JP2007210977A - Anti-ageing agent, and slimming agent, and skin cosmetic - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an anti-ageing agent and a slimming agent each containing an extract of Callicarpa nudiflora Hook. et Arn., and to provide a skin cosmetic containing the agents. <P>SOLUTION: This anti-ageing agent having an anti-ageing action, and the slimming agent having a slimming action, each contains the extract of Callicarpa nudiflora Hook. et Arn. This anti-ageing action is preferably at least one embodiment selected from an estrogen-like action, a hyaluronic acid production-promoting action, and a skin kelatinocyte-proliferating action, and the slimming action is preferably an embodiment of a cyclic AMP phosphodiesterase-inhibiting action. The skin cosmetic is characterized by containing the extract of Callicarpa nudiflora Hook. et Arn. as an active ingredient. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an anti-aging agent and a slimming agent containing an extract of rakash, and a skin cosmetic containing these.

The dermis and epidermis of the skin are composed of epidermal cells, fibroblasts, and extracellular matrices such as elastin and collagen that are outside these cells and support the skin structure. In young skin, the interaction between these skin tissues is kept constant, so moisture retention, flexibility, elasticity, etc. are ensured, and the skin is also stretchy and glossy in appearance, maintaining a fresh state. .
However, when affected by certain external factors such as ultraviolet rays, significant dryness, excessive skin washing, etc., or when aging progresses, the production of collagen, which is a major component of the extracellular matrix, decreases, and crosslinking occurs. Reduced elasticity due to. Elastin also undergoes degradation and alteration. Furthermore, the influence of external factors and a decrease in the growth rate of fibroblasts with aging also result in a decrease in the production of collagen and a decrease in the production of hyaluronic acid, a natural moisturizing factor. As a result, the elasticity and moisturizing function of the skin decreases, the keratin causes abnormal peeling, the skin loses its tension and gloss, and exhibits aging symptoms such as roughening, wrinkles, and dullness.

  Reduction and degeneration of collagen and hyaluronic acid are involved in wrinkles, dullness, disappearance of texture, decrease in elasticity, and the like accompanying such skin aging. In recent years, ultraviolet rays and the like are considered to be a factor for inducing this change, and are considered to be a major factor such as skin wrinkle formation. Therefore, promotion of collagen production and hyaluronic acid production is important in preventing and improving skin aging. Therefore, attempts have been made to extract substances having a collagen production promoting action, hyaluronic acid production promoting action, epidermal keratinocyte proliferation action, and fibroblast proliferation promotion action from natural products (Patent Documents 1 and 2). And non-patent document 1).

  Moreover, the cause of skin aging accompanying aging is also due to a decrease in the secretion of estrogen, a type of female hormone. Estrogens are deeply involved in maintaining the health of adult women, and their lack of secretion leads to various medical illnesses and can cause unwanted skin changes such as skin sensitivities, decreased elasticity, and reduced moisture. It has been known. Therefore, a substance (estrogenic agent) having the same action as estrogen is transcutaneously or orally administered to women in the menopause or later in which estrogen secretion declines. As such estrogen-like agents, for example, steroidal estrogens, non-steroidal estrogens, flavone compounds and the like are used (see Patent Documents 3 to 5).

In addition, it is considered effective for prevention of obesity to suppress the action of cyclic AMP phosphodiesterase, which is an enzyme that degrades cyclic AMP involved in promoting fat metabolism. In fact, it is known that when the action of cyclic AMP phosphodiesterase is suppressed, the concentration of intracellular cyclic AMP increases, lipid metabolism becomes active, and obesity is resolved.
Therefore, attempts have been made to extract substances having a cyclic AMP phosphodiesterase inhibitory action from natural products, such as Fuji tea extract (see Patent Document 6), maple plant extract (see Patent Document 7), and the like. Has been reported.

  However, it is excellent in safety and productivity, can be used on a daily basis, and is inexpensive, but has an excellent estrogen-like action, hyaluronic acid production promoting action, epidermal keratinocyte proliferation action, and cyclic AMP phosphodiesterase inhibitory action The demands of customers for various natural preparations having at least one of the above are extremely strong, and there are currently no sufficiently satisfactory products.

JP 2002-226323 A JP 2003-137801 A JP 2001-316240 A JP 2002-226323 A JP 2003-055245 A JP 2003-12532 A JP 2003-1113068 A "Fragrance Journal" 1992, No. 11, p43

An object of the present invention is to solve the conventional problems and achieve the following objects. That is, the present invention firstly has an anti-aging agent that has at least one selected from an estrogenic action, a hyaluronic acid production promoting action, and an epidermal keratinocyte proliferation action, and can prevent and improve skin aging. And a slimming agent having a cyclic AMP phosphodiesterase inhibitory action and capable of preventing obesity.
In addition, the present invention secondly includes at least one of the anti-aging agent and the slimming agent as an active ingredient, and prevents and improves the reduction of skin wrinkles and elasticity, and the roughening of the skin due to skin dryness. An object of the present invention is to provide a skin cosmetic that can prevent obesity and further prevent obesity.

  As a result of intensive studies by the present inventors in order to solve the above problems, the extract of Lakash is at least one selected from an excellent estrogen-like action, hyaluronic acid production promoting action, and epidermal keratinocyte proliferation action. It is useful as an anti-aging agent that can prevent and ameliorate skin aging, and has an excellent cyclic AMP phosphodiesterase inhibitory action and is also useful as a slimming agent that can prevent obesity. I found each one.

The present invention is based on the above findings of the present inventors, and means for solving the above problems are as follows. That is,
<1> An anti-aging agent characterized by containing an extract of rakashish.
<2> The anti-aging agent according to <1>, which has at least one selected from an estrogen-like action, a hyaluronic acid production promoting action, and an epidermal keratinocyte proliferation action.
<3> A slimming agent characterized by containing an extract of Lakashish.
<4> The slimming agent according to <3>, which has a cyclic AMP phosphodiesterase inhibitory action.
<5> A skin cosmetic comprising the Lakashish extract according to any one of <1> to <4> as an active ingredient.

According to the anti-aging agent of the present invention, it is possible to prevent and improve the reduction of skin wrinkles and elasticity through at least one selected from an excellent estrogenic action, hyaluronic acid production promoting action, and epidermal keratinocyte proliferation action. Can do.
According to the slimming agent of the present invention, lipid metabolism becomes active and obesity can be prevented through excellent cyclic AMP phosphodiesterase inhibitory action.
In addition, the anti-aging agent and slimming agent of the present invention are suitable for blending into skin cosmetics because they are excellent in feeling of use and safety.

(Anti-aging agent and slimming agent)
The anti-aging agent and slimming agent of the present invention contain an extract of rakash and further contain other components as necessary.
The anti-aging agent preferably has at least one selected from an estrogenic action, a hyaluronic acid production promoting action, and an epidermal keratinocyte proliferation action as an anti-aging action.
The slimming agent preferably has a cyclic AMP phosphodiesterase inhibitory action as a slimming action.

The Lakashish (Naked Flower Purple Pearl, Scientific Name: Callicarpa nudiflora Hook. EtArn. ) Is a shrub or sub-high tree that belongs to the family Pinaceae. The shoots and inflorescences have rough braided star hairs, and the branches have grayish yellow skin. The leaves are egg-shaped lanceolates, the upper surface is dark green, black when dry, and there are glands. This rakashish, also known as white flower tea, kanfusai, tsusetetsukou, huntingyou, etc., is distributed in southern China (Guangdong, Guangxi, Hainan) and is readily available from these regions.
Lakash is known to have hemostatic, antibacterial and analgesic effects, but has estrogen-like action, hyaluronic acid production promoting action, epidermal keratinocyte proliferation action, and cyclic AMP phosphodiesterase inhibitory action. However, it has never been known to be effective as an anti-aging agent and a slimming agent, and these are new findings by the present inventors.

  The details of the substance having at least one of anti-aging action and slimming action of the Lakashish extract are unknown, but can be easily obtained by a method generally used for plant extraction. The Lakashish extract includes Lakashish extract, a dried product obtained by drying a diluted solution of the extract, or a crude product or a purified product thereof.

  The raw material for the extraction of Lakashish is not particularly limited and can be appropriately selected according to the purpose.For example, components such as leaves, stems, roots, and flower parts can be used, and among these, The above-ground part (leaf part, stem part, flower part) is particularly preferable.

  Lakash which is the raw material for extraction can be obtained by drying or pulverizing it as it is or using a crusher and subjecting it to solvent extraction. Drying may be performed in the sun or may be performed using a commonly used dryer. The rakash may be used as an extraction raw material after pretreatment such as degreasing with a nonpolar solvent such as hexane or benzene. In addition, by performing pretreatments such as degreasing, extraction with a polar solvent of Lakash can be performed efficiently.

As the solvent used for the extraction, it is preferable to use water, a hydrophilic organic solvent, or a mixed solvent thereof at a temperature from room temperature to the boiling point of the solvent.
Examples of water that can be used as the extraction solvent include pure water, tap water, well water, mineral spring water, mineral water, hot spring water, spring water, fresh water, and the like, as well as water that has been subjected to various treatments. Examples of the treatment applied to water include purification, heating, sterilization, filtration, ion exchange, adjustment of osmotic pressure, buffering, and the like. Therefore, the water that can be used as the extraction solvent includes purified water, hot water, ion exchange water, physiological saline, phosphate buffer, phosphate buffered saline, and the like.

Examples of the hydrophilic organic solvent include lower alcohols having 1 to 5 carbon atoms such as methanol, ethanol, propyl alcohol, and isopropyl alcohol; lower aliphatic ketones such as acetone and methyl ethyl ketone; 1,3-butylene glycol, propylene glycol, Examples thereof include polyhydric alcohols having 2 to 5 carbon atoms such as glycerin, and a mixed solvent of these hydrophilic organic solvents and water can be used.
In addition, when using the mixed solvent of the said water and a hydrophilic organic solvent, in the case of a lower alcohol, it is 1-90 mass parts with respect to 10 mass parts of water, and in the case of a lower aliphatic ketone, it is 10 mass parts of water. It is preferable to add 1-40 mass parts with respect to it. In the case of a polyhydric alcohol, it is preferable to add 1 to 90 parts by mass with respect to 10 parts by mass of water.

  In the present invention, it is not necessary to adopt a special extraction method for extracting a substance having at least one of an anti-aging action and a slimming action from rakash, which is an extraction raw material, and any extraction device at room temperature or under reflux heating Can be extracted.

  Specifically, in the processing tank filled with the extraction solvent, the above-ground part of rakash is used as the extraction raw material, and further, with occasional stirring as necessary, it is allowed to stand for 30 minutes to 2 hours to elute soluble components. Then, the solid matter is removed by filtration, the extraction solvent is distilled off from the obtained extract, and the extract is obtained by drying. The amount of extraction solvent is usually 5 to 15 times (mass ratio) of the extraction raw material. The extraction conditions are usually about 1 to 4 hours at 50 to 95 ° C. when water is used as the extraction solvent. Moreover, when using the mixed solvent of water and ethanol as an extraction solvent, it is about 30 minutes-about 4 hours at 40-80 degreeC normally. In addition, the extraction liquid obtained by extracting with a solvent can be used as it is as an anti-aging agent and a slimming agent of the present invention as long as the extraction solvent is highly safe.

  The resulting Lakashish extract is diluted, concentrated, dried, purified, etc. according to conventional methods to obtain a diluted or concentrated solution of the extract, a dried product of the extract, or a crudely purified product or purified product thereof. You may perform the process of.

  The obtained Lakashish extract can be used as it is as an anti-aging agent and slimming agent, but a concentrated solution or a dried product thereof is easier to use. In obtaining a dried extract, a carrier such as dextrin or cyclodextrin may be added to improve hygroscopicity. In addition, since the Lakashish has a peculiar odor, it can be purified for the purpose of decolorization, deodorization, etc. within a range that does not cause a decrease in its physiological activity. Is not used in large quantities, so there is no practical problem even if it is not purified. Specifically, purification can be performed by activated carbon treatment, adsorption resin treatment, ion exchange resin treatment, or the like.

The anti-aging agent of the present invention is useful for preventing and improving skin wrinkles and a decrease in elasticity through at least one of an excellent estrogenic action, hyaluronic acid production promoting action, and epidermal keratinocyte proliferation action, High safety.
The slimming agent of the present invention is capable of preventing obesity through active lipid metabolism through excellent cyclic AMP phosphodiesterase inhibitory action.
Therefore, the anti-aging agent and slimming agent of the present invention have at least one of the above-mentioned anti-aging action and slimming action, and are excellent in feeling of use and safety. It is suitable for blending into the material.

(Skin cosmetic)
The skin cosmetic of the present invention contains at least one of the anti-aging agent and the slimming agent of the present invention as an active ingredient, and further contains other components appropriately selected as necessary.

  Here, the use of the skin cosmetic is not particularly limited and can be appropriately selected from various uses. For example, ointment, cream, emulsion, lotion, pack, jelly, lip balm, lipstick, bath additive, astringent , Etc.

  The blending amount of the anti-aging agent or slimming agent with respect to the entire skin cosmetic can be adjusted as appropriate depending on the type of skin cosmetic, physiological activity of the extract, etc., but it is 0 in terms of the Lakashish extract. 0.0001-10 mass% is preferable and 0.001-1 mass% is more preferable.

The above-mentioned skin cosmetic can further contain various main ingredients and auxiliaries usually used in the production of the skin cosmetic as long as the effects of the present invention are not impaired as required.
The other components are not particularly limited as long as they do not hinder the anti-aging effect and the slimming effect, and include components appropriately selected according to the purpose. For example, astringents, bactericides, antibacterial agents, ultraviolet absorption Agents, cell activators, antioxidants, active oxygen scavengers, fats and oils, waxes, hydrocarbons, fatty acids, alcohols, esters, surfactants, fragrances, and the like. These components, when used in combination with the Lakash extract, may act synergistically and provide superior effects than would normally be expected.

  The skin cosmetic of the present invention has high safety when used on the skin, and has at least one of an excellent estrogenic action, hyaluronic acid production promoting action, epidermal keratinocyte proliferation action, and cyclic AMP phosphodiesterase inhibitory action. It is useful for preventing and improving wrinkles and elasticity of skin, preventing rough skin due to drying, and preventing obesity.

  The anti-aging agent, slimming agent, and skin cosmetic of the present invention are preferably applied to humans, but may be applied to animals other than humans as long as their respective effects are exhibited. You can also

  Examples of the present invention will be described below, but the present invention is not limited to these examples.

(Production Example 1)
-Preparation of water extract of Lakashish-
2 L of water was added to 200 g of the dried portion of the dried portion of the ground portion of Rakashish, heated and extracted at 80 ° C. for 2 hours with a reflux extractor, and filtered while hot. The same extraction treatment was further performed on the residue. The obtained two extracts were combined, concentrated under reduced pressure, and dried to obtain a water extract of Lakashish. The yield of the obtained extract is shown in Table 1.

(Production Example 2)
-Preparation of 50% by weight ethanol extract of Lakashish-
2L of 50 mass% ethanol (mass ratio of water and ethanol 1: 1) was added to 200 g of the dried portion of the dry portion of the ground portion of Rakashish, heated at 80 ° C. for 2 hours with a reflux extractor, and filtered while hot . The same extraction treatment was further performed on the residue. The obtained two extracts were combined, concentrated under reduced pressure, and dried to obtain a 50% by mass ethanol extract of Lakash. The yield of the obtained extract is shown in Table 1.

(Production Example 3)
-Preparation of ethanol extract of Lakashish-
Ethanol (2 L) was added to 200 g of the dried portion of the dried portion of the ground portion of Rakashish, heated at 80 ° C. for 2 hours with a reflux extractor, and filtered while hot. The same extraction treatment was further performed on the residue. The obtained two extracts were combined, concentrated under reduced pressure, and dried to obtain an ethanol extract of Lakashish. The yield of the obtained extract is shown in Table 1.

Example 1
-Estrogen-like action test-
As the test sample, the extract of Lakashish of Production Examples 1 to 3 was used, and estrogenic action was tested as follows.
The test was conducted according to the method of Thomas et al. (In Vitro Cell. Dev. Biol. 28A, 595-602, 1992), which examines the influence on the proliferation of estrogen-dependent cells.
MCF-7 cells derived from human breast cancer are cultured in a 75 cm ² flask until confluent, and the MCF-7 cells are collected by trypsin treatment. 10% by mass FBS (activated carbon), 1% by mass NEAA and 1 mM pyruvate Using a MEM (minimum essential medium) medium containing sodium and no phenol red (hereinafter abbreviated as “MEM medium”), the concentration was adjusted to 3 × 10 ⁴ cells / mL.
The prepared MCF-7 cells were seeded at 0.9 mL each in a 24-well plate, and cultured at 37 ° C. under 5% CO ₂ -95% air to establish this. Six hours later (Day 0), 100 μL of each sample solution prepared to a concentration 10 times the final concentration in MEM medium was added to the plate, and the culture was continued.
On the sixth day from the start of the culture, the medium was replaced with a MEM medium containing 0.97 mmol / L of MTT (3- (4,5-Dimethyl-2-thiazolyl) -2,5-diphenyl-2H-tetrazolium Bromide), After culturing for 2 hours, the medium was replaced with isopropanol, and blue formazan produced in the cells was extracted. For the isopropanol containing the eluted blue formazan, the absorbance at 570 nm where the absorption maximum of blue formazan is present was measured.
In order to correct the influence of adherent cells, the absorbance at 650 nm was also measured at the same time, and the difference between the two absorbances was taken as a value proportional to the amount of blue formazan produced (the absorbance in Equation 1 below is this corrected absorbance). .
As a positive control, 10 ⁻⁹ mol / L ethinylestradiol was used. The strength of the estrogen-like action (estrogen-dependent growth action) was calculated by the following formula 1 with the absorbance when no sample was added as 100%. The results when the sample concentration is 50 μg / mL are shown in Table 2.
<Formula 1>
Estrogen-like action (%) = (A / B) × 100
In Formula 1, A represents the absorbance when the sample was added, and B represents the absorbance when the sample was not added.

表２の結果から、製造例１〜３のラカシシュの抽出物が強いエストロゲン様作用を有することが確認できた。

From the results in Table 2, it was confirmed that the extract of Lakashish of Production Examples 1 to 3 had a strong estrogen-like action.

(Example 2)
-Hyaluronic acid production promoting effect test-
As the test sample, the Lakashish extract of Production Examples 1 to 3 was used, and the hyaluronic acid production promoting effect was tested as follows.
After normal human skin fibroblasts (NB1RGB) were cultured using α-MEM (minimum essential medium) containing 10% by mass FBS, the cells were collected by trypsin treatment. The collected cells were diluted with α-MEM containing 0.5 mass% FBS to a concentration of 2.2 × 10 ⁵ cells / mL, then seeded at 100 μL per well in a 96-well plate, and cultured overnight. After completion of the culture, 100 μL of each test sample dissolved in α-MEM containing 0.5 mass% FBS was added to each well and cultured for 3 days. After the culture, the amount of hyaluronic acid in the medium of each well was measured by an indirect ELISA method.
From the measurement results, hyaluronic acid production promoting action (%) was determined by the following mathematical formula 2. The results when the sample concentration is 100 μg / mL are shown in Table 3.
<Formula 2>
Hyaluronic acid production promotion rate (%) = (A / B) × 100
However, in the said Numerical formula 2, A represents the amount of hyaluronic acid at the time of test sample addition. B represents the amount of hyaluronic acid when no test sample is added.

表３の結果から、製造例１〜３のラカシシュの抽出物がヒアルロン酸産生促進作用を有することが確認できた。

From the results shown in Table 3, it was confirmed that the extract of Lakashish of Production Examples 1 to 3 has a hyaluronic acid production promoting action.

(Example 3)
-Skin keratinocyte proliferation promoting effect test-
As the test sample, the Lacashish extract of Production Examples 1 to 3 was used, and the keratinocyte proliferation promoting action was tested as follows.
Normal human neonatal foreskin keratinocytes (NHEK) were cultured using a growth medium for long-term culture of normal human epidermal keratinocytes (EpiLife-KG2), and then cells were collected by trypsin treatment. The collected cells were diluted with EpiLife-KG2 to a concentration of 1.5 × 10 ⁴ cells / ml and then seeded at 100 μL per well on a collagen-coated 96-well plate and cultured overnight. After completion of the culture, 100 μL of each test sample dissolved in EpiLife-KG2 was added to each well and cultured for 3 days.
The keratinocyte proliferation effect was measured using the MTT assay. That is, after completion of the culture, the medium was removed and MTT (3- (4,5-Dimethyl-2-thiazolyl) -2,5-diphenyl-2H-tetrazolium dissolved in PBS (−) at a final concentration of 0.4 mg / mL. Bromide) was added to each well at 100 μL. After culturing for 2 hours, blue formazan produced in the cells was extracted with 100 μL of 2-propanol. After extraction, the absorbance at a wavelength of 570 nm was measured. At the same time, the absorbance at a wavelength of 650 nm was measured as turbidity, and the difference between the two was used as the amount of blue formazan produced. In addition, a blank test was performed and corrected in the same manner.
From these results, the keratinocyte proliferation promotion rate was determined by the following formula 3. The results when the sample solution has a concentration of 3.125 μg / mL are shown in Table 4.

<Formula 3>
Epidermal keratinocyte proliferation promotion rate (%) = (St / Ct) × 100
However, in the numerical formula 3, St represents the absorbance in the cells to which the test sample is added. Ct represents the absorbance in cells to which no test sample is added.

表４の結果から、製造例１〜３のラカシシュの抽出物が表皮角化細胞増殖促進作用を有することが確認できた。

From the results of Table 4, it was confirmed that the extract of Lakashish of Production Examples 1 to 3 has an action to promote epidermal keratinocyte proliferation.

Example 4
-Cyclic AMP phosphodiesterase inhibitory action test-
As the test sample, the Lakashish extract of Production Examples 1 to 3 was used, and the cyclic AMP phosphodiesterase inhibitory action was tested as follows.
0.2 mL of 50 mmol / L Tris-HCl buffer (pH 7.5) containing 5 mmol / L magnesium chloride, 0.1 mL of 2.5 mg / mL bovine serum albumin solution, and 0.1 mL of 0.1 mg / mL phosphodiesterase solution Then, 0.05 mL of each test sample solution was added and pre-reacted at 37 ° C. for 5 minutes. To this was added 0.05 mL of a 0.5 mg / mL cAMP solution and reacted at 37 ° C. for 30 minutes. The reaction was stopped by boiling on a boiling water bath for 3 minutes. This was centrifuged (2260 × g, 10 minutes, 4 ° C.), and the supernatant was analyzed as a test sample reaction solution under the following conditions. A blank test was performed and corrected in the same manner.
[HPLC conditions]
・ Colim: Wakosil _C18- ODS 5μm
・ Mobile: 1 mM TBAP in 25 mM KH ₂ PO ₄ : CH ₃ CN = 90: 10
・ Flow rate: 1.0 mL / min
・ Detector: 260nm
・ Atten: 32-64

Next, from the peak area of the obtained cAMP, the cyclic AMP phosphodiesterase activity inhibition rate (%) was calculated based on the following formula 4.
<Formula 4>
Phosphodiesterase activity inhibition rate (%) = (1−A / B) × 100
However, in the said Numerical formula 4, A represents the peak area of cAMP by test sample addition. B represents the peak area of cAMP in the control.

表５の結果から、製造例１〜３のラカシシュの抽出物がサイクリックＡＭＰホスホジエステラーゼ阻害作用を有することが確認された。 Subsequently, the cyclic AMP phosphodiesterase activity inhibition rate is measured by gradually reducing the sample concentration of the test sample, and the sample concentration (μg / mL) that inhibits the cyclic AMP phosphodiesterase activity activity by 50% is interpolated. Determined by The results are shown in Table 5.

From the results in Table 5, it was confirmed that the extract of Lakash from Production Examples 1 to 3 had a cyclic AMP phosphodiesterase inhibitory action.

(Formulation Example 1)
-Emulsion-
An emulsion having the following composition was produced by a conventional method.
-Jojoba oil: 4.0 g
・ Placenta extract ... 0.1g
・ Olive oil ... 2.0g
・ Squalane ... 2.0g
・ Cetanol ... 2.0g
・ Glyceryl monostearate ... 2.0g
・ Polyoxyethylene cetyl ether (20E.O) ... 2.5g
・ Oleic acid polyoxyethylene sorbitan (20E.O) ... 2.0g
・ 1,3-Butylene glycol ・ ・ ・ 3.0g
・ Hinokitiol 0.15g
・ Fragrance ... 0.05g
・ Lakashish ethanol extract (Production Example 3) 0.01g
・ Purified water: remainder (the total amount is 100 g)

(Formulation Example 2)
-Cream-
A cream having the following composition was produced by a conventional method.
-Liquid paraffin: 5.0 g
・ Salax beeswax ... 4.0g
・ Cetanol ... 3.0g
・ Squalane ... 10.0g
・ Lanoline ... 2.0g
・ Stearic acid: 1.0 g
・ Oleic acid polyoxyethylene sorbitan (20E.O) ... 1.5g
・ Glyceryl monostearate ... 3.0 g
・ 1,3-Butylene glycol ・ ・ ・ 6.0g
・ Methyl paraoxybenzoate 1.5g
・ Fragrance ... 0.1g
・ 50% ethanol extract of Lakashish (Production Example 2) ... 0.1g
・ Purified water: remainder (the total amount is 100 g)

(Formulation Example 3)
−Pack−
A pack having the following composition was produced by a conventional method.
・ Polyvinyl alcohol ... 15g
・ Polyethylene glycol 3g
・ Propylene glycol ・ ・ ・ 7g
・ Ethanol ... 10g
・ Ethyl paraoxybenzoate 0.05g
・ Fragrance ... 0.05g
・ Rakashish water extract (Production Example 1) 0.05g
・ Purified water: remainder (the total amount is 100 g)

Skin cosmetics containing at least one of the anti-aging agent and slimming agent of the present invention are useful for prevention and improvement of skin wrinkles and reduction in elasticity, prevention of rough skin, prevention of rough skin, prevention of obesity, for example , Ointments, creams, emulsions, lotions, packs, jellies, lip balms, lipsticks, bath salts, astringents, etc.

Claims (5)

  An anti-aging agent comprising an extract of rakash.   The anti-aging agent according to claim 1, which has at least one selected from an estrogen-like action, a hyaluronic acid production promoting action, and an epidermal keratinocyte proliferation action.   A slimming agent comprising an extract of Lakashish.   The slimming agent according to claim 3, which has a cyclic AMP phosphodiesterase inhibitory action. A skin cosmetic comprising the Lakashish extract according to any one of claims 1 to 4 as an active ingredient.