WO2008078905A1 - Compositions for external use containing minoxidil for hair growth which have an improved skin permeability - Google Patents
Compositions for external use containing minoxidil for hair growth which have an improved skin permeability Download PDFInfo
- Publication number
- WO2008078905A1 WO2008078905A1 PCT/KR2007/006681 KR2007006681W WO2008078905A1 WO 2008078905 A1 WO2008078905 A1 WO 2008078905A1 KR 2007006681 W KR2007006681 W KR 2007006681W WO 2008078905 A1 WO2008078905 A1 WO 2008078905A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- minoxidil
- composition
- external use
- hair growth
- use containing
- Prior art date
Links
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 title claims abstract description 49
- 229960003632 minoxidil Drugs 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims abstract description 46
- 230000003779 hair growth Effects 0.000 title claims abstract description 14
- 231100000245 skin permeability Toxicity 0.000 title abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 43
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000004094 surface-active agent Substances 0.000 claims abstract description 18
- 239000004480 active ingredient Substances 0.000 claims abstract description 12
- 235000011187 glycerol Nutrition 0.000 claims abstract description 11
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 claims abstract description 10
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims abstract description 10
- 229940068968 polysorbate 80 Drugs 0.000 claims abstract description 10
- 229920000053 polysorbate 80 Polymers 0.000 claims abstract description 10
- 235000013772 propylene glycol Nutrition 0.000 claims abstract description 8
- 229960004063 propylene glycol Drugs 0.000 claims abstract description 8
- 229920001213 Polysorbate 20 Polymers 0.000 claims abstract description 7
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 claims abstract description 7
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 claims abstract description 7
- 229940068977 polysorbate 20 Drugs 0.000 claims abstract description 7
- 235000019441 ethanol Nutrition 0.000 claims abstract description 4
- 150000003839 salts Chemical class 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000008213 purified water Substances 0.000 claims description 17
- -1 pH regulators Substances 0.000 claims description 4
- 239000003906 humectant Substances 0.000 claims description 3
- 239000003755 preservative agent Substances 0.000 claims description 3
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 14
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 8
- 235000004866 D-panthenol Nutrition 0.000 description 8
- 239000011703 D-panthenol Substances 0.000 description 8
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 0.000 description 8
- 229960003949 dexpanthenol Drugs 0.000 description 8
- 239000003814 drug Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 7
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 7
- 229960002216 methylparaben Drugs 0.000 description 7
- 229940079593 drug Drugs 0.000 description 6
- 239000002953 phosphate buffered saline Substances 0.000 description 6
- 238000005070 sampling Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 229940108325 retinyl palmitate Drugs 0.000 description 4
- 235000019172 retinyl palmitate Nutrition 0.000 description 4
- 239000011769 retinyl palmitate Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 231100000274 skin absorption Toxicity 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 2
- 210000001015 abdomen Anatomy 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 210000002374 sebum Anatomy 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 230000037384 skin absorption Effects 0.000 description 2
- 230000036962 time dependent Effects 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- OIQOAYVCKAHSEJ-UHFFFAOYSA-N 2-[2,3-bis(2-hydroxyethoxy)propoxy]ethanol;hexadecanoic acid;octadecanoic acid Chemical compound OCCOCC(OCCO)COCCO.CCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O OIQOAYVCKAHSEJ-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- 206010012426 Dermal cyst Diseases 0.000 description 1
- 208000010305 Epidermal Cyst Diseases 0.000 description 1
- 206010020864 Hypertrichosis Diseases 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
- 229960000878 docusate sodium Drugs 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000004526 pharmaceutical effect Effects 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 208000015412 proliferating trichilemmal cyst Diseases 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229940107889 rogaine Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4993—Derivatives containing from 2 to 10 oxyalkylene groups
Definitions
- the present invention relates to a composition for external use containing minoxidil for hair growth, more particularly a composition for external use containing minoxidil for hair growth that has so excellent skin permeability that the effective ingredient minoxidil is delivered effectively to target skin tissues.
- Minoxidil was approved by FDA (USA), as a hypertension treatment agent for oral administration in 1979. Later during the clinical tests for the treatment of hypertension, minoxidil was confirmed to cause hypertrichosis as a side effect. Since then, minoxidil has been used as an agent for hair growth. A drug containing Minoxidil by 2% was approved by FDA (USA) as a prescribed drug in 1988, as a medicine in 1996 and a drug containing minoxidil by 5% was approved by FDA as a medicine in 1997 (fraprance journal, 233-37(2000)).
- Minoxidil liquid in which aqueous solvents such as propyleneglycol that has high solubility for minoxidil, ethanol and water are mixed, has been used as a general minoxidil solution preparation.
- this formulation does not have affinity with sebum, the oil component surrounding pilar cyst on skin, suggesting low skin permeability.
- 0352088 (2002.09.12) describes that skin absorption is improved by using lipophilic oil components castor oil (product name: Cremophor), poly oxy ethylene stearate ester (product name: Myrj), and reactant of trans -es- terification of natural vegetable oil triglyceride and polyalkylene polyol (product name : Labrafil M).
- lipophilic oil components castor oil product name: Cremophor
- Myrj poly oxy ethylene stearate ester
- Labrafil M reactant of trans -es- terification of natural vegetable oil triglyceride and polyalkylene polyol
- composition for external use containing a co- surfactant and a surfactant selected from the group consisting of polysorbate-20 or polysorbate-80 can be fast absorbed through skin by contacting moisture on skin when it is applied on the skin. Disclosure of Invention Technical Problem
- the present invention provides a composition for external use containing minoxidil for hair growth comprising:
- composition of the present invention has optimal skin permeability so that the active ingredient can be delivered effectively to the target skin tissues when it is applied on the skin.
- the active ingredient for the composition of the present invention includes minoxidil, its derivatives and its salts.
- the content of the active ingredient in the composition of the present invention is preferably 1-7 w/v% based on the total weight of the composition, and more preferably 2-5 w/v%. If the content of the active ingredient is less than 1 w/v%, its pharmaceutical effect will be in doubt. If the content of the active ingredient is more than 7 w/v%, solubility will be so low that crystals are educed and side effects such as hair growing on the non-target area can be brought.
- the co-surfactant used for the composition of the present invention is a solvent that has both hydrophilicity and lipophilicity, which favors solution of the active ingredient and maintaining the composition regularly.
- the co-surfactant to meet the above object is exemplified by glycerin, propyleneglycol, and ethanol, and particularly glycerin or ethanol is more preferred. These compounds can be used independently or as a mixture of the two or more.
- the content of the co-surfactant in the total weight of the composition of the invention may be preferably 30-90 w/v% and more preferably 50-80 w/v%. If the content of the co-surfactant is less than 30 w/v%, it appears to have a problem with a solubility of major components. If the content is more than 90 w/v%, also solubility will be a problem.
- the surfactant of the invention is used to maintain the composition as regular as possible by using lipophilic oil components, and may be a various types of surfactants including a pharmaceutically acceptable anionic, cationic, non-ionic or amphoteric surfactants. Particularly, polysorbate-20 and polysorbate-80 are preferred for the composition of the invention.
- the content of the surfactant in the total weight of the composition may be preferably 2-30 w/v%, more preferably 5-20 w/v%. If the content of the surfactant is less than 2 w/v%, it is very difficult to maintain the liquid composition stably. If the content is more than 30 w/v%, a subject might feel something sticky and foreign body sensation when it is applied.
- the composition of the present invention can additionally contains humectants, antioxidants, pH regulators, preserving agents, viscosity modifiers and purified water as long as the effect of the composition is not damaged.
- the humectant is exemplified by dexpanthenol
- the preserving agent is exemplified by methylparaffin
- the pH regulator is exemplified by citric acid
- the viscosity modifier is exemplified by pytosterol, but not always limited thereto.
- Figure 1 is a graph illustrating the results of skin permeability tests with the composition for external use of the present invention and the control.
- Figure 2 is a graph of calibration over concentrations using the minoxidil standard.
- composition for external use containing minoxidil for hair growth was prepared by mixing and dissolving the following components.
- the composition for external use containing minoxidil for hair growth of the present invention has excellent skin permeability and thus the active ingredient of the composition, minoxidil, can reach the target skin tissues effectively when applied on the skin.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention relates to a composition for external use containing minoxidil for hair growth with improved skin permeability. The composition of the invention contains one or more active ingredients selected from the group consisting of minoxidil, its derivatives and its salts; one or more co-surfactants selected from the group consisting of glycerin, propyleneglycol and ethanol; and one or more surfactants selected from the group consisting of polysorbate-20 and polysorbate-80, at a required ratio, so that it has excellent skin permeability, compared with the conventional composition for external use for hair growth comprising minoxidil, so as to deliver the active ingredient to target skin tissues more effectively, when it is applied on the skin.
Description
Description
COMPOSITIONS FOR EXTERNAL USE CONTAINING
MINOXIDIL FOR HAIR GROWTH WHICH HAVE AN
IMPROVED SKIN PERMEABILITY
Technical Field
[1] The present invention relates to a composition for external use containing minoxidil for hair growth, more particularly a composition for external use containing minoxidil for hair growth that has so excellent skin permeability that the effective ingredient minoxidil is delivered effectively to target skin tissues. Background Art
[2] Minoxidil was approved by FDA (USA), as a hypertension treatment agent for oral administration in 1979. Later during the clinical tests for the treatment of hypertension, minoxidil was confirmed to cause hypertrichosis as a side effect. Since then, minoxidil has been used as an agent for hair growth. A drug containing Minoxidil by 2% was approved by FDA (USA) as a prescribed drug in 1988, as a medicine in 1996 and a drug containing minoxidil by 5% was approved by FDA as a medicine in 1997 (fraprance journal, 233-37(2000)).
[3] Minoxidil liquid, in which aqueous solvents such as propyleneglycol that has high solubility for minoxidil, ethanol and water are mixed, has been used as a general minoxidil solution preparation. However, this formulation does not have affinity with sebum, the oil component surrounding pilar cyst on skin, suggesting low skin permeability.
[4] To overcome the problem of low skin permeability, European Patent No. 3156488
(1942.1.4) describes the use of such a nonaqueous solvent as silicon oil that is able to dissolve sebum and Japanese Patent Publication No. 0262818A (1990.3.2) describes the use of such a nonaqueous solvent as glycerin fatty acid ester. Japanese Patent Publication No. 62-230710 (1987.10.9) describes the use of such a nonaqueous solvent as fatty acid alcohol and fatty acid alkylester. These solvents seemed to have better effect on skin absorption than water-soluble solvents but the effect was not satisfactory. Korean Patent No. 0352088 (2002.09.12) describes that skin absorption is improved by using lipophilic oil components castor oil (product name: Cremophor), poly oxy ethylene stearate ester (product name: Myrj), and reactant of trans -es- terification of natural vegetable oil triglyceride and polyalkylene polyol (product name : Labrafil M). However, these compositions also have a problem of feeling something sticky and foreign body sensation owing to their oily, high molecular substances when they are applied.
[5] Thus, the present inventors have studied to develop a composition for external use containing minoxidil for hair growth that has improved skin permeability to bring satisfactory skin absorption effect. As a result, the present inventors completed this invention by confirming that the composition for external use containing a co- surfactant and a surfactant selected from the group consisting of polysorbate-20 or polysorbate-80 can be fast absorbed through skin by contacting moisture on skin when it is applied on the skin. Disclosure of Invention Technical Problem
[6] It is an object of the present invention to provide a composition for external use containing minoxidil for hair growth that has excellent skin permeability. Technical Solution
[7] The above object of the present invention can be achieved by the following embodiments of the present invention.
[8] The present invention is described in detail hereinafter.
[9] To achieve the above object, the present invention provides a composition for external use containing minoxidil for hair growth comprising:
[10] 1 - 7 w/v% of one or more active ingredients selected from the group consisting of minoxidil, its derivatives and its salts;
[11] 30 - 90 w/v% of one or more co- surfactants selected from the group consisting of glycerin, propyleneglycol and ethanol; and
[12] 2 - 30 w/v% of one or more surfactants selected from the group consisting of polysorbate-20 and polysorbate-80.
[13] The composition of the present invention has optimal skin permeability so that the active ingredient can be delivered effectively to the target skin tissues when it is applied on the skin.
[14] Hereinafter, the kinds and characteristics of components of the composition of the invention are described in detail.
[15] (l) Active ingredient
[16] The active ingredient for the composition of the present invention includes minoxidil, its derivatives and its salts. The content of the active ingredient in the composition of the present invention is preferably 1-7 w/v% based on the total weight of the composition, and more preferably 2-5 w/v%. If the content of the active ingredient is less than 1 w/v%, its pharmaceutical effect will be in doubt. If the content of the active ingredient is more than 7 w/v%, solubility will be so low that crystals are educed and side effects such as hair growing on the non-target area can be brought.
[17] (2) Co-surfactant
[18] The co-surfactant used for the composition of the present invention is a solvent that has both hydrophilicity and lipophilicity, which favors solution of the active ingredient and maintaining the composition regularly. The co-surfactant to meet the above object is exemplified by glycerin, propyleneglycol, and ethanol, and particularly glycerin or ethanol is more preferred. These compounds can be used independently or as a mixture of the two or more. The content of the co-surfactant in the total weight of the composition of the invention may be preferably 30-90 w/v% and more preferably 50-80 w/v%. If the content of the co-surfactant is less than 30 w/v%, it appears to have a problem with a solubility of major components. If the content is more than 90 w/v%, also solubility will be a problem.
[19] (3) Surfactant
[20] The surfactant of the invention is used to maintain the composition as regular as possible by using lipophilic oil components, and may be a various types of surfactants including a pharmaceutically acceptable anionic, cationic, non-ionic or amphoteric surfactants. Particularly, polysorbate-20 and polysorbate-80 are preferred for the composition of the invention. The content of the surfactant in the total weight of the composition may be preferably 2-30 w/v%, more preferably 5-20 w/v%. If the content of the surfactant is less than 2 w/v%, it is very difficult to maintain the liquid composition stably. If the content is more than 30 w/v%, a subject might feel something sticky and foreign body sensation when it is applied.
[21] The composition of the present invention can additionally contains humectants, antioxidants, pH regulators, preserving agents, viscosity modifiers and purified water as long as the effect of the composition is not damaged. The humectant is exemplified by dexpanthenol, the preserving agent is exemplified by methylparaffin, the pH regulator is exemplified by citric acid and the viscosity modifier is exemplified by pytosterol, but not always limited thereto. Brief Description of the Drawings
[22] The application of the preferred embodiments of the present invention is best understood with reference to the accompanying drawings, wherein:
[23]
[24] Figure 1 is a graph illustrating the results of skin permeability tests with the composition for external use of the present invention and the control.
[25] Figure 2 is a graph of calibration over concentrations using the minoxidil standard.
Best Mode for Carrying Out the Invention
[26] Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples.
[27] However, it will be appreciated that those skilled in the art, on consideration of this
disclosure, may make modifications and improvements within the spirit and scope of the present invention. [28]
[29] <Example 1>
[30] 100 ml of the composition for external use containing minoxidil for hair growth was prepared by mixing and dissolving the following components.
[31] Minoxidil 5.0 g
[32] Dexpanthenol 0.004 g
[33] Glycerin 24.5 g
[34] Polysorbate80 7.6 g
[35] Ethanol 44.2 g
[36] Methylparaben 0.09 g
[37] Pytosterol 0.0004 g
[38] Retinol palmitate 0.05 g
[39] Purified water 18.0 g [40]
[41] <Example 2>
[42] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water.
[43] Minoxidil 5.0 g
[44] Dexpanthenol 0.004 g
[45] Glycerin 24.5 g
[46] Polysorbate20 7.6 g
[47] Ethanol 44.2 g
[48] Methylparaben 0.09 g
[49] Pytosterol 0.0004 g
[50] Retinol palmitate 0.05 g
[51] Purified water 18.0 g [52]
[53] <Example 3>
[54] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water.
[55] Minoxidil 5.0 g
[56] Dexpanthenol 0.004 g
[57] Propyleneglycol 24.5 g
[58] Polysorbate80 7.6 g
[59] Ethanol 44.2 g
[60] Methylparaben 0.09 g
[61] Pytosterol 0.0004 g
[62] Purified water 18.0 g
[63]
[64] <Example 4>
[65] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water.
[66] Minoxidil 5.0 g
[67] Dexpanthenol 0.004 g
[68] Propyleneglycol 24.5 g
[69] Polysorbate20 7.6 g
[70] Ethanol 44.2 g
[71 ] Methylparaben 0.09 g
[72] Pytosterol 0.0004 g
[73] Purified water 18.0 g [74]
[75] <Example 5>
[76] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water.
[77] Minoxidil 5.0 g
[78] Dexpanthenol 0.004 g
[79] Glycerin 24.5 g
[80] Polysorbate80 7.6 g
[81] Ethanol 44.2 g
[82] Methylparaben 0.09 g
[83] Pytosterol 0.0004 g
[84] Retinol palmitate 0.05 g
[85] Citric acid 0.05 g
[86] Purified water 18.0 g [87]
[88] <Example 6>
[89] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water.
[90] Minoxidil 2.0 g
[91 ] Dexpanthenol 0.004 g
[92] Glycerin 24.5 g
[93] Polysorbate80 7.6 g
[94] Ethanol 44.2 g
[95] Methylparaben 0.09 g
[96] Pytosterol 0.0004 g
[97] Retinol palmitate 0.05 g
[98] Purified water 18.0 g
[99]
[100] <Example 7>
[101] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water. [102] Minoxidil 2.0 g
[103] Dexpanthenol 0.004 g
[104] Glycerin 24.5 g
[105] Polysorbate80 7.6 g
[106] Ethanol 44.2 g
[107] Methylparaben 0.09 g
[108] Pytosterol 0.0004 g
[109] Rretinol palmitate 0.05 g
[110] Citric acid 0.05 g
[111] Purified water 18.0 g
[112]
[113] <Comparative Example 1> [Control drug: Rogaine (Pfizer)]
[114] 100 ml of the composition for external use containing minoxidil was prepared by mixing and dissolving the following components in purified water. [115] Minoxidil 5.0 g
[116] Ethanol 26.1 g
[117] Propylenegly col 52.8 g
[118] Purified water 18.0 g
[119]
[120] Experimental Example 1> In vitro skin permeability test using hairless mice
[121] To investigate skin permeability of the composition for external use of the invention, in vitro skin permeability test was performed using hairless mice. [122] The composition for external use of the invention prepared in example 1 was used as a test drug. The composition prepared in comparative example 1 was used as a control drug. All experiments were repeated twice. [123] Hairless mice (9 weeks, male, 25~30g) were anesthetized by ether, and skin tissues of the abdomen were cut off, which were used as a Franz cell (r=0.75 cm, vessel volume=5.5 ml) membrane and PBS (phosphate buffered saline : pH 7.2) was used as a vessel solution. [124] The experiment procedure is described in detail hereinafter. After applying 1 ml (50 mg) of minoxidil, the bottom of skin tissues were fully contacted with PBS in beaker,
followed by stirring at 600 rpm. Sampling was performed over the time (samples were taken at the time points of 0, 0.5, 1, 2, 4, 6, 9 and 24 hour) by 0.3 ml and the equal amount of PBS was supplemented every time. The samples were stored at 40C, and time dependent concentration curve was made by HPLC. The experimental group and the control group having equal content of minoxidil and the water bath were maintained at 370C and circulated.
[125] <Apparatus>
[126] ® HPLC 2690 (Waters, USA)
[127] © Franz-type diffusion cell (Korea)
[128] ® Shaking water bath
[129] <Analysis condition>
[130] - Mobile phase: Methanol, water and acetic acid were mixed at the ratio of
700:300:10. 3.0 g of Docusate sodium (Fluka co. 86139) was added thereto. PH was adjusted to 3.0 with perchloric acid, followed by filtering using 0.22 D filter and degas.
[131] - Detector: waters 996, Photodiode Array, 254 nm
[132] - Colum: Nova-Pak, C18 3.9 x 150 mm, 4D
[133] - Flow rate: 1.0 ml/min
[134] The standard minoxidil (Sigma M 1430) was dissolved in HPLC moving phase (1 mg/ml) and diluted serially to 100, 50, 25, 12.5, 6.25, 3.125, 1.563, and 0.78 D/ml, with which calibration curve was obtained.
[135] <Time dependent skin permeability concentration of 5% minoxidil tested with hairless mice>
[136] Sampling dilution ratios were calculated by measuring the minoxidil concentrations over the time according to the standard curve shown in Figure 2.
[137] Particularly, from the first 5.5 ml of PBS, 0.3 ml of sample was taken at the sampling hour 1 and 0.3 ml of PBS was supplemented thereto. So, HPLC value obtained therefrom was multiplied by 1.05. The HPLC value obtained from the sampling hour 2 was multiplied again by 1.05. This procedure was repeated to calculate the sampling dilution ratios.
[138] The results are shown in Table 1 and Figure 1.
[140] The abdomen skin tissue sections of the hairless mouse were divided into two groups (right and left) and the results were compared. As shown in Table 1 and Figure 1, it was confirmed that the composition of example 1 demonstrated 3 - 4 fold higher skin permeability from the sampling hour 6, compared with that of comparative example 1.
Industrial Applicability
[141] As explained hereinbefore, the composition for external use containing minoxidil for hair growth of the present invention has excellent skin permeability and thus the active ingredient of the composition, minoxidil, can reach the target skin tissues effectively when applied on the skin.
[142] [143] Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.
Claims
Claims
[1] A composition for external use containing minoxidil for hair growth comprising:
1 - 7 w/v% of one or more active ingredients selected from the group consisting of minoxidil, its derivatives and its salts;
30 - 90 w/v% of one or more co-surfactants selected from the group consisting of glycerin, propyleneglycol and ethanol; and
2 - 30 w/v% of one or more surfactants selected from the group consisting of polysorbate-20 and polysorbate-80. [2] The composition for external use containing minoxidil for hair growth according to claim 1, wherein the composition can additionally further contains humectants, antioxidants, pH regulators, preserving agents, viscosity modifiers or purified water.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020060132255A KR100893469B1 (en) | 2006-12-22 | 2006-12-22 | External solution for hair regrowth containing minoxidil with excellent skin permeability |
KR10-2006-0132255 | 2006-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008078905A1 true WO2008078905A1 (en) | 2008-07-03 |
Family
ID=39562664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2007/006681 WO2008078905A1 (en) | 2006-12-22 | 2007-12-20 | Compositions for external use containing minoxidil for hair growth which have an improved skin permeability |
Country Status (2)
Country | Link |
---|---|
KR (1) | KR100893469B1 (en) |
WO (1) | WO2008078905A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012051374A3 (en) * | 2010-10-15 | 2012-08-09 | The Procter & Gamble Company | Use of monoamine oxidase inhibitors to improve epithelial biology |
US8309142B1 (en) * | 2010-06-11 | 2012-11-13 | RMV Trademarks, LLC | Formulations and methods for preventing eyebrow hair loss |
WO2011081861A3 (en) * | 2009-12-15 | 2013-04-11 | Mcneil-Ppc, Inc. | Hair growth and / or regrowth compositions |
EP2857002A4 (en) * | 2012-05-30 | 2015-12-09 | Asahi Glass Co Ltd | COMPOSITION FOR CAPILLARY GROWTH |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100878198B1 (en) * | 2008-05-06 | 2009-01-13 | 현대약품 주식회사 | Gel Composition Containing Minoxidil |
KR20240147009A (en) * | 2023-03-30 | 2024-10-08 | 신신제약 주식회사 | A Composition for treatment of alopecia comprising minoxidil |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2733980B2 (en) * | 1988-08-26 | 1998-03-30 | 大正製薬株式会社 | Hair restoration composition |
KR20030021707A (en) * | 2001-09-07 | 2003-03-15 | 주식회사 엘지생활건강 | O/o/w multiple emulsion containing minoxidil |
US20050037060A1 (en) * | 1998-04-22 | 2005-02-17 | Connetics Corporation | Pharmaceutical composition |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030021706A (en) * | 2001-09-07 | 2003-03-15 | 주식회사 엘지생활건강 | W/o/w multiple emulsion containing minoxidil |
-
2006
- 2006-12-22 KR KR1020060132255A patent/KR100893469B1/en not_active Expired - Fee Related
-
2007
- 2007-12-20 WO PCT/KR2007/006681 patent/WO2008078905A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2733980B2 (en) * | 1988-08-26 | 1998-03-30 | 大正製薬株式会社 | Hair restoration composition |
US20050037060A1 (en) * | 1998-04-22 | 2005-02-17 | Connetics Corporation | Pharmaceutical composition |
KR20030021707A (en) * | 2001-09-07 | 2003-03-15 | 주식회사 엘지생활건강 | O/o/w multiple emulsion containing minoxidil |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011081861A3 (en) * | 2009-12-15 | 2013-04-11 | Mcneil-Ppc, Inc. | Hair growth and / or regrowth compositions |
US8470833B2 (en) | 2009-12-15 | 2013-06-25 | Mcneil-Ppc, Inc. | Hair growth and/or regrowth compositions |
US8877762B2 (en) | 2009-12-15 | 2014-11-04 | Mcneil-Ppc, Inc. | Hair growth and/or regrowth compositions |
US8927554B2 (en) | 2009-12-15 | 2015-01-06 | Mcneil-Ppc, Inc. | Hair growth and/or regrowth compositions |
US8309142B1 (en) * | 2010-06-11 | 2012-11-13 | RMV Trademarks, LLC | Formulations and methods for preventing eyebrow hair loss |
WO2012051374A3 (en) * | 2010-10-15 | 2012-08-09 | The Procter & Gamble Company | Use of monoamine oxidase inhibitors to improve epithelial biology |
US8986664B2 (en) | 2010-10-15 | 2015-03-24 | The Procter & Gamble Company | Use of monoamine oxidase inhibitors to improve epithelial biology |
EP2857002A4 (en) * | 2012-05-30 | 2015-12-09 | Asahi Glass Co Ltd | COMPOSITION FOR CAPILLARY GROWTH |
Also Published As
Publication number | Publication date |
---|---|
KR20080058516A (en) | 2008-06-26 |
KR100893469B1 (en) | 2009-04-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0315648B1 (en) | Sebum-dissolving nonaqueous minoxidil formulation | |
EP1265617B1 (en) | Novel topical oestroprogestational compositions with systemic effect | |
DE69820973T2 (en) | BIPHASE MEDICINE DOSAGE FORM OF MANY COMPONENTS, CONTAINING SUBSTANCES THAT CAN AFFECT THE DISTRIBUTION OF THE MEDICINAL PRODUCTS | |
US20220273627A1 (en) | Topical composition comprising tacrolimus | |
CA2458448A1 (en) | Spontaneous emulsions containing cyclosporine | |
WO2008078905A1 (en) | Compositions for external use containing minoxidil for hair growth which have an improved skin permeability | |
JP2008533153A (en) | Enhancement of macrolide penetration through human skin | |
WO2009091541A1 (en) | Imiquimod formulation | |
KR20010003063A (en) | Dermal emulsion composition comprising minoxidil | |
WO1995004551A1 (en) | Percutaneously absorbable preparation | |
CN113425620A (en) | Liposome for wrapping active component, preparation method and application thereof | |
KR20180057714A (en) | Non-rinse chemical foams containing triparotene, and uses thereof in the treatment of acne | |
US9295675B2 (en) | Testosterone gel compositions and related methods | |
JP4430889B2 (en) | Preparations for topical skin containing sparingly soluble materials | |
EP0221208A1 (en) | Hair growth promoting compositions | |
JP5897299B2 (en) | Lotion preparation | |
KR100341203B1 (en) | Pharmaceutical Composition Comprising Oily Vitamin and process for the preparation thereof | |
JP2700990B2 (en) | Percutaneous absorption enhancer and skin external preparation composition | |
JP4774691B2 (en) | Dimethylisopropylazulene external preparation | |
JPH0256429A (en) | External drug containing morphines | |
CA2156396A1 (en) | Stable dermatologic preparation containing mycophenolic acid | |
JP2014152135A (en) | Pharmaceutical compositions | |
JP2000119197A (en) | Local treating preparation | |
CN111954526A (en) | Pharmaceutical composition containing (R) -N- [1- (3, 5-difluoro-4-methanesulfonyl-phenyl) -ethyl ] -3- (2-propyl-6-trifluoromethyl-pyridin-3-yl) -acrylamide and method for inhibiting crystal formation thereof | |
HK1186118A (en) | Dermal composition comprising polymeric reversed micelle, and method for producing same |
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: 07851647 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 07851647 Country of ref document: EP Kind code of ref document: A1 |