WO2014054841A1 - Composition comprising material for controlling expression of abh antigen - Google Patents

Composition comprising material for controlling expression of abh antigen Download PDF

Info

Publication number
WO2014054841A1
WO2014054841A1 PCT/KR2013/001756 KR2013001756W WO2014054841A1 WO 2014054841 A1 WO2014054841 A1 WO 2014054841A1 KR 2013001756 W KR2013001756 W KR 2013001756W WO 2014054841 A1 WO2014054841 A1 WO 2014054841A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
expression
acid
abh antigen
substance
Prior art date
Application number
PCT/KR2013/001756
Other languages
French (fr)
Korean (ko)
Inventor
홍용덕
신송석
한상훈
김겸손
정진호
오장희
Original Assignee
(주)아모레퍼시픽
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by (주)아모레퍼시픽 filed Critical (주)아모레퍼시픽
Publication of WO2014054841A1 publication Critical patent/WO2014054841A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A61K31/225Polycarboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/366Lactones having six-membered rings, e.g. delta-lactones
    • A61K31/37Coumarins, e.g. psoralen
    • 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
    • A61K8/362Polycarboxylic 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
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • 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
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations

Definitions

  • a composition comprising a substance that modulates the expression of an ABH antigen
  • the present invention relates to an anti-aging or moisturizing composition.
  • Blood type antigens refer to specific antigenic striking structures found in glycoproteins or glycolipids on the surface of blood red blood cells. Representative examples include AB0 blood type antigens (ABH antigens) and Lewis type blood type antigens. Blood types are determined according to the glycosylation terminal group structure of a specific structure. AB0 blood type antigens and Lewis blood type antigens are not only expressed in red blood cells, but are found in various parts of the human body. In particular, AB0 blood type antigens are expressed in the epithelium of the esophagus, stomach, and small intestine, depending on the individual's blood type. It is known and is expressed in the granular layer of the epidermis in the skin.
  • the expression of the granular layer of the epidermis of the AB0 blood group antigen is shown in the outermost layer of the skin anatomically and is closely related to skin-related diseases, particularly inflammatory diseases.
  • AB0 blood group antigens are very important antigens for the rejection of blood transfusions and organ transplants, but since their discovery in 1900, little has been studied on physiological functions other than rejection.
  • the inventors of the present invention have confirmed that the substance regulating the expression of the ABH antigen not only has an anti-aging effect, but also has a skin moisturizing effect, thereby completing the present invention.
  • An object of the present invention is to provide a composition that brings anti-aging or moisturizing efficacy.
  • the present invention provides a composition for anti-aging comprising a substance for regulating the expression of the ABH antigen as an active ingredient.
  • the present invention also provides a moisturizing composition comprising a substance for regulating the expression of the ABH antigen as an active ingredient.
  • composition according to the present invention contains a substance for regulating the expression of the ABH antigen as an active ingredient, has an excellent anti-aging and moisturizing effect.
  • the composition of the present invention is also MMP-1 It can be usefully used to alleviate or improve wrinkles by inhibiting expression.
  • Figure 1 shows the structure of the ABH antigen and Lewis blood type antigen.
  • Figure 2 is a result of confirming that the expression of B antigens in HaCaT cell line is increased by a substance that controls the expression of ABH antigens.
  • MMP-1 collagenase
  • Figure 4 shows the effect of inhibiting the expression of MMP-1 (collagenase) in HaCaT cells.
  • the present invention relates to an anti-aging composition
  • an anti-aging composition comprising, as an active ingredient, a substance that controls the expression of an ABH antigen.
  • ABS antigen 'glycoprotein black on the surface of red blood cells of the blood refers to a specific antigenic structure expressed in glycolipids, typically ABH antigen is represented ABB antigen represented in Figure 1, Lewis It is used to include all aggregates of ABH antigen analogues, such as blood-type antigens, etc.
  • ABH antigen analogues are substances to which monosaccharides, amino acids, etc. are additionally bound, and mean substances having the same functions as the original functions of ABH antigens.
  • Figure 1 shows the structure of the ABH antigen and Lewis type blood type antigen.
  • anti-aging 'means to slow the change of the body that changes over time, and specifically, examples of improving wrinkles, reducing wrinkles or reducing color deposition such as blotch
  • aging may be delayed by inhibiting the expression of MMP.
  • active ingredient means a component that can exhibit activity alone or in combination with a carrier having no desired activity.
  • the agent for controlling the expression of the ABH antigen includes a substance for increasing the expression of the ABH antigen. Increasing the expression of such ABH antigen may be specifically expressed through increased expression of B antigen in HaCaT cell line.
  • the agent for controlling the expression of the ABH antigen is 1,3-dicaffeoylquinic acid (1,3-dicaffeoylquinic acid), 1,5-dicapeo At least one compound selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable Salts thereof.
  • derivative means any compound that is changed into another substituent at a substitutable position of the compound, and there is no limitation in the kind of such substituents.
  • pharmaceutically acceptable means a conventional medical dosage (medicinal can be approved or approved by the government or equivalent regulatory body for use in animals, more specifically in humans, by avoiding significant toxic effects when used in dosage form, or as listed in a pharmacopeia or other general pharmacopeia. It means to be.
  • the salt is formed by (1) an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfuric acid nitrate, or the like; Or acetic acid, propionic acid, nucleoanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3- (4- Hydroxybenzoyl) benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane- disulfonic acid, 2-hydroxyethanesulfonic acid, benzenebenzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2 Naphthalenesulfonic acid, 4-tolu
  • the composition may include a substance for controlling the expression of the ABH antigen in an amount of 0.001% to 20% by weight based on the total weight of the composition.
  • the substance that controls the expression of the ABH antigen is used in the above range, it is not only suitable for showing the anti-aging effect of the anti-aging and anti-wrinkle, as intended by the present invention, and also satisfies both the stability and safety of the composition. This is useful in terms of cost effectiveness.
  • the composition of the present invention is 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, 0.02% by weight relative to the total weight of the substance composition for controlling the expression of the ABH antigen % To 18% by weight, 0.025% to 17.5% by weight, 0.03% to 17% by weight, 0.035% to 16.5% by weight, 0.04% to 16% by weight, or 0.045% to 15.5% by weight. have.
  • the composition is MMP1
  • the composition of the present invention can inhibit the expression of matrix metal loproteinases.
  • the composition of the present invention may inhibit or inhibit the expression of the MMP1 gene, or may inhibit the activity of the MMP1 protein by inhibiting its activity.
  • the present invention relates to a moisturizing composition comprising, as another active ingredient, a substance that controls the expression of the ABH antigen.
  • composition of the present invention can increase the skin moisturizing power by increasing the expression of the ABH antigen.
  • the material for controlling the expression of the ABH antigen may be a substance that increases the expression of the ABH antigen.
  • the material for controlling the expression of the ABH antigen is 1,3-dicaffeoylquinic acid (1,3-dicaffeoylquinic acid), 1,5-dicafeoylqui And one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof.
  • the composition modulates the expression of an ABH antigen.
  • the material to be degraded may comprise from 0.001 weight 3 ⁇ 4 to 20 weight percent relative to the total weight of the composition.
  • the present invention is not only suitable for exhibiting the intended moisturizing effect, but also satisfies both the stability and safety of the composition, and the aspect of cost-effectiveness.
  • the composition of the present invention is a substance that controls the expression of the ABH antigen , 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, 0.02 to the total weight of the composition Weight% to 18 weight%, 0.025 weight% to 17.5 weight%, 0.03 weight% to 17 weight 3 ⁇ 4, 0.035 weight% to 16.5 weight%, 0.04 weight% to 16 weight% or 0.045 weight% to 15.5 weight 3 ⁇ 4 Can be.
  • the composition may be a cosmetic composition.
  • the cosmetic composition is not particularly limited in formulation, and may be appropriately selected according to the purpose.
  • supple cream skin lotion and milk lotion
  • nourishing cream essence
  • nourishing cream massage cream pack
  • gel essence
  • eye cream eye essence
  • cleansing cream cleansing foam
  • cleansing water cleansing water
  • pack powder
  • the cosmetic composition may include using the formulation of the external preparation for skin in the form of an ointment, a patch.
  • Cosmetic compositions according to the invention may be provided in all formulations suitable for topical application.
  • it can be provided in the form of a formulation of emulsion, suspension, solid, gel, powder, paste, foam or aerosol composition obtained by dispersing the oil phase in a solution, aqueous phase. have.
  • Compositions of such formulations may be prepared according to conventional methods in the art.
  • the cosmetic composition according to the present invention may include other ingredients in addition to the above-mentioned substances within the range of not impairing the main effect, preferably synergistic effects on the main effect.
  • the cosmetic composition according to the present invention is a moisturizing agent, emollient, purple.
  • the sun absorber, preservatives, fungicides, antioxidants, pH adjusting agents, organic and inorganic pigments, fragrances, coolants or limiting agents may be further included.
  • the blending amount of the above components can be easily selected by those skilled in the art within the range that does not impair the object and effect of the present invention, the blending amount is 0.01 to 5% by weight, specifically 0.01 to 3% by weight based on the total weight of the composition Can be.
  • the composition may be a pharmaceutical composition.
  • the formulation of the pharmaceutical composition according to the present invention may be a solution, a suspension, an emulsion, a gel, a drop, a suppository, a patch or a spray, but is not limited thereto.
  • the formulations can be easily prepared according to conventional methods in the art, and include excipients, wetting agents, emulsifying accelerators, suspending agents, salts or buffers for controlling osmotic pressure, colorants, spices, stabilizing agents, preservatives, preservatives. Or other commercially available adjuvants may be used as appropriate.
  • the active ingredient of the pharmaceutical composition of the present invention will vary depending on the age, sex, weight, pathology and severity of the subject to be administered, the route of administration or the judgment of the prescriber. Determination of dosage based on these factors is within the level of one skilled in the art, and its daily dosage is, for example, 0.000025 mg / g / day to 0.025 mg / g / day, more specifically 0.00025 mg / g / day to 0.01 m g / g / day, but is not limited thereto.
  • the pharmaceutical composition of the present invention may be administered orally or transdermally, but is not limited thereto.
  • the present invention relates to an anti-aging method of administering to a subject an effective amount of a substance that regulates the expression of A ⁇ antigen. Applying the method to a subject can inhibit or delay aging of the subject's skin.
  • the agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen.
  • a substance for regulating the expression of the ABH antigen 1,3-dicafeoylquinic acid (1,3-dicafeoylquinic acid), 1,5-dicafeoylquinic acid and amentoflavone
  • 1,3-dicafeoylquinic acid 1,3-dicafeoylquinic acid
  • 1,5-dicafeoylquinic acid and amentoflavone It may include, but is not limited to, one or more compounds selected from the group consisting of (amentoflavon), derivatives thereof or pharmaceutically acceptable salts thereof.
  • the agent for controlling the expression of the ABH antigen may be administered to the subject in the form of a composition, wherein the composition is a substance for controlling the expression of the ABH antigen It may comprise from 0.001% by weight to 20% by weight relative to the total weight of the composition.
  • the composition administered in the anti-aging method of one aspect of the present invention is a substance that controls the expression of the ABH antigen is 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight relative to the total weight of the composition, 0.015 wt% to 18.5 wt%, 0.02 wt% 3 ⁇ 4 to 18 wt%, 0.025 wt% to 17.5 wt%, 0.03 wt% to 17 wt%, 0.035 wt% to 16.5 wt%, 0.04 wt% to 16 wt%, or 0.045 It may be included in the weight% to 15.5% by weight.
  • the substance regulating the expression of the ABH antigen can inhibit the expression of matrix metal loproteinase (MMP1).
  • MMP1 matrix metal loproteinase
  • the present invention relates to a method of moisturizing skin, comprising administering to a subject an effective amount of a substance that modulates the expression of an ABH antigen.
  • the agent for controlling the expression of the ABH antigen may be a substance for increasing the expression of the ABH antigen, and specifically, 1,3-dicafeoylquinic acid ( 1,3-dicaffeoylquinic acid), 1,5-dicafeoylquinic acid (1,5 ⁇ dicafeoylquinic acid) and one or more compounds selected from the group consisting of amentoflavon, derivatives thereof or pharmaceutically acceptable Its salts may be included.
  • a substance that controls the expression of the ABH antigen may be administered to a subject in the form of a composition, and the composition may include a substance that modulates the expression of the ABH antigen. It may comprise from 0.001% to 20% by weight relative to the total weight.
  • a substance that modulates the expression of the ABH antigen is used in the above range, it is not only suitable to exhibit the moisturizing effect intended by the present invention, but also the composition of the composition. Both qualitative and safety can be satisfied and it is useful in terms of cost effectiveness.
  • the composition of the present invention comprises 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, based on the total weight of the composition 0.02 wt% to 18 wt%, 0.025 wt% to 17.5 wt%, 0.03 wt% to 17 wt%, 0.035 wt% to 16.5 wt%, 0.04 wt% to 16 wt% or 0.045 wt% to 15.5 wt% Can be.
  • the present invention may be a substance that controls the expression of an ABH antigen for use in anti-aging.
  • the agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3- dicaffeoylquinic acid (1,3- dicaffeoylquinic acid), 1,5—decaffeinated One or more compounds selected from the group consisting of oilquinic acid (1,5-dicafeoylquinic acid) and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof, but are not limited thereto.
  • Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
  • MMP1 matrix metalloproteinase
  • the present invention may be a substance that modulates the expression of an ABH antigen for use in moisturizing the skin.
  • the agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3- dicaf feoylquinic acid (1,3-dicaf feoylquinic acid), 1,5 ⁇ It may be, but is not limited to, one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof.
  • Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
  • MMP1 matrix metalloproteinase
  • the present invention may relate to the anti-aging use of a substance that modulates the expression of an ABH antigen.
  • the agent for regulating the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3-dicafeoylquinic acid (1,3-dicaf feoylquinic acid), 1,5 one It may be, but is not limited to, one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof.
  • a substance that regulates the expression of the ABH antigen can inhibit the expression of matrix PI (matrix metalloproteinase).
  • the present invention may relate to a skin moisturizing use of a substance that modulates the expression of an ABH antigen.
  • the agent for regulating the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, and specifically 1,3-dicafeoylquinic acid (1,3—dicaffeoylquinic acid), 1,5 dicafe One or more compounds selected from the group consisting of oilquinic acid (1,5-dicafeoylquinic acid) and amentoflavon. Water, its derivatives or pharmaceutically acceptable salts thereof, but is not limited thereto.
  • Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
  • MMP1 matrix metalloproteinase
  • HaCaT cells provided by Prof. Dr. N.E. Fusenig, DKFZ Heidelberg, Germany
  • 10% FBS-DMEM in 35 mm dish and starvated with 0% FBS-DMEM for 24 hours.
  • Proteins were extracted from the cells, and the cells were lysed in the same amount, and the expression of type B antigen was examined by Western blot. Alpha-leuulin protein was used as a control.
  • FBS-DMEM Dulbecco's Modified Eagle's Media
  • DMEM Dulbecco's Modified Eagle's Media
  • PBS Pulbecco's Modified Eagle's Media
  • 1,3-dicaf feoylquinic acid, 1,5-dicafeoylquinic acid and amento were changed again with medium of 0% FBS-DMEM.
  • Each flavone (amentoflavon) was treated at a concentration of 2 ug / ml and then incubated for 48 hours (control treated with DMS0).
  • the medium was collected and loaded with the same amount of medium to confirm MMP-1 by Western blot.
  • the protein was extracted from the cells and the same amount of cell lysate was loaded to confirm the expression of alpha-tubulin by Western blot.
  • MIiP-1 Collagenase
  • test substance 0.2% of the substance that controls the expression of ABH antigen was diluted. Glycerine 5% was used as a positive control.
  • the skin moisture content at the beginning, after 2 days, after 7 days, and after 11 days of the test substance was measured according to the following method with a coronometer (Corneometer CM825 (C + KGmbH, Germany)), and the results are shown in Table 1 below. .
  • the amount of moisture present in the skin's epidermis is measured by electrical measurement, and the moisture level is measured by numerically calculating the amount of moisture.
  • ⁇ ? 6> 1. Place the probe of the Koniometer on the area of skin to be measured.
  • the electrical conductivity of the skin is quantified through the sensor and displayed on the screen.
  • the average value is obtained by repeating the measurement three times at each site.
  • the composition containing a substance that regulates the expression of the ABH antigen according to the present invention was found to have excellent skin moisturizing power by effectively preserving the moisture of the skin after application.
  • a lotion is prepared according to a conventional method using the composition shown in the table below.
  • a nutritious cream is prepared according to a conventional method with the composition shown in the table below.
  • Massage cream is prepared according to a conventional method with the composition described in the table below.
  • the pack is prepared according to a conventional method with the composition shown in the table below.
  • Ointments were prepared in a conventional manner with the compositions shown in the table below.
  • (1,5-dicafeoylquinic acid) and one or more compounds in the group consisting of amentoflavon 0.0025g, vitamin C 0.0025g, red ginseng extract 50 mg, palm oil 2 mg, palm frond 8 mg of sulfur oil, 4 mg of lead, and 6 mg of lecithin were mixed and layered by 400 mg per 1 capsule according to a conventional method to prepare a soft capsule.
  • 1,3-diaffeoylquinic acid (l, 3-dicaffeoykiuinic acid), 1,5-dicafeoylquinic acid
  • one or more compounds containing 150 mg, 150 mg of vitamin C, 100 mg of glucose, 50 mg of hepatic ginseng extract and 600 mg of starch are mixed and 30% ethanol 100 mg of the granules were formed, followed by drying at 60 ° C. to form granules, which were then laminated to the fabric.
  • the final weight of the content was 1 g.
  • the composition according to the present invention contains a substance regulating the expression of the ABH antigen as an active ingredient, and has an excellent anti-aging and moisturizing effect.
  • the composition of the present invention can also be usefully used to alleviate or improve wrinkles by inhibiting MMP-1 expression.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Dermatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The present invention relates to an anti-aging or skin moisturizing composition. The composition according to the present invention contains, as an active ingredient, a material for controlling the expression of ABH antigen, and therefore, has superior anti-aging and skin moisturizing effects. Further, the composition of the preset invention may inhibit the expression of MMP-1, and therefore, can be effectively used in reducing wrinkles or improving the appearance thereof.

Description

【명세서】  【Specification】
【발명의 명칭】  [Name of invention]
ABH항원의 발현을 조절하는 물질을 포함하는 조성물  A composition comprising a substance that modulates the expression of an ABH antigen
【기술분야】  Technical Field
<ι> 본 발명은 항노화용 또는 보습용 조성물에 관한 것이다.  The present invention relates to an anti-aging or moisturizing composition.
【배경기술】  Background Art
<2> 혈액형 항원은 혈액의 적혈구 표면의 당단백질 혹은 당지질에서 발견된 특정 한 항원성올 띄는 구조를 말한다. 대표적으로 AB0식 혈액형 항원 (ABH 항원), Lewis식 혈액형 항원 등이 있으며, 특정구조의 당질화 말단기 구조에 따라 혈액형 이 결정된다. AB0식 혈액형 항원 및 Lewis식 혈액형 항원은 적혈구에서만 발현되는 것이 아니라, 인체의 다양한 부위에서 발견되며, 특히 AB0식 혈액형 항원은 개인의 혈액형에 따라 몸 안의 식도, 위장, 소장 등의 상피에서도 발현되는 것이 알려져 있으며, 피부에서는 표피의 과립층에 발현된다.  Blood type antigens refer to specific antigenic striking structures found in glycoproteins or glycolipids on the surface of blood red blood cells. Representative examples include AB0 blood type antigens (ABH antigens) and Lewis type blood type antigens. Blood types are determined according to the glycosylation terminal group structure of a specific structure. AB0 blood type antigens and Lewis blood type antigens are not only expressed in red blood cells, but are found in various parts of the human body. In particular, AB0 blood type antigens are expressed in the epithelium of the esophagus, stomach, and small intestine, depending on the individual's blood type. It is known and is expressed in the granular layer of the epidermis in the skin.
<3> AB0식 혈액형 항원의 표피의 과립층 발현은, 해부학적인 위치상 피부의 가장 바깥층에서 나타나므로, 피부관련 질환 특히 염증 질환과 밀접한 관계가 있다. The expression of the granular layer of the epidermis of the AB0 blood group antigen is shown in the outermost layer of the skin anatomically and is closely related to skin-related diseases, particularly inflammatory diseases.
<4> AB0식 혈액형 항원은 수혈과 장기이식의 거부반응의 주원인이 되는 매우 중 요한 항원이지만 1900년에 발견된 이래로 아직까지 거부반응 이외의 생리적 기능 에 대해서는 연구된 바가 거의 없다. AB0 blood group antigens are very important antigens for the rejection of blood transfusions and organ transplants, but since their discovery in 1900, little has been studied on physiological functions other than rejection.
<5> 본 발명자들은 ABH 항원의 발현을 조절하는 물질이 항노화 효능을 가질 뿐 아니라, 피부 보습 효과를 가짐을 확인하고 본 발명을 완성하게 되었다. The inventors of the present invention have confirmed that the substance regulating the expression of the ABH antigen not only has an anti-aging effect, but also has a skin moisturizing effect, thereby completing the present invention.
【발명의 상세한 설명】  [Detailed Description of the Invention]
【기술적 과제】  [Technical problem]
<6> 본 발명의 목적은 항노화 또는 보습 효능을 가져오는 조성물을 제공하는 것 이다.  An object of the present invention is to provide a composition that brings anti-aging or moisturizing efficacy.
【기술적 해결방법】  Technical Solution
<7> 상기 목적을 달성하기 위하여 본 발명은 ABH 항원의 발현을 조절하는 물질을 유효성분으로 포함하는 항노화용 조성물을 제공한다.  In order to achieve the above object, the present invention provides a composition for anti-aging comprising a substance for regulating the expression of the ABH antigen as an active ingredient.
<8> 본 발명은 또한 ABH 항원의 발현을 조절하는 물질을 유효성분으로 포함하는 보습용 조성물을 제공한다. <8> The present invention also provides a moisturizing composition comprising a substance for regulating the expression of the ABH antigen as an active ingredient.
【유리한 효과】  Advantageous Effects
<9> 본 발명에 따른 조성물은 ABH 항원의 발현을 조절하는 물질을 유효성분으로 함유하여, 우수한 항노화 및 보습 효과를 가진다. 본 발명의 조성물은 또한 MMP-1 발현을 억제하여 주름의 완화 또는 개선을 위해 유용하게 사용될 수 있다. <9> The composition according to the present invention contains a substance for regulating the expression of the ABH antigen as an active ingredient, has an excellent anti-aging and moisturizing effect. The composition of the present invention is also MMP-1 It can be usefully used to alleviate or improve wrinkles by inhibiting expression.
【도면의 간단한 설명】  [Brief Description of Drawings]
<ιο> 도 1은 ABH항원 및 Lewis 식 혈액형 항원의 구조를 나타낸 것이다.  Figure 1 shows the structure of the ABH antigen and Lewis blood type antigen.
<ιι> 도 2는 ABH항원의 발현을 조절하는 물질에 의해 HaCaT세포주에서 B항원의 발현이 증가되는 것을 확인한 결과이다.  <ιι> Figure 2 is a result of confirming that the expression of B antigens in HaCaT cell line is increased by a substance that controls the expression of ABH antigens.
<12> 도 3은 사람피부 섬유아세포에서의 MMP-1 (콜라게네이즈) 의 발현 억제 효과 를 나타낸다. 3 shows the effect of inhibiting the expression of MMP-1 (collagenase) in human skin fibroblasts.
<13> 도 4는 HaCaT세포에서의 MMP-1 (콜라게네이즈) 의 발현 억제 효과를 나타낸 다.  Figure 4 shows the effect of inhibiting the expression of MMP-1 (collagenase) in HaCaT cells.
【발명의 실시를 위한 최선의 형태】  [Best form for implementation of the invention]
<14> 본 발명은 일 관점에서, ABH 항원의 발현을 조절하는 물질을 유효성분으로 포함하는 항노화용 조성물에 관한 것이다.  In one aspect, the present invention relates to an anti-aging composition comprising, as an active ingredient, a substance that controls the expression of an ABH antigen.
<15> 본 명세서에서, "ABH항원' '은 혈액의 적혈구 표면의 당단백질 흑은 당지질에 서 발현된 특정한 항원성을 띄는 구조를 말하며, 대표적으로 ABH 항원은 그림 1로 표현된 ABH 항원, Lewis식 혈액형 항원등 ABH 항원 유사체의 집합체를 모두 포함하 는 의미로 사용한다. ABH 항원 유사체는 단당류, 아미노산 등이 추가로 결합되어 있는 물질로서 ABH 항원 본래의 기능과 동일한 기능을 하는 물질을 의미한다. 도 1 에 ABH항원 및 Lewis 식 혈액형 항원의 구조를 나타내었다.  In the present specification, "ABH antigen" 'glycoprotein black on the surface of red blood cells of the blood refers to a specific antigenic structure expressed in glycolipids, typically ABH antigen is represented ABB antigen represented in Figure 1, Lewis It is used to include all aggregates of ABH antigen analogues, such as blood-type antigens, etc. ABH antigen analogues are substances to which monosaccharides, amino acids, etc. are additionally bound, and mean substances having the same functions as the original functions of ABH antigens. Figure 1 shows the structure of the ABH antigen and Lewis type blood type antigen.
<16> 본 명세서에서, "항노화' '는 시간이 흐름에 따라 변화하는 신체의 변화를 늦 추어 주는 것을 의미하며, 구체적으로, 주름 개선, 주름 감소 또는 검버섯 등의 색 소침착 완화 등의 예를 들 수 있으나 이에 제한되는 것은 아니다. 본 명세서에서는 구체적으로, MMP의 발현을 억제함에 의하여 노화를 지연시킬 수 있다.  In the present specification, "anti-aging" 'means to slow the change of the body that changes over time, and specifically, examples of improving wrinkles, reducing wrinkles or reducing color deposition such as blotch In the present specification, aging may be delayed by inhibiting the expression of MMP.
<17> 본 명세서에서 "유효성분"은 단독으로 목적하는 활성을 나타내거나 또는 그 자체 활성이 없는 담체와 함께 활성을 나타낼 수 있는 성분을 의미하는 것이다. As used herein, the term "active ingredient" means a component that can exhibit activity alone or in combination with a carrier having no desired activity.
<18> 본 발명의 일 관점인 항노화용 조성물에 있어서, 상기 ABH항원의 발현을 조 절하는 물질은 ABH항원의 발현을 증가시키는 물질을 포함한다. 이러한 ABH 항원의 발현 증가는 구체적으로 HaCaT 세포주에서의 B 항원의 발현 증가를 통하여 나타나 는 것일 수 있다. In the anti-aging composition according to the aspect of the present invention, the agent for controlling the expression of the ABH antigen includes a substance for increasing the expression of the ABH antigen. Increasing the expression of such ABH antigen may be specifically expressed through increased expression of B antigen in HaCaT cell line.
<19> 본 발명의 일 관점인 항노화용 조성물에 있어서, 상기 ABH항원의 발현을 조 절하는 물질은 1,3-디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5—디카페오 일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentof lavon) 으로 구성 된 군에서 선택되는 하나 이상의 화합물, 그의 유도체 또는 약학적으로 허용가능한 그의 염을 포함한다. In the anti-aging composition of the present invention, the agent for controlling the expression of the ABH antigen is 1,3-dicaffeoylquinic acid (1,3-dicaffeoylquinic acid), 1,5-dicapeo At least one compound selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable Salts thereof.
【화학식 1]  [Formula 1]
Figure imgf000005_0001
Figure imgf000005_0001
1 ,3-dicafTeoylquinic acid  1,3-dicafTeoylquinic acid
【화학식 2】 [Formula 2]
Figure imgf000005_0002
Figure imgf000005_0002
,5-dicaffeoylquinic acid  , 5-dicaffeoylquinic acid
【화학식 3】 [Formula 3]
Figure imgf000005_0003
Figure imgf000005_0003
amentoflavon  amentoflavon
<25>  <25>
<26> 본 명세서에서 "유도체' '는 상기 화합물의 치환 가능한 위치에서 다른 치환기 로 변경되는 모든 화합물을 의미하는 것이며, 이러한 치환기의 종류에는 제한이 없 다.  As used herein, the term "derivative" means any compound that is changed into another substituent at a substitutable position of the compound, and there is no limitation in the kind of such substituents.
<27> 본 명세서에서 "약학적으로 허용 가능"이란 통상의 의약적 복용량 (medicinal dosage)으로 이용할 때 상당한 독성 효과를 피함으로써, 동물, 더 구체적으로는 인 간에게 사용할 수 있다는 정부 또는 이에 준하는 규제 기구의 승인을 받을 수 있거 나 승인 받거나, 또는 약전에 열거되거나 기타 일반적인 약전으로 인지되는 것을 의미한다. <27> As used herein, "pharmaceutically acceptable" means a conventional medical dosage (medicinal can be approved or approved by the government or equivalent regulatory body for use in animals, more specifically in humans, by avoiding significant toxic effects when used in dosage form, or as listed in a pharmacopeia or other general pharmacopeia. It means to be.
<28> 본 명세서에서 "약학적으로 허용 가능한 염"은 약학적으로 허용 가능하고 모  <28> As used herein, "pharmaceutically acceptable salts" are pharmaceutically acceptable and parental.
화합물 (parent compound)의 바람직한 약리 활성을 갖는 본 발명의 일 관점에 따른 염을 의미한다. 상기 염은 (1) 염산, 브롬화수소산, 황산, 질산ᅳ 인산 등과 같은 무기산으로 형성되거나; 또는 아세트산, 프로파이온산, 핵사노산, 시클로펜테인프 로피온산, 글라이콜산, 피루브산, 락트산, 말론산, 숙신산, 말산, 말레산, 푸마르 산, 타르타르산, 시트르산, 벤조산, 3-(4-히드록시벤조일) 벤조산, 신남산, 만델 산, 메테인설폰산, 에테인설폰산, 1,2-에테인—디설폰산, 2-히드록시에테인설폰산, ᅳ벤젠설폰산, 4-클로로벤젠설폰산, 2-나프탈렌설폰산, 4-톨루엔설폰산, 캄퍼설폰산, 4-메틸바이시클로 [2,2,2]-0 -2-엔-1—카르복실산, 글루코헵톤산, 3-페닐프로파이 온산, 트리메틸아세트산, tert—부틸아세트산, 라우릴 황산, 글루콘산, 글루탐산, 히드록시나프토산, 살리실산, 스테아르산, 뮤콘산과 같은 유기산으로 형성되는 산 부가염 (acid addition salt); 또는 (2) 모 화합물에 존재하는 산성 프로톤이 치환 될 때 형성되는 염을 포함할 수 있다.  A salt according to one aspect of the invention having the desired pharmacological activity of a parent compound. The salt is formed by (1) an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfuric acid nitrate, or the like; Or acetic acid, propionic acid, nucleoanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3- (4- Hydroxybenzoyl) benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane- disulfonic acid, 2-hydroxyethanesulfonic acid, benzenebenzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2 Naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo [2,2,2] -0-2-ene-1—carboxylic acid, glucoheptonic acid, 3-phenylpropyionic acid Acid addition salts formed with organic acids such as trimethylacetic acid, tert-butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid and muconic acid; Or (2) salts formed when the acidic protons present in the parent compound are substituted.
<29> 본 발명의 일 관점인 항노화용 조성물에 있어서, 상기 조성물은 ABH 항원의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.001 중량 % 내지 20 중량 %로 포 함할 수 있다.  In the anti-aging composition of one aspect of the present invention, the composition may include a substance for controlling the expression of the ABH antigen in an amount of 0.001% to 20% by weight based on the total weight of the composition.
<30> 상기 ABH항원의 발현을 조절하는 물질을 상기 범위로 사용할 경우 본 발명 이 의도하는 안티에이징, 주름 개선 둥의 항노화 효과를 나타내기에 적절할 뿐만 아니라, 조성물의 안정성 및 안전성을 모두 만족할 수 있으며, 비용 대비 효과의 측면에서 유용하다. 상기와 같은 관점에서, 본 발명의 조성물은 ABH 항원의 발현을 조절하는 물질올 조성물 총중량에 대하여 0.005 중량 % 내지 19.5 중량 ¾, 0.01 중량 % 내지 19 중량 %, 0.015 중량 % 내지 18.5 중량 %, 0.02 중량 % 내지 18 중량 %, 0.025 중량 % 내지 17.5 중량 %, 0.03 중량 % 내지 17 중량 %, 0.035 중량 % 내지 16.5 중량 ¾>, 0.04중량 % 내지 16중량 %또는 0.045중량 % 내지 15.5중량 %로 포함할 수 있다. When the substance that controls the expression of the ABH antigen is used in the above range, it is not only suitable for showing the anti-aging effect of the anti-aging and anti-wrinkle, as intended by the present invention, and also satisfies both the stability and safety of the composition. This is useful in terms of cost effectiveness. In view of the above, the composition of the present invention is 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, 0.02% by weight relative to the total weight of the substance composition for controlling the expression of the ABH antigen % To 18% by weight, 0.025% to 17.5% by weight, 0.03% to 17% by weight, 0.035% to 16.5% by weight, 0.04% to 16% by weight, or 0.045% to 15.5% by weight. have.
<3i> 본 발명의 일 관점인 항노화용 조성물에 있어서, 상기 조성물은 MMP1 <3i> In the antiaging composition according to one aspect of the present invention, the composition is MMP1
(matrix metal loproteinase)의 발현을 억제할 수 있다. 구체적으로 본 발명의 조성 물은 MMP1 유전자의 발현을 방해하여 억제 또는 저해시키거나, MMP1 단백질의 활성 을 저해하여 그 작용을 방해할 수 있다. <32> 본 발명은 다른 관점에서 ABH 항원의 발현을 조절하는 물질을 유효성분으로 포함하는 보습용 조성물에 관한 것이다. can inhibit the expression of matrix metal loproteinases. Specifically, the composition of the present invention may inhibit or inhibit the expression of the MMP1 gene, or may inhibit the activity of the MMP1 protein by inhibiting its activity. The present invention relates to a moisturizing composition comprising, as another active ingredient, a substance that controls the expression of the ABH antigen.
<33> 본 발명의 조성물은 ABH 항원의 발현을 증가시켜서 피부 보습력을 증가시킬 수 있다. The composition of the present invention can increase the skin moisturizing power by increasing the expression of the ABH antigen.
<34> 본 발명의 일 관점인 조성물에 있어서, 상기 ABH항원의 발현을 조절하는 물 질은 ABH항원의 발현을 증가시키는 물질일 수 있다.  In a composition of one aspect of the present invention, the material for controlling the expression of the ABH antigen may be a substance that increases the expression of the ABH antigen.
<35> 본 발명의 일 관점인 조성물에 있어서, 상기 ABH항원의 발현을 조절하는 물 질은 1,3-디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5-디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentof lavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그의 유도체 또는 약학적으로 허용가능한 그의 염을 포함할 수 있다.  In a composition of one aspect of the present invention, the material for controlling the expression of the ABH antigen is 1,3-dicaffeoylquinic acid (1,3-dicaffeoylquinic acid), 1,5-dicafeoylqui And one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof.
<36> 본 발명의 일 관점인 조성물에 있어서, 상기 조성물은 ABH항원의 발현을 조  In a composition according to one aspect of the invention, the composition modulates the expression of an ABH antigen.
절하는 물질을 조성물 총중량에 대하여 0.001 중량 ¾ 내지 20 중량 %로 포함할 수 있 다.  The material to be degraded may comprise from 0.001 weight ¾ to 20 weight percent relative to the total weight of the composition.
<37> 상기 ABH항원의 발현을 조절하는 물질을 상기 범위로 사용할 경우ᅳ 본 발명 이 의도하는 보습 효과를 나타내기에 적절할 뿐만 아니라, 조성물의 안정성 및 안 전성을 모두 만족할 수 있으며, 비용 대비 효과의 측면에서 유용하다. 상기와 같은 관점에서, 본 발명의 조성물은 ABH 항원의 ,발현을 조절하는 물질을 조성물 총중량 에 대하여 0.005 증량 % 내지 19.5 중량 %, 0.01 중량 % 내지 19 중량 %, 0.015 중량 % 내지 18.5 중량 %, 0.02 중량 % 내지 18 중량 %, 0.025 중량 % 내지 17.5 중량 %, 0.03 증량 % 내지 17 중량 ¾, 0.035 중량 % 내지 16.5 중량 %, 0.04 증량 % 내지 16 중량 % 또 는 0.045중량 % 내지 15.5중량 ¾로 포함할 수 있다. In the case of using a substance that regulates the expression of the ABH antigen in the above range, the present invention is not only suitable for exhibiting the intended moisturizing effect, but also satisfies both the stability and safety of the composition, and the aspect of cost-effectiveness. Useful at In view of the above, the composition of the present invention is a substance that controls the expression of the ABH antigen , 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, 0.02 to the total weight of the composition Weight% to 18 weight%, 0.025 weight% to 17.5 weight%, 0.03 weight% to 17 weight ¾, 0.035 weight% to 16.5 weight%, 0.04 weight% to 16 weight% or 0.045 weight% to 15.5 weight ¾ Can be.
<38> 본 발명의 일 관점인 조성물에 있어서, 상기 조성물은 화장료 조성물일 수 있다.  In a composition which is one aspect of the present invention, the composition may be a cosmetic composition.
<39> 상기 화장료 조성물은 제형이 특별히 한정되지 않으며, 목적하는 바에 따라 적절히 선택할 수 있다. 예를 들어, 유연화장수 (스킨로션 및 밀크로션), 영양화장 수, 에센스, 영양크림, 마사지크림 팩, 젤, 에센스, 아이크림, 아이에센스, 클렌 징크림, 클렌징폼, 클렌징워터, 팩, 파우더, 보디로션, 보디크림, 보디오일 및 보 디 에센스로 이루어진 군으로부터 선택된 어느 하나 이상의 제형으로 제조될 수 있 으나, 이에 제한되는 것은 아니다. 아울러, 상기 화장료 조성물은 연고, 패치 등의 형태로 피부 외용제의 제형으로 사용하는 것을 포함할 수 있다.  The cosmetic composition is not particularly limited in formulation, and may be appropriately selected according to the purpose. For example, supple cream (skin lotion and milk lotion), nourishing cream, essence, nourishing cream, massage cream pack, gel, essence, eye cream, eye essence, cleansing cream, cleansing foam, cleansing water, pack, powder It may be prepared in any one or more formulations selected from the group consisting of body lotion, body cream, body oil and body essence, but is not limited thereto. In addition, the cosmetic composition may include using the formulation of the external preparation for skin in the form of an ointment, a patch.
<40> 본 발명에 따른 화장료 조성물은 국소 적용에 적합한 모든 제형으로 제공될 수 있다. 예를 들면, 용액, 수상에 유상을 분산시켜 얻은 에멀견, 유상에 수상을 분산시켜 얻은 에멀견, 현탁액, 고체, 겔, 분말, 페이스트, 포말 (foam) 또는 에어 로졸 조성물의 제형으로 제공될 수 있다. 이러한 제형의 조성물은 당해 분야의 통 상적인 방법에 따라 제조될 수 있다. Cosmetic compositions according to the invention may be provided in all formulations suitable for topical application. Can be. For example, it can be provided in the form of a formulation of emulsion, suspension, solid, gel, powder, paste, foam or aerosol composition obtained by dispersing the oil phase in a solution, aqueous phase. have. Compositions of such formulations may be prepared according to conventional methods in the art.
<41> 본 발명에 따른 화장료 조성물은 상기한 물질 이외에 주 효과를 손상시키지 않는 범위 내에서, 바람직하게는 주 효과에 상승 효과를 줄 수 있는 다른 성분들을 포함할 수 있다. 또한 본 발명에 따른 화장료 조성물은 보습제, 에몰리언트제 , 자 . 외선 흡수제, 방부제, 살균제, 산화 방지제, pH 조정제, 유기 및 무기 안료, 향료, 냉감제 또는 제한제를 더 포함할 수 있다. 상기 성분의 배합량은 본 발명의 목적 및 효과를 손상시키지 않는 범위 내에서 당업자가 용이하게 선정 가능하며, 그 배 합량은 조성물 전체 중량을 기준으로 0.01 내지 5 중량 ¾, 구체적으로 0.01 내지 3 중량 %일 수 있다. The cosmetic composition according to the present invention may include other ingredients in addition to the above-mentioned substances within the range of not impairing the main effect, preferably synergistic effects on the main effect. In addition, the cosmetic composition according to the present invention is a moisturizing agent, emollient, purple. The sun absorber, preservatives, fungicides, antioxidants, pH adjusting agents, organic and inorganic pigments, fragrances, coolants or limiting agents may be further included. The blending amount of the above components can be easily selected by those skilled in the art within the range that does not impair the object and effect of the present invention, the blending amount is 0.01 to 5% by weight, specifically 0.01 to 3% by weight based on the total weight of the composition Can be.
<42> 본 발명의 일 관점인 조성물에 있어서, 상기 조성물은 약학 조성물일 수 있 다.  In a composition of one aspect of the present invention, the composition may be a pharmaceutical composition.
<43> 본 발명에 따른 약학 조성물의 제형은 용액제, 현탁제, 유액제, 겔, 점적제, 좌제, 패취 또는 분무제일 수 있으나, 이에 제한되는 것은 아니다. 상기 제형은 당 해 분야의 통상적인 방법에 따라 용이하게 제조될 수 있으며 , 부형제, 수화제, 유 화 촉진제, 현탁제, 삼투압 조절을 위한 염 또는 완층제, 착색제, 향신료, 안정화 거 1, 방부제 , 보존제 또는 기타 상용하는 보조제를 적당히 사용할 수 있다.  The formulation of the pharmaceutical composition according to the present invention may be a solution, a suspension, an emulsion, a gel, a drop, a suppository, a patch or a spray, but is not limited thereto. The formulations can be easily prepared according to conventional methods in the art, and include excipients, wetting agents, emulsifying accelerators, suspending agents, salts or buffers for controlling osmotic pressure, colorants, spices, stabilizing agents, preservatives, preservatives. Or other commercially available adjuvants may be used as appropriate.
<44> 본 발명의 약학 조성물의 유효 성분은 투여 받을 대상의 연령, 성별, 체중, 병리 상태 및 그 심각도, 투여 경로 또는 처방자의 판단에 따라 달라질 것이다. 이 러한 인자에 기초한 적용량 결정은 당업자의 수준 내에 있으며, 이의 1일 투여 용 량은 예를 들어 0.000025mg/g/일 내지 0.025mg/g/일, 보다 구체적으로는 0.00025mg /g/일 내지 0.01mg/g/일이 될 수 있으나, 이에 제한되는 것은 아니다. The active ingredient of the pharmaceutical composition of the present invention will vary depending on the age, sex, weight, pathology and severity of the subject to be administered, the route of administration or the judgment of the prescriber. Determination of dosage based on these factors is within the level of one skilled in the art, and its daily dosage is, for example, 0.000025 mg / g / day to 0.025 mg / g / day, more specifically 0.00025 mg / g / day to 0.01 m g / g / day, but is not limited thereto.
<45> 본 발명의 약학 조성물은 경구 또는 경피로 투여될 수 있으나, 이에 제한되 는 것은 아니다. The pharmaceutical composition of the present invention may be administered orally or transdermally, but is not limited thereto.
<46>  <46>
<47> 본 발명은 또 다른 관점에서 ΑΒΗ·항원의 발현을 조절하는 물질을 대상에 유 효량으로 투여하는 안티 에이징 방법에 관한 것이다. 상기 방법을 대상에 적용하면 대상 피부의 노화가 억제 또는 지연될 수 있다.  In another aspect, the present invention relates to an anti-aging method of administering to a subject an effective amount of a substance that regulates the expression of AβΗ antigen. Applying the method to a subject can inhibit or delay aging of the subject's skin.
<48> 본 발명의 일 관점인 안티 에이징 방법에 있어서, 상기 ABH 항원의 발현을 조절하는 물질은 ABH 항원의 발현을 증가시키는 물질을 포함할 수 있다. 구체적으 로 상기 ABH 항원의 발현을 조절하는 물질은 1,3-디카페오일퀴닉산 (1,3- dicaffeoylquinic acid), 1,5-디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염을 포함할 수 있으나, 이에 제한되 는 것은 아니다. In the anti-aging method of one aspect of the present invention, the agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen. Specifically As a substance for regulating the expression of the ABH antigen, 1,3-dicafeoylquinic acid (1,3-dicafeoylquinic acid), 1,5-dicafeoylquinic acid and amentoflavone It may include, but is not limited to, one or more compounds selected from the group consisting of (amentoflavon), derivatives thereof or pharmaceutically acceptable salts thereof.
<49> 본 발명의 일 관점인 안티 에이징 방법에 있어서, 상기 ABH 항원의 발현을 조절하는 물질은 조성물의 형태로 대상에게 투여할 수 있고ᅳ 이 때, 상기 조성물은 ABH 항원의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.001 증량 % 내지 20 중량 %로 포함할 수 있다. 상기 ABH 항원의 발현을 조절하는 물질을 상기 범위로 사 용할 경우, 본 발명이 꾀도하는 안티 에이징 효과를 나타내기에 적절할 뿐만 아니 라, 조성물의 안정성 및 안전성을 모두 만족할 수 있으며, 비용 대비 효과의 측면 에서 유용하다. 상기와 같은 관점에서, 본 발명의 일 관점인 안티 에이징 방법에서 투여하는 조성물은 ABH 항원의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.005 중량 % 내지 19.5 중량 %, 0.01 중량 ¾> 내지 19 중량 %, 0.015 증량 % 내지 18.5 증량 ¾>, 0.02 중량 ¾ 내지 18 중량 %, 0.025 중량 % 내지 17.5 증량 %, 0.03 증량 % 내지 17 중량 %, 0.035 중량 % 내지 16.5 중량 %, 0.04 중량 % 내지 16 중량 %또는 0.045 중 량% 내지 15.5 중량 %로 포함할 수 있다.  In the anti-aging method of one aspect of the present invention, the agent for controlling the expression of the ABH antigen may be administered to the subject in the form of a composition, wherein the composition is a substance for controlling the expression of the ABH antigen It may comprise from 0.001% by weight to 20% by weight relative to the total weight of the composition. When using a substance that modulates the expression of the ABH antigen in the above range, not only is it suitable for showing the anti-aging effect of the present invention, but also satisfies both the stability and safety of the composition, and cost-effectiveness aspects Useful at In view of the above, the composition administered in the anti-aging method of one aspect of the present invention is a substance that controls the expression of the ABH antigen is 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight relative to the total weight of the composition, 0.015 wt% to 18.5 wt%, 0.02 wt% ¾ to 18 wt%, 0.025 wt% to 17.5 wt%, 0.03 wt% to 17 wt%, 0.035 wt% to 16.5 wt%, 0.04 wt% to 16 wt%, or 0.045 It may be included in the weight% to 15.5% by weight.
<50> 본 발명의 일 관점인 안티 에이징 방법에 있어서, 상기 ABH 항원의 발현을 조절하는 물질은 MMP1 (matrix metal loproteinase)의 발현을 억제할 수 있다.  In the anti-aging method of one aspect of the present invention, the substance regulating the expression of the ABH antigen can inhibit the expression of matrix metal loproteinase (MMP1).
<5i> 본 발명은 또 다른 관점에서 대상에 ABH 항원의 발현을 조절하는 물질을 유 효량으로 투여하는 것을 포함하는 피부 보습 방법에 관한 것이다.  In another aspect, the present invention relates to a method of moisturizing skin, comprising administering to a subject an effective amount of a substance that modulates the expression of an ABH antigen.
<52> 본 발명의 일 관점인 피부 보습 방법에 있어서, 상기 ABH 항원의 발현을 조 절하는 물질은 ABH 항원의 발현을 증가시키는 물질일 수 있고, 구체적으로 1,3-디 카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5-디카페오일퀴닉산 (1,5ᅳ dicafeoylquinic acid) 및 아맨토플라본 (amentoflavon) 으로 구성된 군에서 선택 되는 하나 이상의 화합물, 그의 유도체 또는 약학적으로 허용가능한 그의 염을 포 함할 수 있다.  In the method of moisturizing the skin, which is an aspect of the present invention, the agent for controlling the expression of the ABH antigen may be a substance for increasing the expression of the ABH antigen, and specifically, 1,3-dicafeoylquinic acid ( 1,3-dicaffeoylquinic acid), 1,5-dicafeoylquinic acid (1,5 ᅳ dicafeoylquinic acid) and one or more compounds selected from the group consisting of amentoflavon, derivatives thereof or pharmaceutically acceptable Its salts may be included.
<53> 본 발명의 일 관점인 피부 보습 방법에 있어서, 상기 ABH 항원의 발현을 조 절하는 물질은 조성물의 형태로 대상에게 투여할 수 있고, 상기 조성물은 ABH 항원 의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.001 중량 % 내지 20 중량 %로 포함할 수 있다. 상기 ABH 항원의 발현을 조절하는 물질을 상기 범위로 사용할 경 우, 본 발명이 의도하는 보습 효과를 나타내기에 적절할 뿐만 아니라, 조성물의 안 정성 및 안전성을 모두 만족할 수 있으며, 비용 대비 효과의 측면에서 유용하다. 상기와 같은 관점에서, 본 발명의 조성물은 ABH 항원의 발현을 조절하는 물질을 조 성물 총중량에 대하여 0.005 중량 % 내지 19.5 중량 %, 0.01 중량 % 내지 19 중량 ¾>, 0.015 중량 % 내지 18.5 중량 %, 0.02 중량 % 내지 18 중량 %, 0.025 중량 % 내지 17.5 중량 %, 0.03 중량 % 내지 17 중량 %, 0.035 중량 % 내지 16.5 중량 %, 0.04중량 % 내지 16증량 %또는 0.045중량 % 내지 15.5중량 %로 포함할 수 있다. In the method of moisturizing the skin, which is an aspect of the present invention, a substance that controls the expression of the ABH antigen may be administered to a subject in the form of a composition, and the composition may include a substance that modulates the expression of the ABH antigen. It may comprise from 0.001% to 20% by weight relative to the total weight. When a substance that modulates the expression of the ABH antigen is used in the above range, it is not only suitable to exhibit the moisturizing effect intended by the present invention, but also the composition of the composition. Both qualitative and safety can be satisfied and it is useful in terms of cost effectiveness. In view of the above, the composition of the present invention comprises 0.005% by weight to 19.5% by weight, 0.01% by weight to 19% by weight, 0.015% by weight to 18.5% by weight, based on the total weight of the composition 0.02 wt% to 18 wt%, 0.025 wt% to 17.5 wt%, 0.03 wt% to 17 wt%, 0.035 wt% to 16.5 wt%, 0.04 wt% to 16 wt% or 0.045 wt% to 15.5 wt% Can be.
<54>  <54>
<55> 본 발명은 또 다른 관점에서 항노화에 사용하기 위한 ABH 항원의 발현을 조 절하는 물질일 수 있다. 상기 ABH항원의 발현을 조절하는 물질은 ABH항원의 발현 을 증가시키는 물질을 포함할 수 있고, 구체적으로 1,3-디카페오일퀴닉산 (1,3- dicaffeoylquinic acid) , 1,5—디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염일 수 있으나, 이에 제한되는 것은 아니다. 상기 ABH 항원의 발현을 조절하는 물질은 MMP1 (matrix metalloproteinase)의 발현을 억제할 수 있다.  In another aspect, the present invention may be a substance that controls the expression of an ABH antigen for use in anti-aging. The agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3- dicaffeoylquinic acid (1,3- dicaffeoylquinic acid), 1,5—decaffeinated One or more compounds selected from the group consisting of oilquinic acid (1,5-dicafeoylquinic acid) and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof, but are not limited thereto. Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
<56> 본 발명은 또 다른 관점에서 피부 보습에 사용하기 위한 ABH 항원의 발현을 조절하는 물질일 수 있다. 상기 ABH 항원의 발현을 조절하는 물질은 ABH 항원의 발 현을 증가시키는 물질을 포함할 수 있고, 구체적으로 1,3-디카페오일퀴닉산 (1,3- dicaf feoylquinic acid) , 1,5一디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플파본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염일 수 있으나, 이에 제한되는 것은 아니다. 상기 ABH 항원의 발현을 조절하는 물질은 MMP1 (matrix metalloproteinase)의 발현을 억제할 수 있다.  In another aspect, the present invention may be a substance that modulates the expression of an ABH antigen for use in moisturizing the skin. The agent for controlling the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3- dicaf feoylquinic acid (1,3-dicaf feoylquinic acid), 1,5 一It may be, but is not limited to, one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof. . Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
<57>  <57>
<58> 본 발명은 또 다른 관점에서 , ABH항원의 발현을 조절하는 물질의 항노화 용 도에 관한 것일 수 있다. 상기 ABH 항원의 발현을 조절하는 물질은 ABH 항원의 발 현을 증가시키는 물질을 포함할 수 있고, 구체적으로 1,3-디카페오일퀴닉산 (1,3- dicaf feoylquinic acid) , 1,5一디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염일 수 있으나, 이에 제한되는 것은 아니다. 상기 ABH 항원의 발현을 조절하는 물질은 腿 PI (matrix metalloproteinase)의 발현을 억제할 수 있다. <59> 본 발명은 또 다른 관점에서 , ABH 항원의 발현을 조절하는 물질의 피부 보습 용도에 관한 것일 수 있다. 상기 ABH 항원의 발현을 조절하는 물질은 ABH 항원의 발현을 증가시키는 물질을 포함할 수 있고, 구체적으로 1,3-디카페오일퀴닉산 (1,3— dicaffeoylquinic acid) , 1,5一디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합 . 물, 그의 유도체 또는 약학적으로 허용가능한 그의 염일 수 있으나, 이에 제한되는 것은 아니다. 상기 ABH 항원의 발현을 조절하는 물질은 MMP1 (matrix metalloproteinase)의 발현을 억제할 수 있다. In another aspect, the present invention may relate to the anti-aging use of a substance that modulates the expression of an ABH antigen. The agent for regulating the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, specifically 1,3-dicafeoylquinic acid (1,3-dicaf feoylquinic acid), 1,5 one It may be, but is not limited to, one or more compounds selected from the group consisting of 1,5-dicafeoylquinic acid and amentoflavon, derivatives thereof or pharmaceutically acceptable salts thereof. A substance that regulates the expression of the ABH antigen can inhibit the expression of matrix PI (matrix metalloproteinase). In another aspect, the present invention may relate to a skin moisturizing use of a substance that modulates the expression of an ABH antigen. The agent for regulating the expression of the ABH antigen may include a substance for increasing the expression of the ABH antigen, and specifically 1,3-dicafeoylquinic acid (1,3—dicaffeoylquinic acid), 1,5 dicafe One or more compounds selected from the group consisting of oilquinic acid (1,5-dicafeoylquinic acid) and amentoflavon. Water, its derivatives or pharmaceutically acceptable salts thereof, but is not limited thereto. Substances that control the expression of the ABH antigen may inhibit the expression of matrix metalloproteinase (MMP1).
<60>  <60>
【발명의 실시를 위한 형태】  [Form for implementation of invention]
<61> 이하, 실시예를 통하여 본 발명을 더욱 상세히 설명하고자 한다. 이들 실시 예는 오로지 본 발명을 예시하기 위한 것으로, 본 발명의 범위가 이들 실시예에 의 해 제한되는 것으로 해석되지 않는 것은 당업계에서 통상의 지식을 가진 자에게 있 어서 자명할 것이다.  Hereinafter, the present invention will be described in more detail with reference to Examples. These examples are only to illustrate the invention, it will be apparent to those of ordinary skill in the art that the scope of the present invention is not to be construed as being limited by these examples.
[실시예 1】  Example 1
<62> HaCaT 세포주에서 B antigen의 발현증가 효과  Increased Expression of B Antigen in HaCaT Cell Lines
<63> 다양한 종류의 화합물이 ABH 항원의 발현에 미치는 영향을 실험하였다. 이를 위하여, HaCaT 세포 (provided by Prof. Dr. N.E. Fusenig, DKFZ Heidelberg, Germany) 를 35 醒 디쉬에 10% FBS-DMEM 으로 배양한 후 24시간 동안 0% FBS-DMEM 으로 starvation 하였다. 다시 0% FBS-DMEM으로 배지를 갈아주면서 1,3-디카페오일 퀴닉산 (1,3-dicaffeoylquinic acid), 1,5-디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon)를 각각 2ug/ml의 농도로 HaCaT 세포에 처리 한 후, 48시간 동안 배양하였다 (대조군은 DMS0를 처리함). 세포에서 단백질을 추출 하여 세포 용해물을 동량 로딩하여 웨스턴 블랏으로 B 형 항원의 발현을 조사하였 다. 대조군으로는 알파-류블린 단백질을 사용하였다.  The effects of various kinds of compounds on the expression of ABH antigens were examined. To this end, HaCaT cells (provided by Prof. Dr. N.E. Fusenig, DKFZ Heidelberg, Germany) were incubated with 10% FBS-DMEM in 35 mm dish and starvated with 0% FBS-DMEM for 24 hours. 1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid and amentoflavones, followed by medium replacement with 0% FBS-DMEM (Amentoflavon) was treated in HaCaT cells at a concentration of 2ug / ml each, and then incubated for 48 hours (control treated with DMS0). Proteins were extracted from the cells, and the cells were lysed in the same amount, and the expression of type B antigen was examined by Western blot. Alpha-leuulin protein was used as a control.
<64> 그 결과 (도 2), 1,3-디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5- 디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon) 모 두 HaCaT세포에서 B형 항원의 발현을 증가시키는 효과가 있음을 확인하였다.  As a result (FIG. 2), 1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid and amentoflavones Both amentoflavon) were found to have an effect of increasing the expression of type B antigen in HaCaT cells.
【실시예 2】  Example 2
<65> 사람피부 섬유아세포에서의 MMP-1 (콜라게네이즈) 의 발현 억제 효과  <65> Inhibitory effect of MMP-1 (collagenase) in human skin fibroblasts
<66> 사람의 섬유'아세포 (KF-4109, 클라보사로부터 입수) 를 60mm 디쉬에서 1W <66> the fibers' fibroblasts (KF-4109, available from Cloud pictorial) of the person in 60mm dish 1W
FBS-DMEM(Dulbecco's Modified Eagle's Media)으로 배양한 후 24시간 동안 0% FBS- DMEM으로 starvation 하였다. PBS로 2회 워싱한 후 자외선올 조사하였다. 다시 0% FBS-DMEM으로 배지를 갈아주면서 1,3-디카페오일퀴닉산 (1,3-dicaf feoylquinic acid), 1,5—디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon) 각각을 2ug/ml의 농도로 처리한 후, 48시간 동안 배양하였다 (대조 군은 DMS0를 처리함). 배지를 모아서 동량의 배지를 로딩하여 웨스턴 블랏으로 MMP-1을 확인하였고, 세포에서 단백질을 추출하여 세포 용해물을 동량 로딩하여 웨 스턴 블랏으로 알파-튜블린의 발현을 확인하였다. After incubation with Dulbecco's Modified Eagle's Media (FBS-DMEM), 0% FBS- Starvation with DMEM. After washing twice with PBS, ultraviolet rays were irradiated. 1,3-dicaf feoylquinic acid, 1,5-dicafeoylquinic acid and amento were changed again with medium of 0% FBS-DMEM. Each flavone (amentoflavon) was treated at a concentration of 2 ug / ml and then incubated for 48 hours (control treated with DMS0). The medium was collected and loaded with the same amount of medium to confirm MMP-1 by Western blot. The protein was extracted from the cells and the same amount of cell lysate was loaded to confirm the expression of alpha-tubulin by Western blot.
<67> 그 결과 (도 3), 1,3—디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5- 디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토폴라본 (amentoflavon)이 모두 MMP-1 (콜라게네이즈) 의 발현을 억제하는 효과가 있음을 확인하였으며, 특히 아멘토플라본 (amentoflavon)의 효과가 우수함을 확인하였다. As a result (FIG. 3), 1,3—dicafeoylquinic acid, 1,5-dicafeoylquinic acid, and amentopolbonone It was confirmed that both (amentoflavon) had an effect of inhibiting the expression of MMP-1 (collagenase), and in particular, it was confirmed that the effect of amentoflavon was excellent.
【실시예 3】  Example 3
<68> HaCaT세포에서의 MIiP-1 (콜라게네이즈) 의 발현 억제 효과  Inhibition Effect of MIiP-1 (Collagenase) in HaCaT Cells
<69> HaCaT 세포 (provided by Prof. Dr. N.E. Fusenig, DKFZ Heidelberg,  HaCaT cells (provided by Prof. Dr. N. E. Fusenig, DKFZ Heidelberg,
Germany)를 60腿 디쉬에서 10% FBS-DMEM(Dulbecco' s Modified Eagle's Media)으로 배양한 후 24시간 동안 0¾ FBS-D EM으로 starvation 하였다: PBS로 2회 워성한 후 자외선을 조사하였다. 다시 0% FBS-DMEM으로 배지를 갈아주면서 각 물질 (1,3- dicaffeoylquinic acid, 1,5-dicafeoylquinic acid, amentoflavon, 시그마로부터 구입)을 2ug/ml의 농도로 처리한 후, 48시간 동안 배양하였다 (대조군은 DMS0를 처 리함). 배지를 모아서 동량의 배지를 로딩하여 웨스턴 블랏으로 MMP-1을 확인하였 고, 세포에서 단백질을 추출하여 cell lysate를 동량 로딩하여 웨스턴 블랏으로 알 파-튜블린의 발현을 확인하였다.  Germany) was incubated with 60% DBS in 10% FBS-DMEM (Dulbecco's Modified Eagle's Media) and starvated with 0¾ FBS-D EM for 24 hours: warmed twice with PBS and irradiated with UV light. Each medium (1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid, amentoflavon, and sigma) was treated at a concentration of 2 ug / ml while changing the medium with 0% FBS-DMEM, followed by incubation for 48 hours. (Control handles DMS0). Collecting the medium and loading the same amount of medium to confirm the MMP-1 by Western blot, the protein was extracted from the cells to load the cell lysate in the same amount to confirm the expression of alpha-tubulin in Western blot.
<70> 그 결과 (도 4), 1,3-디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5- 디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon)이 모두 MMP-1 (콜라게네이즈) 의 발현을 억제하는 효과가 있음을 확인하였으며, 특히 아멘토플라본 (amentoflavon)의 효과가 우수함을 확인하였다. As a result (Fig. 4), 1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid and amentoflavones It was confirmed that both amentoflavon) had an effect of suppressing the expression of MMP-1 (collagenase), and in particular, the effect of amentoflavon was excellent.
【실시예 4】  Example 4
<71> 피부 보습 효과 평가  <71> Evaluation of Skin Moisturizing Effect
<72> ABH 항원의 발현을 조절하는 물질의 피부 보습 효과를 알아보기 위하여 건강 한 20~30대 성인 남녀 14명 (남자 7명, 여자 7명)에게 시험물질을 하박 내측면에 3X3cm 정사각형의 3부위에 도포하도록 하였다.  <72> To examine the skin moisturizing effect of a substance that regulates the expression of the ABH antigen, a test substance was applied to 14 healthy males and females (7 males and 7 females) in their 20s to 30s. It was applied to the site.
<73> 시험물질로는 ABH 항원의 발현을 조절하는 물질을 0.2% 농도로 희석하여 사 용하고, 양성 대조군으로 글리세린 5%를 사용하였다. 시험물질의 초기, 2일 후, 7 일 후, 11일 후의 피부 수분량을 코니오미터 (Corneometer CM825(C+KGmbH, Germany))로 하기 방법에 따라측정하였고, 그 결과를 하기 표 1에 나타내었다.<73> As the test substance, 0.2% of the substance that controls the expression of ABH antigen was diluted. Glycerine 5% was used as a positive control. The skin moisture content at the beginning, after 2 days, after 7 days, and after 11 days of the test substance was measured according to the following method with a coronometer (Corneometer CM825 (C + KGmbH, Germany)), and the results are shown in Table 1 below. .
<74> <코니오미터 측정 방법 > <74> <Method of measuring Koniometer>
<75> 원리: 피부의 표피 내에 존재하는 수분의 양을 전기적 측정법을 이용하여 수 분의 이온 정도를 측정, 이를 수치화하여 수분의 양을 계산함으로써 보습력을 측정 한다.  Principle: The amount of moisture present in the skin's epidermis is measured by electrical measurement, and the moisture level is measured by numerically calculating the amount of moisture.
<?6> 1. 측정하고자 하는 피부 부위에 코니오미터의 프로브 (probe)를 올려놓는다. <? 6> 1. Place the probe of the Koniometer on the area of skin to be measured.
<77> 2. 프로브를 피부에 누르면 센서를 통하여 피부의 전기 전도도를 수치화하여 화면에 표시된다. 2. When the probe is pressed on the skin, the electrical conductivity of the skin is quantified through the sensor and displayed on the screen.
<78> 3. 각 부위에서 3회 반복 측정하여 평균값을 구한다. 3. The average value is obtained by repeating the measurement three times at each site.
<79> 【표 1】 <79> [Table 1]
Figure imgf000014_0001
Figure imgf000014_0001
<80> 상기 표 1에서 확인할 수 있듯이, 본 발명에 따른 ABH항원의 발현을 조절하 는 물질을 피부에 도포할 경우, 피부 수분량이 통계적으로 유의하게 증가하는 경향 (paired T-test, p<0.01)을 나타내었고 도포 11일 후에도 피부 수분량이 유지되었 다. 그러므로, 본 발명에 따른 ABH 항원의 발현을 조절하는 물질를 함유하는 조성 물은 도포 후 피부의 수분을 효과적으로 보존하여 피부 보습력이 뛰어남을 알 수 있었다ᅳ  As can be seen in Table 1 above, when the substance regulating the expression of the ABH antigen according to the present invention is applied to the skin, the skin moisture content tends to increase statistically (paired T-test, p <0.01 ) And skin moisture was maintained 11 days after application. Therefore, the composition containing a substance that regulates the expression of the ABH antigen according to the present invention was found to have excellent skin moisturizing power by effectively preserving the moisture of the skin after application.
<81> 이하, 본 발명에 따른 조성물의 제형예를 설명하나 약학 조성물 및 화장료 조성물은 여러 가지 제형으로 웅용 가능하며, 이는 본 발명을 한정하고자 함이 아 닌 단지 구체적으로 설명하고자 함이다.  Hereinafter, the formulation example of the composition according to the present invention will be described, but the pharmaceutical composition and the cosmetic composition can be used in various formulations, which is intended to explain in detail only and not intended to limit the present invention.
<82> [제형예 1] 화장수  <82> [Formulation Example 1] lotion
<83> 아래 표에 기재된 조성으로 통상의 방법에 따라 화장수를 제조한다.  <83> A lotion is prepared according to a conventional method using the composition shown in the table below.
<84> 【표 2】  <84> [Table 2]
Figure imgf000014_0002
<85> [제형예 2] 영양 크림
Figure imgf000014_0002
<85> [Formulation Example 2] Nutrition Cream
<86> 아래 표에 기재된 조성으로 통상의 방법에 따라 영양 크림을 제조한다. A nutritious cream is prepared according to a conventional method with the composition shown in the table below.
<87> 【표 3】<87> [Table 3]
Figure imgf000015_0001
Figure imgf000015_0001
[제형예 3] 마사지 크림  Formulation Example 3 Massage Cream
아래 표에 기재된 조성으로 통상의 방법에 따라 마사지 크림을 제조한다. Massage cream is prepared according to a conventional method with the composition described in the table below.
<90> 【표 4】
Figure imgf000016_0001
<90> [Table 4]
Figure imgf000016_0001
<91> [제형예 4] 팩  <91> [Formulation Example 4] Pack
<92> 아래 표에 기재된 조성으로 통상의 방법에 따라 팩을 제조한다. The pack is prepared according to a conventional method with the composition shown in the table below.
<93> 【표 5】<93> [Table 5]
Figure imgf000016_0002
Figure imgf000016_0002
<94> [제형예 5] 젤  <94> [Formulation Example 5] Gel
<95> 아래 표에 기재된 조성으로 통상의 방법에 따라 젤을 제조한다. <96> 【표 6】 Gels are prepared according to conventional methods using the compositions shown in the table below. <96> [Table 6]
Figure imgf000017_0001
Figure imgf000017_0001
<97> [제형예 6] 연고  <97> [Formulation Example 6] Ointment
<98> 아래 표에 기재된 조성으로 통상적인 방법으로 연고를 제조하였다.  Ointments were prepared in a conventional manner with the compositions shown in the table below.
<99> 【표 7】  <99> [Table 7]
Figure imgf000017_0002
Figure imgf000017_0002
<ιοο> [제제예 1] 연질캅셀제  <ιοο> [Example 1] soft capsule
<ιοι> 1,3-디카페오일퀴닉산 (1,3-dicaf feoylquinic acid), 1,5-디카페오일퀴닉산  <ιοι> 1,3-diccafeoylquinic acid, 1,5-dicafeoylquinic acid
(1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentoflavon)로 구성된 군에서 하 나 이상의 화합물 0.0025g, 비타민 C 0.0025g, 홍삼추출물 50 mg, 팜유 2 mg, 팜경 화유 8 mg, 황납 4 mg 및 레시틴 6 mg을 흔합하고, 통상의 방법에 따라 1 캡술당 400 mg씩 층진하여 연질캅셀을 제조하였다. (1,5-dicafeoylquinic acid) and one or more compounds in the group consisting of amentoflavon 0.0025g, vitamin C 0.0025g, red ginseng extract 50 mg, palm oil 2 mg, palm frond 8 mg of sulfur oil, 4 mg of lead, and 6 mg of lecithin were mixed and layered by 400 mg per 1 capsule according to a conventional method to prepare a soft capsule.
<102> [제제예 2] 정제 Preparation Example 2 Tablet
<103> 1,3-디카페오일퀴닉산 (l,3-dicaffeoykiuinic acid), 1,5-디카페오일퀴닉산  1,3-diaffeoylquinic acid (l, 3-dicaffeoykiuinic acid), 1,5-dicafeoylquinic acid
(1,5-dicafeoylquinic acid) 및 아멘토플라본 ( anient oflavon)로 구성된 군에서 하 나 이상의 화합물 0.0025g, 비타민 C 0.0025g, 포도당 100 mg, 흥삼추출물 50 mg, 전분 96 mg 및 마그네슘 스테아레이트 4 mg을 흔합하고 30% 에탄올을 40 mg 첨가하 여 과립을 형성한 후, 60°C에서 건조하고 타정기를 이용하여 정제로 타정하였다.In the group consisting of (1,5-dicafeoylquinic acid) and amentoflavones (0.0025 g), one or more compounds 0.0025 g, vitamin C 0.0025 g, glucose 100 mg, heungsam extract 50 mg, starch 96 mg and magnesium stearate 4 mg The mixture was added, 40 mg of 30% ethanol was added to form granules, dried at 60 ° C., and compressed into tablets using a tablet press.
<104> [제제예 3] 과립제 Preparation Example 3 Granules
<105> 1,3ᅳ디카페오일퀴닉산 (1,3-dicaffeoykiuimc acid), 1,5-디카페오일퀴닉산  <105> 1,3-dicaffeoyyl quinic acid (1,3-dicaffeoykiuimc acid), 1,5-dicafeoyl quinic acid
(1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentof lavon)로 구성된 군에서 하 나 이상의 화합물 150 mg, 비타민 C 150 mg, 포도당 100 mg, 흥삼추출물 50 mg 및 전분 600 mg을 흔합하고 30% 에탄올을 100 mg 첨가하여 과립을 형성한 후, 60°C에 서 건조하여 과립올 형성한 다음 포에 층진하였다. 내용물의 최종 중량은 1 g으로 하였다.  In a group consisting of (1,5-dicafeoylquinic acid) and amentoflavon, one or more compounds containing 150 mg, 150 mg of vitamin C, 100 mg of glucose, 50 mg of hepatic ginseng extract and 600 mg of starch are mixed and 30% ethanol 100 mg of the granules were formed, followed by drying at 60 ° C. to form granules, which were then laminated to the fabric. The final weight of the content was 1 g.
<106> [제제예 4] 드링크제  <Example 4> Preparation Example 4 Drinks
<107> 1,3ᅳ디카페오일퀴닉산 (1,3-dicaffeoylquinic acid), 1,5-디카페오일퀴닉산  1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid
(1,5-dicafeoylquinic acid) 및 아멘토플라본 (amentof lavon)로 구성된 군에서 하 나 이상의 화합물 0.0025g, 비타민 C 0.0025g, 포도당 10 g, 홍삼추출물 50 mg, 구 연산 2 g 및 정제수 187.8 g을 흔합하고 병에 충진하였다. 내용물의 최종 용량은 200 ml로 하였다.  In the group consisting of (1,5-dicafeoylquinic acid) and amentoflavon, 0.0025 g of one or more compounds, 0.0025 g of vitamin C, 10 g of glucose, 50 mg of red ginseng extract, 2 g of citric acid and 187.8 g of purified water Were mixed and filled in bottles. The final dose of the contents was 200 ml.
<108> 이상으로 본 발명 내용의 특정한 부분을 상세히 기술하였는 바, 당업계의 통 상의 지식을 가진 자에게 있어서 이러한 구체적 기술은 단지 바람직한 실시태양일 뿐이며, 이에 의해 본 발명의 범위가 제한되는 것이 아닌 점은 명백할 것이다. 따 라서, 본 발명의 실질적인 범위는 첨부된 청구항들과 그것들의 등가물에 의하여 정 의된다고 할 것이다.  Having described the specific part of the present invention in detail, such a specific description is only a preferred embodiment for those skilled in the art, and thus the scope of the present invention is not limited thereto. The point will be obvious. Therefore, the substantial scope of the present invention will be defined by the appended claims and their equivalents.
<109>  <109>
【산업상 이용가능성】  Industrial Applicability
<πο> 본 발명에 따른 조성물은 ABH 항원의 발현을 조절하는 물질을 유효성분으로 함유하여, 우수한 항노화 및 보습 효과를 가진다. 본 발명의 조성물은 또한 MMP-1 발현을 억제하여 주름의 완화 또는 개선을 위해 유용하게 사용될 수 있다.  <πο> The composition according to the present invention contains a substance regulating the expression of the ABH antigen as an active ingredient, and has an excellent anti-aging and moisturizing effect. The composition of the present invention can also be usefully used to alleviate or improve wrinkles by inhibiting MMP-1 expression.

Claims

【청구의 범위】  [Range of request]
【청구항 11  [Claim 11
ABH 항원의 발현을 조절하는 물질을 유효성분으로 포함하는 항노화용 조성 물.  Anti-aging composition comprising a substance that controls the expression of the ABH antigen as an active ingredient.
【청구항 2】  [Claim 2]
제 1항에 있어서,  The method of claim 1,
상기 유효성분은 ABH항원의 발현을 증가시키는 물질인, 항노화용 조성물. 【청구항 3]  The active ingredient is a substance for increasing the expression of the ABH antigen, anti-aging composition. [Claim 3]
제 1항에 있어서,  The method of claim 1,
상기 ABH 항원의 발현을 조절하는 물질은 1, Substances that regulate the expression of the ABH antigen are 1,
3—디카페오일퀴닉산 (1ᅳ 3- dicaf feoylquinic acid) , 1,5—디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염인, 항노화용 조성물. One or more compounds selected from the group consisting of 1—3-dicaf feoylquinic acid, 1,5-dicafeoylquinic acid, and amentoflavon Or a derivative thereof or a pharmaceutically acceptable salt thereof.
【청구항 4】  [Claim 4]
제 1항에 있어서,  The method of claim 1,
상기 조성물은 ABH 항원의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.001중량 %내지 20중량 %로 포함하는, 항노화용 조성물.  The composition comprises an agent for controlling the expression of the ABH antigen in an amount of 0.001% to 20% by weight based on the total weight of the composition, anti-aging composition.
【청구항 5】  [Claim 5]
제 1항에 있어서,  The method of claim 1,
상기 유효성분은 MMP1 (matrix 111^31101)1"^ 11336)의 발현을 억제하는, 항노 화용 조성물. The active ingredient inhibits the expression of MMP1 (matrix 111 ^ 31101) 1 " ^ 11336), anti-aging composition.
【청구항 6】  [Claim 6]
ABH항원의 발현을 조절하는 물질을 유효성분으로 포함하는 보습용 조성물.  Moisturizing composition comprising a substance that controls the expression of the ABH antigen as an active ingredient.
【청구항 7】 [Claim 7]
제 6항에 있어서,  The method of claim 6,
상기 유효성분은 ABH항원의 발현을 증가시키는 물질인, 보습용 조성물.  The active ingredient is a substance that increases the expression of the ABH antigen, moisturizing composition.
【청구항 8】 [Claim 8]
제 6항에 있어서,  The method of claim 6,
상기 ABH 항원의 발현을 조절하는 물질은 1,3-디카페오일퀴닉산 (1,3- dicaf feoylquinic acid) , 1,5—디카페오일퀴닉산 (1,5-dicafeoylquinic acid) 및 아 멘토플라본 (amentoflavon) 으로 구성된 군에서 선택되는 하나 이상의 화합물, 그 의 유도체 또는 약학적으로 허용가능한 그의 염인, 보습용 조성물. Substances that regulate the expression of the ABH antigen are 1,3-dicaffeoylquinic acid, 1,5-dicafeoylquinic acid, and amentoflavones. A moisturizing composition, which is at least one compound selected from the group consisting of (amentoflavon), derivatives thereof or pharmaceutically acceptable salts thereof.
【청구항 9】 [Claim 9]
제 6항에 있어서,  The method of claim 6,
상기 조성물은 ABH 항원의 발현을 조절하는 물질을 조성물 총중량에 대하여 0.001 중량 % 내지 20 중량 %로 포함하는, 보습용 조성물.  The composition is a moisturizing composition comprising a substance that controls the expression of the ABH antigen in an amount of 0.001% to 20% by weight relative to the total weight of the composition.
【청구항 10]  [Claim 10]
제 1항 내지 제 9항 중 어느 한 항에 있어서, 상기 조성물은 화장료 조성물인ᅳ 조성물.  The composition according to any one of claims 1 to 9, wherein the composition is a cosmetic composition.
[청구항 11】  [Claim 11]
제 1항 내지 제 9항 중 어느 한 항에 있어서, 상기 조성물은 약학 조성물인, 조성물.  The composition of claim 1, wherein the composition is a pharmaceutical composition.
PCT/KR2013/001756 2012-10-05 2013-03-05 Composition comprising material for controlling expression of abh antigen WO2014054841A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2012-0110418 2012-10-05
KR1020120110418A KR101449129B1 (en) 2012-10-05 2012-10-05 Composition Containing Compound of Regulation for ABH Antigen

Publications (1)

Publication Number Publication Date
WO2014054841A1 true WO2014054841A1 (en) 2014-04-10

Family

ID=50435153

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2013/001756 WO2014054841A1 (en) 2012-10-05 2013-03-05 Composition comprising material for controlling expression of abh antigen

Country Status (2)

Country Link
KR (1) KR101449129B1 (en)
WO (1) WO2014054841A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023001385A1 (en) * 2021-07-23 2023-01-26 Symrise Ag Compositions of dicaffeoylquinic acids with tocopherol

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170239159A1 (en) * 2014-10-15 2017-08-24 Amorepacific Corporation Composition containing material for regulating expression of abh antigens
KR102199884B1 (en) * 2014-10-15 2021-01-08 (주)아모레퍼시픽 Composition for controlling sebum containing a substance related to regulation of ABH antigen expression
KR102224110B1 (en) * 2014-10-15 2021-03-09 (주)아모레퍼시픽 Composition for reducing the skin pore containing a substance related to regulation of ABH antigen expression

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20100012892A (en) * 2010-01-21 2010-02-08 (주)아모레퍼시픽 Method and kit for diagnosis of skin aging
KR20100082709A (en) * 2009-01-09 2010-07-19 서울대학교산학협력단 Composition for improving inflammatory disorder using abh antigen

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100665313B1 (en) * 2003-06-26 2007-01-09 한국과학기술연구원 Compound showing anti-oxidant and anti-viral activity and extract of Chrysanthemum indicum comprising the same
KR20120009953A (en) * 2010-07-23 2012-02-02 (주)아모레퍼시픽 Composition containging amentoflavone for preventing uv-induced skin cell damage

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20100082709A (en) * 2009-01-09 2010-07-19 서울대학교산학협력단 Composition for improving inflammatory disorder using abh antigen
KR20100012892A (en) * 2010-01-21 2010-02-08 (주)아모레퍼시픽 Method and kit for diagnosis of skin aging

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DABELSTEEN, E.: "ABO blood group antigens in oral mucosa. What is new?", JOURNAL OF ORAL PATHOLOGY & MEDICINE, vol. 31, 2002, pages 65 - 70 *
DANINO, O. ET AL.: "Antioxidant activity of 1,3-dicaffeoylquinic acid isolated from Inula viscosa", FOOD RESEARCH INTERNATIONAL, vol. 42, 2009, pages 1273 - 1280 *
LEE, CHAN-WOO ET AL.: "Biflavonoids isolated from Selaginella tamariscina regulate the expression of matrix metalloproteinase in human skin fibroblasts", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 16, 2008, pages 732 - 738 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023001385A1 (en) * 2021-07-23 2023-01-26 Symrise Ag Compositions of dicaffeoylquinic acids with tocopherol

Also Published As

Publication number Publication date
KR20140044454A (en) 2014-04-15
KR101449129B1 (en) 2014-10-08

Similar Documents

Publication Publication Date Title
JP2018109054A (en) Topical oil composition for treatment of fungal infection
KR20150025286A (en) Cmposition for treating or preventing atopic dermatitis or skin wound comprising phytosphingosine-1-phosphate or its derivatives
WO2014054841A1 (en) Composition comprising material for controlling expression of abh antigen
KR20210107560A (en) Composition for treating allergic skin disease or skin pruritis comprising colchicine
US10500187B2 (en) Composition comprising plant phenols for preventing or reducing TEWL and associated disorders and diseases
US20190142721A1 (en) Composition containing substance for regulating expresson of abh antigens
KR101965590B1 (en) Composition for skin whitening containing compound of regulation for ABH antigen
US20070275093A1 (en) Methods for Treating Non-Microbial Inflammatory Skin Conditioners
KR102199884B1 (en) Composition for controlling sebum containing a substance related to regulation of ABH antigen expression
KR20160113474A (en) Compositions for Inhibition, Improvement or Alleviation of Itching
KR101548254B1 (en) Composition for treating skin disease comprising sulfur, alum and vinegar
US20240225973A1 (en) Cosmetic composition for improving sensitive skin
KR20130077953A (en) Elastase inhibitors containing carnosic acid or derivatives thereof
KR101567735B1 (en) Composition for preventing or improving or treating psoriasis comprising immunomodulating agent and glucosamine
KR101438376B1 (en) Composition for skin external containing fructose 1,6-diphosphate stabilized by pH control
KR20160066733A (en) COMPOSITION FOR MOISTURIZING THE SKIN CONTAINING (2S)-1-O-LINOLENOYL-3-O-β-D-GALACTOPYRANOSYL-SN-GLYCEROL
KR102224110B1 (en) Composition for reducing the skin pore containing a substance related to regulation of ABH antigen expression
KR20160067428A (en) COMPOSITION FOR MOISTURIZING THE SKIN CONTAINING (2S)-1-O-LINOLENOYL-2-O-LINOLENOYL-3-O-β-D-GALACTOPYRANOSYL-SN-GLYCEROL
KR20130052243A (en) Agent for reducing skin irritation comprising carnosic acid or derivatives thereof
US20190175601A1 (en) Composition for inhibiting or alleviating itching including riboflavin
KR102215170B1 (en) Composition for moisturizing the skin containing acetic acid 16-hydroxy-octadeca-9,17-diene-12,14-diynyl ester
KR102286681B1 (en) Composition for moisturizing the skin containing ginsenoyne A
KR20160064499A (en) Composition for moisturizing the skin containing icariside B6
KR20160066736A (en) COMPOSITION FOR MOISTURIZING THE SKIN CONTAINING (2S)-1-O-LINOLEOYL-3-O-β-D-GALACTOPYRANOSYL-SN-GLYCEROL
KR20160068193A (en) Composition for moisturizing the skin containing (-)-eudesmin

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13844220

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205A DATED 04/08/2015)

122 Ep: pct application non-entry in european phase

Ref document number: 13844220

Country of ref document: EP

Kind code of ref document: A1