WO2022191551A1 - Composition comprenant du cannabigérol - Google Patents
Composition comprenant du cannabigérol Download PDFInfo
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- WO2022191551A1 WO2022191551A1 PCT/KR2022/003210 KR2022003210W WO2022191551A1 WO 2022191551 A1 WO2022191551 A1 WO 2022191551A1 KR 2022003210 W KR2022003210 W KR 2022003210W WO 2022191551 A1 WO2022191551 A1 WO 2022191551A1
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- WO
- WIPO (PCT)
- Prior art keywords
- hair
- composition
- lotion
- ginseng
- extract
- Prior art date
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Classifications
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- A61K2800/78—Enzyme modulators, e.g. Enzyme agonists
- A61K2800/782—Enzyme inhibitors; Enzyme antagonists
Definitions
- the present invention cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, Ginseng saponin, and one or more selected from the group consisting of propolis; a composition comprising, specifically, for moisturizing the skin including the composition as an active ingredient; for anti-inflammatory or skin soothing; Or it relates to a composition for whitening.
- Cannabigerol is a trace amount of active ingredient that can be obtained from the seeds of cannabis sativa. Cannabigerol is not a psychotropic substance and is known to have various effects.
- the present inventors have prepared cannabigerol; isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, When combined with one or more selected from the group consisting of vitamin C (vitamin C), panthenol, adenosine, cedrol, ginseng saponin, and propolis, HAS than using each component alone
- vitamin C vitamin C
- panthenol panthenol
- adenosine cedrol
- ginseng saponin ginseng saponin
- propolis HAS than using each component alone
- the present invention was completed by confirming that -2 (Hyaluronan Synthase 2) or AQP3 (Aquaporin 3) expression increase, NO production inhibition, and tyrosinase activity inhibition effects were significantly superior.
- the present invention is a cosmetic, for a quasi-drug composition, cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides a composition comprising ginseng saponin, and one or more selected from the group consisting of propolis as an active ingredient.
- cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides a skin moisturizing, anti-inflammatory or skin soothing, or skin whitening method comprising the step of treating the skin with a composition comprising ginseng saponin, and propolis as an active ingredient.
- cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides a skin moisturizing, anti-inflammatory or skin soothing, or skin whitening method comprising administering to a subject a composition comprising ginseng saponin, and propolis as an active ingredient.
- skin moisturizing, anti-inflammatory or skin soothing, or skin whitening cosmetic In order to achieve the above object, skin moisturizing, anti-inflammatory or skin soothing, or skin whitening cosmetic; Or quasi-drugs; Cannabigerol for manufacturing; and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides the use of a composition comprising ginseng saponin, and propolis as an active ingredient.
- composition according to the present invention has an effect of increasing the expression of HAS-2 or AQP3, inhibiting the production of NO, and inhibiting tyrosinase activity, and has a synergistic effect due to the combination of the present invention, as a cosmetic or quasi-drug composition can be used effectively.
- Increased expression of HAS-2 or AQP3, inhibition of NO production, and inhibition of tyrosinase activity are all more effective than cannabigerol alone, isopulegol, ginseng extract, centella asiatica extract, niacinamide (niacinamide), hyaluronic acid (hyaluronic acid), vitamin C (vitamin C), panthenol (panthenol), adenosine (adenosine), cedrol (cedrol), one or more selected from the group consisting of ginseng saponin and propolis; It was confirmed that a synergistic effect occurred when combined with
- the present invention cannabigerol (Cannabigerol); and
- cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides a skin moisturizing, anti-inflammatory or skin soothing, or skin whitening method comprising the step of treating the skin with a composition comprising ginseng saponin, and propolis as an active ingredient.
- cannabigerol (Cannabigerol); and isopulegol, ginseng extract, centella asiatica extract, niacinamide, hyaluronic acid, vitamin C, panthenol, adenosine, cedrol, It provides a skin moisturizing, anti-inflammatory or skin soothing, or skin whitening method comprising administering to a subject a composition comprising ginseng saponin, and propolis as an active ingredient.
- the active ingredients (Cannabigerol, isopulegol, ginseng extract, Centella asiatica extract, niacinamide, hyaluronic acid, vitamin C (vitamin C), panthenol (panthenol), Adenosine (adenosine), cedrol (cedrol), ginseng saponin, and propolis) Legally permitted commercial products or commercial ingredients of the active ingredient may be used.
- the "extract" of the present invention is an extract obtained by the extraction treatment of the plant material, a diluted or concentrated liquid of the extract, a dried product obtained by drying the extract, a prepared or purified product of the extract, or a mixture thereof, such as the extract itself and extracts of all formulations that can be formed using the extract.
- the extract of the present invention may be prepared and used in the form of a dry powder after extraction.
- any part of ginseng or Centella asiatica such as an outpost, leaf, root, fruit, stem, etc. of ginseng or Centella asiatica may be used.
- the "ginseng saponin” of the present invention is a saponin present in the ginseng extract before purification, and refers to all of the saponin contained in ginseng, a substance represented by saponin, a substance to be changed to saponin, or a substance presumed to be saponin.
- the saponins contained in ginseng are panaxadiol-based saponins (Ra1, G-Ra2, G-Ra3, G-Rb1, G-Rb2, Rb3, G-Re, G-Rd, G-Rs1, G-Rs2, Rg3 ( 20 S), G-Rg3(20R), G-Rh2, G-Rs3, Rs4, G-Rg5, G-F4,Q-R1, N-R4, Rg6, etc.)
- Panaxatriol-based saponins Ros, Rf , Rg1, Rg2(20 S), Rg2(20 R), Rh1(20 S), Rh2(20 R), 20-glc-Rf, N-R1, Rh4, Rf2, etc.
- oleic saponins G-R, etc.
- G-R, etc. etc.
- the ginseng saponin of the present invention may be a mixture of several types of ginseng saponins mentioned above or not mentioned, or may be a single type of ginseng saponin, and ginsenoside, pseudoginsenoside, or its It may be other ginseng saponins.
- the composition may be a cosmetic or quasi-drug.
- the cosmetics include lotion, essence, lotion, cream, pack, gel, powder, foundation, balm, ointment, detergent, hair shampoo, hair tonic, hair conditioner, hair lotion, hair nourishing lotion, hair treatment, hair essence , hair pack, hair liquid, non-aerosol mousse, non-aerosol spray, aerosol mousse or aerosol spray formulation, but is not limited thereto.
- “Moisturizing skin” of the present invention means to increase the feeling of moisture in the skin and to maintain a moist state by suppressing moisture loss.
- the skin moisturizing effect was confirmed by increasing the expression of HAS-2 (Hyaluronan Synthase 2) or AQP3 (Aquaporin 3).
- composition may have an effect of increasing the expression of HAS-2 or AQP3.
- anti-inflammatory refers to inhibiting inflammation, and the inflammation is one of the defense responses of a living tissue to a certain stimulus, and refers to a complex lesion that combines three types: tissue deterioration, circulatory disorder and exudation, and tissue proliferation. More specifically, inflammation is part of innate immunity, and as in other animals, human innate immunity recognizes patterns on the surface of cells that are specific to pathogens. Phagocytes recognize cells with such a surface as non-self and attack pathogens. If pathogens break through the body's physical barriers, an inflammatory response occurs. The inflammatory response is a non-specific defense action that creates a hostile environment for microorganisms that invade the wound site.
- the white blood cells responsible for the early stage immune response flock and express cytokines. Therefore, the expression level of intracellular cytokines is an indicator of inflammatory response activation.
- skin diseases associated with inflammation include atopic dermatitis, psoriasis, erythematous diseases triggered by radiation, chemicals, burns, etc., acid burns, bullous dermatosis, lichenoid type disease, itching due to allergy, seborrheic eczema, acne on roses, pemphigus vulgaris, erythema multiforme, erythema nodosum, balanitis, vulvitis, inflammatory hair loss such as alopecia areata, cutaneous T-cell lymphoma, and the like.
- the anti-inflammatory effect of the present invention for example, it may have an effect of improving skin troubles such as acne.
- the anti-inflammatory hair loss such as alopecia areata, cutaneous T-cell lymphoma, and the like.
- skin soothing means alleviating or reducing inflammation, or itching, redness, pain, burning, or swelling caused by inflammation.
- the skin soothing may mean a skin soothing effect by reducing or inhibiting inflammation.
- the composition may have an effect of inhibiting the production of NO.
- Whitening of the present invention means not only to brighten skin tone by inhibiting the synthesis of melanin, but also to inhibit or prevent melanin deposition (hyperpigmentation), to relieve or to relieve freckles caused by UV rays, hormones, or heredity. It means any action that improves.
- melanin deposition hyperpigmentation
- tyrosinase activity was confirmed.
- the composition may have a tyrosinase activity inhibitory effect.
- the "cosmetics composition” of the present invention may be in the form of general emulsified formulations and solubilized formulations.
- lotions such as flexible lotions or nourishing lotions, emulsions such as facial lotions and body lotions, creams such as nourishing creams, moisture creams, and eye creams, essences, cosmetic ointments, balms, sprays, gels, packs, sunscreens , makeup base, liquid type, solid type or spray type foundation, powder, cleansing cream, cleansing lotion, makeup remover such as cleansing oil, cleansing agent such as cleansing foam, soap, body wash, etc., but is limited thereto it's not going to be
- the cosmetic includes a fatty substance, an organic solvent, a solubilizer, a thickening agent and a gelling agent, an emollient, an antioxidant, a suspending agent, a stabilizer, a foaming agent, a fragrance, a surfactant, water, Ionic or nonionic emulsifiers, fillers, sequestering and chelating agents, preservatives, vitamins, blocking agents, wetting agents, essential oils, dyes, pigments, hydrophilic or lipophilic actives, lipid vesicles or any conventionally used in cosmetics It may contain adjuvants commonly used in the field of cosmetology such as other ingredients of
- the cosmetic formulation may include a relatively high concentration of the composition of the present invention in the case of a wash-off type cosmetic such as a makeup remover or a detergent in which the active ingredient stays on the skin within a short period of time.
- a wash-off type cosmetic such as a makeup remover or a detergent
- leave-on type cosmetics such as lotions, emulsions, creams, and essences
- the composition of the present invention at a lower concentration than the wash-off type cosmetics. would be free to include.
- the composition comprises 0.000001% to 10% by weight (preferably 0.000001% to 1% by weight) of the composition of the present invention based on the total weight of the composition.
- composition of the present invention contains less than 0.000001% by weight of the composition of the present invention, sufficient moisturizing, anti-inflammatory or skin soothing and whitening effects cannot be expected, and when it contains more than 10% by weight, unwanted reactions such as allergies This is to prevent this from occurring or there may be problems with skin safety.
- the "quasi-drug composition" of the present invention refers to an article that is used for the purpose of diagnosing, treating, alleviating, treating or preventing diseases of humans or animals, but has a milder effect on the human body than pharmaceuticals, and is not an instrument, machine or device among articles It means a composition for articles other than instruments, machines, or devices among articles used for the purpose of pharmacologically affecting the structure and function of humans or animals. Except for articles used for pharmaceutical purposes according to the Pharmaceutical Affairs Act, one embodiment may include, but is not limited to, external preparations for skin, personal care products, or preparations for internal use. Components and the like may be appropriately selected from conventional techniques known in the art.
- compositions of the present invention may be included in the composition of the present invention, preferably within a range not exceeding the maximum amount specified in the norms stipulated by the respective national governments.
- the cosmetic composition of the present invention may be added to the cosmetic composition of the present invention within a range that does not exceed the maximum amount specified in the Cosmetic Safety Act stipulated by each country or the “Cosmeceutical Safety Technical Specification” stipulated by the Chinese government. may be included.
- Ginseng (Panax ginseng) roots were extracted with 70% ethanol aqueous solution corresponding to 30 times the mass at room temperature for 3 days, and then filtered under reduced pressure. The filtered extract was concentrated and dried with a rotary evaporator (Buchi, Switzerland) to prepare an extract.
- Centella asiatica leaves were extracted with 70% ethanol aqueous solution corresponding to 30 times the mass at room temperature for 3 days, and then filtered under reduced pressure. The filtered extract was concentrated and dried with a rotary evaporator (Buchi, Switzerland) to prepare an extract.
- the prepared ginseng extract was extracted three times with a solvent in which equal amounts of water and saturated butanol were mixed, and the saturated butanol layers were combined and concentrated under reduced pressure using a rotary evaporator (Buchi, Switzerland).
- Example 1 Cannabigerol (CBG)
- Example 2 isopuregol
- Ginseng Extract Example 4 Centella asiatica extract
- Niacinamide Example 6 hyaluronic acid
- Example 7 vitamin c
- Example 8 panthenol
- Example 9 adenosine
- Example 10 cedrol
- Example 11 ginseng saponin
- Example 12 propolis
- Fibroblasts were seeded and cultured at a concentration of 2-5 x 10 4 cells/ml using DMEM (Dulbecco's Modified Eagle's Medium, Gibco) supplemented with 10% FBS (Fetal Bovine Serum) as a basal medium. After the cultured cells were transferred to DMEM medium not containing 10% FBS and calcium ions, Examples and Comparative Examples were treated alone or in combination at concentrations corresponding to Table 2 below and cultured for 24 hours.
- DMEM Dulbecco's Modified Eagle's Medium, Gibco
- FBS Fetal Bovine Serum
- TaqMan® Universal Master Mix II (Thermo Fisher, catalog number 4440043) with TaqMan® GeneExpression Assays (Thermo Fisher, catalog number 4331348), HAS2 primer (5'-CCCAAAATGTGAAGCTTGGT -3'), AQP3 primer (5'-AGACAGCCCCTTCAGGATTT-3' ) was used. Quantitative real time PCR was performed using the StepOnePlus® Realtime PCR System (Applied Biosystems, catalog number 4376600). The experimental results were calculated using the ⁇ Ct method based on the housekeeping gene Glyceraldehyde-3-phosphate dehydrogenase (GAPDH, 5'-TGCACCACCAACTGCTTAGC-3').
- Example 1 0.0001% 8.54 7.66
- Example 2 0.001% 2.25 29.81 11.40 25.14
- Example 3 0.01% 16.73 43.15 4.49 19.06
- Example 4 0.01% 15.00 32.95 2.51 20.93
- Example 5 0.001% 6.72 18.10 8.97 18.14
- Example 6 0.001% 6.41 33.79 3.78 12.76
- Example 7 0.001% 18.32 46.31 7.88 20.28
- Example 8 0.001% 3.17 16.95 2.48 20.53
- Example 9 0.001% 2.51 31.24 6.23 22.25
- Example 10 0.001% 8.06 22.67 0.98 16.59
- Example 11 0.01% 5.83 44.25 4.26 20.72
- Example 12 0.01% 6.09 35.54 4.90 23.94
- the NO production inhibitory effect was measured using a mouse macrophage cell line, Raw 264.7 cells (ATCC, catalog number CRL-2788). 10% FBS was added to DMEM and used as a growth medium. Raw264.7 cells were seeded at a concentration of 1 to 2 x 10 5 cells/ml and cultured in a 5% CO 2 incubator for one day. After removing the medium and starvation with a serum-free medium for 12 hours, Examples and Comparative Examples were treated alone or in combination at the concentrations corresponding to Table 3 below and pre-treated for 30 minutes.
- Example 1 sample number sample concentration NO production inhibition ability (%) Use of each sample alone Combination with Example 1 Comparative Example 1 0.00 Comparative Example 2 53.02
- Example 1 0.0001% 26.21
- Example 2 0.001% 13.50 59.04
- Example 3 0.01% 27.18 62.38
- Example 4 0.01% 27.53 57.73
- Example 5 0.001% 9.84 53.67
- Example 6 0.001% 24.09 60.74
- Example 7 0.001% 37.81 66.90
- Example 8 0.001% 21.42 57.97
- Example 9 0.001% 24.12 60.91
- Example 10 0.001% 12.47 52.72
- Example 11 0.01% 19.42 60.70
- Example 12 0.01% 25.63 57.80
- MNT-1 melanoma cells (ATCC, catalog number CRL-3450) were seeded in DMEM medium containing 10% FBS at a concentration of 1 to 2 x 10 5 cells/ml and cultured for 24 hours. Examples and Comparative Examples were treated alone or in combination on melanocytes cultured at the concentration corresponding to Table 4 below and cultured for 72 hours, and then the cells were recovered. After centrifugation at 13,000 rpm for 1 minute and removing the supernatant, 300 ⁇ l of 0.5% triton X-100 solution was added to the pellet to lyse the cells.
- Example 1 sample number sample concentration Tyrosinase activity (%) Use of each sample alone Combination with Example 1 Comparative Example 1 100 Comparative Example 2 57.94 Example 1 0.0001% 89.75 Example 2 0.001% 98.23 72.79 Example 3 0.01% 89.34 70.10 Example 4 0.01% 80.93 61.28 Example 5 0.001% 77.25 60.99 Example 6 0.001% 88.98 66.99 Example 7 0.001% 73.84 51.77 Example 8 0.001% 98.59 75.48 Example 9 0.001% 77.91 50.05 Example 10 0.001% 95.68 76.77 Example 11 0.01% 84.42 71.39 Example 12 0.01% 92.26 77.44
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- Birds (AREA)
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- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Abstract
La présente invention se rapporte à une composition comprenant : du cannabigérol ; et un ou plusieurs composants choisis dans le groupe constitué par l'isopulégol, un extrait de ginseng, un extrait de Centella asiatica, le niacinamide, l'acide hyaluronique, la vitamine C, le panthénol, l'adénosine, le cédrol, la saponine brute de ginseng et la propolis et, plus particulièrement, à une composition hydratante pour la peau, anti-inflammatoire ou de soin apaisant pour la peau et de blanchiment comprenant la composition en tant que matière active. De plus, il a été confirmé qu'en termes de tous les effets hydratants, anti-inflammatoires ou apaisant la peau et de blanchiment, la composition selon la présente invention avait un effet synergique une fois combinée à un ou plusieurs composants choisis dans le groupe constitué par l'isopulégol, un extrait de ginseng, un extrait de Centella asiatica, le niacinamide, l'acide hyaluronique, la vitamine C, le panthénol, l'adénosine, le cédrol, la saponine brute de ginseng et la propolis, par comparaison au cannabigérol seul.
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KR10-2021-0030241 | 2021-03-08 | ||
KR20210030241 | 2021-03-08 |
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WO2022191551A1 true WO2022191551A1 (fr) | 2022-09-15 |
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PCT/KR2022/003210 WO2022191551A1 (fr) | 2021-03-08 | 2022-03-07 | Composition comprenant du cannabigérol |
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WO (1) | WO2022191551A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN115778828A (zh) * | 2023-02-10 | 2023-03-14 | 安婕妤化妆品科技股份有限公司 | 一种含有富勒烯的化妆品组合物 |
Citations (5)
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US10206888B2 (en) * | 2017-06-06 | 2019-02-19 | Cmg Partners, Inc. | Cannabis-based therapeutic product for treatment of chronic pain |
KR20190034576A (ko) * | 2016-08-03 | 2019-04-02 | 젤다 테라퓨틱스 오퍼레이션즈 피티와이 엘티디 | 카나비스 조성물 |
US20200188325A1 (en) * | 2015-02-16 | 2020-06-18 | Axim Biotechnologies, Inc. | Cosmetic and topical compositions comprising cannabigerol |
WO2020249184A1 (fr) * | 2019-06-11 | 2020-12-17 | Symrise Ag | Synthèse et purification de cannabigérol et son utilisation |
KR20210008327A (ko) * | 2018-01-13 | 2021-01-21 | 트루티바 인코포레이티드 | 노화 방지 및 피부 톤 미백 조성물 및 이를 위한 방법 |
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2022
- 2022-03-07 KR KR1020220028843A patent/KR20220126653A/ko unknown
- 2022-03-07 WO PCT/KR2022/003210 patent/WO2022191551A1/fr active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20200188325A1 (en) * | 2015-02-16 | 2020-06-18 | Axim Biotechnologies, Inc. | Cosmetic and topical compositions comprising cannabigerol |
KR20190034576A (ko) * | 2016-08-03 | 2019-04-02 | 젤다 테라퓨틱스 오퍼레이션즈 피티와이 엘티디 | 카나비스 조성물 |
US10206888B2 (en) * | 2017-06-06 | 2019-02-19 | Cmg Partners, Inc. | Cannabis-based therapeutic product for treatment of chronic pain |
KR20210008327A (ko) * | 2018-01-13 | 2021-01-21 | 트루티바 인코포레이티드 | 노화 방지 및 피부 톤 미백 조성물 및 이를 위한 방법 |
WO2020249184A1 (fr) * | 2019-06-11 | 2020-12-17 | Symrise Ag | Synthèse et purification de cannabigérol et son utilisation |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115778828A (zh) * | 2023-02-10 | 2023-03-14 | 安婕妤化妆品科技股份有限公司 | 一种含有富勒烯的化妆品组合物 |
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