tendons and bones are sweet and heal and blood flow, bleeding, healing Nagwa and Changyang. Plant in the field.
  • the present invention includes a natural medicinal herb extract comprising essentially the golden extract and hyeonghyeong extract, the natural medicinal extract is an amount within the range of 0.1 to 5.0% by weight based on the total weight of oral composition for inhibiting bad breath according to the present invention It is preferable for the bad breath inhibitory effect to be contained.
  • the oral composition for inhibiting bad breath according to the present invention further comprises tocopherol acetate and malic acid in addition to the above-mentioned natural herbal extracts.
  • the tocopherol acetate is a vitamin E acetate is different from the free vitamin E, the molecular formula is C 31 H 52 0 3 , molecular weight 472.73 is a light yellow, viscous liquid.
  • Acetate acetate is not affected by oxidizing agents such as air, light and ultraviolet light. Insoluble in water, soluble in acetone, chloroform and ether, slightly soluble in alcohol.
  • Tocopherol is a vitamin E oil that not only acts as a natural antioxidant, but also has the effect of aging skin and cell regeneration, so it is mainly used in capsule form in skin.
  • teeth have such a function, and it is known that the addition of an effective amount is effective in the prevention of gingivitis, periodontitis (alveolar pylori), and the prevention of periodontal and gingival diseases.
  • the tocopherol acetate is preferably used in an amount within the range of 0.01 to 1.0% by weight based on the total weight of oral composition for inhibiting bad breath according to the present invention.
  • the malic acid (Malic Acid) is also referred to as umseongumum otherwise. It is a colorless acicular crystal with the chemical formula C 4 H 6 O 5 , one asymmetric carbon atom, and D-, L-, and DL-3 optical isomers. Left-rotating L-malic acid is found in natural fruits and vegetables, such as apples and grapes. Deliquescent, molecular weight 134.09, specific gravity 1.595, melting point 100 °C, boiling point 140 °C. Compared to citric acid, citric acid, which has the same acidity, is not only cheaper in price, but also elegant and refined high-quality acidity and long-lasting acidity make people's appetite more pleasant and sour.
  • the malic acid is preferably used in an amount within the range of 0.01 to 1.0% by weight based on the total weight of the oral composition for inhibiting bad breath according to the present invention.
  • the natural medicinal herb extract ranges from 0.1 to 5.0% by weight, based on the total weight of the oral composition for inhibiting bad breath according to the present invention, the extract selected from the group consisting of duct bridge extract, gold silver extract, gilyeong extract and a mixture of two or more thereof It is especially preferable for the bad breath inhibitory effect to contain in the quantity within the below.
  • the Yeongyo extract is an extract of the fruit of the Forsythia forsythia and the same plant belonging to the ash family called Yeongyo.
  • Yeon-gyo's temper is bitter and cold, and the ear canal is known to act on the heart, menopause and liver.
  • it is known to have the effects of sweating, clearing, drainage, antipyretic, antibacterial, anti-inflammatory, fever, headache, dry mouth, seawater, sore throat, boils, vomiting, vasodilation and blood flow improvement.
  • the sterling silver extract is a semi-heterophyllum vine plant of the genus Rosaceae, and is an extract of the plant of the cedar. From ancient times, when it is stuffy and thirsty, treatment of boils, skin is loose, organ inflammation and pus discharge, skin necrosis by dysentery or heat poisoning, mumps or conjunctivitis, and tonsils, sore throat, bronchitis It was mainly used for the treatment of inflammation such as cystitis. According to classical medicine, the nature of honeysuckle is cold, sweet and bitter, acts on the heart and menopause, lowers the heat, releases the poison, improves the meridians, has excellent effects on various inflammatory diseases, It is said that heals boils and boils.
  • the Giltyeong extract is an extract of Giltyeong, ie Bellflower.
  • Bellflower is native to Korea and is common enough to be recognized as one of the three color herbs that are edible a lot of bellflowers, bellflowers, etc. Old bellflower is better than wild ginseng. ” Indeed, the excellent alkaline food bellflower is rich in dietary fiber as well as minerals such as calcium, iron and potassium, as well as beneficial amino acids such as vitamins B1, B2, vitamin C and tyrosine and tryptophan. It is said that there are 278 records about the efficacy of bellflower. Bellflower is a perennial plant belonging to the lantern family.
  • the root is mainly used as a medicine, which is taken in the fall, peeled and dried in the sun, and then the stem is removed and used.
  • the root contains saponins, Platicodin and Platicodigenin.
  • the bellflower is commonly used for cough and phlegm.
  • the bellflower contains about 2g per 100g of bitter saponin, which is known as the main ingredient of ginseng, and triterpenoid-based saponins show efficacy in respiratory diseases. It is known to increase mucus secretion of the respiratory mucosa and to cut phlegm.
  • Bellflower juice which is a mixture of bellflower and pears, is widely used as a winter preventive medicine.
  • the main ingredient of Yonggaksan famous for cough and phlegm, is bellflower.
  • bellflower Especially in oriental medicine, it is known to be effective as drainage, expectorant, tonsillitis, oily, cough, purulent boil, expectorant of asthma and pulmonary tuberculosis, and pleurisy.
  • Bellflower is known to be beneficial for people with high blood pressure and diabetes who weigh a lot because it lowers blood pressure and blood sugar.
  • Bellflower is known to help people with hyperlipidemia because it increases the secretion of steroids and galic acid in the body, leading to a decrease in cholesterol in the body.
  • Oral composition for inhibiting bad breath preferably further comprises citric acid in an amount within the range of 0.01 to 1.0% by weight in addition to the malic acid.
  • the oral composition for inhibiting bad breath is preferably used in an amount such that the pH is within the range of 6 to 8, preferably neutral.
  • Oral composition containing the extract or compound of the present invention in the present invention can be used to prepare a paste and liquid, preferably, the bad breath control oral composition may be a paste, but is not limited thereto.
  • the oral composition of the present invention may be formulated as a toothpaste, mouthwash or mouthwash.
  • the toothpaste may comprise a composition selected from the group consisting of abrasives, caking agents, moisturizers, active ingredients, foaming agents, sweeteners, flavoring agents as the formulation ingredients, the formulation ingredients for formulation to these toothpastes are It can be understood as known.
  • abrasive examples include aluminum hydroxide, silicic anhydride, aluminum silicate, dicalcium phosphate, dihydrate and anhydride, tricalcium phosphate, calcium carbonate, calcium pyrophosphate, insoluble sodium metaphosphate, magnesium triphosphate, magnesium carbonate, and sulfuric acid.
  • Calcium, polymethyl methacrylate, and other synthetic resins may be used in combination of one or two or more of them in an amount of about 20 to 90% by weight of the total composition (in the case of paste toothpaste, it may be within the range of 20 to 60% by weight). Can be).
  • binder examples include carrageenan, various incremental cellulose derivatives, xanthan gum, gums such as tragacanth gum, polyvinyl alcohol, sodium polyacrylate, polyacrylic acid / maleic acid copolymer, and carboxyvinyl polymer.
  • organic binders such as a polymer derivative
  • inorganic binders such as a silica and a laponite
  • 1 type, or 2 or more types can be mix
  • the moisturizing agent may include one or two or more of about 10 to 70% of sorbitol, glycerin, ethylene glycol, propylene glycol, polyether glycol, polypropylene glycol, etc. It can be used in combination.
  • sweeteners such as sodium saccharin, stevioside, aspartame, D-Xylose, and the like may be used in combination in amounts ranging from 0 to 1%, preferably 0.01 to 0.5% by weight of the total composition. .
  • anionic surfactants include sodium lauryl sulfate, sodium alkyl sulfate such as myristyl sulfate, sodium N-lauroyl sarcosinate, sodium N-miristyl sarcosinate, and the like.
  • Sodium N-acylsarcosinate may be used, and non-ionic surfactants, sugar fatty acid esters such as sugar fatty acid esters, maltose fatty acid esters, lactose fatty acid esters, polyoxyethylene Cured castor oil, polyoxyethylene higher alcohol ether, polyoxyethylene polyoxypropylene copolymer, polyoxyethylene polypropylene fatty acid ester and the like can be used.
  • sugar fatty acid esters such as sugar fatty acid esters, maltose fatty acid esters, lactose fatty acid esters, polyoxyethylene Cured castor oil, polyoxyethylene higher alcohol ether, polyoxyethylene polyoxypropylene copolymer, polyoxyethylene polypropylene fatty acid ester and the like can be used.
  • Zwitterionic surfactants include N-alkyl diaminoethylglycine, such as N-lauryl di aminoethylglycine, N-myristyl diaminoethylglycine, N-alkyl-N-carboxy methyl ammonium betaine, 2-alkyl-1 -Hydroxy ethyl imidazoline betaine sodium, etc. can be used. And pluron-based and poloxamer-based surfactants may be used. In this case, anionic surfactants are mainly used as foaming components, and sodium alkyl sulfates such as sodium lauryl sulfate are most widely used. In addition, these surfactant is used individually by 1 type or in mixture of 2 or more types, The compounding quantity is used in the range of 0.01-0.5 weight%, More preferably, 0.05-0.3 weight% of the whole composition normally.
  • oral compositions of the present invention include various nutrients, vitamins, minerals (electrolytes), flavors such as synthetic and natural flavors, colorants and neutralizing agents (such as cheese, chocolate), pectic acid and salts thereof, alginic acid and Salts, organic acids, protective colloid thickeners, stabilizers, preservatives, glycerin, alcohols, carbonation agents used in carbonated drinks, and the like.
  • the oral compositions of the present invention may contain flesh for the production of natural fruit juices and fruit juice beverages and vegetable beverages. These components can be used independently or in combination. The proportion of such additives is not so critical but is generally selected in the range of 0 to 20 parts by weight per 100 parts by weight of the composition of the present invention.
  • the mouthwash or mouthwash may also include suitable formulation ingredients, and formulating ingredients for formulation into these mouthwashes or mouthwashes will be understood by those skilled in the art, for example, carriers. It may include water to maintain a liquid at room temperature, lower alcohols having 1 to 4 carbon atoms, polyhydric alcohols, etc., and may further include other colorants, flavors, flavors, sweeteners and the like.
  • the oral composition for inhibiting bad breath may be filled in a double container having a septum.
  • a double container having such a diaphragm it may be desirable to satisfy the preference of the consumer to have the same composition on both sides based on the diaphragm of the double container, but filled with different colors.
  • Example 1 described in Table 1 below is an oral composition comprising a natural medicinal herb extract and tocopherol acetate and malic acid as essential, including a golden extract and a mold extract according to the present invention
  • Example 2 is a natural medicinal herbs in addition to Example 1
  • the extract further comprises an equivalent amount of Yeongyo extract, Geumgumhwa extract and Gilgyeong extract.
  • the oral composition of Comparative Example 1 is an oral composition, which is configured in the same manner as in Example 1, except that in Example 1 it does not contain the golden extract, mold extract, tocopherol acetate and malic acid.
  • the oral compositions of Comparative Example 1 and Examples 1 and 2 were formulated with toothpaste, and 2 g of the oral composition formulated with toothpaste was suspended and diluted in 9 g of sterile phosphate buffer solution.
  • Example 1 Amorphous sorbitol 30 30 30 30 Polyethylene Glycol 300 2 2 2 Carboxymethyl Cellulose One One One Tocopherol Acetate - 0.1 0.1 Zaccarin Sodium 0.22 0.22 0.22 Apple and mountain - 0.1 0.1 Calcium Phosphate Dichloride 0.1 0.1 0.1 Sedimentation Silica 30 30 30 Sedimentation silica (for increasing) 3 3 3 Sodium Lauryl Sulfate 1.55 1.55 1.55 Sodium fluoride 0.22 0.22 0.22 Golden extract - 0.5 0.5 Mold extract - 0.5 0.5 Duct extract - - 0.5 Gold Coin Extract - - 0.5 Gilt Extract - - 0.5 Yellow No.
  • the diluted suspension was serially diluted 2-fold with BHI (Brain heart infusion) medium and injected into 1 ml of 48 well plates.
  • BHI Brain heart infusion
  • one Streptococcus mutans (ATCC 25175) colony was suspended in 20 ml BHI medium in an agar medium and additionally injected into the diluted 48-well plate and incubated at 37 ° C. for 24 hours.
  • MIC minimum inhibition concentration
  • natural herbal extracts including golden extract and mold extract and oral composition comprising tocopherol acetate and malic acid (Example 1) and Yeongyo extract, Geummi extract and Gilpyeong extract in addition to Example 1 were further added. It was confirmed that the oral composition (Example 2) containing the superior antimicrobial activity compared to Comparative Example 1 otherwise.
  • oral compositions containing herbal prescriptions were shown to be similar to Comparative Example 1 in antibacterial activity, but they also exhibited antibacterial activity against Popuromonas gingivavalis which is a periodontitis-inducing bacterium. It is also expected to be excellent in inhibiting periodontal inflammation.
  • Example 4 Amorphous sorbitol 30 30 30 30 Polyethylene Glycol 300 2 2 2 Carboxymethyl Cellulose One One One Tocopherol Acetate - 0.1 0.1 Zaccarin Sodium 0.22 0.22 0.22 Apple and mountain - 0.1 0.1 Calcium Phosphate Dichloride 0.1 0.1 0.1 Golden extract 0.5 0.5 Mold extract 0.5 0.5 Duct extract - 0.5 Gold Coin Extract - 0.5 Gilt Extract - 0.5 Titanium dioxide 0.1 0.1 0.1 Sodium monophosphate 0.1 0.1 0.1 0.1 Sodium monophosphate 0.1 0.1 0.1 0.1 Trisodium Phosphate 0.05 0.05 0.05 Purified water 66.43 65.23 63.73
  • Fibroblasts were cultured to see the inhibitory activity of MMP-3 and treated with the oral composition.
  • Human gum fibroblasts (Human Gingvial Fibroblast) were collected from healthy tissues of humans without a history of periodontitis and used for the first culture.
  • Fetal bovine serum fetal bovine serum
  • GibcoBRL GibcoBRL, USA
  • antibiotics / antimycotics 100 U / ml penicillin, 25 ⁇ g / ml amphotericin
  • DMEM Dulbecco's modified Eagle's medium
  • Gum fibroblasts from humans cultured in cultured with 1% FBS were incubated for 24 hours, followed by sodium monofluorophosphate, sodium lauryl sulfate, paraoxybenzoic acid and mint B70097, which may cause cell toxicity.
  • the other oral compositions were treated with phosphate buffer at a concentration of 200 ppm and 500 ppm for 30 minutes, followed by addition of interleukin-1 ⁇ (100 ng / ml) and incubated for 48 hours (MMP-3). Supernatant only by centrifugation during MMP-3 activity was measured using an ELISA kit (Amersham Bioscience, UK), and the results are shown in Table 7.
  • gyeonghyang extract including the gyeonghyang extract (Example 3) is shown to be more effective than the comparative example 2, Yeongyo extract, gyeonghyang extract as the main inhibitor component It seems to work.
  • the composition of herbal medicine containing Yeongyo extract, hyunggwa extract, gilding extract, gilyeong extract (Example 4) is a little better MMP-3 inhibitory effect than Example 3, so the gilge extract, gilyeong extract is yeonkyo extract, hyunggae The extract and synergistic effect are considered to be indicative.
  • the mixture was left for 3 minutes and centrifuged at 14000 rpm for 15 minutes.
  • the supernatant containing ribonucleic acid was transferred to a new tube and mixed with 500 ⁇ l of isopropyl alcohol. After 10 minutes, the supernatant was discarded again by centrifugation, 1 ml of 75% ethanol was added to the precipitate, and centrifuged at 10000 rpm for 5 minutes, the supernatant was discarded, and the precipitated ribonucleic acid was dried at room temperature for 20 minutes. The dried ribonucleic acid was suspended in distilled water treated with DEPC (Diethylpyrocarbonate, Sigma).
  • cDNA complementary nucleic acid
  • RT-PreMix RT-PreMix
  • Synthesized cDNA was used as a template to mix interleukin-1 ⁇ and cyclooxygenase-2 primers, and the expression level of ribonucleic acid was confirmed using PCR Premix (AccuPower PCR PreMix, Bioneer).
  • COX-2 primers were mixed with the synthesized cDNA template, and the expression level of ribonucleic acid was confirmed using PCR Premix (AccuPower PCR PreMix, Bioneer). Quantitative analysis was performed using a densitometer (Image Gauge V 3.46, Koshin Graphic Systems, Fuji Photo Film Co., Japan).
  • the composition comprising a herbal prescription (combination extract, formulation containing a hyunggae extract) (Examples 3 and 4)
  • a herbal prescription combination extract, formulation containing a hyunggae extract
  • Comparative Example 2 it was confirmed that the interleukin-1 ⁇ and cyclooxygenase-2 gene expression more effectively suppressed.
  • the expression inhibition rate of cyclooxygenase-2 was confirmed to be significantly reduced by 50% or more in Example 3, 4 500ppm.
  • the suppression rate of the oral composition (Examples 3 and 4) containing an herbal prescription according to this invention is excellent. From this, it was confirmed that the herbal composition prescribed according to the present invention is very effective in inhibiting periodontal anti-inflammatory.
  • Example 1 of the present invention All oral compositions of Example 1 of the present invention, including herbal prescription, effectively inhibit the growth of dental caries, bad breath-causing and periodontitis-causing bacteria, MMP-3 directly involved in periodontal tissue destruction, interleukin-1 ⁇ and cycloox It was confirmed to effectively inhibit the gene genease-2 expression.
  • the present invention can be used in the industry of manufacturing hygiene products, especially oral compositions such as toothpaste or mouthwashes.

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Abstract

The present invention relates to an oral composition which has excellent effects in halitosis inhibition, dental caries inhibition and peridontal disease inhibition, the oral composition comprising natural medicinal ingredient extracts essentially comprising Scutellariae Radix extract and Nepetae Spica extract, and additionally comprising forsythia fruit extract, lonicer aflower extract and platycodi radix extract, etc., and the oral composition further comprising tocopheryl acetate and malic acid. The oral composition comprises 0.1 to 5.0 % by weight of a mixture of the natural medicinal ingredient extracts including Scutellariae Radix extract and Nepetae Spica extract, 0.01 to 1.0 % by weight of tocopheryl acetate, and 0.01 to 1.0 % by weight of malic acid.

Description

구취 억제용 구강 조성물Oral composition for bad breath
본 발명은 구취 억제용 구강 조성물에 관한 것으로 특히, 황금 추출물 및 형개 추출물을 필수로 포함하고, 그리고, 거기에 더해 연교 추출물, 금은화 추출물 및 길경 추출물 등을 포함하는 천연 약재 추출물을 포함하고, 거기에 더해 초산 토코페롤 및 사과산을 더 포함하여 구취 억제, 치아우식증 억제 및 치주질환 억제 효과가 뛰어난 구강 조성물에 관한 것이다.The present invention relates to an oral composition for inhibiting bad breath, and in particular, it comprises a golden extract and a mold extract, and in addition to the natural medicinal extract including a duct extract, gold silver extract, gilyeong extract, etc. In addition, the present invention relates to an oral composition excellent in inhibiting bad breath, inhibiting dental caries and inhibiting periodontal disease, further including tocopherol acetate and malic acid.
충치란 치은연상 및 치은연하의 치면세균막에 존재하는 미생물들에 의해 음식물 중의 탄수화물이 대사되어, 국소적으로 생산된 유기산의 작용으로 인해 치아의 경조직이 파괴되는 질환으로, 그 예방은 우리나라 뿐만 아니라 세계적인 관심사 중 하나이다. 충치는 인간의 생명에는 직접적인 관계가 없다고 하나, 음식물의 저작기능이 저하되므로, 소화계통의 질병에 직간접으로 영향을 미친다. 충지의 이환율은 특히 어린이에게 많은데, 5세 어린이의 85%에 이르고 있을 정도로 누구나 충치로 인한 고통을 경험했거나 경험한다. 이러한 충치는 구강 내의 미생물들 중 특히 스트렙토코커스 뮤탄스(Streptococcs mutans: S. mutans) 에 의해 발생되는데, 그 미생물에 의한 충치유발 작용기전을 살펴보면 다음과 같다. 스트렙토코커스 뮤탄스는 그람 양성 통성 혐기성 세균으로, 구강 내 치면세균막에 상주하며, 음식물에 포함된 탄수화물, 특히 포도당, 과당 등을 분해하고, 그 대사과정에서 발생하는 부산물인 유기산, 주로 젖산을 세균 외로 방출하여 치아의 법랑질을 파괴한다(김종배 외, 공중구강보건학, 고문사, pp 68-84, 1991).Tooth decay is a disease in which carbohydrates in food are metabolized by microorganisms in the gingival and subgingival bacterial membranes, and the hard tissues of teeth are destroyed by the action of locally produced organic acids. One of the concerns. Tooth decay does not have a direct relationship to human life, but the chewing function of food deteriorates, so it directly or indirectly affects diseases of the digestive system. The prevalence of tooth decay is especially high in children, with 85% of children aged 5 or older experiencing or experiencing pain from tooth decay. This tooth decay is caused by Streptococcs mutans ( S. mutans ), among the microorganisms in the oral cavity. The mechanism of caries induced by the microorganisms is as follows. Streptococcus mutans is a Gram-positive anaerobic bacterium that resides in the dental plaque in the oral cavity. To destroy enamel of teeth (Kim Jong-bae et al., Public Oral Health Science, Advisor, pp. 68-84, 1991).
구취는 대부분의 경우, 구강 내에서 숙주성분과 음식 잔류물이 세균에 의해 부패된 결과로 85% 이상이 구강 내에 원인이 있다고 보고 있다. 구강 내 원인들로는 설태, 치주질환, 불결한 구강 위생상태, 음식물 잔사, 부적절한 보철물, 비위생적인 의치, 구강암종 등 여러 원인들이 있으나, 현재 구취의 가장 중요한 원인으로 설태와 치주질환이 언급되고 있다. 휘발성 황화합물(volatile sulfur compounds; VSC)이 구취의 주된 원인 인자로, 황화수소(hydrogen sulfide: H2S), 메틸머캅탄(methyl mercaptan: CH3SH), 디메틸설파이드(dimethyl sulfide: CH3SCH3) 등이 있으며, 이중 황화수소와 메틸머캅틴이 90% 가량 차지한다고 하였다. 이러한 VSC는 주로 치은열구액, 타액, 음식물 잔사 내에 포함된 단백질(특히 시스테인(cysteine)과 메티오닌(methionine)을 포함하는 것들), 펩타이드, 아미노산 등을 기질로 이용한 구강 내 혐기성 세균의 부패활동에 의해 생성된다. 대표적인 그람 음성 혐기성 세균은 포르피로모나스 진지발리스(Porphyromonas gingivalis), 프레보텔라 인터미디아(Prevotella intermedia), 후소박테리움 뉴클레아툼(Fusobacterium nucleatum) 등이 있으며, 많은 양의 황화수소와 메틸머캅탄이 생성됨이 보고되고 있다. 결과적으로, 치주질환 세균이 구취유발에 중요한 역할을 할 것으로 보고하였다. 많은 연구들에서 휘발성 황화합물이 치주조직에 유해한 작용을 가짐이 밝혀졌는데, VSC가 조직에 미치는 작용으로, 점막의 투과성 증가, 콜라겐(collagen) 분해 증가, 치은섬유아세포와 치주인대세포의 활성 변화, 창상 치유 지연 효과 등이 실험적으로 입증되었다(권진희 등, 대한치주과학회지 2000).In most cases, bad breath causes more than 85% of the root causes of oral disease as a result of bacterial decay of host components and food residues in the oral cavity. Intraoral causes include tongue, periodontal disease, dirty oral hygiene, food residues, inadequate prostheses, unsanitary dentures, oral carcinoma, but the most important causes of bad breath are tongue and periodontal disease. Volatile sulfur compounds (VSC) are the main cause of bad breath: hydrogen sulfide (H 2 S), methyl mercaptan (CH 3 SH), dimethyl sulfide (CH 3 SCH 3 ) And hydrogen sulfide and methyl mercaptin account for about 90%. These VSCs are mainly caused by the decay activity of anaerobic bacteria in the oral cavity using gingival fissure, saliva, proteins in food residues (particularly those containing cysteine and methionine), peptides and amino acids as substrates. Is generated. Representative Gram-negative anaerobic bacteria include Porphyromonas gingivalis , Prevotella intermedia , Fusobacterium nucleatum , and large amounts of hydrogen sulfide and methylmercaptan. Is being reported. As a result, it has been reported that periodontal disease bacteria play an important role in inducing bad breath. Many studies have shown that volatile sulfur compounds have a detrimental effect on periodontal tissues. VSC's action on tissues increases mucosal permeability, collagen breakdown, changes in gingival fibroblasts and periodontal ligament cells, and wounds. The effects of delayed healing have been experimentally demonstrated (Kwon Jin-hee et al., The Korean Periodontological Society 2000).
세포 내 기질단백질인 MMP3는 만성 염증성 질환, 류마티스 관절염, 피부질환, 암과 같은 여러 질환에서 조직파괴와 조직 재구성에 관여하는 중요한 단백질분해효소로 간주되고 있으며, 치주질환과 관련된 다형핵 백혈구, 섬유아세포, 대식세포, 상피세포 등에서 발현되어 치주염의 원인효소로 알려져 있다(조종희 등 대한치주과학회지 1999).MMP3, an intracellular matrix protein, is considered to be an important protease involved in tissue destruction and tissue reorganization in various diseases such as chronic inflammatory disease, rheumatoid arthritis, skin disease, and cancer, and polymorphonuclear leukocytes and fibroblasts associated with periodontal disease It is expressed in macrophages, epithelial cells, etc. and is known as the causative enzyme of periodontitis (Cho Jong-Hee et al 1999).
치주염은 치은, 치주인대, 백악질 그리고 치조골과 같은 치아-지지 조직의 파괴를 초래하는 염증성 질환이다. 치주염은 인터류킨 1β(interleukin-1β: IL-1β) 같은 사이토카인(cytokines)의 존재와 강하게 연관된다. 그리고 생리적으로 사이클로옥시게나아제(cyclooxygenases: COX)의 활성화는 치주염과도 밀접히 연관되어 있다. 특히 COX-2는 염증 전 사이토카인과 세균에 의한 생산물에 의해 활성이 유도된다(김선우 등 대한치주과학회지 2007).Periodontitis is an inflammatory disease that results in the destruction of tooth-supporting tissues such as gingiva, periodontal ligament, chalky and alveolar bone. Periodontitis is strongly associated with the presence of cytokines such as interleukin-1β (IL-1β). Physiologically, the activation of cyclooxygenases (COX) is closely related to periodontitis. In particular, COX-2 is induced by the production of cytokines and bacteria before inflammation (Kim, Sun-Woo et al. 2007).
한편, 예로부터 구강질환의 예방이나 치료를 위해 여러 생약제를 이용한 기록을 볼 수 있으며, 벌꿀, 장미유, 구운 소금, 한약제재 등과 같은 여러 획득가능한 물질들을 구강 질환의 예방이나 치료에 사용하여 왔다는 것이 여러 기록들을 통하여 밝혀지고 있으나, 여전히 구취 억제, 치아우식증 억제 및 치주질환 억제 효과가 뛰어난 구강 조성물의 개발이 요구되고 있는 실정이다.On the other hand, the record of using various herbal medicines for the prevention or treatment of oral diseases has been seen from the past, and it has been said that various obtainable substances such as honey, rose oil, roasted salt, and herbal medicines have been used for the prevention or treatment of oral diseases. Although it is revealed through the records, there is still a need for the development of oral compositions excellent in inhibiting bad breath, inhibiting dental caries and periodontal disease.
본 발명은 위와 같은 종래 기술의 문제점을 해결하기 위하여 예의 연구한 결과, 황금 추출물 및 형개 추출물을 필수로 포함하고, 그리고, 거기에 더해 연교 추출물, 금은화 추출물 및 길경 추출물 등을 포함하는 천연 약재 추출물을 포함하고, 거기에 더해 초산 토코페롤 및 사과산을 더 포함하여 구취 억제, 치아우식증 억제 및 치주질환 억제 효과가 뛰어난 구강 조성물을 제공할 수 있음을 확인하고, 본 발명을 완성하기에 이른 것이다.The present invention has been conducted in order to solve the problems of the prior art, as a result, it is essential to include a golden extract and a mold extract, and, in addition to the natural medicinal extracts including yeongyo extract, gold silver extract and Gilyeong extract, etc. In addition, tocopherol acetate and malic acid were further included, and it was confirmed that it can provide the oral composition which is excellent in the bad breath suppression, the dental caries suppression, and the periodontal disease suppression effect, and came to complete this invention.
특히, pH를 바람직하게는 6 내지 8, 보다 바람직하게는 타액과 같은 중성으로 유지할 수 있도록 하는 조성의 구강 조성물을 제공함을 목적으로 한다.In particular, it is an object to provide an oral composition having a composition such that the pH is preferably maintained at 6 to 8, more preferably neutral such as saliva.
본 발명에 따른 구취 억제용 구강 조성물은, 황금 추출물 및 형개 추출물을 포함하는 천연 약재 추출물의 혼합물 0.1 내지 5.0중량%, 초산 토코페롤 0.01 내지 1.0중량%, 사과산 0.01 내지 1.0중량%를 포함한다.Oral composition for inhibiting bad breath according to the present invention, 0.1 to 5.0% by weight of the mixture of natural medicinal extracts, including golden extract and mold extract, 0.01 to 1.0% by weight of tocopherol acetate, 0.01 to 1.0% by weight of malic acid.
바람직하게는, 상기 천연 약재 추출물은 연교 추출물, 금은화 추출물, 길경 추출물 및 이들 중 2이상의 혼합물로 이루어지는 군으로부터 선택되는 추출물 0.1 내지 5.0중량%을 더 포함할 수 있다.Preferably, the natural medicinal herb extract may further comprise 0.1 to 5.0% by weight of an extract selected from the group consisting of duct bridge extract, gilding extract, gilyeong extract and a mixture of two or more thereof.
바람직하게는, 상기 구취 억제용 구강 조성물은 6 내지 8의 범위 이내의 pH를 가질 수 있으며, 보다 바람직하게는 중성일 수 있다.Preferably, the oral composition for inhibiting bad breath may have a pH within the range of 6 to 8, more preferably may be neutral.
상기 구취 억제용 구강 조성물은 페이스트상일 수 있으며, 특히, 치약, 구강 청정제 또는 구강 세정제로 제형화된 것일 수 있다.The oral composition for inhibiting bad breath may be a paste, and in particular, may be formulated with a toothpaste, mouthwash or mouthwash.
상기 구취 억제용 구강 조성물은, 바람직하게는, 격막이 있는 이중용기 내에 충진된 것일 수 있다.The oral composition for inhibiting bad breath, preferably, may be filled in a double container having a septum.
본 발명에 따르면, 황금 추출물 및 형개 추출물을 필수로 포함하고, 그리고, 거기에 더해 연교 추출물, 금은화 추출물 및 길경 추출물 등을 포함하는 천연 약재 추출물을 포함하고, 거기에 더해 초산 토코페롤 및 사과산을 더 포함하여 구취 억제, 치아우식증 억제 및 치주질환 억제 효과가 뛰어난 구강 조성물을 제공하는 효과가 있다.According to the present invention, essential extracts include golden extracts and mold extracts, and in addition, natural herbal extracts, including duct extracts, gold and silver extracts, and gil dynasty extracts, and the like, and further include tocopherol acetate and malic acid. Therefore, there is an effect of providing an oral composition excellent in inhibiting bad breath, inhibiting dental caries and periodontal disease.
도 1은 본 발명에 따른 구강 조성물의 인터류킨 1β 유전자 발현 억제 효과를 대조군 및 비교예들과 비교하여 나타내는 그래프이다.1 is a graph showing the interleukin 1β gene expression inhibitory effect of the oral composition according to the present invention in comparison with the control and comparative examples.
도 2는 본 발명에 따른 구강 조성물의 사이클로옥시게나아제-2(COX-2) 유전자 발현 억제 효과를 대조군 및 비교예들과 비교하여 나타내는 그래프이다.Figure 2 is a graph showing the cyclooxygenase-2 (COX-2) gene expression inhibitory effect of the oral composition according to the present invention in comparison with the control and comparative examples.
이하, 본 발명의 구체적인 실시예를 첨부한 도면을 참조하여 상세히 설명한다.Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings.
본 발명에 따른 구취 억제용 구강 조성물은, 황금 추출물 및 형개 추출물을 포함하는 천연 약재 추출물의 혼합물 0.1 내지 5.0중량%, 초산 토코페롤 0.01 내지 1.0중량%, 사과산 0.01 내지 1.0중량%를 포함함을 특징으로 한다.Oral composition for inhibiting bad breath according to the present invention, characterized in that it comprises 0.1 to 5.0% by weight of the mixture of natural medicinal extracts, including golden extract and mold extract, 0.01 to 1.0% by weight of tocopherol acetate, 0.01 to 1.0% by weight of malic acid do.
본 발명에서 사용되는 상기 금은화 추출물, 연교 추출물, 형개 추출물, 길경 추출물들은 당업계에 널리 알려진 통상적인 추출방법으로 추출한 것을 사용할 수 있으며, 바람직하게는 열수추출방법이나 에탄올 혹은 물과 에탄을 혼합하여 추출한 것을 사용할 수 있다.The sterling silver extract, duct bridge extract, mold extract, gilyeong extracts used in the present invention may be extracted by conventional extraction methods well known in the art, preferably hot water extraction method or extracted by mixing ethanol or water and ethane Can be used.
상기 천연 약재 추출물 중의 황금 추출물은 꿀풀과에 속하는 여러해살이 초본식물인 황금(Scutellaria baicalensis GEORGE)의 뿌리의 추출물이다. 상기 초본식물인 황금은 각지에서 재배하여 널리 약용으로 쓰이고 있고, 약효성분은 바이카레인(Baicalein), 바이카린(Baicalin), 워고닌(Wogonin), 워고노사이드(Wogonoside) 등이 알려져 있다. 맛은 쓰고 약성은 차다. 효능은 실화(實火)를 내려주므로, 신체에 열이 많고 번조와 갈증을 심하게 나타내면서 심하면 의식이 혼몽한 증상을 개선시킨다. 감기로 인한 고열에서부터 일반적인 전염성질환의 고열에 해열효과가 높은 것으로 알려져 있다. 폐에 열이 쌓여서 일어나는 해소에 현저한 반응을 보이는데, 이것은 급성폐렴이나 급성기관지염의 고열해소, 천식에 탁월한 반응을 나타내는 것이다. 위장에 열이 있으면서 소화장애가 심하고 더 악화되면 입 안이 헤지고 구내염이 발생하면서 음식물을 먹을 수 없는 증상에도 활용되며 급성황달에도 효력을 보인다고 알려져 있다. 체내에 열이 과다하게 쌓여서 일어나는 안구충혈과 동통을 제거하고, 고혈압, 두통, 코피, 자궁출혈에도 활용되며, 피부발적 종기에도 효력이 있다. 이와 같은 효능은 찬 약성이 열을 내리므로 증상을 완화시키기 때문인 것으로 알려져 있다. 열이 심하여 일어나는 갈증을 풀어주고, 전신의 관절마디마다 열이 나고 아픈 증상을 해소시킨다. 약리실험에서는 항염증반응, 항병원미생물작용, 해열, 이뇨, 혈압강하작용, 혈당과 고지혈증강하, 담즙분비촉진, 진정작용 등이 나타났다.The golden extract of the natural medicinal extract is an extract of the root of golden ( Scutellaria baicalensis GEORGE ), which is a perennial herbaceous plant belonging to the Lamiaceae. Gold is a herbaceous plant cultivated in various places and is widely used for medicinal, the active ingredient is known as Baikalein (Baicalein), Baikalin (Baicalin), wogonin (Wogonin), wogonoside (Wogonoside) and the like. The taste is bitter and weak. Efficacy is a fact that lowers (實 火), so the body has a lot of fever and hunger and thirst severely, if you improve the symptoms of conscious confusion. It is known that antipyretic effect is high from high fever due to cold to high fever of general infectious disease. Responds to the accumulation of heat in the lungs, which is a remarkable response to acute pneumonia, acute bronchitis, high fever and asthma is an excellent response. If gastrointestinal fever is severe and worsens digestive disorders, it is known to be effective in acute jaundice as well as symptoms of mouthache and stomatitis. Eliminates ocular hyperemia and pain caused by excessive heat build up in the body, high blood pressure, headache, nosebleeds, uterine bleeding, and is effective in skin boils. Such efficacy is known to be because cold medicine relieves symptoms because it lowers the fever. To quench the thirst caused by severe fever, and to relieve the symptoms of fever and pain in every joint joint. In pharmacological experiments, anti-inflammatory reactions, anti-pathogenic microorganisms, antipyretics, diuresis, lowering blood pressure, lowering blood sugar and hyperlipidemia, promoting bile secretion, and sedation were shown.
상기 형개 추출물은 형개라는 꿀풀과에 속하는 한해살이풀의 추출물로서, 형개는 가소라고 불릴 정도로 자줏빛이 나는 차조기와 모양과 색깔이 비슷하며, 식용보다는 약용으로 주로 사용된다. 한방에서는 형개의 전초와 그 꽃이 달린 이삭을 형개수라고 하여 약재로 사용하고 있다. 동의보감 본초에 따르면 “성질이 따뜻하고 맛이 매우면서 쓰며 독이 없다. 악풍, 적풍, 온몸에 감각이 없는 것, 상한으로 머리가 아프고 힘줄과 뼈가 달면서 아픈 것과 혈로, 풍기를 치료하며 나력과 창양을 낫게 한다. 밭에 심는다. 어릴 때는 향기롭고 맛이 맵기 때문에 채소로 먹을 수 있는데, 생으로도 먹고 익혀서도 먹는다. 또한 달여 차를 만들어 먹으면 머리와 눈이 시원하다. 꽃과 씨로 이삭을 이룬 것을 베서 햇볕에 말려 약으로 쓴다. 본래 이름은 가소라고 하는데 그것은 냄새와 맛이 차조기 비슷하기 때문이다.”라고 기재하고 있다. 동의보감 단방에 따르면 형개 효능 및 먹는법으로 “머리가 핑핑 돌고 눈 앞이 어지러운 것을 치료하는데 두풍증에 중요하게 쓰는 약이다. 달여 먹거나 가루를 내어 먹어도 다 좋다. 두풍을 치료하는데 형개수와 석고(달군 것)를 각각 같은 양으로 하여 가루를 내서 한번에 8g씩 생강이나 파를 달인 물에 타 먹는다. 일명 형개산이라고도 한다. 땀이 나게 한다. 또한 혈풍도 치료하는데 물에 달여서 먹는다. 손과 발의 힘줄이 땅기는 것을 치료한다. 물에 달여 먹는다. 만문한 것으로 생절이를 해 먹어도 좋다. 중풍으로 입과 눈이 비뚤어지고 저린 것과 모든 풍증을 치료한다. 물에 달여 먹는다. 짓찧어 식초에 개어 정창에 붙이면 효과가 좋다. 물에 진하게 달여서 먹어도 좋다. 상한으로 머리가 아플 때에 형개수 40g을 진하게 달여 먹는다. 땀을 나게 하여 표를 푼다. 물에 달여 먹는다. 붕루가 멎지 않는 것을 치료한다. 약성이 남게 태워 가루내어 한번에 8g씩 먹는다.”라고 기재하고 있다. The hyunggae extract is an extract of the annual herb belonging to the family Lamiaceae called hyeonggae, hyeonggae is called purple, so the shape and color is similar to a purple tea, it is mainly used for medicinal rather than edible. In oriental medicine, Hyeonggae's outpost and the flowered ear are used as medicine for Hyeonggaesu. According to Dongbobom Herb, “The quality is warm, the taste is very bitter, and it is poisonous. Bad winds, red winds, lack of sensation all over the body, upper head hurts, tendons and bones are sweet and heal and blood flow, bleeding, healing Nagwa and Changyang. Plant in the field. When you are young, you can eat vegetables because they are fragrant and spicy. You can eat them raw or cooked. Also, if you make a tea over moon, your head and eyes will be cool. Cut the ears of flowers and seeds, dry them in the sun, and use them as medicine. The original name is Kaso because it smells and tastes like a perilla. ” According to Dongbogam, one of the most effective medicines for diaphragm is to treat dizziness and dizziness in front of eyes. It's good to eat decocted or powdered. To heal the swelling in the same amount of mold and gypsum (dalgun), each powder is powdered 8g at a time to eat ginger or green onions in water. Also known as Hyeonggae Mountain. Makes you sweat It also treats the blood breeze, which is eaten in water. Heals the tendons of hands and feet. Eat decoction in water. You can eat raw foods in full. The stroke causes the mouth and eyes to be crooked and swept away and to heal all the symptoms. Eat decoction in water. Squeeze it into the vinegar and paste it on the window. It is good to eat it by thickening it in water. When the head hurts to the upper limit, 40g of gyeonghyeong number is thickly eaten. Make yourself sweat and solve the ticket. Eat decoction in water. Heal what does not break. The drug is burned and the powder is eaten 8g at a time. ”
본 발명에서는 상기 황금 추출물과 형개 추출물을 필수적으로 포함하는 천연 약재 추출물을 포함하며, 상기 천연 약재 추출물은 본 발명에 따른 구취 억제용 구강 조성물 총 중량을 기준으로 0.1 내지 5.0중량%의 범위 이내의 양으로 포함되는 것이 구취 억제 효과에 바람직하다.The present invention includes a natural medicinal herb extract comprising essentially the golden extract and hyeonghyeong extract, the natural medicinal extract is an amount within the range of 0.1 to 5.0% by weight based on the total weight of oral composition for inhibiting bad breath according to the present invention It is preferable for the bad breath inhibitory effect to be contained.
본 발명에 따른 상기 구취 억제용 구강 조성물은 상기한 천연 약재 추출물에 더해 초산 토코페롤과 사과산을 더 포함한다.The oral composition for inhibiting bad breath according to the present invention further comprises tocopherol acetate and malic acid in addition to the above-mentioned natural herbal extracts.
상기 초산 토코페롤(tocopherol acetate)은 비타민 E 아세테이트로 유리형 비타민 E와는 다르고, 분자식은 C31H5203, 분자량 472.73으로 연황색, 점성의 액체이다. 초산 아세테이트는 공기, 광, 자외선 등의 산화제에 의해서 영향을 받지 않는다. 물에 녹지 않으며, 아세톤, 클로로포름, 에테르에는 가용하고, 알코올에도 조금은 녹는다. 토코페롤은 비타민 E 오일로 천연 산화방지제 역할 뿐만 아니라, 노화피부 및 세포재생의 효능이 있어서 피부에서는 주로 캡슐 형태로 활용된다. 특히 치아에서도 이러한 기능이 있어서 유효한 일정량을 첨가하면 치은염, 치주염(치조농루)의 예방, 치주 및 치은질환의 예방에 효과가 있는 것으로 알려져 있다. 상기 초산 토코페롤은 본 발명에 따른 구취 억제용 구강 조성물 총 중량을 기준으로 0.01 내지 1.0중량%의 범위 이내의 양으로 사용되는 것이 바람직하다.The tocopherol acetate (tocopherol acetate) is a vitamin E acetate is different from the free vitamin E, the molecular formula is C 31 H 52 0 3 , molecular weight 472.73 is a light yellow, viscous liquid. Acetate acetate is not affected by oxidizing agents such as air, light and ultraviolet light. Insoluble in water, soluble in acetone, chloroform and ether, slightly soluble in alcohol. Tocopherol is a vitamin E oil that not only acts as a natural antioxidant, but also has the effect of aging skin and cell regeneration, so it is mainly used in capsule form in skin. In particular, teeth have such a function, and it is known that the addition of an effective amount is effective in the prevention of gingivitis, periodontitis (alveolar pylori), and the prevention of periodontal and gingival diseases. The tocopherol acetate is preferably used in an amount within the range of 0.01 to 1.0% by weight based on the total weight of oral composition for inhibiting bad breath according to the present invention.
상기 사과산(Malic Acid)은 달리 능금산이라고도 한다. 무색의 침상결정으로 화학식은 C4H6O5, 비대칭탄소원자를 1개 가지고 있으며, D-, L- 및 DL- 3종의 광학이성질체가 존재한다. 좌회전성인 L-말산은 사과, 포도 등 천연 과일과 야채 등에 함유되어 있다. 조해성이 있으며, 분자량 134.09, 비중 1.595, 녹는점 100℃, 끓는점 140℃ 이다. 같은 산미제인 구연산에 비해 산도가 강하고, 가격도 저렴할 뿐만 아니라, 우아하고 세련된 고급 산미를 나타내고 산미(酸味) 지속이 훨씬 길어 사람의 입맛을 한층 즐겁게 하여 청량음료에 신맛을 나게 하는 데 사용한다. 사람의 탄수화물 신진대사에 필요한 산미제이기도 하며, 특히 구강에서는 산성의 산미로서 구취를 감소 및 억제시키거나 pH 조절제로서 작용을 한다. 상기 사과산은 본 발명에 따른 구취 억제용 구강 조성물 총 중량을 기준으로 0.01 내지 1.0중량%의 범위 이내의 양으로 사용되는 것이 바람직하다.The malic acid (Malic Acid) is also referred to as umseongumum otherwise. It is a colorless acicular crystal with the chemical formula C 4 H 6 O 5 , one asymmetric carbon atom, and D-, L-, and DL-3 optical isomers. Left-rotating L-malic acid is found in natural fruits and vegetables, such as apples and grapes. Deliquescent, molecular weight 134.09, specific gravity 1.595, melting point 100 ℃, boiling point 140 ℃. Compared to citric acid, citric acid, which has the same acidity, is not only cheaper in price, but also elegant and refined high-quality acidity and long-lasting acidity make people's appetite more pleasant and sour. It is also an acidic agent necessary for carbohydrate metabolism in humans, and especially in the oral cavity, it is an acidic acid, which reduces and inhibits bad breath and acts as a pH regulator. The malic acid is preferably used in an amount within the range of 0.01 to 1.0% by weight based on the total weight of the oral composition for inhibiting bad breath according to the present invention.
달리, 상기 천연 약재 추출물에는 연교 추출물, 금은화 추출물, 길경 추출물 및 이들 중 2이상의 혼합물로 이루어지는 군으로부터 선택되는 추출물을 본 발명에 따른 구취 억제용 구강 조성물 총 중량을 기준으로 0.1 내지 5.0중량%의 범위 이내의 양으로 더 포함하는 것이 구취 억제 효과에 특히 바람직하다.In contrast, the natural medicinal herb extract ranges from 0.1 to 5.0% by weight, based on the total weight of the oral composition for inhibiting bad breath according to the present invention, the extract selected from the group consisting of duct bridge extract, gold silver extract, gilyeong extract and a mixture of two or more thereof It is especially preferable for the bad breath inhibitory effect to contain in the quantity within the below.
상기 연교 추출물은 연교라는 물푸레나무과에 속하는 의성개나리 및 동속식물의 열매의 추출물이다. 연교의 성미는 쓰고 차가우며, 귀경은 심경, 폐경, 간경에 작용하는 것으로 알려져 있다. 또한, 발한, 청열작용, 배농해독, 해열작용, 항균, 소염, 발열, 두통, 구갈, 해수, 인후통, 종기류, 구토억제, 혈관확장 및 혈류개선작용 등의 효능이 있는 것으로 알려져 있다. 또한, 이뇨작용(소변을 잘 나오게함), 강심이뇨작용(심장을 튼튼하게하고 소변을 잘 나오게함), 청열해독(열을 식히며 독소를 제거함), 소종산결(종기를 가라앉히고 뭉친 것을 풀어줌)의 효과가 있는 것으로 알려져 있다.The Yeongyo extract is an extract of the fruit of the Forsythia forsythia and the same plant belonging to the ash family called Yeongyo. Yeon-gyo's temper is bitter and cold, and the ear canal is known to act on the heart, menopause and liver. In addition, it is known to have the effects of sweating, clearing, drainage, antipyretic, antibacterial, anti-inflammatory, fever, headache, dry mouth, seawater, sore throat, boils, vomiting, vasodilation and blood flow improvement. In addition, diuretic effect (to make urine well), cardiac diuresis (to strengthen the heart and urine well), clearing detoxification (cools the heat, removes toxins), small squirt (to cool the boil and loosen the masses) It is known that there is an effect.
상기 금은화 추출물은 금은화라는 인동과의 반상록 덩굴식물로서, 쌍떡잎식물의 꼭두서니목의 식물의 추출물이다. 예로부터, 답답하고 갈증이 심할 때, 종기의 치료, 피부가 헐어 있거나, 장기의 염증 및 농을 배출시킬 때, 이질이나 열독에 의한 피부괴사에, 유행성 이하선염이나 결막염에, 그리고 편도선, 인후염, 기관지염, 방광염 등의 염증의 치료에 주로 사용하였다. 고전의학서들에 따르면 인동덩굴의 성질은 차고 맛은 달며 조금 쓰고, 심경, 폐경에 작용하며, 열을 내리고, 독을 풀어주고, 경맥을 잘 통하게 하며, 여러 가지 염증질환에 탁월한 효과가 있으며, 창상과 종기, 부스럼을 고친다고 전해지고 있다.The sterling silver extract is a semi-heterophyllum vine plant of the genus Rosaceae, and is an extract of the plant of the cedar. From ancient times, when it is stuffy and thirsty, treatment of boils, skin is loose, organ inflammation and pus discharge, skin necrosis by dysentery or heat poisoning, mumps or conjunctivitis, and tonsils, sore throat, bronchitis It was mainly used for the treatment of inflammation such as cystitis. According to classical medicine, the nature of honeysuckle is cold, sweet and bitter, acts on the heart and menopause, lowers the heat, releases the poison, improves the meridians, has excellent effects on various inflammatory diseases, It is said that heals boils and boils.
상기 길경 추출물은 길경, 즉 도라지의 추출물이다. 도라지는 우리나라 전역에서 자생하며, 도라지생채, 도라지나물 등으로 많이 식용하고, 제사상에도 올라가는 삼색 나물 가운데 하나로 인정할 만큼 흔한 재료이다. 오래된 도라지는 산삼보다도 낫다’는 얘기가 있습니다. 실제로 우수한 알칼리성 식품인 도라지에는 식이섬유는 물론 칼슘, 철분, 칼륨 등의 미네랄과 비타민B1, B2, 비타민C 그리고 티로신, 트립토판 등의 유익한 아미노산이 풍부하게 함유되어 있다. 이 같은 영양성분 때문인지 동의보감에는 도라지의 효능에 관한 기록이 278종이나 된다고 한다. 도라지는 초롱과에 속하는 여러해살이 풀이다. 생약명으로 길경, 방도, 백약, 경초, 고경, 이여라고도 부른다. 주로 뿌리를 약으로 사용하는데, 가을에 채취하여 껍질을 벗겨서 햇볕에 말린 후, 꼭지를 따 버리고 사용한다. 뿌리에 사포닌의 일종인 플라티코딘, 플라티코디게닌이 함유되어 있다. 일반적으로 도라지는 기침, 가래에 쓰인다고 많이 알려져 있다. 특히 도라지에는 인삼의 주요 성분으로 알려진 쌉쌀한 맛의 사포닌이 약 100g당 2g 정도 들어 있는데, 트리테르페노이드(triterpenoid)계 사포닌의 경우, 호흡기 질환에 효능을 보인다. 호흡기 점막의 점액분비를 늘려주고, 가래도 삭혀준다고 알려져 있다. 도라지와 배를 혼합한 도라지배즙은 겨울철 목감기 예방약으로 널리 사용되고 있다. 기침과 가래 약으로 유명한 용각산의 주재료도 바로 도라지이다. 특히 한방에서는 배농, 거담, 편도선염, 최유, 진해, 화농성 종기, 천식 및 폐결핵의 거담제로서, 그리고 늑막염 등에도 효과가 있는 것으로 알려져 있다. 도라지는 혈압과 혈당을 낮춰주는 기능이 있어 체중이 많이 나가는 고혈압 환자나 당뇨병 환자들이 먹으면 유익하다고 알려져 있다. 도라지는 체내 스테로이드와 갈릭산(galic acid)의 분비를 증강시켜서 체내 콜레스테롤 감소를 유도하기 때문에 고지혈증 환자들이 먹으면 도움이 된다고 알려져 있다. 최근에는 도라지에서 종양을 억제하는 물질이 분리되었고, 항돌연변이 효과도 확인되었다. 도라지를 에틸아세테이트로 추출한 물질을 간암세포에 반응시키면 강한 항산화효과를 나타내 산화적 스트레스로 인해 세포가 암에 걸리지 않도록 보호할 수 있다는 사실도 밝혀졌다.The Giltyeong extract is an extract of Giltyeong, ie Bellflower. Bellflower is native to Korea and is common enough to be recognized as one of the three color herbs that are edible a lot of bellflowers, bellflowers, etc. Old bellflower is better than wild ginseng. ” Indeed, the excellent alkaline food bellflower is rich in dietary fiber as well as minerals such as calcium, iron and potassium, as well as beneficial amino acids such as vitamins B1, B2, vitamin C and tyrosine and tryptophan. It is said that there are 278 records about the efficacy of bellflower. Bellflower is a perennial plant belonging to the lantern family. In the name of the herbal medicine, Gilgyeong, Bangdo, Paekak, Goryeo, Kogyeong, also called Yeo. The root is mainly used as a medicine, which is taken in the fall, peeled and dried in the sun, and then the stem is removed and used. The root contains saponins, Platicodin and Platicodigenin. The bellflower is commonly used for cough and phlegm. In particular, the bellflower contains about 2g per 100g of bitter saponin, which is known as the main ingredient of ginseng, and triterpenoid-based saponins show efficacy in respiratory diseases. It is known to increase mucus secretion of the respiratory mucosa and to cut phlegm. Bellflower juice, which is a mixture of bellflower and pears, is widely used as a winter preventive medicine. The main ingredient of Yonggaksan, famous for cough and phlegm, is bellflower. Especially in oriental medicine, it is known to be effective as drainage, expectorant, tonsillitis, oily, cough, purulent boil, expectorant of asthma and pulmonary tuberculosis, and pleurisy. Bellflower is known to be beneficial for people with high blood pressure and diabetes who weigh a lot because it lowers blood pressure and blood sugar. Bellflower is known to help people with hyperlipidemia because it increases the secretion of steroids and galic acid in the body, leading to a decrease in cholesterol in the body. Recently, tumor suppressors have been isolated from bellflower, and antimutagenic effects have been identified. It was also found that when the bellflower extract was extracted with ethyl acetate, hepatic cancer cells reacted with a strong antioxidant effect, protecting the cells from cancer by oxidative stress.
달리 본 발명에 따른 구취 억제용 구강 조성물은 상기 사과산에 더해 구연산을 0.01 내지 1.0중량%의 범위 이내의 양으로 더 포함하는 것이 바람직하다.Oral composition for inhibiting bad breath according to the present invention preferably further comprises citric acid in an amount within the range of 0.01 to 1.0% by weight in addition to the malic acid.
상기 구취 억제용 구강 조성물은 6 내지 8의 범위 이내의 pH, 바람직하게는 중성이 되도록 하는 양으로 사용되는 것이 바람직하다.The oral composition for inhibiting bad breath is preferably used in an amount such that the pH is within the range of 6 to 8, preferably neutral.
본 발명에서 본 발명의 추출물 또는 화합물을 함유하는 구강조성물은 페이스트 및 액상 제조하여 사용할 수 있으며, 바람직하게는 상기 구취 억제용 구강 조성물은 페이스트상인 것일 수 있으나, 이에 한정하는 것은 아니다.Oral composition containing the extract or compound of the present invention in the present invention can be used to prepare a paste and liquid, preferably, the bad breath control oral composition may be a paste, but is not limited thereto.
본 발명의 구강 조성물은 치약, 구강 청정제 또는 구강 세정제로 제형화될 수 있다. 특히, 상기 치약은 제형화 성분으로서 연마제, 점결제, 보습제, 유효성분, 발포제, 감미료, 향미제로 이루어진 군에서 선택된 조성물을 포함할 수 있으며, 이들 치약으로의 제형화를 위한 제형화 성분들은 당업자에게는 공지된 것으로 이해될 수 있는 것이다. The oral composition of the present invention may be formulated as a toothpaste, mouthwash or mouthwash. In particular, the toothpaste may comprise a composition selected from the group consisting of abrasives, caking agents, moisturizers, active ingredients, foaming agents, sweeteners, flavoring agents as the formulation ingredients, the formulation ingredients for formulation to these toothpastes are It can be understood as known.
상기 연마제로는 수산화알루미늄, 무수규산, 규산알루미늄, 제2인산칼슘, 제2수산화물 및 무수물, 제3인산칼슘, 탄산칼슘, 피로인산칼슘, 불용성 메타인산나트륨, 제3인산마그네슘, 탄산마그네슘, 황산칼슘, 폴리메타아크릴산메틸, 기타 합성수지 등에서 1종 또는 2종 이상을 전체 조성물의 약 20 내지 90중량%의 양으로 배합하여 사용할 수 있다(페이스트 치약의 경우에는 20 내지 60중량%의 범위 이내가 될 수 있다).Examples of the abrasive include aluminum hydroxide, silicic anhydride, aluminum silicate, dicalcium phosphate, dihydrate and anhydride, tricalcium phosphate, calcium carbonate, calcium pyrophosphate, insoluble sodium metaphosphate, magnesium triphosphate, magnesium carbonate, and sulfuric acid. Calcium, polymethyl methacrylate, and other synthetic resins may be used in combination of one or two or more of them in an amount of about 20 to 90% by weight of the total composition (in the case of paste toothpaste, it may be within the range of 20 to 60% by weight). Can be).
상기 점결제로는 카라기닌, 각종 점증용 셀룰로오스 유도체, 잔탄검, 트라가칸트 검(Tragacanth gum) 등의 검류, 폴리비닐 알콜, 폴리아크릴산 나트륨, 폴리아크릴산/말레인산 공중합체, 카르복시비닐 폴리머 등의 합성고분자 유도체 등의 유기계 점결제와 실리카, 라포나이트 등의 무기계 점결제에서 1종 또는 2종 이상을 전체 조성물의 약 0.3 내지 5중량%의 범위 이내의 양으로 배합하여 사용할 수 있다.Examples of the binder include carrageenan, various incremental cellulose derivatives, xanthan gum, gums such as tragacanth gum, polyvinyl alcohol, sodium polyacrylate, polyacrylic acid / maleic acid copolymer, and carboxyvinyl polymer. In organic binders, such as a polymer derivative, and inorganic binders, such as a silica and a laponite, 1 type, or 2 or more types can be mix | blended and used in the quantity within the range of about 0.3 to 5 weight% of the whole composition.
상기 보습제로는 페이스트상과 액상 구강용 조성물에서는 그 제조 시 보습제로 솔비톨, 글리세린, 에틸렌글리콜, 프로필렌글리콜, 폴리에테르글리콜, 폴리프로필렌글리콜 등에서 1종 또는 2종 이상을 전체 조성물의 약 10 내지 70%의 양으로 배합하여 사용할 수 있다.In the pasty and liquid oral composition, the moisturizing agent may include one or two or more of about 10 to 70% of sorbitol, glycerin, ethylene glycol, propylene glycol, polyether glycol, polypropylene glycol, etc. It can be used in combination.
또한 사카린나트륨, 스테비오사이드, 아스파탐, D-자일로스(D-Xylose) 등과 같은 감미제 등을 전체 조성물의 0 내지 1%, 바람직하게는 0.01 내지 0.5중량%의 범위 이내의 양으로 배합하여 사용할 수 있다.In addition, sweeteners such as sodium saccharin, stevioside, aspartame, D-Xylose, and the like may be used in combination in amounts ranging from 0 to 1%, preferably 0.01 to 0.5% by weight of the total composition. .
또한 본 발명의 구강 조성물에서 발포성분으로 사용하는 계면활성제로는 음이온 계면활성제, 비이온계면활성제, 양성이온 계면활성제 및/또는 플루론계(Pluron),폴록사머계(Poloxamer) 계면 활성제를 사용할 수 있다. 여기에서, 음이온 계면활성제로는 라우릴황산나트륨, 미리스틸황산나트륨 등의 알킬황산나트륨, N-라우로일사르코신산나트륨(Sodium N-Lauroylsarcosinate), N-미리스틸사르코신산나트륨(Sodium N-miristyl sarcosinate) 등의 N-아실사르코신산나트륨(Sodium N-acylsarcosinate) 등을 사용할 수 있고, 비이온 계면활성제로는 슈가지방산 에스테르, 말토스 지방산 에스테르, 락토스 지방산 에스테르 등과 같은 당(糖)유래 지방산 에스테르, 폴리옥시에틸렌 경화 피마자유, 폴리옥시에틸렌고급알콜 에테르, 폴리옥시에틸렌 폴리옥시프로필렌 공중합체, 폴리옥시에틸렌 폴리프로필렌지방산 에스테르 등을 사용할 수 있다. 양성이온 계면활성제로는 N-라우릴 디 아미노에틸글리신, N-미리스틸 디아미노에틸글리신 등과 같은 N-알킬 디 아미노에틸글리신, N-알킬-N-카르복시 메틸 암모늄 베타인, 2-알킬-1-하이드록시 에틸 이미다조린 베타인 나트륨 등을 사용할 수 있다. 그리고 플루론계,폴록사머계 계면 활성제 등을 사용할 수 있다. 이 경우, 발포성분으로는 음이온 계면활성제를 주로 사용하며, 대표적인 것으로는 라우릴황산나트륨과 같은 알킬황산나트륨을 가장 널리 사용하고 있다. 또한 이들 계면활성제는 1종 단독 또는 2종 이상 혼합하여 사용하며, 배합량은 통상 전체 조성물의 0.01 내지 0.5중량%, 보다 바람직하게는 0.05 내지 0.3중량%의 범위 이내의 양을 사용한다.In addition, as the surfactant used in the oral composition of the present invention as a foaming component, anionic surfactants, nonionic surfactants, zwitterionic surfactants and / or Pluron-based and poloxamer-based surfactants may be used. . Here, the anionic surfactants include sodium lauryl sulfate, sodium alkyl sulfate such as myristyl sulfate, sodium N-lauroyl sarcosinate, sodium N-miristyl sarcosinate, and the like. Sodium N-acylsarcosinate (Sodium N-acylsarcosinate) may be used, and non-ionic surfactants, sugar fatty acid esters such as sugar fatty acid esters, maltose fatty acid esters, lactose fatty acid esters, polyoxyethylene Cured castor oil, polyoxyethylene higher alcohol ether, polyoxyethylene polyoxypropylene copolymer, polyoxyethylene polypropylene fatty acid ester and the like can be used. Zwitterionic surfactants include N-alkyl diaminoethylglycine, such as N-lauryl di aminoethylglycine, N-myristyl diaminoethylglycine, N-alkyl-N-carboxy methyl ammonium betaine, 2-alkyl-1 -Hydroxy ethyl imidazoline betaine sodium, etc. can be used. And pluron-based and poloxamer-based surfactants may be used. In this case, anionic surfactants are mainly used as foaming components, and sodium alkyl sulfates such as sodium lauryl sulfate are most widely used. In addition, these surfactant is used individually by 1 type or in mixture of 2 or more types, The compounding quantity is used in the range of 0.01-0.5 weight%, More preferably, 0.05-0.3 weight% of the whole composition normally.
상기 외에 본 발명의 구강 조성물은 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 중진제(치즈, 초콜릿 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, 안정화제, 방부제, 글리세린, 알코올, 탄산음료에 사용되는 탄산화제 등을 함유할 수 있다. 그밖에 본 발명의 구강 조성물들은 천연 과일 쥬스 및 과일 쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 이러한 첨가제의 비율은 그렇게 중요하진 않지만 본 발명의 조성물 100중량부 당 0 내지 20중량부의 범위에서 선택되는 것이 일반적이다.In addition to the above, oral compositions of the present invention include various nutrients, vitamins, minerals (electrolytes), flavors such as synthetic and natural flavors, colorants and neutralizing agents (such as cheese, chocolate), pectic acid and salts thereof, alginic acid and Salts, organic acids, protective colloid thickeners, stabilizers, preservatives, glycerin, alcohols, carbonation agents used in carbonated drinks, and the like. In addition, the oral compositions of the present invention may contain flesh for the production of natural fruit juices and fruit juice beverages and vegetable beverages. These components can be used independently or in combination. The proportion of such additives is not so critical but is generally selected in the range of 0 to 20 parts by weight per 100 parts by weight of the composition of the present invention.
상기 구강 청정제 또는 구강 세정제 역시 적절한 제형화 성분들을 포함할 수 있으며, 이들 구강 청정제 또는 구강 세정제로로의 제형화를 위한 제형화 성분들은 당업자에게는 공지된 것으로 이해될 수 있는 것이며, 예를 들면, 담체로서 상온에서 액상을 유지하는 물, 탄소수 1 내지 4의 저급 알코올, 다가 알코올 등을 포함할 수 있으며, 기타, 착색제, 착향제, 향미제, 감미료 등을 더 포함할 수 있다.The mouthwash or mouthwash may also include suitable formulation ingredients, and formulating ingredients for formulation into these mouthwashes or mouthwashes will be understood by those skilled in the art, for example, carriers. It may include water to maintain a liquid at room temperature, lower alcohols having 1 to 4 carbon atoms, polyhydric alcohols, etc., and may further include other colorants, flavors, flavors, sweeteners and the like.
상기 구취 억제용 구강 조성물은 격막이 있는 이중용기 내에 충진된 것일 수 있다. 이러한 격막이 있는 이중용기 내에 충진되는 경우, 이중용기의 격막을 기준으로 양측에 동일한 조성을 가지나, 색상 만을 달리하여 충진되는 것이 소비자의 기호도를 만족시키는 데 바람직할 수 있다.The oral composition for inhibiting bad breath may be filled in a double container having a septum. When filled in a double container having such a diaphragm, it may be desirable to satisfy the preference of the consumer to have the same composition on both sides based on the diaphragm of the double container, but filled with different colors.
이하에서 본 발명의 바람직한 실시예 및 비교예들이 기술되어질 것이다.Hereinafter, preferred embodiments and comparative examples of the present invention will be described.
이하의 실시예들은 본 발명을 예증하기 위한 것으로서 본 발명의 범위를 국한시키는 것으로 이해되어져서는 안될 것이다.The following examples are intended to illustrate the invention and should not be understood as limiting the scope of the invention.
하기 표 1 기재의 실시예 1은 본 발명에 따라 황금 추출물 및 형개 추출물을 포함하는 천연 약재 추출물과 초산 토코페롤 및 사과산을 필수로 포함하는 구강 조성물이고, 실시예 2는 상기 실시예 1에 더해 천연 약재 추출물로서 연교 추출물, 금은화 추출물 및 길경 추출물을 등량으로 더 포함하는 것을 제외하고는 상기 실시예 1과 동일한 구강 조성물이다. 한편, 비교예 1의 구강 조성물은 상기 실시예 1에서 황금 추출물, 형개 추출물, 초산 토코페롤 및 사과산을 포함하지 않는 것을 제외하고는 상기 실시예 1과 동일하게 구성된 구강 조성물이다.Example 1 described in Table 1 below is an oral composition comprising a natural medicinal herb extract and tocopherol acetate and malic acid as essential, including a golden extract and a mold extract according to the present invention, Example 2 is a natural medicinal herbs in addition to Example 1 It is the same oral composition as in Example 1, except that the extract further comprises an equivalent amount of Yeongyo extract, Geumgumhwa extract and Gilgyeong extract. On the other hand, the oral composition of Comparative Example 1 is an oral composition, which is configured in the same manner as in Example 1, except that in Example 1 it does not contain the golden extract, mold extract, tocopherol acetate and malic acid.
하기 표들의 조성과 함량으로 정확히 칭량하고 혼합한 후, 일반적인 치약의 제조방법으로 치약으로 제조하였다.After precisely weighing and mixing the composition and content of the following tables, it was prepared as a toothpaste by a general toothpaste manufacturing method.
<실험예 1> 스트렙토코커스 뮤탄스(Streptococcus mutans)의 항균력 시험Experimental Example 1 Antibacterial Activity Test of Streptococcus mutans
상기 비교예 1, 그리고 실시예 1 및 2의 구강 조성물을 치약으로 제형화하고, 치약으로 제형화된 구강 조성물 2g을 멸균된 인산완충액 9g에 희석 현탁시켜 하기와 같은 방법으로 실험을 실시하였다.The oral compositions of Comparative Example 1 and Examples 1 and 2 were formulated with toothpaste, and 2 g of the oral composition formulated with toothpaste was suspended and diluted in 9 g of sterile phosphate buffer solution.
표 1
원료명 비교예 1 실시예 1 실시예 2
비결정 솔비톨 30 30 30
폴리에틸렌글리콜 300 2 2 2
카르복시메틸셀룰로오스 1 1 1
초산 토코페롤 - 0.1 0.1
삭카린나트륨 0.22 0.22 0.22
사 과 산 - 0.1 0.1
칼슘인산염이염화물 0.1 0.1 0.1
침강실리카(연마제용) 30 30 30
침강실리카(점증용) 3 3 3
라우릴황산나트륨 1.55 1.55 1.55
불화나트륨 0.22 0.22 0.22
황금 추출물 - 0.5 0.5
형개 추출물 - 0.5 0.5
연교 추출물 - - 0.5
금은화 추출물 - - 0.5
길경 추출물 - - 0.5
황색4호(FDC#5) 0.002 0.002 0.002
녹색3호(FDC#5) 0.0005 0.0005 0.0005
치약향(Flavor) 1.05 1.05 1.05
이산화티탄 0.1 0.1 0.1
제1인산나트륨 0.1 0.1 0.1
제3인산나트륨 0.05 0.05 0.05
정제수 30.6075 29.4075 27.9075
Table 1
Raw material name Comparative Example 1 Example 1 Example 2
Amorphous sorbitol 30 30 30
Polyethylene Glycol 300 2 2 2
Carboxymethyl Cellulose One One One
Tocopherol Acetate - 0.1 0.1
Zaccarin Sodium 0.22 0.22 0.22
Apple and mountain - 0.1 0.1
Calcium Phosphate Dichloride 0.1 0.1 0.1
Sedimentation Silica 30 30 30
Sedimentation silica (for increasing) 3 3 3
Sodium Lauryl Sulfate 1.55 1.55 1.55
Sodium fluoride 0.22 0.22 0.22
Golden extract - 0.5 0.5
Mold extract - 0.5 0.5
Duct extract - - 0.5
Gold Coin Extract - - 0.5
Gilt Extract - - 0.5
Yellow No. 4 (FDC # 5) 0.002 0.002 0.002
Green No. 3 (FDC # 5) 0.0005 0.0005 0.0005
Toothpaste Flavor 1.05 1.05 1.05
Titanium dioxide 0.1 0.1 0.1
Sodium monophosphate 0.1 0.1 0.1
Trisodium Phosphate 0.05 0.05 0.05
Purified water 30.6075 29.4075 27.9075
상기 희석된 현탁액을 BHI(Brain heart infusion) 배지로 2배씩 연속 희석시켜 48웰 플레이트(well plate)에 1㎖씩 주입하였다. 그리고 한천배지에서 스트렙토코커스 뮤탄스(Streptococcus mutans, ATCC 25175) 콜로니(colony) 1개를 20㎖ BHI 배지에 현탁시킨 다음 상기 희석시킨 48웰 플레이트에 추가적으로 주입하여 37℃에서 24시간 배양한 후, 항균력을 MIC(minimal inhibition concentration)로 측정하였으며, 그 결과를 하기 표 2에 나타내었다.The diluted suspension was serially diluted 2-fold with BHI (Brain heart infusion) medium and injected into 1 ml of 48 well plates. In addition, one Streptococcus mutans (ATCC 25175) colony was suspended in 20 ml BHI medium in an agar medium and additionally injected into the diluted 48-well plate and incubated at 37 ° C. for 24 hours. Was measured by MIC (minimal inhibition concentration), and the results are shown in Table 2 below.
표 2
종류 비교예 1 실시예 1 실시예 2
㎎/㎖ 12.5 6.25 6.25
TABLE 2
Kinds Comparative Example 1 Example 1 Example 2
Mg / ml 12.5 6.25 6.25
그 결과, 본 발명에 따라 황금 추출물 및 형개 추출물을 포함하는 천연 약재 추출물 그리고 초산 토코페롤 및 사과산을 포함하는 구강 조성물(실시예 1) 및 상기 실시예 1에 더해 연교 추출물, 금은화 추출물 및 길경 추출물을 더 포함하는 구강 조성물(실시예 2)이 그렇지 않은 비교예 1에 비하여 항균력이 더 우수한 것을 확인할 수 있었다.As a result, according to the present invention, natural herbal extracts including golden extract and mold extract and oral composition comprising tocopherol acetate and malic acid (Example 1) and Yeongyo extract, Geummi extract and Gilpyeong extract in addition to Example 1 were further added. It was confirmed that the oral composition (Example 2) containing the superior antimicrobial activity compared to Comparative Example 1 otherwise.
<실험예 2> 혐기성 미생물에서의 항균력 시험Experimental Example 2 Antimicrobial Activity Test in Anaerobic Microorganisms
실험예 1에서처럼 비교예와 실시예들의 구강 조성물 2g을 멸균된 인산완충액 9g에 희석 현탁시켜 하기와 같은 방법으로 실험을 실시하였다. MIC방법은 실험예 1과 동일하게 시행하였다. 다만, 혐기성 미생물이 산소가 있는 상태에서는 자라지 않기 때문에 5% 수소(H2)와 95% 질소(N2)가 공급되는 혐기성 배양기(Sheldon Manufactoring Bac 2-2E)에서 배양하여 실험에 사용하였으며, 그 결과를 하기 표 3에 나타내었다.As in Experiment 1, 2g of the oral composition of Comparative Example and Examples was diluted and suspended in 9g of sterile phosphate buffer, and the experiment was carried out as follows. MIC method was carried out in the same manner as in Experiment 1. However, because anaerobic microorganisms do not grow in the presence of oxygen, they were cultured in an anaerobic incubator (Sheldon Manufactoring Bac 2-2E) supplied with 5% hydrogen (H 2 ) and 95% nitrogen (N 2 ). The results are shown in Table 3 below.
표 3
균주(㎎/㎖) 비교예 1 실시예 1 실시예 2
포퓨로모나스 진지발리스ATCC 33277 12.50 6.50 6.50
프리보텔라 인터메디아ATCC 25611 6.50 6.50 6.50
후소박테리움 뉴클레아툼ATCC 25586 6.50 6.50 6.50
TABLE 3
Strain (mg / ml) Comparative Example 1 Example 1 Example 2
Popuromonas Serious Bally ATCC 33277 12.50 6.50 6.50
Prebotella Intermediate ATCC 25611 6.50 6.50 6.50
Husobacterium nucleatumATCC 25586 6.50 6.50 6.50
그 결과, 본 발명에 따라 한방처방을 함유한 구강 조성물(실시예 1, 2)들이 항균력에서는 비교예 1과 유사하게 나타났으나, 치주염 유발균인 포퓨로모나스 진지발리스에도 항균력을 나타내는 것으로 보아 치주염증억제에도 우수할 것으로 판단된다.As a result, according to the present invention, oral compositions containing herbal prescriptions (Examples 1 and 2) were shown to be similar to Comparative Example 1 in antibacterial activity, but they also exhibited antibacterial activity against Popuromonas gingivavalis which is a periodontitis-inducing bacterium. It is also expected to be excellent in inhibiting periodontal inflammation.
<실험예 3> MMP-3의 활성저해능 평가Experimental Example 3 Evaluation of Activity Inhibitory Activity of MMP-3
하기 표 4와 같이 상기 비교예 1 및 실시예 1 및 2의 구강 조성물에서 불화나트륨, 라우릴황산나트륨, 향(flavor), 색소 등을 제외한 처방을 사용(비교예 2 및 실시예 3 및 4)하여 MMP-3의 활성저해능을 평가하였다.In the oral compositions of Comparative Example 1 and Examples 1 and 2, as shown in Table 4, using the formulation except for sodium fluoride, sodium lauryl sulfate, flavor, pigment, etc. (Comparative Examples 2 and 3 and 4) The inhibitory activity of MMP-3 was evaluated.
표 4
원료명 비교예 2 실시예 3 실시예 4
비결정 솔비톨 30 30 30
폴리에틸렌글리콜 300 2 2 2
카르복시메틸셀룰로오스 1 1 1
초산 토코페롤 - 0.1 0.1
삭카린나트륨 0.22 0.22 0.22
사 과 산 - 0.1 0.1
칼슘인산염이염화물 0.1 0.1 0.1
황금 추출물 0.5 0.5
형개 추출물 0.5 0.5
연교 추출물 - 0.5
금은화 추출물 - 0.5
길경 추출물 - 0.5
이산화티탄 0.1 0.1 0.1
제1인산나트륨 0.1 0.1 0.1
제3인산나트륨 0.05 0.05 0.05
정제수 66.43 65.23 63.73
Table 4
Raw material name Comparative Example 2 Example 3 Example 4
Amorphous sorbitol 30 30 30
Polyethylene Glycol 300 2 2 2
Carboxymethyl Cellulose One One One
Tocopherol Acetate - 0.1 0.1
Zaccarin Sodium 0.22 0.22 0.22
Apple and mountain - 0.1 0.1
Calcium Phosphate Dichloride 0.1 0.1 0.1
Golden extract 0.5 0.5
Mold extract 0.5 0.5
Duct extract - 0.5
Gold Coin Extract - 0.5
Gilt Extract - 0.5
Titanium dioxide 0.1 0.1 0.1
Sodium monophosphate 0.1 0.1 0.1
Trisodium Phosphate 0.05 0.05 0.05
Purified water 66.43 65.23 63.73
MMP-3의 활성저해능을 보기 위해 섬유아세포를 배양하고, 상기 구강 조성물로 처리하여 아래와 같이 실시하였다. 사람의 잇몸 섬유아세포(Human Gingvial Fibroblast)는 치주염 병력이 없는 사람의 건강한 조직에서 채취하여 1차 배양하여 실험에 사용하였다. 10% FBS(Fetal bovine serum; 우태혈청)(GibcoBRL, USA)와 1% 항생물질(antibiotics)/항균성 물질(antimycotics)(100U/㎖의 페니실린(penicillin), 25㎍/㎖의 암포테르신(amphotericin) D 및 100㎍/㎖의 스트렙토마이신(streptomycin)이 함유된 DMEM(Dulbecco's modified Eagle's medium)(GibcoBRL, USA) 배지를 이용하여 37℃, 5% 이산화탄소(CO2) 항온기에서 배양하였다. 100㎜ 접시에서 배양한 사람의 잇몸 섬유아세포를 1% FBS가 함유된 배양액으로 교환하여 24시간 배양한 다음, 세포의 독성을 유발할 수 있는 일불소인산나트륨, 라우릴황산나트륨, 파라옥시안식향산매칠 및 민트향 B70097을 제외한 구강 조성물들을 인산완충액을 이용 200ppm, 500ppm농도로 하여 30분간 전처리를 하여 인터루킨-1β(100ng/㎖)를 첨가, 48시간(MMP-3) 배양하였다. 배양 후에는 배양액을 모아 1500rpm/5분 동안 원심 분리하여 상층액 만을 실험에 사용하였으며, MMP-3 활성도는 ELISA키트(Amersham Bioscience, UK)를 이용하여 측정하였으며, 그 결과를 표 7에 나타내었다.Fibroblasts were cultured to see the inhibitory activity of MMP-3 and treated with the oral composition. Human gum fibroblasts (Human Gingvial Fibroblast) were collected from healthy tissues of humans without a history of periodontitis and used for the first culture. Fetal bovine serum (fetal bovine serum) (GibcoBRL, USA) and 1% antibiotics / antimycotics (100 U / ml penicillin, 25 µg / ml amphotericin) Cultured in a 37 ° C., 5% carbon dioxide (CO 2 ) incubator using Dulbecco's modified Eagle's medium (DMEM) medium containing D) and 100 μg / ml streptomycin. Gum fibroblasts from humans cultured in cultured with 1% FBS were incubated for 24 hours, followed by sodium monofluorophosphate, sodium lauryl sulfate, paraoxybenzoic acid and mint B70097, which may cause cell toxicity. The other oral compositions were treated with phosphate buffer at a concentration of 200 ppm and 500 ppm for 30 minutes, followed by addition of interleukin-1β (100 ng / ml) and incubated for 48 hours (MMP-3). Supernatant only by centrifugation during MMP-3 activity was measured using an ELISA kit (Amersham Bioscience, UK), and the results are shown in Table 7.
표 5
MMP-3 활성(ng/㎖) 무처리군 IL-1β 비교예 2+ IL-1β 실시예 3+ IL-1β 실시예 4+ IL-1β
200ppm 4.25 17.50 16.36 9.25 8.95
500ppm 4.67 18.10 14.56 4.76 4.50
Table 5
MMP-3 Activity (ng / ml) No treatment group IL-1β Comparative Example 2+ IL-1β Example 3+ IL-1β Example 4+ IL-1β
200 ppm 4.25 17.50 16.36 9.25 8.95
500 ppm 4.67 18.10 14.56 4.76 4.50
본 발명에 따라 연교 추출물, 형개 추출물을 포함하는 한방처방의 조성물(실시예 3)이 그렇지 않은 비교예 2에 비해 효과가 높은 것으로 나타남에 기초하여 볼 때, 연교 추출물, 형개 추출물이 주요 억제 성분으로 작용하는 것으로 판단된다. 또한 연교 추출물, 형개 추출물, 금은화 추출물, 길경추출물을 포함하는 한방처방의 조성물(실시예 4)이 실시예 3보다 MMP-3억제 효과가 조금 더 우수한 것으로 보아 금은화 추출물, 길경추출물이 연교 추출물, 형개 추출물과 상승효과가 나타내는 것으로 판단된다.According to the present invention, based on the composition of the herbal prescription, gyeonghyang extract, including the gyeonghyang extract (Example 3) is shown to be more effective than the comparative example 2, Yeongyo extract, gyeonghyang extract as the main inhibitor component It seems to work. In addition, the composition of herbal medicine containing Yeongyo extract, hyunggwa extract, gilding extract, gilyeong extract (Example 4) is a little better MMP-3 inhibitory effect than Example 3, so the gilge extract, gilyeong extract is yeonkyo extract, hyunggae The extract and synergistic effect are considered to be indicative.
<실험예 4> 항염증 지표인 인터류킨-1β와 사이클로옥시게나아제-2(cox-2)의 발현 억제시험(RT-PCR)Experimental Example 4 Anti-inflammatory Indices Interleukin-1β and Cyclooxygenase-2 (cox-2) Expression Inhibition Test (RT-PCR)
100㎜ 페트리디쉬에 1×106개의 Raw264.7 세포주를 분주하고, 배합 조성물에서 세포의 독성을 유발할 수 있는 일불소인산나트륨, 라우릴황산나트륨, 파라옥시안식향산메칠 및 민트향 B70097을 제외한 구강 조성물을 인산완충액을 이용 200ppm, 500ppm농도로 처리하고 LPS로 염증을 유도시켜 24시간 배양한 후, 배지를 제거한 다음, 세포를 배양용기로부터 떼어내어 리보핵산 추출 용액(Invitrogen, CA, USA)을 사용하여 세포를 균질화 하였다. 5분 후에 세포를 모아서 원심분리관에 옮기고, 200㎕의 클로로포름을 넣고 15초간 완전히 섞어준 후, 3분간 방치한 다음 14000rpm에서 15분간 원심분리하였다. 리보핵산을 포함하는 상등액을 새로운 관에 옮겨 담고, 아이소프로필알코올 500㎕와 혼합하였다. 10분 후, 다시 원심분리를 하여 상등액은 버리고, 침천물에 75% 에탄올 1㎖을 넣고 10000rpm에서 5분간 원심분리한 후, 상등액을 버리고, 침전된 리보핵산을 20분간 상온에서 건조시켰다. 건조된 리보핵산은 DEPC(Diethylpyrocarbonate, Sigma)가 처리된 증류수로 현탁하였다. 리보핵산은 정량 후, RT-PreMix(AccuPower RT PreMix, 바이오니아)를 이용하여 상보적 핵산(cDNA)을 합성하였다. 합성된 cDNA를 주형(template)으로 인터류킨-1β와 사이클로옥시게나아제-2 프라이머를 각각 혼합한 후, PCR Premix(AccuPower PCR PreMix, 바이오니아)를 사용하여 리보핵산의 발현 정도를 확인하였다. 합성된 cDNA를 주형으로 COX-2 프라이머를 혼합하고, PCR Premix(AccuPower PCR PreMix, 바이오니아)를 사용하여 리보핵산의 발현 정도를 확인하였다. 정량 분석은 덴시토미터(densitometer: Image Gauge V 3.46, Koshin Graphic Systems, Fuji Photo Film Co., Japan)을 이용하여 시행되었다. Dispense 1 × 10 6 Raw264.7 cell lines into 100 mm Petri dishes and remove the oral composition except sodium monofluorophosphate, sodium lauryl sulfate, paraoxybenzoic acid methyl, and mint B70097, which may cause cellular toxicity in the formulation. Treatment with phosphate buffer at 200ppm, 500ppm concentration, induce inflammation with LPS, incubate for 24 hours, remove the medium, remove the cells from the culture vessel, and use the ribonucleic acid extract solution (Invitrogen, CA, USA) Was homogenized. After 5 minutes, the cells were collected and transferred to a centrifuge tube. 200 μl of chloroform was added and mixed thoroughly for 15 seconds. The mixture was left for 3 minutes and centrifuged at 14000 rpm for 15 minutes. The supernatant containing ribonucleic acid was transferred to a new tube and mixed with 500 μl of isopropyl alcohol. After 10 minutes, the supernatant was discarded again by centrifugation, 1 ml of 75% ethanol was added to the precipitate, and centrifuged at 10000 rpm for 5 minutes, the supernatant was discarded, and the precipitated ribonucleic acid was dried at room temperature for 20 minutes. The dried ribonucleic acid was suspended in distilled water treated with DEPC (Diethylpyrocarbonate, Sigma). After quantification of ribonucleic acid, complementary nucleic acid (cDNA) was synthesized using RT-PreMix (AccuPower RT PreMix, Bioneer). Synthesized cDNA was used as a template to mix interleukin-1β and cyclooxygenase-2 primers, and the expression level of ribonucleic acid was confirmed using PCR Premix (AccuPower PCR PreMix, Bioneer). COX-2 primers were mixed with the synthesized cDNA template, and the expression level of ribonucleic acid was confirmed using PCR Premix (AccuPower PCR PreMix, Bioneer). Quantitative analysis was performed using a densitometer (Image Gauge V 3.46, Koshin Graphic Systems, Fuji Photo Film Co., Japan).
그 결과, 도 1 및 도 2에 나타난 바와 같이, LPS 처리한 군의 상대적인 발현 저해율을 조사한 결과, 본 발명에 따라 한방처방(연교 추출물, 형개 추출물 포함 처방)로 포함하는 조성물(실시예 3 및 4)에서 비교예 2 보다 인터류킨-1β와 사이클로옥시게나아제-2 유전자 발현을 효과적으로 억제함을 확인할 수 있었다. 특히 사이클로옥시게나아제-2의 발현 억제율은 실시예 3, 4 500ppm에서 50% 이상 현저히 감소하는 것을 확인하였다. 이 결과에서, 본 발명에 따라 한방처방을 포함하는 구강 조성물(실시예 3, 4)의 억제률이 우수한 것으로 판단된다. 이로부터 본 발명에 따라 한방처방된 구강 조성물이 치주항염증억제에 아주 효과적임을 확인할 수 있었다.As a result, as shown in Figures 1 and 2, as a result of examining the relative expression inhibition rate of the LPS-treated group, according to the present invention, the composition comprising a herbal prescription (combination extract, formulation containing a hyunggae extract) (Examples 3 and 4) In Comparative Example 2 it was confirmed that the interleukin-1β and cyclooxygenase-2 gene expression more effectively suppressed. In particular, the expression inhibition rate of cyclooxygenase-2 was confirmed to be significantly reduced by 50% or more in Example 3, 4 500ppm. In this result, it is judged that the suppression rate of the oral composition (Examples 3 and 4) containing an herbal prescription according to this invention is excellent. From this, it was confirmed that the herbal composition prescribed according to the present invention is very effective in inhibiting periodontal anti-inflammatory.
한방처방을 포함하는 본 발명의 실시예 1의 구강 조성물 모두 치아우식증, 구취유발 및 치주염 원인균을 효과적으로 성장을 억제하고 치주조직파괴에 직접 관여하는 MMP-3와 염증억제 지표인 인터류킨-1β와 사이클로옥시게나아제-2 유전자 발현을 효과적으로 억제하는 것을 확인하였다.All oral compositions of Example 1 of the present invention, including herbal prescription, effectively inhibit the growth of dental caries, bad breath-causing and periodontitis-causing bacteria, MMP-3 directly involved in periodontal tissue destruction, interleukin-1β and cycloox It was confirmed to effectively inhibit the gene genease-2 expression.
본 발명은 위생제품, 특히 치약이나 구강 세정제 등과 같은 구강 조성물을 제조하는 산업에서 이용될 수 있다.The present invention can be used in the industry of manufacturing hygiene products, especially oral compositions such as toothpaste or mouthwashes.
이상에서 본 발명은 기재된 구체예에 대해서만 상세히 설명되었지만 본 발명의 기술사상 범위 내에서 다양한 변형 및 수정이 가능함은 당업자에게 있어서 명백한 것이며, 이러한 변형 및 수정이 첨부된 특허청구범위에 속함은 당연한 것이다.Although the present invention has been described in detail only with respect to the described embodiments, it will be apparent to those skilled in the art that various modifications and variations are possible within the technical scope of the present invention, and such modifications and modifications are within the scope of the appended claims.

Claims (7)

  1. 황금 추출물 및 형개 추출물을 포함하는 천연 약재 추출물의 혼합물 0.1 내지 5.0중량%, 초산 토코페롤 0.01 내지 1.0중량%, 사과산 0.01 내지 1.0중량%를 포함함을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath, characterized in that it comprises 0.1 to 5.0% by weight of the mixture of natural medicinal extracts, including golden extract and mold extract, 0.01 to 1.0% by weight of tocopherol acetate, 0.01 to 1.0% by weight of malic acid.
  2. 제 1 항에 있어서, The method of claim 1,
    상기 천연 약재 추출물이 연교 추출물, 금은화 추출물, 길경 추출물 및 이들 중 2이상의 혼합물로 이루어지는 군으로부터 선택되는 추출물 0.1 내지 5.0중량%을 더 포함함을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath, characterized in that the natural medicinal extract further comprises 0.1 to 5.0% by weight of the extract selected from the group consisting of Yeongyo extract, Geumhwa extract, Gilgeung extract and a mixture of two or more thereof.
  3. 제 1 항에 있어서,The method of claim 1,
    상기 구취 억제용 구강 조성물이 6 내지 8의 범위 이내의 pH의 범위 이내임을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath, characterized in that within the range of pH within the range of 6 to 8.
  4. 제 3 항에 있어서,The method of claim 3, wherein
    상기 구취 억제용 구강 조성물이 중성임을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath, characterized in that the oral composition for inhibiting bad breath.
  5. 제 1 항에 있어서,The method of claim 1,
    상기 구취 억제용 구강 조성물이 페이스트상인 것을 특징으로 하는 구취 억제용 구강 조성물.The bad breath suppression oral composition is characterized in that the paste is a bad breath suppressor.
  6. 제 1 항에 있어서,The method of claim 1,
    상기 구취 억제용 구강 조성물이 치약, 구강 청정제 또는 구강 세정제로 제형화된 것임을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath, characterized in that formulated with toothpaste, mouthwash or mouthwash.
  7. 제 1 항에 있어서,The method of claim 1,
    상기 구취 억제용 구강 조성물이 격막이 있는 이중용기 내에 충진된 것임을 특징으로 하는 구취 억제용 구강 조성물.Oral composition for inhibiting bad breath is characterized in that the oral cavity is filled in a double container with a diaphragm.
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