KR101569431B1 - Skin enhancement method comprising six steps using cosmetic composition, especially cosmetic composition comprising illite eluate haved skin whitening function and anti-wrinkles effect - Google Patents

Abstract

The present invention relates to a six-step skin caring and improving method using a cosmetic composition including an illite eluent having excellent skin-whitening and anti-wrinkle effects. The method includes: a face washing step of washing the face with a facial cleanser to remove foreign matters on the surface of skin; a lifting pack coating step of applying a lifting pack on the face to capillaries and decomposing the subcutaneous fat to enable the skin to easily absorb the nutrients; an eye cream coating step of applying eye cream around eyes to alleviate the eye wrinkles and decomposing the fat under the eyes; an essence coating step of applying an essence to the face to brighten the skin and provide nutrients thereto; and a nourishing cream coating step of coating a nourishing cream onto the face to provide nutrients to the skin; and a BB cream coating step of coating a BB cream onto the face to produce a healthy and bright skin tone while correcting the skin flaws. The essence includes a composition which includes: 30 to 35% wt% of illite elution propylene glycol; 30 to 35% wt% of N-methyl-pyrrolidone; and 30-40 wt% of vitamin C, thereby enhancing the skin-whitening effects, anti-wrinkle effects, and skin inflammation alleviating effects. The method can improve the skin through the skin-whitening anti-wrinkle, skin elasticity enhancing, and blemish removing effects. The present invention enables more beautiful skin without skin troubles.

Description

TECHNICAL FIELD [0001] The present invention relates to a cosmetic composition comprising a sunlight extract which is excellent in skin whitening and wrinkle improving effect, ANTI-WRINKLES EFFECT}

The present invention relates to a skin improving method, and more particularly, to a skin improving cosmetic composition which exhibits a good effect on the skin, and more particularly to a cosmetic composition containing a sunlight extract which is excellent in skin whitening and wrinkle- And an improvement method.

Skin with human body protection function has sensory function, body temperature control and maintenance, synthesis of vitamin D, absorption of external substances and control of volatilization of body components.

However, as time passes, waste accumulates, and as the aging progresses, fine wrinkles occur and elasticity decreases.

To solve this problem, the skin is cleaned and cosmetics having various functions such as basic cosmetics, functional cosmetics, or color cosmetics are used.

However, as described above, various cosmetics have a good effect on the skin according to their respective characteristics, but the function of each cosmetics is not completely applied to the skin by using a plurality of cosmetics in combination. That is, one cosmetic may interfere with the skin absorption of another cosmetic, or one cosmetic may interfere with the function of another.

In addition, a large number of cosmetics are used in combination, resulting in side effects such as skin trouble. This is due to toxic substances that can cause skin irritation when mixed with cosmetics, so users should always be careful to avoid this problem.

As a result, no matter how good cosmetics are used, users are not satisfied and waste unnecessary costs.

Korean Patent No. 10-0897364 Korean Patent Publication No. 10-2008-0083596 Korean Patent Publication No. 10-2005-0034005 Korean Patent No. 10-1210371 Korean Patent Publication No. 10-2006-0103790

The present invention has been made to solve the above-mentioned problems, and it is an object of the present invention to provide a skin improvement method by effectively managing the skin by minimizing side effects while optimizing the inherent functions and effects of each cosmetic.

According to an aspect of the present invention,

A cleansing step of cleansing the skin surface with a cleanser to remove impurities;

Applying a lifting pack to the face, releasing micro-blood vessels, decomposing subcutaneous fat, and allowing the skin to easily absorb nutrients;

Applying an eye cream to the eyes to soften the wrinkles of the eyes and dissolve the fat layer under the eye;

Applying an essence to the face, applying an essence to whiten and provide nutrients to the skin;

Apply nutrition cream to the face to provide nutrients to the skin; And

The method comprising the steps of: applying a face cream to the face to produce a healthy and bright skin tone and complementing the defects of the skin;

Wherein the essence comprises a composition comprising 30 to 35% by weight of propylene glycol eluting with anilite, 30 to 35% by weight of N-methylpyrrolidone and 30 to 40% by weight of vitamin C, Thereby providing a skin improvement method.

In the skin improving method according to the present invention as described above, the sunlight-extracted propylene glycol may be prepared by heating the sunlight and propylene glycol in a heating furnace and heating the propylene glycol vapor to condense the generated propylene glycol vapor, It can be obtained by condensing the following vapor.

In the method for improving skin according to the present invention as described above, it is more preferable to use a dry skin such as dry garlic, dried black gum, dried gum, dried gum, dried gum, Dried gum, and mixtures thereof. The present invention further provides a method for producing a hair cosmetic composition, comprising the steps of:

In the skin improving method according to the present invention as described above, it is more preferably selected from the group consisting of basalt, crushed soil, and mixture thereof, which is ground to the same particle size as Ilright when the ILIT is eluted with propylene glycol And further includes any one of them.

In the method for improving skin according to the present invention as described above, it is most preferable that when the sunlight is eluted with propylene glycol, the dried sunflower, dried black gum, dried gum, dried gum, Dried plums, basalt, marine clay, and mixtures thereof.

In the skin improvement method as described above, the cleanser includes a base, a herbal medicine ingredient, chamomile, alkoxyglycerol, hyaluronic acid, aloe vera extract, arginine, grape seed oil, tea trioyl, skin moisturizer and perfume can do.

In the skin improving method according to the present invention as described above, the herbal medicine ingredient of the cleanser may be at least one selected from the group consisting of meplopsis japonica makino, bletilla strrata reic jenbach fil, acorus gramires soland, There are two kinds of white beans: dolichos lablab L, ansu semen, prunus japonic thunb, artemisia vulgaris L, sophora angustifolia siebolt, bomyx mori line), bank (ginko: gingko, tetrapanx papyriferum, a radicle, mentha arvensis L, mung bean phasolus raiatus L, bamboo-salt, And rhinoceros (cnidii rhozoma).

In the skin improving method according to the present invention as described above, the lifting pack may be at least one selected from the group consisting of purified water, carbomer, yeast beta-glucan, caffeine, hinoki extract, green tea extract, Extract, peach tree leaf extract, ginkgo leaf extract, and phenoxyethanol.

In order to adjust the pH of the lifting pack to 3.5 +/- 0.5 when applying skin to the skin according to the present invention as described above, sodium oxide (Na ₂ O), silicon dioxide (SiO ₂ ) And sodium silicate are preferably added to the lifting pack.

In the skin improving method according to the present invention as described above, the eye cream may be at least one selected from the group consisting of purified water, glyceryl acrylate / acrylic acid copolymer, glycerin, propylene glycol, butylene glycol, betaine, PEG-8 dimethicone, But are not limited to, chicone, polysorbate 20, PPG-26-butes-26, cyclopentasiloxane cyclotetrasiloxane, dimethicone, dipotassium glycyrrhizate, platelet extract, sodium hyaluronate, PEG-40 Hydrogenated Castor Oil, Triethanolamine, Adenosine, Pethoxyethanol, 1,2-Hexanediol, Diazolidinyl Urea, and Fragrances, including, but not limited to, Peptide-8, Cappertree Peptide-1, Palmitoylpentapeptide-4, can do.

In the skin improvement method according to the present invention as described above, the nutritional cream may be selected from the group consisting of purified water, dipropylene glycol, cetyl hexyl hexanoate, PEG-10 dimethicone, squalane, glyceryl stearate, dimethicone, -Hexanediol, stearyl alcohol, meadowfoam seed oil, polysorbate 60, ethoxydiglycol, trimethylpentanediol, hydrogenated lecithin, sodium hydrogencarbonate tallow oil glutamate, cetyl alcohol, tocopheryl acetate, Carboxymethylcellulose, carboxymethylcellulose, xanthan gum, sodium heparuronate, capper tripeptide-1, palmitoylpentapeptide-4, acetylhexapeptide-8, dipotassium glycyrrhizate, sodium polyacrylate, yeast betaglucan, C13-14 iso Paraffin, laureth-7, polyacrylamide, adenosine, aldec-oligopeptide-1, triethanolamine, tetrasodium EDTA and fragrances.

In the skin improvement method as described above, the bibby cream may be at least one selected from the group consisting of purified water, caprylic, titanium dioxide, propylene glycol, squalane, cetyl PEG, arbutin, butyleneglycol dicaprylate, Aloe vera leaf juice, endosperm extract, nylon-12, distearmonium hectorite, triethanolamine, triethanolamine, triethanolamine, triethanolamine, Beeswax, polymethylmethacrylate, tocopheryl acetate, cellulose gum, dimethicone, DMDM hydantoin, phenoxyethanol, red iron oxide, yellow iron oxide, black iron oxide, ultramarine, sodium lauro Sunglutamate, aluminum hydroxide, and fragrances.

The skin improvement method through efficient management according to the present invention greatly improves the skin whitening effect, such as skin whitening, skin elasticity, wrinkle removal, and dirt removal. Therefore, when making up the skin through the skin improvement method according to the present invention, more beautiful skin can be obtained without skin trouble.

In addition, the skin improvement method according to the present invention can increase the satisfaction of the cosmetics user through the beautiful skin deformation, thereby increasing the sales volume of the cosmetics used in the skin improvement method according to the present invention, And exhibits a very excellent effect even in the case of

1 is a cross-sectional view of a cleansing tool according to the present invention.
2 and 3 are views showing the use state of the cleanser according to the present invention.

Hereinafter, referring to the accompanying drawings and the like, the skin is efficiently managed in six steps according to the present invention, and a method for improving the skin will be described in detail.

Cleansing step

Cleanse with a cleanser to remove foreign substances from the skin surface.

The cleanser can be used without any particular limitations as long as it is widely known in the art to which the present invention belongs. In the present invention, especially, a cleanser base comprising 75% by weight of a seed oil and 25% And the remaining ingredients are 22 herbal medicine ingredients and a combination of Chamomile, Alkoxy Glycerol, Hyaluronic Acid, Aloe Vera Extract, Arginine, Grape Seed Oil, Oil, Tea Tree Oil, a skin moisturizer, and a fragrance.

The cleaner was composed of 93.4% by weight of base, 2.0% by weight of herbal medicine ingredient, 0.5% by weight of chamomile, 0.3% by weight of alkoxyglycerol, 0.2% by weight of hyaluronic acid, 0.4% by weight of aloe vera extract, 0.4 wt% of tea trioyl, 1.0 wt% of a skin moisturizer, and 1.0 wt% of a perfume.

Herein, the herbal medicine includes meplopsis japonica makino, bletilla strriate reic jenbach fil, acorus gramires soland, white lentil dolichos lablab L, ansu semen Prinus japonic thunb, artemisia vulgaris L, sophora angustifolia siebolt, bomyx mori line, ginko biloba, gingko, tetrapanx papyriferum, a radicle, mentha arvensis L, mung bean phasolus raiatus L, bamboo-salt, And cynidium rhizoma (cnidii rhizoma).

Such a cleanser is excellent in removal of dirt and debris, thereby making the skin transparent after cleansing, providing elasticity to the skin, and keeping the skin always moisturized. In addition, the cleanser removes bruises and folliculitis, has excellent whitening effect on spots and freckles, and is effective in treating acne and inflammation. Furthermore, the cleanser is also effective in the treatment of atopic dermatitis due to the sterilizing action.

On the other hand, the cleansing agent may be prepared in the form of a soap using a soap base, or a cleansing foam base may be used to make a cleansing foam.

In the present invention, cleansing may be performed through a cleansing tool in the cleansing step. The cleansing tool will be described with reference to FIG. 1, which is a sectional view.

The facial cleanser comprises a lower pad 100, an upper protrusion 200, a lower protrusion 300, a nanofiber 400, a middle pad 500, a loess ball 600, and an upper pad 700.

The lower pad 100 is provided at an upper portion of the room 110 for the loess ball water number and is opened at the upper portion. The lower pad 100 is provided at the lower portion of the loessroom ball room space 110 and is formed through the upper and lower rooms. A plurality of upper through-holes 120 communicating with the upper through-holes 120 and 110, a flow space 130 communicating with the upper through-holes 120 at a lower portion of the upper through-holes 120, And a plurality of lower through holes 140 which are located at the lower portion of the flow space 130 and communicated with the flow space 130 and arranged in a zigzag manner with the upper through holes 120. At this time, the lower pad 100 is preferably made of a soft and elastic material, except for the bonding surface with the middle pad 500.

A plurality of the upper protrusions 200 are provided at a lower portion of the space 110 for the loess balls in the lower pad 100.

A plurality of the lower protrusions 300 are provided in a lower portion of the flow space 130 of the lower pad 100.

A plurality of the nanofibers 400 are provided at a lower portion of the lower pad 100 so as not to close the lower through hole 140 of the lower pad 100.

The middle pad 500 is made of an elastic material and closes the space 110 for the loess ball water of the lower pad 100.

A plurality of the upper pads 600 are accommodated in a space 110 for the number of loess balls of the lower pad 100.

The upper pad 700 is installed at one end of the middle pad 500 so as to form a holding space 710.

When cleansing using such a cleansing tool, the skin wastes are sufficiently removed and the skin becomes optimal for absorbing cosmetics and the like, which can double the effect of the lifting pack and cosmetic application step for skin improvement.

2 and 3 are views showing the action of the cleanser according to the present invention, and the operation of the cleanser according to the present invention will be described with reference to FIGS. 2 and 3. FIG.

2 and 3, arrows represent the flow of the wash water, and the flow of the wash water is expressed to facilitate identification of the drawings.

When the user puts his / her hand into the facial cleanser and then applies facial cleansing while pressing the middle pad 500 of the facial cleanser lightly, the nanofiber 400 cleans the pores using the cleansing soap bubble. 2, the cleansing water flows into the flow space 130 of the lower pad 100 through the lower through hole 140 of the lower pad 100 and then flows into the upper through hole 120 of the lower pad 100, Into the space 110 for the yellowing of the lower pad 100. [ When the cleansing water flows into the space 110 for the loess balls in the lower pad 100, the cleansing water comes into contact with the loess ball 600, and the beneficial component of the loess ball 600 is contained in the cleansing water.

At this time, when the cleansing water flows into the loess bowl watering space 110 to some extent, the cleanser presses the middle pad 500 more strongly with fingers.

3, the cleansing water passes through the upper through hole 120 of the lower pad 100 in the space 110 for the loess ball water of the lower pad 100, and then passes through the lower through hole 120 of the lower pad 100 140, respectively. The cleansing water is discharged from the upper through hole 120 of the lower pad 100 and vibrates the lower pad 100 to generate a flow while bumping against the lower protrusion 300 of the lower pad 100, ). Since the upper through hole 120 and the lower through hole 140 of the lower pad 100 are disposed so as to be staggered with respect to each other, they are not directly discharged from the upper through hole 120 to the lower through hole 140 when the cleansing water moves The vibration of the lower pad 100 is more effectively generated.

Therefore, when cleansing with a facial cleanser, the nanofibers 400 remove foreign substances from the face as if the face is massaged, thereby effectively removing foreign substances from the face.

When the foreign objects on the face are removed, cosmetics are applied to every corner of the skin when the cosmetics are put on the skin after the cleansing, so that the functions of the cosmetics are sufficiently exhibited and the skin can be further improved.

lifting  Pack application step

In the present invention, the lifting pack is used to easily absorb the nutrients of the skin. The lifting pack is not limited to any particular one as long as it is widely known as a lifting pack in the field to which the present invention belongs.

The most suitable lifting packs for use in the present invention include purified water, Carbomer, Yeast Beta-Glucan, Caffeine, Hovenia Dulcis Fruit Extract, Camellia Sinensis Leaf Extract, Lonicera Japonica (Honeysuckle Flower Extract), Paeonia albiflora Root Extract, Sophora Angustifolia Root Extract, Scutellaria Baicalensis Root Extract, Rhus Semialata Gall Extract, , Peach Leaf Extract, Ginkgo Biloba Leaf Extract, Acetyl Hexapeptide-8, Copper Tripeptide-1, p- P-Anisic Acid, Caprylyl Glycol, and Phenoxyethanol.

The lifting pack contained 91.592 wt% of purified water, 2 wt% of carbomer, 1.2 wt% of yeast beta-glucan, 1.2 wt% of caffeine, 0.6 wt% of Hovenia dulcis extract, 0.6 wt% of green tea extract, 0.5 wt% 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% 0.002% by weight, 0.3% by weight of p-anic acid, 0.2% by weight of caprylyl glycol and 0.3% by weight of phenoxyethanol.

Herein, the lifting pack may be any one of the group consisting of acetyl hexapeptide-8, capper tripeptide-1, p-phenylacetic acid and caprylic glycol as well as known pack preparations, All packagings for the pack can be excluded. At this time, if the known pack material is excluded, the remaining composition ratio of the lifting pack is adjusted as needed.

Such a lifting pack relaxes the hardened collagen layer and fine blood vessels and decomposes and burns subcutaneous fat in the skin. Thus, the skin is in a state of breathing and accepting nutrients. In addition, as the ingredients contained in the lifting pack infiltrate into the skin, strong lifting, wrinkling, anti-aging, whitening, promoting blood circulation, lipolysis, and pore reduction are exhibited.

Meanwhile, in the present invention, the lifting pack is preferably adjusted to have a pH of 3.5 ± 0.5, and it is preferable to mix at least one selected from the group consisting of sodium oxide (Na ₂ O), silicon dioxide (SiO ₂ ), and liquid sodium silicate can do. When the lifting pack is mixed with any one selected from the group consisting of sodium oxide, silicon dioxide, and liquid sodium silicate, the lifting pack is more stably dried when applied to the skin. At this time, the mixing of sodium oxide, silicon dioxide, and liquid sodium silicate is performed immediately before application to the skin, and it is preferable to use the lifting pack.

The lifting pack of the present invention is applied to the skin, especially the face, in the form of a cream, an emulsion or a liquid, unlike the conventional patch type formulation, and is dried and cured by contact with the air over time. It releases the microvessels and breaks down the subcutaneous fat, making the skin breathing and making it easy to absorb the nutrients it gives in subsequent products or stages, restoring skin elasticity.

Eye Cream  Application step

The eye cream is used to alleviate the wrinkles of the eyes and to decompose the fat layer under the eyes. The present invention can be used without any particular limitation as long as it is known as eye cream in the technical field of the present invention.

The most suitable eye cream for use in the present invention may be selected from the group consisting of purified water, glyceryl acrylate / acrylic acid copolymer, glycerin, propylene glycol, butylene glycol, PEG-8 Dimethicone, Phenyl Trimethicone, Polysorbate 20, PPG-26-Buteth-26, PEG-8 dimethicone, 26), Cyclopentasiloxane, Cyclotetrasiloxane, Dimethiconol, Dipotassium Glycyrrhizate, Hovenia Dulcis Fruit Extract, Sodium Hyaluronate Sodium Hyaluronate, Yeast Beta-Glucan, Acetyl Hexapeptide-8, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, ), PEG-40 Hydrogenerated Cass PEG-40 hydrogenated caster oil, Human Oligo Peptide-1, Triethanolamine, Adenosine, Phenoxyethanol, 1,2-hexanediol (1, 2-hexanediol, diazolidinyl urea, and perfume.

The eye cream contains 37.615% by weight of purified water, 30% by weight of glyceryl acrylate / acrylic acid copolymer, 20% by weight of glycerin, 5% by weight of propylene glycol, 3% by weight of butylene glycol, 1% by weight of betaine, 0.2% by weight of cyclopentasiloxane, 0.25% by weight of cyclotetrasiloxane, 0.2% by weight of cyclopentasiloxane, 0.1% by weight of cyclopentasiloxane, 0.2% 0.1% by weight of dipotassium glycyrrhizate, 0.1% by weight of diapause extract, 0.05% by weight of sodium hyaluronate, 0.01% by weight of yeast beta-glucan, 0.02% by weight of acetylhexapeptide-8, 1 0.012% by weight, palmitoyl pentapeptide-4 0.008% by weight, PEG-40 hydrogenated castor oil 0.2% by weight, triethanolamine 0.01% by weight, adenosine 0.04% by weight, 0.3 wt% of diol, 0.025 wt% of diazolidinyl urea, and 0.0 1% by weight.

Herein, the eye cream may contain at least one selected from the group consisting of propylene glycol, butylene glycol, betaine, PEG-8 dimethicone, polysorbate 20, PPG-26-butes-26, cyclopentasiloxane, cyclotetrasiloxane, di Methicone, and di-potassium glycyrrhizate, and may preferably include all of the above components. At this time, if the known eye cream component is excluded, the remaining composition ratio of the eye cream is adjusted as needed.

These eye creams improve wrinkles, exfoliate the skin, exfoliate the rough and dry areas around the eyes, and improve the elasticity around the eyes. In addition, the eye cream removes wastes from the skin, maintains a balance of skin oil / moisture, and allows human-friendly skin penetration quickly.

In the present invention, it is preferable that the eye cream has a specific gravity of 1.2 ± 0.05 and a viscosity of 12,000 ± 3,000.

Essence application step

In the present invention, the wrinkles on the eyes are relieved through the eye cream, the fat layer under the eyes is disintegrated, and then the nutritional cream is applied to the face, thereby relieving the inflammation caused in the skin and facilitating the active ingredient of the nutritional cream Skin whitening, skin clearness, and skin cell activation.

For the above-mentioned reasons, the present invention uses an essence comprising 30 to 35% by weight of propylene glycol eluting with light, 30 to 35% by weight of N-methylpyrrolidone and 30 to 40% by weight of vitamin C do.

This essence is characterized by a high concentration of vitamin C essence containing up to 40% by weight of vitamin C. To this end, a mixed solvent of propylene glycol and N-methylpyrrolidone is used as a solvent, and vitamin C It is chemically stabilized even when used at a high concentration. In addition, by using a mixed solvent of propylene glycol and N-methylpyrrolidone, the skin irritation caused when only N-methylpyrrolidone is used is improved and stability as an essence is enhanced.

In addition, propylene glycol was used instead of propylene glycol to elaborate the effects of skin lightening, wrinkle prevention, improvement of skin inflammation, activation of skin cells through various minerals, and skin moisturizing effect. Dried light ginseng, dried ginseng, dried ginseng, dried ginseng, dried ginseng, and a mixture thereof.

Also, various tests of the present inventors have found that the addition of any one selected from the group consisting of basalt, corrosion-resistant soil and mixtures thereof to minerals such as skin whitening, anti-wrinkle, skin inflammation, various minerals The skin cell activation and the skin moisturizing effect can be further enhanced.

The illite used in the present invention is one of clay minerals and is a fine mica-type mineral which is generated in volcanic tuffs which are not rich in aluminum. In terms of chemical composition, SiO ₂ , MgO and H ₂ O are relatively abundant and K ₂ O is relatively small although there are some muscovite. It is a kind of minerals such as dolomite. Hardness 1 ~ 2, specific gravity 2.6 ~ 2.9. The cleavage is complete with [001], streaking color is white, and earthy shine. There is an opinion that it is a mixed mineral containing different components, not an independent mineral in terms of chemical composition or crystal structure. It is produced in aluminum-rich heterogeneous or tuffaceous sedimentary rocks and is produced as altered minerals in hydrothermal ore deposits.

Basalt is a volcanic rock composed mainly of basic plagioclase, pyroxene and olivine, and it is a black-colored eruption rock and generally contains less than 52% by weight of SiO ₂ . Because of this low silica content, the basalt lava flows are less viscous and flow faster and flow more than 20 km from the crater. Basalt is generally divided into the Tholeiiti basalt, Highalumina basalt and alkaline basalt. The most common basaltic rocks in the eruption rocks form the majority of the oceanic crust. In Korea, it is distributed in Jeju Island, Mt. Paektu, Cheorwon in Gangwon Province, Ulleungdo in Gyeongsangbukdo, and Hantan River in Gyeonggi Province. Globally, on the Deccan Plateau in India, an 800m thick lava stone plateau is formed over 500,000 ㎢. The basalt rock of the Columbia River in the United States is about 1,800 meters thick. Basalt is mostly black-black or black when it is fresh, fine-grained, and sometimes porous.

In addition, the soil to be used in the present invention generally refers to a black soil containing 20% or more of humus. Because it is suitable for plant cultivation, it is used for cultivation of drinking water and flower plant. The soil and the fluid of flora and fauna integrated in the soil and the corrosion caused by them are corroded by the action of microorganisms in the soil. In general, the soil rich in corrosion is rich in organic matter, fertile, and black or dark brown. It is mainly developed in the surface part of the northwestern region of the temperate zone. Peat is a kind of corroded soil, and coal is a deteriorated corroded ground.

The propylene glycol derived from illytic solute can be prepared by the following process.

The method for producing the ilite effluent according to the present invention comprises a crushing step, an elution step and a condensing step.

In the pulverizing step, the ilite mineral is pulverized so that the effective component extraction of ilite can be performed more easily in the leaching step. For this purpose, the size of the pulverized ilite is suitably 0.1-0.5 mm. If it is less than 0.1 mm, there is a problem that the burden of pulverization is increased. If it is more than 0.5 mm, there is a problem that the surface area in contact with the solvent is relatively small and the elution is not properly performed. The milling of the ilite mineral may be carried out by a conventional milling method of minerals.

The leaching step is the step of leaching and releasing the effective component of ilite mineral. The dissolution method can be roughly classified into two types.

In the first method, the lignite and propylene glycol which are ground in the pulverization step are put into a heating furnace and heat is applied to elute the active ingredient from the pulverized ilite mineral.

It is preferable that the heating furnace temperature during elution is maintained at 185 to 400 ° C. 185 deg. C is the temperature at which propylene glycol starts to boil. When the temperature is lower than the temperature, extraction of the extracted minerals is hardly performed. When the temperature is higher than 400 deg. C, there is a problem that daily light is denatured. The duration of the extraction step is not particularly limited, but it is preferable to proceed for 30 minutes to 2 hours.

The second method is a method in which the propylene glycol is separately boiled to generate steam, and the generated propylene glycol vapor is contacted with pulverized ilite to elute an effective component of ilite.

At this time, the elution time is not particularly limited, but it is preferable to proceed for about 30 minutes to 2 hours.

Finally, in the condensation stage, the vapor generated in the elution step is condensed, and the high-temperature steam is liquefied through the condensation stage, resulting in the desired light-eluting propylene glycol.

Also, in order to enhance the efficacy of the propylene glycol according to the present invention, any one selected from the group consisting of dry seaweed, dried black gum, dried gum liquor, dried gum, dried gum, And may further include one.

 When the composition further contains one of the fishes selected from the group consisting of dry seaweed, dried black gum, dried gum, dried gum, dried gum, and mixtures thereof, the propylene glycol used in the present invention may contain various skin whitening ingredients, In addition, it can further contain bacalin, niacazone, licoritinapioside, black ginsap saponin and the like, so that it can have a better effect than when eluting only ilite.

In order to enhance the efficacy of the propylene glycol derived from ilite according to the present invention, it may further include any one selected from the group consisting of basalt, crustaceans, and mixtures thereof, which are ground to the same particle size as Illight. The active ingredient such as minerals eluted is further increased, and it is possible to obtain a more excellent effect than when eluting only ilite.

The essence according to the present invention prepared as described above can be used without any particular limitation as long as it can increase the effect without containing water. However, the range of the essence is to keep the vitamin C content at least 30% by weight desirable.

Nutrition cream application step

The nutritional cream in the present invention is intended to provide nutrients to the entire facial skin and can be used without any particular limitation as long as it is widely known as a nutritional cream in the technical field to which the present invention belongs. Examples of nutritional creams most suitable for use in the present invention are as follows same.

The nutritional cream may be selected from the group consisting of purified water, Dipropylene Glycol, Cetyl Ethylhexanoate, PEG-10 Dimethicone / Vinyl Dimethicone Crosspolymer, Squalane ), Glyceryl stearate, dimethicone, 1,2-hexanediol, stearyl alcohol, meadowfoam seed oil, poly Polysorbate 60, Ethoxydiglycol, Trimethylpentanediol / Adipic Acid Copolymer, Hydrogenated Lecithin, Sodium Hydrogenated Tallow Oil, Sodium Hydrogenated Tallowoyl Glutamate, Cetyl Alcohol, Tocopheryl Acetate, Carbomer, Xanthan Gum, Sodium Hyaluronate, (Copper Tripeptide-1), Palmitoyl Pentapeptide-4, Acetyl Hexapeptide-8, Dipotassium Glycyrrhizate, Sodium Polyacrylate Sodium Polyacrylate, Yeast Beta-Glucan, C13-14 Isoparaffin, Laureth-7, Polyacrylamide, Adenosine, Human Oligopeptide-1, Triethanolamine, Tetrasodium EDTA, and Perfume.

The nutritional cream contained 70.35% by weight of purified water, 8% by weight of dipropylene glycol, 5% by weight of cetylhexylhexanoate, 2% by weight of PEG-10 dimethicone / vinyl dimethicone crosspolymer, 3% by weight of squalane, 1.5 weight% of dimethicone, 1 weight% of 1,2hexanediol, 1.2 weight% of stearyl alcohol, 1.5 weight% of meadowfoam seed oil, 0.6 weight% of polysorbate 60, 1 weight% of ethoxydiglycol 1 0.5% by weight of trimethylpentanediol / adipic acid copolymer, 0.4% by weight of hydrogenated lecithin, 0.2% by weight of sodium hydrogencarbonate tallow oil glutamate, 0.3% by weight of cetyl alcohol, 0.1% by weight of tocopheryl acetate, 0.1% by weight of xanthan gum, 0.05% by weight of xanthan gum, 0.05% by weight of sodium heparonate, 0.022% by weight of caprate tripeptide-1, 0.0035% by weight of palmitoylpentapeptide-4, 0.004% by weight of acetylhexapeptide- 0.01% by weight of silicate, sodium poly 0.05% by weight of acrylate, 0.1% by weight of yeast beta-glucan, 0.8% by weight of C13-14 isoparaffin, 0.3% by weight of Laureth-7, 0.2% by weight of polyacrylamide, 0.04% by weight of adenosine, By weight, 0.1% by weight of triethanolamine, 0.02% by weight of tetrasodium EDTA, and 0.2% by weight of fragrance. Herein, the nutritional cream may be prepared by selecting only a part of the constituents as necessary and adjusting the respective composition ratios.

These nutritional creams can maximize skin and wrinkle improvement, promote cell regeneration, and have excellent anti-aging effects.

Meanwhile, the nutritional cream of the present invention is adjusted to pH 6.0 ± 0.5 and has a specific gravity of 1.10 ± 0.05 and a viscosity of 20,000 ± 5,000.

The nutritional cream of the present invention may further comprise EFG (Epidermal Growth Factor). The EGF (epidermal growth factor) is a growth factor that regenerates skin elasticity and promotes cell division. The nutritional cream of the present invention has high concentration of high-performance EGF, that is, 50 ppb or higher, preferably 70 ppb, 100 ppb or more. These EGFs are involved in cell division that is the basis of skin improvement activity and are known to supply the energy used for cell division.

Bibby Cream  Application step

In the present invention, nutrition is supplied to the entire face skin through a nutrition cream, and then a facial cleansing cream is applied to the facial skin to produce a healthy and bright skin tone and complement the defects of the skin. The cleansing cream is well known in the art If it is, it can be used without special proposal, and the most suitable example to be used in the invention is as follows.

The most suitable bibby cream for use in the present invention may be selected from the group consisting of purified water, Caprylic / Capric Triglyceride, Titanium Dioxide, Propylene Glycol, Squalane, Cetyl PEG / PPG-10/1-dimethicone, Arbutin, Butylene Glycol Dicaprylate / Dicaprate, sorbitan sesquioleate, Sorbitan Sesquioleate, Magnesium Sulfate, Calcium Stearate and Microcrystalline wax, Benincasa Cerifera Fruit Extract, Butylene Glycol, Portulaca Oleracea Extract, Aloe Barbadensis Leaf Juice, Hovenia Dulcis Fruit Extract, Nylon-12, Disteardimonium Hectorite, , Triethoxycaprylylsilane, beeswax, polymethyl methacrylate, tocopheryl acetate, cellulose gum, dimethicone, capers, and the like. (Copper Tripeptide-1), Acetyl Hexapeptide-8, Palmitoyl Pentapeptide-4, DMDM Hydantoin, Phenoxyethanol Phenoxyethanol), red iron oxide (CI 77491), yellow iron oxide (CI 77492), black iron oxide (CI 77499), Ultramarines, Sodium Lauroyl Glutamate, Aluminum Hydroxide, And Perfume.

The bibby cream contained 61.02 wt% of purified water, 13.2 wt% of caprylic / capric triglyceride, 5.2 wt% of titanium dioxide, 5 wt% of propylene glycol, 2.5 wt% of squalane, cetyl PEG / PPG- 2.2% by weight of dimethicone, 2.0% by weight of arbutin, 1.3% by weight of butyleneglycol dicaprylate / dicaprate, 0.9% by weight of sorbitan sesquioleate, 0.7% by weight of magnesium sulfate, 0.5% by weight of calcium stearate, 0.5% by weight of talline wax, 0.5% by weight of an extract from Donghua fruit, 0.5% by weight of butylene glycol, 0.2% by weight of extracts of horseradish, 0.2% by weight of aloe vera leaf juice, 0.4% 0.1% by weight of teadimonium hectorite, 0.2% by weight of triethoxycaprylylsilane, 0.2% by weight of beads wax, 0.05% by weight of polymethylmethacrylate, 0.05% by weight of tocopheryl acetate, 0.02% by weight of cellulose gum, 0.1% by weight, DMDMH 0.3% by weight of phenol ethoxylate, 0.3% by weight of phenoxyethanol, 0.15% by weight of red iron oxide, 0.8% by weight of yellow iron oxide, 0.02% by weight of black iron oxide, 0.01% by weight of ultramarine, 0.2% by weight of sodium lauroyl glutamate, 0.2 wt%, and flavor 0.15 wt%. Herein, the bibby cream can be prepared by selecting only a part of the constituent components as necessary and controlling the composition ratios of the components.

These bibby creams are excellent for the treatment of spots, dullness, acne marks, sunburn, allergic reactions, wound inflammation and the like.

Meanwhile, the beef cream of the present invention is preferably adjusted to have a pH of 6.0 ± 1.0, a specific gravity of 1.20 ± 0.05 and a viscosity of 25,000 ± 5,000.

Hereinafter, the present invention will be described in detail with reference to Examples, Comparative Examples and Experimental Examples. EXAMPLES The specific examples are intended to illustrate the invention and are not intended to be limiting.

<Essence according to the present invention Example  And Test Example >

< Manufacturing example  1>

The intrinsic minerals were pulverized to a diameter of 0.3 mm and 300 g of pulverized ilite minerals and 500 g of propylene glycol were placed in a heating furnace and heated for 20 minutes under a condition of 2 atm and 200 캜 to generate pilophylene glycol vapor , And the generated vapor was condensed to obtain one light propylene glycol. After cooling to room temperature, an essence consisting of 30% by weight of propylene glycol eluted with 1-liter light, 30% by weight of N-methylpyrrolidone and 40% by weight of vitamin C was prepared.

< Manufacturing example  2>

Production Example 2 was carried out in the same manner as in Production Example 1 except that 50 g of dry sodium chloride, 50 g of dried black gum, 50 g of dry licorice, 50 g of dried gold and 50 g of dried gum were further added and the amount of ilite was reduced to 150 g Was prepared in the same manner as in Preparation Example 1.

< Manufacturing example  3>

500 g of propylene glycol was passed through a heating furnace at 2 atm and 200 ° C, and the resulting vapor, which had been passed through the column, was condensed and condensed to give a light propylene glycol And the total time was 20 minutes. After cooling to room temperature, an essence consisting of 30% by weight of propylene glycol eluted with 1-liter light, 30% by weight of N-methylpyrrolidone and 40% by weight of vitamin C was prepared.

< Manufacturing example  4>

Production Example 4 was repeated except that 50 g of dry sodium chloride, 50 g of dried black gum, 50 g of dry licorice, 50 g of dried gold and 50 g of dry gum were pulverized to the same particle size as the ilite mineral and the amount of ilite was reduced to 150 g Was prepared in the same manner as in Production Example 3.

< Manufacturing example  5>

Production Example 5 was prepared in the same manner as in Production Example 3, except that 300 g of ground basalt crushed to the same particle size as the ilite mineral was further added and the amount of ilite was reduced to 150 g.

< Manufacturing example  6>

Production Example 6 was prepared in the same manner as in Production Example 3, except that 300 g of the ground powder crushed to the same particle size as the ilite mineral was further contained and the amount of the ilite was reduced to 150 g.

<Safety test: skin irritation test>

Selection Criteria

* Adult men and women aged 20 to 55

* Those who understand the purpose and content of the test and express their intention to participate voluntarily

* A person who understands possible adverse reactions and signs written consent

* Applicants who can be trained during the test period

Criteria for excluding test subjects

* If you have eczematous skin disease

* In case of infectious skin disease

* Allergic specificity

* Cosmetics, medicines, and daily irritation or allergy to daylight exposure

 Selection of test subjects

* We conducted physicochemical tests and questionnaires on dermatologists' skin for voluntary test subjects, and selected 30 individuals who met the criteria and did not qualify as exclusion criteria.

Skin patch  exam( patch test ) Safety evaluation by human body application test

The subjects were visited 4 times (before the start of the test, on the day of removing the patch, after 24 hours, after 48 hours after the removal of the patch, and after 48 hours after the removal of the patch) during the period of application of the human body, and skin irritation was judged by the dermatologist.

At the first visit, subjects were tested for skin patches on their backs using IQ chambers (Chemotechnique Diagnostics, Sweden). The subjects were applied to the shoulder bones and waist line around the spine using an IQ chamber.

The test site was wiped with distilled water and dried. Then, 35 μl of the test sample prepared in accordance with Table 1 and Table 2 was dropped in the IQ chamber, and the test sample was fixed on the test site.

After 24 hours, the test area was marked with a marking pen. After 30 minutes, 24 hours, and 48 hours, the test site was observed.

Skin responses were graded according to the criteria of the International Society for Contact Dermatology (ICDRG) (see Table 1). The mean score was calculated according to the formula for calculating the average skin reactivity, and the skin patch test results were evaluated according to the judgment table (see Table 2).

sign score Criteria for Skin Response - 0 No stimulation ± 0.5 Missile: mild or slightly erythematous erythema + One Light Stimulation: Clear borders but weak erythema, edema and palsy ++ 2 Moderate irritation: marked erythema, papules and small follicles +++ 3 Stimulation of the river: severe swelling and alveoli, scab formation

<Average Skin Reactivity Calculation Formula>

Grade mean score Unstimulated (1) 0.00 to 0.75 Unstable (2) 0.76 to 1.50 Light stimulus (3) 1.51 to 2.50 Medium Stimulus (4) 2.51 to 4.00 Stimulants stimulating (5) 4.01 ~

Test result

As shown in the following Table 3, the essence of Preparation Example 1 according to the present invention was judged to be non-stimulated because the reaction could not be observed at 30 minutes, 24 hours and 48 hours after the removal of the patch, After 24 hours and 48 hours, significant erythema was found, and it was judged as a moderate stimulus. In Comparative Example, 40% by weight of vitamin C and 40% by weight of N-methylpyrrolidone were used.

sample
Number of reactants
Reactivity Average skin response
30 minutes 24 hours 48 hours Production Example 1 0 0 0 0 0 Comparative Example 28 3.57 3.26 2.99 3.27

According to the test results, it can be seen that the essence according to the present invention is a non-irritant essence without skin irritation when compared with the conventional vitamin C cosmetic composition.

<Vitamin C Potency  Measurement>

The initial potency of vitamin C was 100, and the potency of vitamin C after 1 month was measured at 25 ° C and 45 ° C. The results are shown in Table 4 below. The comparative example is prepared by 40% by weight of vitamin C and 40% by weight of N-methylpyrrolidone.

The measurement was performed using a Waters SunFire C18 5,100 A, 150 X 4.6 mm column. At this time, the wavelength of the detector was set to 254 nm, and the mobile phase was measured with a flow rate of 0.6 mL / min using 25 mM KH ₂ PO ₄ buffer (pH 2.5).

Remarks Production Example 1 Production Example 2 Production Example 3 Production Example 4 Production Example 5 Production Example 6 Comparative Example 25 ℃ 99 98 99 99 99 99 97 45 ° C 90 91 91 92 91 92 89

As shown in Table 4, it was confirmed that the reversibility of vitamin C was sufficiently maintained in both the cosmetic composition according to the present invention and the cosmetic composition according to the prior art. Therefore, it was confirmed that the composition according to the present invention has chemical stability that is not inferior to the prior art composition.

<Stability test: discoloration, Fling >

For stability of the formulation, it was stored in an opaque glass container in a thermostat kept constant at 45 ° C for 12 weeks and stored in an opaque glass container in a fully lighted refrigerator maintained at 4 ° C for 12 weeks After that, discoloration and degree of change were measured. The results are shown in Table 5 below. The comparative example is prepared by 40% by weight of vitamin C and 40% by weight of N-methylpyrrolidone.

At this time, the degree of product discoloration and degree of detachment was classified into the following six grades and evaluated.

0: No change 1: Extremely small

2: a little bit 3: a bit badly

4: Severely 5: Extremely severe

sample discoloration Fling
Production Example 1 45 ° C 0.1 0.1 4 ℃ 0 0
Production Example 2 45 ° C 0.5 0.15 4 ℃ 0 0
Production Example 3 45 ° C 0.1 0.15 4 ℃ 0 0
Production Example 4 45 ° C 0.15 0.1 4 ℃ 0 0
Production Example 5 45 ° C 0.1 0.1 4 ℃ 0 0
Production Example 6 45 ° C 0.1 0.1 45 ° C 0 0
Comparative Example 45 ° C 0.1 0.1 4 ℃ 0 0

As shown in Table 5, it was found that there was almost no color change or peeling at 45 DEG C in the cosmetic composition according to the present invention and the prior art. Accordingly, it was found that the cosmetic composition according to the present invention had a formulation stability comparable to that of the conventional cosmetic composition.

&Lt; Evaluation of anti-wrinkle efficacy: Measurement of elastase inhibitory activity &

● Experimental method

 Prepare each test solution at a constant concentration. 40 μl of each test solution was added with 40 μL of a solution of proporcine pancreas elastase (2.5 U / ㎖) dissolved in 50 mM Tris-HCl buffer (pH 8.6), and the substrate was dissolved in 50 mM Tris-HCl buffer (pH 8.6) L-Ala) 3-p-nitroanilide (0.5 mg / ml) was added and mixed. After incubation at 37 ° C for 30 minutes, absorbance is measured at 410 nm. Elastase inhibitory activity was expressed as the absorbance reduction rate of the sample solution added and no added sample solution.

Inhibition rate (%) = 1- (absorbance of sample addition group / absorbance of sample addition group) x 100

● Experimental results

The elastase present in the neutrophil granulocyte of human body is known as the main enzyme of wrinkle formation by decomposing elastin which is insoluble elastic fiber protein of animal connective tissue and breaking the network structure of dermal tissue of skin. Whether the elastase of Preparation Examples 1 and 6 had an inhibitory activity on such elastase was examined, and the results are shown in Table 6. &lt; tb &gt;&lt; TABLE &gt;

sample Concentration (500 mu g / ml) Production Example 1 81.1 ± 0.8 Production Example 2 90.0 ± 2.2 Production Example 3 85.1 ± 0.8 Production Example 4 93.1 ± 2.2 Production Example 5 89.1 ± 2.2 Production Example 6 93.3 ± 2.2 oleanolic acid 81.6 ± 0.5

As shown in Table 6, it was confirmed that elastase inhibition activity was observed at 1 to 6 in all of the preparations and elastase inhibitory activity was as high as that of oleanolic acid, which is a positive control, so that the essence according to the present invention has a highly excellent anti-wrinkle effect.

<Skin Whitening Effect: Melanin ( melanin ) Biosynthesis Low performance  Evaluation>

Melanoma cell line B16F10 cells were purchased from Korean Cell Line Bank, and Dulbecco's modified Eagle's (Gibco, USA) containing 1% antibiotic (Gibco, USA) and 10% fetal bovine serum (DMEM) medium at 37 ° C in a 5% CO ₂ incubator and subcultured once every four days.

B16F10 cells cultured in DMEM medium were added to a 24 well plate at a concentration of 2.0 × 10 ⁴ cells / well. After culturing for 24 hours, the samples were added at various concentrations and washed with phosphate buffer solution (pH 7.4) 48 hours later. Then, 1N NaOH was added to melanin and reacted at 80 ° C for 1 hour, and the absorbance was measured at 405 nm in a spectrophotometer. The inhibition of melanin biosynthesis was calculated by the absorbance reduction ratio of the sample solution added and the no-added solution, and the results are shown in Table 7.

sample Melanin biosynthesis inhibition
(Absorbance reduction rate%) α-MSH (-) - α-MSH (+) 100 Kojic acid 55.7 ± 1.6 Arbutin 51.9 ± 1.4  Production Example 1 47.8 ± 0.8  Production Example 2 49.1 ± 0.3  Production Example 3 48.5 ± 0.5  Production Example 4 49.1 ± 0.9  Production Example 5 48.9 ± 0.3  Production Example 6 49.2 ± 0.9

As can be seen from the results of Table 7, the essence according to the present invention shows superior melanin production inhibitory ability to B16F10 melanoma cells as compared with kojic acid and arbutin, which are known whitening substances, It can be seen that the whitening effect is excellent.

<Antibacterial effect against acne bacteria>

The antimicrobial effect was measured using the Minimal inhibitory concentration (MIC) test for the Illiate dissolution products of the above preparation examples.

MIC test This is a method to measure the growth of the test organism after the raw material having the antimicrobial effect is added in a stepwise concentration in the liquid medium, the inoculum of the various test organisms is inoculated thereto, the shake culture is carried out at 25 ° C for 24 hours.

To 10 ml of yeast peptone dextrose broth was added 10 ml of Propionibacterium acnes, acnes KCTC3314) is cultured at 25 ° C for 48 hours, and the microorganisms are inoculated so that each cultured microorganism becomes 10 ⁴ cells in 3 ml of medium. 2.0% by weight of the Illitol dissolution product prepared in each medium is added. The prepared test tube was incubated at 25 DEG C for 48 hours, and the degree of growth of the microorganism was observed. The results are shown in Table 8.

sample Propionate bacterium acnes Production Example 1 - Production Example 2 - Production Example 3 - Production Example 4 - Production Example 5 - Production Example 6 - +: Microbial growth appears
-: No microbial growth due to antimicrobial activity

As shown in Table 8, all of Production Examples 1 to 6 showed antibacterial effects and no growth of microorganisms was observed.

&Lt; The skin improvement method according to the present invention Example  And Test Example >

Example  1: skin improvement method according to the present invention

Cleanse with cleansing soap to remove foreign matter on skin surface.

At this time, the cleansing soap was composed of 93.4% by weight of soap base, 2.0% by weight of herbal medicine ingredient, 0.5% by weight of chamomile, 0.3% by weight of alkoxyglycerol, 0.2% by weight of hyaluronic acid, 0.4% by weight of aloe vera extract, 0.5 wt.%, Tea trioyl 0.4 wt.%, Glycerin (skin moisturizer) 1.0 wt.%, And apricot flower natural fragrance 1.0 wt.

Then apply a lifting pack to the face, allowing the skin to absorb nutrients easily.

The lifting pack contained 91.592 wt% of purified water, 2 wt% of carbomer, 1.2 wt% of yeast beta-glucan, 1.2 wt% of caffeine, 0.6 wt% of Hovenia dulcis extract, 0.6 wt% of green tea extract, 0.5 wt% 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% by weight of Ganoderma lucidum extract, 0.2% 0.002% by weight, 0.3% by weight of p-anic acid, 0.2% by weight of caprylyl glycol and 0.3% by weight of phenoxyethanol.

Then apply eye cream to the eye area to alleviate the wrinkles in the eyes, and disassemble the fat layer under the eyes.

The eye cream contains 37.615% by weight of purified water, 30% by weight of glyceryl acrylate / acrylic acid copolymer, 20% by weight of glycerin, 5% by weight of propylene glycol, 3% by weight of butylene glycol, 1% by weight of betaine, 0.2% by weight of cyclopentasiloxane, 0.25% by weight of cyclotetrasiloxane, 0.2% by weight of cyclopentasiloxane, 0.1% by weight of cyclopentasiloxane, 0.2% 0.1% by weight of dipotassium glycyrrhizate, 0.1% by weight of diapause extract, 0.05% by weight of sodium hyaluronate, 0.01% by weight of yeast beta-glucan, 0.02% by weight of acetylhexapeptide-8, 1 0.012% by weight, palmitoyl pentapeptide-4 0.008% by weight, PEG-40 hydrogenated castor oil 0.2% by weight, triethanolamine 0.01% by weight, adenosine 0.04% by weight, 0.3% by weight of diol, 0.025% by weight of diazolidinyl urea, And 0.01% by weight of a natural perfume.

And apply an essence on the face, whitening the skin and providing nutrients.

At this time, the essence is prepared so as to be composed of 30% by weight of propylene glycol eluted with 1-light, 30% by weight of N-methylpyrrolidone and 40% by weight of vitamins.

Continue to apply nutrient cream to your face to provide nutrients to your skin.

Wherein the nutritional cream comprises 70.35% by weight of purified water, 8% by weight of dipropylene glycol, 5% by weight of cetylhexylhexanoate, 2% by weight of PEG-10 dimethicone, 3% by weight squalane, 1.5% by weight of glyceryl stearate, 1% by weight of chicone, 1% by weight of 1,2-hexanediol, 1.2% by weight of stearyl alcohol, 1.5% by weight of meadowfoam oil, 0.6% by weight of polysorbate 60, 1% by weight of ethoxydiglycol, 0.5 wt% of diol, 0.4 wt% of hydrogenated lecithin, 0.2 wt% of sodium hydrogenated tallow oil glutamate, 0.3 wt% of cetyl alcohol, 0.1 wt% of tocopheryl acetate, 0.1 wt% of carbomer, 0.05 wt% of xanthan gum, 0.05% by weight of sodium hyaluronate, 0.022% by weight of caprate tripeptide-1, 0.0035% by weight of palmitoylpentapeptide-4, 0.004% by weight of acetylhexapeptide-8, 0.01% by weight of dipotassium glycyrrhizate, 0.05% by weight, yeast beta-glucan 0.1% by weight, 0.8% by weight of C13-14 isoparaffin, 0.3% by weight of Laureth-7, 0.2% by weight of polyacrylamide, 0.04% by weight of adenosine, 0.0005% by weight of Al-oligo peptide-1, 0.1% by weight of triethanolamine, By weight, and 0.2% by weight, respectively.

Afterwards, apply the cream to the face and produce a healthy and bright skin tone and complement the defects of the skin.

The bibby cream contained 61.02 wt% of purified water, 13.2 wt% of caprylic, 5.2 wt% of titanium dioxide, 5 wt% of propylene glycol, 2.5 wt% of squalane, 2.2 wt% of cetyl PEG, 2.0 wt% of arbutin, A mixture of 1.3% by weight of cocidicaprylate, 0.9% by weight of sorbitan sesquioleate, 0.7% by weight of magnesium sulfate, 0.5% by weight of calcium stearate, 0.5% by weight of microcrystalline wax, 0.5% 0.5% by weight of Lycopersicon esculentum, 0.2% by weight of Lycopersicon esculentum extract, 0.2% by weight of Aloe vera leaf juice, 0.4% by weight of Leaflet extract, 0.28% by weight of Nylon-12, 0.15% by weight of Distearmonium hectorite, 0.2 wt% of beeswax, 0.05 wt% of polymethylmethacrylate, 0.05 wt% of tocopheryl acetate, 0.02 wt% of cellulose gum, 0.1 wt% of dimethicone, 0.3 wt% of DMDM hydantoin, 0.3 wt% of phenoxyethanol % By weight, red iron oxide 0.15 , 0.2 wt% of sodium lauroyl glutamate, 0.2 wt% of aluminum hydroxide, and 0.15 wt% of natural fragrance of apricot flower, in an amount of 0.1 wt%, yellow iron oxide of 0.8 wt%, black iron oxide of 0.02 wt%, ultramarine of 0.01 wt% do.

Example  2: skin improvement method according to the present invention

The second embodiment is the same as the first embodiment except that the face is cleaned using the facial cleanser of the present invention shown in Fig.

Comparative Example  1: Make-up method using known cosmetics

After cleansing with a known cleanser, applying a known lifting pack, applying a known nutrition cream, applying the known eye cream again, applying the known essence, and applying the known cleansing cream. Herein, the term &quot; known &quot; refers to a product sold on the market, and in this embodiment, a medium-priced product is used as a known cosmetic product from Innisfree (cosmetics trade name). If Innisfree's cosmetics are not available at this time, middle-priced products of Misha (cosmetics brand name) products are available.

Experimental Example  1: Depending on the skin improvement method Skin tone  Improvement evaluation

Comparative Example 1 and Examples 1 to 2 were evaluated for skin tone improvement.

Table 8 shows changes in the skin tone of 10 respondents by observing directly before and after the make-up on the 15th, 30th, 45th, and 60th days after the makeup. , The degree of skin tone improvement was expressed as a relative multiple based on the makeup. At this time, the degree of improvement was evaluated by the evaluator and the evaluation score was taken as the average score of 10 evaluation members.

Makeup
before Make-up
After 15 days Make-up
After 30 days Make-up
After 45 days Make-up
60 days later Comparative Example 1 1.0 1.2 1.4 1.4 1.4 Example 1 1.0 2.9 3.0 3.2 3.2 Example 2 1.0 3.2 3.5 3.8 3.8

As shown in Table 9, it can be seen that the skin improvement method of the present invention according to Examples 1 and 2 has an excellent skin tone improving effect. That is, the conventional method (Comparative Example 1) does not have a large effect of improving the skin tone, and the effect of improving the skin tone is not exhibited well after 30 days after the makeup. On the other hand, the skin improvement method (Examples 1 to 2) of the present invention is excellent in improving the skin tone, and the effect of improving the skin tone after makeup is increased for a long period (up to 45 days).

Experimental Example  2: Evaluation of skin elasticity improvement according to skin improvement method

Skin elasticity improvement evaluation was performed for Comparative Example 1 and Examples 1 to 2.

Table 9 shows the evaluation of the skin elasticity improvement for the experimenters who passed 60 days after the cremation. In this case, the original restoration time before the makeup was set to 10, and the original restoration time of Comparative Example 1 and Examples 1 to 2 was expressed as a relative multiple based on the original restoration time before the makeup.

Before makeup 60 days after makeup Comparative Example 1 10 8.3 Example 1 10 4.3 Example 2 10 3.9

As can be seen from Table 10, the skin improvement method of the present invention according to Examples 1 and 2 has excellent skin elasticity improving effect. That is, the conventional method (Comparative Example 1) has a small effect of improving skin elasticity, but the skin improvement method of the present invention (Examples 1 to 2) is remarkably superior in improving skin elasticity.

Experimental Example  3: Example  1

As a result of observing the skin changes of Examples 1 to 6 using the skin care method according to Example 1 for at least one month, it was confirmed that increase in gloss, restoration of skin elasticity, whitening and dulling were observed in Case 1, The wrinkles were completely improved, the skin was smooth, the pores were reduced, and the elasticity of the skin was restored. According to Case 3, forehead wrinkles, wrinkles and wrinkles were alleviated, skin elasticity was increased, and wounds were restored. In Example 4, the effect of whitening, lowering of the under eye area and reduction of wrinkles in the wrist was confirmed. In Example 5, the color of the blood was transparent, the skin texture was improved, and the wrinkles under the eyes and wrinkles of the wrists were alleviated. According to Case 6, the skin was regenerated, blood circulation, skin tone improved, and skin elasticity increased.

As described above, the skin improvement method through efficient management according to the present invention greatly improves the effect of improving skin such as relieving inflammation symptoms, skin whitening, skin elasticity, wrinkle removal, dirt removal,

Therefore, when making up the skin through the skin improvement method according to the present invention, more beautiful skin can be obtained without skin trouble.

In addition, the skin improvement method according to the present invention can increase the satisfaction of the cosmetics user through the beautiful skin deformation, thereby increasing the sales volume of the cosmetics used in the skin improvement method according to the present invention, .

100; Lower pad 110; Space for yellow soil
120; An upper through hole 130; Flow space
140; A lower through hole 200; Upper projection
300; Lower protrusion 400; Nanofiber
500; A central pad 600; Loess ball
700; Top pad 710; Phage space

Claims (5)

A cleansing step of cleansing the skin surface with a cleanser to remove impurities;
Applying a lifting pack to the face, releasing micro-blood vessels, decomposing subcutaneous fat, and allowing the skin to easily absorb nutrients;
Applying an eye cream to the eyes to soften the wrinkles of the eyes and dissolve the fat layer under the eye;
Applying an essence to the face, applying an essence to whiten and provide nutrients to the skin;
Apply nutrition cream to the face to provide nutrients to the skin; And
The method comprising the steps of: applying a face cream to the face to produce a healthy and bright skin tone and complementing the defects of the skin;
Wherein the essence is a mixture of ilite and marine soil. The composition according to claim 1, comprising 30 to 35% by weight of propylene glycol, 30 to 35% by weight of N-methylpyrrolidone and 30 to 40% A method of improving skin through efficient management.
The method according to claim 1,
The propylene glycol derived from illylite is obtained by condensing propylene glycol vapor generated by heating a mixture of propylene glycol with a mixture of ilite and propylene glycol in a heating furnace or by passing propylene glycol vapor through a mixture of ilite and marine soil and then condensing the vapor Wherein the skin is cleaned by the skin.
3. The method of claim 2,
Dried liquorice, dry golden liquor, dried liquorice, and mixtures thereof when the mixture of the ilite and the humus soil is eluted with propylene glycol at the same particle size as that of unidirectional light The method of skin improvement through efficient management consisting of 6 steps.
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