WO2021201310A1 - 비타민과 덱스판테놀이 봉입된 에토좀 조성물 및 이의 제조방법 - Google Patents
비타민과 덱스판테놀이 봉입된 에토좀 조성물 및 이의 제조방법 Download PDFInfo
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/14—Liposomes; Vesicles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
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- 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
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- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
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- 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
- A61K8/55—Phosphorus compounds
- A61K8/553—Phospholipids, e.g. lecithin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
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- 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
- A61K8/67—Vitamins
- A61K8/673—Vitamin B group
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- 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
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
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- 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
- A61K8/67—Vitamins
- A61K8/678—Tocopherol, i.e. vitamin E
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
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- 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
Definitions
- the present invention is an ethosome composition
- an ethosome composition comprising an etosome encapsulated with vitamins and dexpanthenol.
- the sparingly soluble substance is effectively permeated into the skin, especially the scalp, and It has an effect and relates to an ethosome composition capable of preventing hair loss and a method for preparing the same.
- Human hair is about 100,000 to 150,000 per person, and hair grows with its own cycle. This cycle is divided into anagen, catagen, and telogen, and according to this cycle, hair growth and hair loss are repeated. In this process, it is a natural phenomenon that an average of 100 hairs fall out per day.
- Hair loss refers to a state in which hair is lost and sparse or lost. Although the mechanism of hair loss has not yet been precisely elucidated, the research so far has shown that excessive sebum production caused by abnormalities in the circulatory system such as endocrine system abnormalities such as hormone imbalance, autonomic nervous system and blood circulation disorders, nutritional deficiency of hair roots, allergy, bacterial infection, Genetic factors and aging are presumed to be the main causes.
- hair loss which was mainly seen in middle-aged people in the past, can be easily found in young people in their 20s and 30s, and the number is also increasing.
- the minoxidil formulation induces a vasodilatory effect by inducing the opening of Ca-channels, and through this, by increasing blood flow, it is a drug that induces hair growth by continuously supplying nutrients to the hair roots.
- the effect is large with respect to hair loss in the crown region.
- hair loss in areas other than the crown it has a disadvantage that it does not have a good effect.
- finasteride inhibits the function of type 2 5-alpha reductase (5 ⁇ -reductase) to prevent the conversion of testosterone to DHT (dihydrotestosterone), thereby inhibiting hair loss.
- DHT dihydrotestosterone
- finasteride shows side effects such as decreased libido and erectile dysfunction in some patients.
- a short-term rapid treatment is possible, but when the use of the therapeutic drug is stopped, it has a fatal problem in that hair loss proceeds immediately.
- finasteride alone does not have a sufficient effect of improving hair loss, and it has a problem that it is difficult to show a continuous hair effect without the help of a DHT inhibitor.
- an ethosome composition capable of efficiently delivering an active ingredient having an effect on hair growth and hair, and a method for preparing the same.
- Patent Document 0001 Republic of Korea Patent No. 10-0352088
- Patent Document 0002 Republic of Korea Patent Publication No. 10-2015-0044029
- An object of the present invention is to provide an ethosome composition capable of efficiently delivering a sparingly soluble active ingredient by penetrating the skin barrier and a method for preparing the same.
- the present invention uses an anti-aging skin active ingredient that has effects such as skin anti-aging, antioxidant, collagen promotion, etc., rather than a hair growth/wool functional active ingredient whose efficacy is recognized for hair growth/hair growth, by enabling efficient delivery to the scalp. , It aims to provide a composition that promotes the hair effect and prevents hair loss.
- the ethosome composition according to the present invention for solving the above-mentioned problems is an ethosome composition comprising an ethosome encapsulated with vitamins and dexpanthenol,
- the ethosome includes ethanol, a peptide, phosphatidyl choline, and an amino acid compound.
- the peptide is pal-GHK, Pal-GQPR, Pal-KTTK, Pal-KTTKS, Biotin-GHK, PAL-KVK (Palmiotyl Tripeptide-5), Palmitoyl tripeptide-38, Palmitoyl-Tripeptide (Pal-RFK) , Human Oligopeptide-20(Val-Gly-Val-Ala-Pro-Gly), GHK-Cu, (AHK)2Cu, AHK-Cu, Myristic acid-KLAKK-CONH2, Hexapeptide-11, Octapeptide-2, Palmitoyl-hexapeptide , Acetyl tetrapeptide-15, Acetyl Hexapeptide 3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-5, Acetyl-Decapeptide-3, Ac-KGHK, rh-Oligopeptide-1(humanEGF) (NSDSECPLSHDGYCLHDGVCMYIEALDKYACN
- the vitamin may be at least one selected from the group consisting of vitamin E, vitamin C, vitamin B, salts thereof, and analogs thereof.
- the amino acid compound may be one or more selected from the group consisting of amino acids and amino acid analogs, and the amino acids and amino acid analogs are NAC (N-Acetyl Cysteine), arginine (Arginin), lolysine, lysine ethyl ester, It may be at least one selected from the group consisting of histidine and histidine ethyl ester.
- the ethosome composition is vitamin 20 to 70 mg/100ml, dexpanthenol 150 to 250 mg/100ml, ethanol 5 to 15 ml/100ml, peptide 0.1 to 10 mg/100ml, phosphatylcholine 10 to 1000 mg/100ml, it may be one containing 10 to 1000 mg/100ml of the amino acid compound.
- the etosome may have an average particle diameter of 90 to 200 nm.
- the etosome may have an absolute value of a surface charge value of 10 to 100 mV.
- the present invention also provides a method for preparing the above-described ethosome composition
- step (d) adding the solution of step (b) to the solution of step (a), followed by mixing;
- step (e) adding the solution of step (c) to the solution of step (d), followed by mixing;
- step (f) adding a pH adjusting agent to the solution of step (e), followed by mixing; It provides a method for producing an ethosome composition comprising a.
- Step (c) may further include one or more selected from the group consisting of surfactants and other active ingredients for wool.
- the pH adjusting agent may include one or more selected from the group consisting of citric acid and salts thereof.
- the step (a) may be to add 80 to 120 g of the amino acid compound to 50 to 70 L of purified water.
- Step (b) may be to add 100 to 300 g of dexpanthenol to 25 to 35 L of purified water.
- the present invention also provides a composition for promoting hair growth and/or hair comprising the etosome composition according to the present invention.
- the present invention also provides a composition for preventing telogen hair loss comprising the etosome composition according to the present invention.
- composition for preventing telogen hair loss may be to prevent telogen hair loss by promoting scalp anti-aging and/or collagen production.
- the present invention also provides a composition for promoting hair growth and/or hair, characterized in that the ethosome composition is a composition for men further comprising oleanolic acid and/or apigenin.
- the etosome composition provides a composition for preventing telogen hair loss, characterized in that the composition for men further comprises oleanolic acid and/or apigenin.
- skin anti-aging active ingredients having effects such as skin anti-aging, antioxidant, and collagen promotion are efficiently delivered to the scalp, thereby promoting hair growth and hair growth, and preventing hair loss.
- the present invention has the effect of increasing the hair growth effect by enabling the efficient delivery of various compositions in addition to the active ingredient for hair growth using the etosome morphology.
- FIG. 1 is a schematic diagram showing a hair cycle
- Figure 6 is a graph showing the test results to confirm the skin penetration rate of Dexpantenol
- Figure 13 is a graph showing the thickness of the skin tissue in the growth phase continuation / telogen inhibitory effect test
- Figure 15 is a photograph recording the difference between each group on the 19th day after the start of the test in the growth phase continuation / telogen inhibitory effect test;
- 16 is a graph in which the growth phase maintenance state of the growth phase continuation/resting phase inhibition effect experiment is scored.
- the etosome composition according to the present invention has an effect of efficiently delivering vitamins and poorly soluble substances such as dexpanthenol by penetrating the skin.
- Hydrophilic substances dissolve well in solvents such as water, but the skin is composed of a hydrophobic protective film, so it is difficult for hydrophilic active ingredients to be delivered into the skin. Therefore, there is a problem that the transfer efficiency using the solvent is lowered because it is not dissolved.
- Etosome is a phospholipid nanovesicle used for skin and transdermal delivery of molecules, and the present invention uses this to form a vesicle like ethosome by using a phospholipid called phosphatidylcholine and encapsulates the active ingredient in the skin.
- a phospholipid called phosphatidylcholine By moving to the protective film, it is configured to allow the active ingredient to penetrate into the skin protective film to efficiently deliver the active ingredient.
- the present invention is not a component known to be effective for hair growth and wool, but an active ingredient for skin aging improvement that has effects such as skin anti-aging, antioxidant, and collagen promotion, and effectively delivers it to the scalp. By inducing aging and antioxidant effects, it promotes hair growth and wool, and has the effect of preventing hair loss.
- the vitamin may be one or more selected from the group consisting of vitamin E, vitamin C, vitamin B, salts thereof, and analogs thereof. As long as it functions as a vitamin, any type may be used regardless of its form, for example, various forms such as vitamin E acetate and fat-soluble vitamin C may be used.
- the ethosome contains ethanol, peptide, phosphatidylcholine, and an amino acid compound, thereby improving the flexibility of the ethosome shell, thereby increasing the skin penetration rate, and thereby, the effect of efficient delivery of active ingredients.
- the peptide is pal-GHK, Pal-GQPR, Pal-KTTK, Pal-KTTKS, Biotin-GHK, PAL-KVK (Palmiotyl Tripeptide-5), Palmitoyl tripeptide-38, Palmitoyl-Tripeptide (Pal-RFK), Human Oligopeptide-20(Val-Gly-Val-Ala-Pro-Gly), GHK-Cu, (AHK)2Cu, AHK-Cu, Myristic acid-KLAKK-CONH2, Hexapeptide-11, Octapeptide-2, Palmitoyl-hexapeptide, Acetyl tetrapeptide-15, Acetyl Hexapeptide 3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-5, Acetyl-Decapeptide-3, Ac-KGHK, rh-Oligopeptide-1 (humanEGF) (NSDSECPLSHDGYCLHDGVCMYIEALDKYACNCVVG
- the peptide has an effect on skin antioxidant, etc., it is not a component known to have an effect on hair growth, wool effect, etc., but in the present invention, by sufficiently efficiently delivering the component into the scalp, the antioxidant / By maximizing the anti-aging effect and controlling the hair growth cycle, the resting period is shortened, and the growth period is continued, thereby inducing hair growth and wool effects.
- the peptide may preferably be pal-GHK.
- the phosphatidyl choline is one of lecithins, and lecithin refers to a group of fatty substances occurring in animal and plant tissues consisting of phosphoric acid, choline, fatty acids, glycerol, glycolipids, triglycerides, and phospholipids.
- phosphatidyl choline is a phospholipid class including choline as a headline, and as it is made of phospholipids such as a skin protective film, it has the advantage of easily penetrating the skin membrane during delivery of an active ingredient.
- the amino acid compound may be one or more selected from the group consisting of amino acids and amino acid analogs, and the amino acids and amino acid analogs are specifically, N-Acetyl Cysteine (NAC), arginine and lysine, lysine ethyl ester, histidine, and histidine. It may include at least one selected from the group consisting of ethyl esters.
- NAC N-Acetyl Cysteine
- arginine and lysine arginine and lysine
- lysine ethyl ester histidine
- histidine histidine
- histidine histidine
- the ethosome composition is vitamin 20 to 70 mg/100ml, dexpanthenol 150 to 250 mg/100ml, ethanol 5 to 15 ml/100ml, peptide 0.1 to 10 mg/100ml, phosphatylcholine 10 to 1000 mg/100ml, may be one containing 10 to 1000 mg/100ml of the amino acid compound.
- the vitamin may preferably be included in an amount of 30 to 60 mg/100ml, and when it is added in excess than the above content, there is a problem of vitamin precipitation during long-term storage, and when added in a small amount than the above content, high skin Despite the penetration rate, there is a problem that it is difficult to exhibit a sufficient effect.
- the dexpanthenol may preferably be included in an amount of 120 to 220 mg/100ml, but when added in excess of the above content, there is a problem of difficult solubilization and poor stability, and when added in a small amount than the above content, effectiveness There is a problem that the effect exerted by the minute is insignificant.
- the ethanol may be included in an amount of 7 to 12 mg/100ml, but when it is added in excess of the above content, there is a problem in that it cannot form an ethosome and becomes a dissolved state, and it is added in a small amount than the above content. In this case, there is a problem that the stability of the formulation of the poorly soluble material is lowered because the ethosome is not formed.
- the peptide may preferably be included in an amount of 0.1 to 10 mg/100ml, when added in excess than the above content, there is a problem in that the manufacturing / production cost increases, and when added in a small amount than the above content , there is a problem in that it is difficult to exhibit a sufficient effect in spite of a high skin penetration rate.
- the phosphatidylcholine may be included in an amount of 10 to 1000 mg/100ml, but when it is added in excess than the above content, an excess material that does not participate in ethosome formation remains and there is a serious problem in turbidity, the content When added in a smaller amount, there is a problem in ethosomizing the active substance.
- the amino acid compound in the case of the amino acid compound, it may be included in an amount of 10 to 1000 mg/100ml, when it is added in excess than the above content, there is a problem of raising or lowering the pH, and when it is added in a small amount than the above content, then a pH adjusting agent There is a problem that must be added in excess.
- the effective ingredient delivery effect of the ethosome composition is particularly excellent, and in particular, in the present invention, the hair growth cycle is controlled through effective delivery to the scalp to shorten the resting period and , characterized in that it has a hair growth and wool effect by continuing the growth phase.
- the ethosome included in the ethosome composition may have an average particle diameter of 90 to 200 nm.
- the size of the particles has a uniform effect, and has a more advantageous effect on effective ingredient delivery by maintaining a stable ethosome composition.
- the etosome may also have an absolute value of a surface charge value of 10 to 100 mV. When it has the above range, the etosomes may be uniformly dispersed in the solution without clumping together.
- the method for preparing an ethosome composition according to the present invention comprises the steps of: (a) solubilizing an amino acid compound in purified water;
- step (c) may further include one or more selected from the group consisting of surfactants and other active ingredients for wool.
- the surfactant may be, for example, a surfactant such as Poloxamer 188, Poloxamer 407, Poloxamer F-127, PEG 60 (hydrogenated cateroil), Polysorbate 80, tween 20, tween 60, tween 80.
- the other active ingredients for wool are not particularly limited and can be used, for example, natural extracts and compounds such as melatonin and cheongpo extract, and the like, may be appropriately added as necessary.
- the pH adjusting agent may include one or more selected from the group consisting of citric acid and salts thereof.
- the step (a) may be to add 80 to 120 g of the amino acid compound to 50 to 70 L of purified water. Preferably, it may be to add 90 to 110 g of the amino acid compound to 55 to 65 L of purified water.
- the step (b) may be to add 100 to 300 g of dexpanthenol to 25 to 35 L of purified water, preferably, to add 150 to 250 g of dexpanthenol to 27 to 32 L of purified water.
- the ethosome composition according to the present invention can be used as a composition for promoting hair growth and/or wool, and as described above, by effectively penetrating the active ingredient having the effect of improving skin aging and anti-aging into the scalp using the ethosome composition. , prevents telogen hair loss by inducing an aging improvement effect of the scalp, and induces hair growth and/or wool effect by sustaining the growth phase.
- a composition for preventing telogen hair loss that can prevent telogen hair loss.
- composition according to the present invention can be used to induce hair growth, hair growth, or to improve or prevent hair loss.
- the present invention can provide a composition for promoting hair growth and/or hair growth and a composition for preventing telogen hair loss, which are optimized according to the gender of the user.
- ethosome composition can be used without distinction between women and men, but by configuring it to further include oleanolic acid and/or apigenin in addition to men, a composition particularly suitable for male users can be provided.
- the oleanolic acid is a triterpenoid saponin, and is a pentacyclic triterpenoid. By using it, it is possible to provide a composition particularly suitable for men.
- test substance was diluted with a 0.2% solution using distilled water and then measured, and measured using a Disposable cell.
- Each sample was stored at 37°C and 70% humidity, and samples were collected and diluted at a predetermined time for measurement.
- Table 4 below shows the stability measurement results for Examples 1 to 5 and 10 to 14 in which ZnO was not added.
- the particle size distribution of the Example prepared according to the manufacturing process was completed with a very even particle size distribution of about 100 nm to 160 nm based on the Z-average size, and in the case of zeta potential, Examples 3 and 14 had the lowest charge Results with values were obtained, suggesting that the formulation has excellent long-term storage stability.
- Examples 1 and 10 there was no change in the particle size distribution as time passed, but it was confirmed that the surface charge value increased, which means that the stability of the ethosome increases after 1 to 2 days or more from the initial stage.
- Test kit Pion's skin pmapa test kit is used.
- Experimental time was measured by using a microplate or by using HPLC to measure the amount of target material that moved toward the acceptor for 6 hours based on 6hr. It was calculated using the formula below.
- composition of the experimental group The experimental group in which the material to be measured was added to the buffer solution provided by Pion was selected as a control group, and the experimental group was comparatively analyzed using the formulation corresponding to the example.
- FIGS. 6 and 7 The experimental results measured using the above test method are shown in FIGS. 6 and 7 .
- the penetration rate of the control group was calculated as 100%, and the relative penetration rate was shown.
- 6 is an experimental result confirming the skin penetration rate for dexpantenol, a hydrophilic material, and it was confirmed that the penetration rate was increased due to the high penetration rate of etosomes when the ethosomal formulation was used despite the water-soluble material.
- the degree of hair growth in each group was visually determined for each animal by the scoring system. According to the degree of hair growth, 0% for 0%, 1 to 25% for 1 point, 26 to 50% for 2 points, and 51 to 75% for hair growth. 3 points, 76 ⁇ 100% were divided into 4 points.
- skin tissue was extracted and fixed in 10% neutral formalin for more than 48 hours while attached to filter paper.
- the fixed tissue was trimmed from the head to the tail to a thickness of 5 to 10 mm, followed by general tissue treatment with alcohol, xylene, and paraffin.
- 4 ⁇ m slices were made using a rotary slicer and stained with hematoxylin and eosin (H&E).
- the thickness of the skin tissue was measured while observing with an optical microscope, and the ratio of growing hair follicles to resting hair follicles among 100 hair follicles for each animal was calculated.
- the C57BL/6 mouse used in this experiment has the advantage of being able to determine whether or not the hair follicle has been introduced into the growth phase just by observing the change in skin color with the naked eye because the melanin production cycle and the growth phase of the hair follicle coincide. Therefore, in this experiment, in order to confirm the hair growth promoting effect of the test substance, the change in skin color and the time at which hair was observed for the first time were measured every day from immediately after application of the test substance.
- FIG. 9 is a photograph of the skin tissue of the experimental group in which the hair was H&E dyed after application of the test substance of Experimental Example 4-1, and FIG. am.
- the thickness measurement result of the skin tissue is shown in FIG. 9 .
- the negative group it was 264.8 ⁇ 17.3 ⁇ m, whereas in the Rogaine group, it was 476.4 ⁇ 95.3 ⁇ m, confirming a clear increase in skin thickness.
- the skin thickness was higher than that of the 6 group (569.9 ⁇ 54.5 ⁇ m) Rogaine group.
- the skin tissue was excised, fixed in 10% neutral formalin, washed with running water 24 hours later, dehydrated with alcohol, xylene, and paraffin, transparent, penetrated, and then embedded in paraffin.
- the embedded tissue was made into 4 ⁇ m slices, stained with hematoxylin and eosin (H&E), and observed under an optical microscope.
- the duration of the growth phase of the test substance was measured.
- the period when skin color pigmentation appears from pink to gray or black is the introduction period of the growth phase, and after hair growth occurs, the skin color change is observed once a day.
- the difference (day) was compared with the time period.
- FIG. 11 is a photograph of the skin tissue after H&E dyeing in Experimental Example 4-2, and FIG. 12 is a photograph recording the state of hair regrowth during the experimental period of Experimental Example 4-2.
- Example 1 was placed in Experimental Group 3 and the experiment was performed.
- groups 4, 5, 8 and 12 showed particularly high scores.
- groups 8 and 12 which showed rapid growth phase transition, hair began to be observed from the 24th and 21st, respectively, and hair began to be observed from the 23rd day in the test group to which Hyundai Pharmaceutical Minoxidil, a positive control, was applied.
- group 4 had an average of 3.1 ⁇ 0.7 points
- group 12 had 2.5 ⁇ 0.7 points or higher, which was higher than Hyundai Pharm Minoxidil’s 2.8 ⁇ 1.3 points.
- the state of hair regrowth was recorded as a photograph at regular intervals after application of the test substance, and the photographic results are shown in FIG. 10 .
- hair was observed uniformly without deviation in group 4, and it was confirmed that hair was observed in a uniform and wide area in the group coated with the test substance of group 12 (Example 18) than in the minoxidil group, which is a positive control group.
- the skin tissue was excised, fixed in 10% neutral formalin, washed with running water 24 hours later, dehydrated with alcohol, xylene, and paraffin, transparent, penetrated, and then embedded in paraffin. After making a 4 ⁇ m-thick section of the embedded tissue, hematoxylin and eosin (H&E) staining was performed and observed under a light microscope to measure the ratio of anagen and resting follicles and the change in skin tissue thickness.
- H&E hematoxylin and eosin
- the purpose of this experiment is an experiment conducted to confirm the effect on the growth phase continuation/resting phase inhibitory effect of Examples.
- Figure 14 is a graph showing the growth phase hair follicle ratio in the anagen period / telogen inhibitory effect test.
- FIG. 15 is a photograph recording the difference between each group on the 19th day after the start of the test in the growth phase continuation / telogen inhibitory effect test, and FIG.
Abstract
Description
Claims (17)
- 비타민과 덱스판테놀이 봉입된 에토좀을 포함하는 에토좀 조성물로서,상기 에토좀은 에탄올, 펩티드, 포스파티틸콜린(Phosphatidyl choline), 아미노산 화합물을 포함하는 에토좀 조성물.
- 제1항에 있어서,상기 펩티드는 pal-GHK, Pal-GQPR, Pal-KTTK, Pal-KTTKS, Biotin-GHK, PAL-KVK (Palmiotyl Tripeptide-5), Palmitoyl tripeptide-38, Palmitoyl-Tripeptide(Pal-RFK), Human Oligopeptide-20(Val-Gly-Val-Ala-Pro-Gly), GHK-Cu, (AHK)2Cu, AHK-Cu, Myristic acid-KLAKK-CONH2, Hexapeptide-11, Octapeptide-2, Palmitoyl-hexapeptide, Acetyl tetrapeptide-15, Acetyl Hexapeptide 3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-5, Acetyl-Decapeptide-3, Ac-KGHK, rh-Oligopeptide-1(humanEGF) (NSDSECPLSHDGYCLHDGVCMYIEALDKYACNCVVG YIGERCQYRDLKWWELR), Snake tripeptide(beta-Ala-Pro-Dab-NHBzl), peptide CK+(Ac-Arg-Lys-Arg-NH2), peptide CK(Arg-Lys-Arg), tripeptide-3(Ala-His-Lys.HCl), Ac-KGHK-NH2, Ac-Tyr-Arg-hexadecylester, Argireline로 이루어진 군에서 선택된 하나 이상인 것을 특징으로 하는 에토좀 조성물.
- 제1항에 있어서,상기 비타민은 비타민 E, 비타민 C, 비타민 B, 이들의 염 및 이들의 유사체로 이루어진 군에서 선택된 하나 이상인 것을 특징으로 하는 에토좀 조성물.
- 제1항에 있어서,상기 아미노산 화합물은 아미노산 및 아미노산 유사체로 이루어진 군에서 선택된 하나 이상의 것이고,상기 아미노산 및 아미노산 유사체는 NAC(N-Acetyl Cysteine), 아르기닌(Arginin), 로라이신, 라이신 에틸에스터, 히스티딘 및 히스티딘 에틸에스터로 이루어진 군에서 선택된 하나 이상인 것을 특징으로 하는 에토좀 조성물.
- 제1항에 있어서,상기 에토좀 조성물은 비타민 20 내지 70 mg/100ml, 덱스판테놀 150 내지 250 mg/100ml, 에탄올 5 내지 15 ml/100ml, 펩티드 0.1 내지 10 mg/100ml, 포스파티틸콜린 10 내지 1000 mg/100ml, 아미노산 화합물 10 내지 1000 mg/100ml를 포함하는 것을 특징으로 하는 에토좀 조성물.
- 제1항에 있어서,상기 에토좀은 평균입경이 90 내지 200 nm인 것을 특징으로 하는 에토좀 조성물.
- 제1항에 있어서,상기 에토좀은 표면전하값의 절대값이 10 내지 100 mV인 것을 특징으로 하는 에토좀 조성물.
- 제1항에 따른 에토좀 조성물의 제조방법으로서,(a) 정제수에 아미노산 화합물을 가용화하는 단계;(b) 정제수에 덱스판테놀을 가용화하는 단계;(c) 에탄올, 비타민, 포스파티딜콜린, 페녹시에탄올을 가용화하는 단계;(d) 상기 (a) 단계의 용액에 상기 (b) 단계의 용액을 첨가한 후, 혼합하는 단계;(e) 상기 (d) 단계의 용액에 상기 (c) 단계의 용액을 첨가한 후, 혼합하는 단계;(f) 상기 (e) 단계의 용액에 pH 조절제를 첨가한 후, 혼합하는 단계; 를 포함하는 에토좀 조성물의 제조방법.
- 제8항에 있어서,상기 (c) 단계는 계면활성제, 기타 양모 유효성분 및 트리테르페노이드 사포닌으로 이루어진 군에서 선택된 하나 이상을 더 포함하는 것을 특징으로 하는 에토좀 조성물의 제조방법.
- 제8항에 있어서,상기 pH 조절제는 시트르산 및 이의 염으로 이루어진 군에서 선택된 하나 이상을 포함하는 것을 특징으로 하는 에토좀 조성물의 제조방법.
- 제8항에 있어서,상기 (a) 단계는 정제수 50 내지 70L에 아미노산 화합물을 80 내지 120g 첨가하는 것을 특징으로 하는 에토좀 조성물의 제조방법.
- 제8항에 있어서,상기 (b) 단계는 정제수 25 내지 35L에 덱스판테놀 100 내지 300 g을 첨가하는 것을 특징으로 하는 에토좀 조성물의 제조방법.
- 제1항 내지 제7항 중 어느 하나에 따른 에토좀 조성물을 포함하는 발모 및/또는 양모 촉진용 조성물.
- 제1항 내지 제7항 중 어느 하나에 따른 에토좀 조성물을 포함하는 휴지기성 탈모 방지용 조성물.
- 제14항에 있어서,상기 휴지기성 탈모 방지용 조성물은 두피 항노화 및/또는 콜라겐 생성 촉진을 통해 휴지기성 탈모를 방지하는 것을 특징으로 하는 휴지기성 탈모 방지용 조성물.
- 제13항에 있어서,상기 에토좀 조성물이 올레아놀산(Oleanolic acid) 및/또는 아피제닌(Apigenin)을 더 포함하는 남성용 조성물인 것을 특징으로 하는 발모 및/또는 양모 촉진용 조성물.
- 제14항에 있어서,상기 에토좀 조성물이 올레아놀산(Oleanolic acid) 및/또는 아피제닌(Apigenin)을 더 포함하는 남성용 조성물인 것을 특징으로 하는 휴지기성 탈모 방지용 조성물.
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