JP2003252740A - Antioxidant, enderonic fibroblast potentiator and epidermal cell potentiator - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a skin care preparation having high antiaging effect and high epidermal homeostasis restorative effect for addressing skin aging symptoms including occurrence of wrinkles and fleckles due to aging and extraneous stress such as ultraviolet radiation and skin elasticity decline and various skin troubles including rough skin. <P>SOLUTION: The skin care preparation having the above-mentioned advantages is obtained by compounding the extract from a plant belonging to Primula L., based on the surprising finding that the extract has marked antioxidative, enderonic fibroblast-potentiating and epidermal cell-potentiating effects as a result of screening substances effectively active in the above effects as indicators. <P>COPYRIGHT: (C)2003,JPO

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to an antioxidant and a cell activator containing an extract of a specific plant as an active ingredient. Furthermore, the present invention relates to an external preparation for skin which contains such an antioxidant and a cell activator as active ingredients and is effective in preventing aging and restoring epidermal homeostasis.

[0002]

2. Description of the Related Art Skin aging symptoms such as wrinkles, age spots, and reduced skin elasticity caused by external stress such as aging and ultraviolet rays are associated with a decrease in the function of fibroblasts in the skin dermis and a decrease or degradation of matrix fibers. Degeneration is an important factor. Therefore, in order to obtain a skin external preparation having anti-aging and improving effects on the skin, a study has been conducted on a component having a fibroblast activation or growth-promoting action and a component having an antioxidant action for eliminating active oxygen species. Has been done.

[0003] For example, with respect to the activation and proliferation promoting action of fibroblasts, loquat extract (Japanese Patent Publication No. 5-127206) and α-hydroxyacetic acid (JP-A-5-112422).
Gazette), sterol ester of α-hydroxy acid (JP-A-8-104632), 6-benzylaminopurine (JP-A-7-233037), specific ribonuclease (JP-A-7-309778), L -Lysyl-L-glycyl-L-histidine (JP-A-7-31
6192), milk-derived fibroblast growth factor (JP-A-8-119867), oxidized coenzyme A.
(Japanese Patent Laid-Open No. 8-175961) and the like are disclosed. As for antioxidants, the genus Hetero (genus Heterologous to Japanese Unexamined Patent Publication No. 11-180886) is known, as well as BHA (butylhydroxyanisole) and BHT.
A compound of a synthetic antioxidant such as (butylhydroxytoluene) and a compound of vitamin E known as a natural antioxidant can be considered.

In addition to aging signs such as wrinkles, skin roughness is also induced by external stress such as aging and ultraviolet rays. This is because the homeostasis of the epidermis is an important factor due to the stress. Is known to exist. To solve this problem, polyols of glycerin tow, mucopolysaccharides such as hyaluronic acid, amino acids, organic acids,
Cosmetics containing humectants such as urea and animal and plant extracts have been used symptomatically.

However, among the components having the above-mentioned effects, there are problems that the action and effect are insufficient and the stability is poor. Therefore, when contained in the skin external preparation base, it is effective. There were some which had to be contained in a considerable amount in order to obtain such effects. In addition, it has unfavorable side effects or irritation, adversely affects the stability of the formulation, is difficult to mix with external preparations in terms of odor or color, and it is difficult to maintain a certain action and quality. There were many things. Among them, many of the ingredients known to improve rough skin have a temporary moisturizing effect, and very few activate the epidermis itself, and the effect of improving the underlying epidermal condition is very rare. It has been desired to develop a skin external preparation having a certain effect, that is, a skin external preparation having an effect of restoring homeostasis of the epidermis.

[0006]

SUMMARY OF THE INVENTION Therefore, the object of the present invention is to prevent wrinkles caused by external stress such as aging and ultraviolet rays.
The purpose of the present invention is to provide an external preparation for the skin, which responds to various skin problems such as skin aging symptoms such as the generation of spots and a decrease in skin elasticity and rough skin, and its specific effects are the anti-aging effect and the epidermal constancy. It is a sexual recovery effect.

[0007]

In order to solve the above-mentioned problems, the present inventors have screened for a substance having an effective activating action using the antioxidant effect and the activating effect of dermal fibroblasts and epidermal cells as indicators. I went. As a result, they have surprisingly found that an extract of a plant of the genus Primrose of the Primula family has a remarkable antioxidant effect and a activating effect on dermal fibroblasts and epidermal cells, and completed the present invention.

That is, the present invention relates to an anti-aging skin external preparation containing an extract of a Primula primrose plant and a skin external preparation for restoring epidermal homeostasis, and an antioxidant containing a Primula Primula plant extract as an active ingredient. Agents and cell activators.

The structure of the present invention will be described in detail below. Examples of the technology relating to the Primrose plant extract of the present invention include technology for stabilizing emulsification by using in combination with lecithin (Japanese Patent Publication No. 07-8333), and technology for whitening agents in combination with kojic acid (JP-A-07-17846) or And technology relating to melanin production promoter (Japanese Patent Application Laid-Open No. 2001-294
516) and the like have already been disclosed, but it has not been known that a Primula plant extract has a remarkable antioxidant effect and cell activating effect, and it was discovered for the first time this time. In addition, regarding the technology relating to the plant extract, an anti-aging skin external preparation and / or a skin external preparation for restoring epidermal homeostasis,
Was not known.

[0010]

BEST MODE FOR CARRYING OUT THE INVENTION The genus Primula ( P
rimula L. ), Primula schikimensis ( P. sikkimensis Hook.
Oka Houshun ( Yohana Hoshun)), Primula Faberi ( P. Faberi Oliv. Gabi Houshun (Emei Hoshun)), Primula Patense ( P. patents T)
urcz. Suinan Houshun (Suinan Hoshun), Primula Shinodenticrata ( P. sinodentici)
lata Balf. f. Tenhoku Kyu Kahoushun ( Henboku Hanahoharu), Primula Vittata ( P. vittata Bur. Et Franc)
h. Joumon Houshun (Articles), Primula,
Kapitata (P.capitata Hook. Himalayan primrose) and, other, Primula Dentikurata (P.denticulata), Primula Studios Arti Lee (P.stuartii), Primula Oburika (P.obliqa), primula macro Philadelphia (P. macrophylla), Primula Konkina (P.concinna), Primula Worasutonii (P.wollastonii), Primula Kuroki Folia (P.crocifolia), Primula cock Bull a two-pole (P.cockburniana), Primula Purorifera (P.prolifera) , Primula Pulverulent
a ), Primula saxtilis ( P. saxtili
s ), Primula Cortusoides ( P. cortuso)
), Primula Vialia ( P. viali )
i ) and the like are preferably used, but the present invention is not limited to these species. These plants are mainly plants that are distributed and grow in the cool climate region of the plateau from Siberia through the inland China to the Himalayas.

The extract of the present invention may be used in any part of flowers, fruits, seeds, leaves, stems, roots and the like of Primula plants, and may be used in the whole plant.

The method for preparing the extract of the above primrose plant used in the present invention is described below.
It is not limited to these extraction solvents and extraction methods. Alcohols such as water, ethanol, methanol, isopropanol, isobutanol, n-hexanol, methylamyl alcohol, 2-ethylbutanol, n-octyl alcohol, glycerin, ethylene glycol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene Polyhydric alcohols such as glycol, propylene glycol monomethyl ether, propylene glycol monoethyl ether, triethylene glycol, 1,3-butylene glycol and hexylene glycol, or derivatives thereof, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl-n-propyl ketone. Such as ketones, ethyl acetate, esters such as isopropyl acetate, ethyl ether, isopropyl ether, n One or more mixed solvents selected from polar solvents such as ethers such as ether can be preferably used, also can be used in phosphate buffered saline. Or petroleum ether,
It is selected from hydrocarbons such as n-hexane, n-pentane, n-butane, n-octane, cyclohexane and squalane, and low polar or non-polar solvents such as carbon tetrachloride, chloroform, dichloromethane, trichloroethylene, benzene and toluene. One solvent or a mixed solvent of two or more solvents can also be suitably used. Furthermore, water, carbon dioxide, ethylene, propylene, ethanol, methanol,
One or more supercritical fluids such as ammonia and subcritical fluids can also be used.

As the extraction method, normal pressure or pressure,
Under reduced pressure, room temperature, a method of impregnating in a cooled or heated state to extract, a method of extracting using a distillation method such as steam distillation, a method of squeezing a Primula plant to obtain an extract, and the like are exemplified, These methods can be used alone or in combination of two or more.

The extract of the Primula genus plant thus obtained can be used as it is,
Purification operations such as deodorization, decolorization, and concentration may be added to the extent that the effect is not lost, and the fractionated product may be obtained by using column chromatography and the like. These extracts, purified products, and fractionated products can be made into a dried product by removing the solvent from them, and can be used in the form of being solubilized in a solvent such as alcohol, or in the form of an emulsion. it can.

The antioxidant and cell activator in the present invention contain the above-mentioned Primula plant extract as an active ingredient.
Further, by incorporating a Primula plant extract, which is an active ingredient of such an antioxidant and a cell activating agent, into an external preparation for skin, it is possible to exhibit an excellent anti-aging effect and an effect of restoring epidermal homeostasis.

The amount of the extract of the Primula genus plant added to the external preparation for skin is generally 0.0001% by weight to 10.0% by weight as a dried product, and preferably 0.001% by weight.
% By weight to 5.0% by weight, more preferably 0.001
% By weight to 1.0% by weight.

As the dosage form of the external preparation for the skin containing the extract of the Primula genus plant, emulsions such as creams and emulsions, water-based cosmetics such as lotion and gel-like cosmetics, soaps and face-washing foams are washed. Examples include cosmetics, peel-off type and wash-off type packs.

Examples of the raw materials which can be used in combination in such an external preparation for skin include the raw materials contained in the following group (A), and these can be used in combination according to the purpose. As a matter of course, the present invention is not limited to the raw materials contained in the (A) group that can be used in combination, and can be used in combination with various raw materials within a range that does not impair the effects of the present invention. (A) Oil, moisturizer, surfactant, thickener, neutralizing agent, preservative, powder component, dye, chelating agent, fragrance, ultraviolet absorber, drug, cell activator,
Antioxidant.

[0019]

EXAMPLES Details of the present invention will be described in detail with reference to examples.

Example 1 A dried product of Primula schikimensis was crushed, and 1.67 kg thereof was impregnated with 10% by weight of 50% ethanol for one week. Then, the residue was removed by filtration, the extract was concentrated under reduced pressure, and further freeze-dried to obtain 0.1 kg of an extract, which was referred to as Example 1.

[Example 2] A dried product of Primula Fabelli was crushed, and 124.0 g thereof was crushed by 10% by weight to 50%.
It was impregnated with ethanol for one week. Then, the residue was removed by filtration, and this was designated as Example 2.

[Example 3] A dried product of Primula Patense was crushed, and 186.0 g of the pulverized product was crushed into 50% by weight of 10 weight times.
It was impregnated with 1,3-butylene glycol for one week. Then, the residue was removed by filtration, and this was designated as Example 3.

Example 4 The dried product of Primula capitata was crushed and impregnated with 1.35 kg of 10-fold amount of n-hexane for 1 week. Then, the residue was removed by filtration and the extract was concentrated under reduced pressure and dried to obtain 8.3 g of an extract, which was referred to as Example 4.

Example 5 The dried product of Primula suartii was crushed and 98.0 g of it was impregnated with 10 weight times of squalane for one week. Then, the residue was removed by filtration to obtain Example 5.

<Evaluation of Antioxidant Effect> 100 μL of the 50% ethanol solution of Example 1 diluted to an arbitrary concentration was added to a 96-well plate. Next, 0.2 mM of 1,1-diphenyl-2-picrylhydrazyl (DPPH) ethanol solution was added to a 96-well microplate in an amount of 100 μL. After standing at room temperature in the dark for 24 hours, the absorbance of light having a wavelength of 516 nm derived from DPPH radical was measured.
The radical scavenging rate of Example 1 can be represented by the following formula (1), where the absorbance in Example 1 is the case without addition (A) and the absorbance of only the sample is (B). Radical scavenging rate = [1− (B) / (A)] × 100 Formula (1) The concentration of Example 1 (IC ₅₀ ) required to eliminate 50% of DPPH radicals obtained from the measurement data, and As a comparative example, dl often used as an existing antioxidant
Table 1 shows IC ₅₀ values of -α-tocopherol. Table 1
As is more apparent, dl-α-tocopherol 0.
Compared with 0062%, Example 1 has a lower concentration of 0.0
It was confirmed that DPPH radicals were scavenged by 50% at a concentration of 039%, which revealed the excellent antioxidant effect of the Primula plant extract.

[0026]

[Table 1]

<Activation of dermal fibroblasts> Normal human dermal fibroblasts were seeded on a 96-well plate so that 2.0 × 10 ⁴ cells were formed per well. As a seeding medium, a commercially available medium D-MEM (manufactured by Nikken Biomedical Research Institute) supplemented with 5% fetal bovine serum was used. After culturing for 24 hours, Example 1 at an arbitrary concentration
The medium was replaced with a D-MEM medium containing 1% fetal bovine serum, and the cells were further cultured for 48 hours. After that, 3- (4,
5-dimethyl-2-thiazolyl) -2,5-diphenyltetrazolium bromide (MTT) 100 μg / mL
The medium was replaced with the added D-MEM medium and the cells were cultured for 2 hours. The formazan generated by the ring opening of the tetrazolium ring was extracted with 2-propanol, and the absorbance at 550 nm was measured. At the same time, the absorbance at 650 nm was measured as the turbidity, and the dermal fibroblast activation effect was evaluated by the difference between the two measured values. The results are shown in Table 2 as a relative value with 100 being the dermal fibroblast activation effect in the case where Example 1 was not added. As is clear from Table 2, 0.025% by weight to 0.
A clear (1% significant) dermal fibroblast activation effect was observed in the concentration range of 05% by weight.

[0028]

[Table 2]

<Epidermal cell activating action> Normal human epidermal keratinocytes were adjusted to 2.0 × 10 ⁴ per well 9
A 6-well plate was seeded. The seeding medium is a commercial medium KG-
2 (made by Kurabo) was used. After culturing for 24 hours, the KG-2 medium supplemented with Example 1 at an arbitrary concentration was exchanged and further cultivated for 24 hours. Then, K added with 100 μg / mL of 3- (4,5-dimethyl-2-thiazolyl) -2,5-diphenyltetrazolium bromide (MTT).
The medium was replaced with a G-2 medium and the cells were cultured for 2 hours. The formazan generated by the opening of the tetrazolium ring was extracted with 2-propanol, and the absorbance at 550 nm was measured. At the same time, the absorbance at 650 nm was measured as the turbidity, and the epidermal cell activation effect was evaluated by the difference between the two measured values. The results are shown in Table 3 as a relative value with 100 being the epidermal cell activating effect in the case where Example 1 was not added. As is clear from Table 3,
In the concentration range of 0.03125% by weight to 0.0625% by weight, a clear (1% significant) epidermal cell activating effect was observed.

[0030]

[Table 3]

[Example 6] Lotion (1) Ethanol 10.00 (wt%) (2) Polyoxyethylene hydrogenated castor oil (60EO) 0.30
(3) Primula plant extract (Example 2) 0.05
(4) Methyl paraoxybenzoate 0.02 (5) Concentrated glycerin 3.00 (6) 1, 3-butylene glycol 1.00 (7) Purified water Remainder manufacturing method: (1) to (2), (3), (4) is added sequentially,
Dissolve evenly to obtain the alcohol phase. (5) and (6) are added to (7) in advance, and the mixture is uniformly mixed with an aqueous phase which has been homogenized while stirring.

[Example 7] Cream (1) Squalane 10.00 (% by weight) (2) Stearic acid 2.00 (3) Hydrogenated palm kernel oil 0.50
(4) Hydrogenated soybean phospholipid 0.10 (5) Cetanol 3.60 (6) Lipophilic glyceryl monostearate 2.00 (7) Glycerin 10.00 (8) Methyl paraoxybenzoate 0.10 (9 ) Carboxyvinyl polymer 0.15 (10) L-arginine 0.10
(11) Primula extract (Example 3) 5.00
(12) Purified water Remainder manufacturing method: The oil phase components of (1) to (6) are dissolved by heating, and the temperature is 80 ° C.
And On the other hand, a part of (7) to (9) and (12) is melted by heating to 80 ° C. After the above oil phase was added to this with stirring, a mixture of (10) dissolved in the rest of (12) and heated to 80 ° C. was added, and the mixture was uniformly emulsified with a homogenizer. After cooling to 30 ° C, (1
Add 1), mix and homogenize.

Example 8 Emulsion (1) Squalane 5.00 (% by weight) (2) Primula plant extract (Example 5) 5.00 (3) Methylphenylpolysiloxane 4.00 (4) Hydrogen Added palm kernel oil 0.50 (5) Polyoxyethylene sorbitan monostearate (20 EO) 1.30 (6) Sorbitan monostearate 1.00 (7) Glycerin
10.00 (8) Methyl paraoxybenzoate 0.10
(9) Carboxyvinyl polymer 0.15 (10) L
-Arginine 0.10 (12) Purified water Remainder manufacturing method: The oil phase components of (1) to (6) are dissolved by heating and the temperature is 80 ° C.
And On the other hand, (7) to (9) and (12) are heated and dissolved (aqueous phase A) and the rest of (10) and (12) are heated (aqueous phase B) to prepare 80 ° C. . Water phase A
Is added to the oil phase while stirring, and then the aqueous phase B is added,
After uniformly emulsifying with a homogenizer, it is cooled.

[Example 9] Peel-off type pack (1) Polyvinyl alcohol 10.00 (% by weight)
(2) Ethanol 2.00 (3) Purified water 50.00
(4) Polyethylene glycol 1500 1.50
(5) 1,3-Butylene glycol 5.00 (6) Methyl paraoxybenzoate 0.10 (7) Primula plant extract (Example 1) 0.20 (8) Polyoxyethylene hydrogenated castor oil (50E. O.) 0.20 (9) Ethanol 8.00 (10) Purified water Remainder method: (2) was added to (1) and moistened, and room temperature (3) was added, and the mixture was slowly stirred. While heating to 80 ° C. After confirming that (1) was uniformly dissolved, 50
Cool to ℃, add (4) and (5), and stir. (4)
After confirming the dissolution of, cool to 30 ° C and
The alcohol layer in which (6) to (8) is dissolved and (10) are sequentially added to the above and stirred uniformly.

[Example 10] Gel cosmetic (1) Dipropylene glycol 10.00 (% by weight)
(2) Carboxyvinyl polymer 0.50 (3) Potassium hydroxide 0.10 (4) Methyl paraoxybenzoate 0.10 (5) Primula plant extract (Example 4)
0.05 (6) Purified water Remainder manufacturing method: After uniformly dissolving (2) in (6), (4) and (5) were dissolved in (1) and added, and then (3) was added. Thicken.

[Example 11] Face wash (1) Myristic acid 24.00 (% by weight) (2) Stearic acid 12.00 (3) Lipophilic glyceryl monostearate 3.00 (4) Concentrated glycerin 15. 00
(5) Purified water 30.00 (6) Potassium hydroxide 7.
80 (7) Primula extract (Example 2) 3.
00 (8) Purified water Remainder production method: (1), (2), (3) and (4) are sequentially weighed in and heated to 80 ° C. To this, (5) in which (6) was dissolved and heated to 80 ° C. was slowly added with stirring. After stirring until homogeneous, cool to 45 ° C., add (7) and (8) and stir until homogeneous.

[Use Test] A use test was conducted using the external preparations for skin (Examples 6 to 10) containing the extracts of the plants of the genus Primula shown in Examples 1 to 5. at the same time,
Examples 1 to 5 compounded in Examples 6 to 10 were replaced with the following, respectively, and Comparative Examples 1 to 1 respectively.
5, the usage test was conducted in the same manner. Example 1 is purified water, Example 2 is 50% ethanol, and Example 3 is 50%.
1,3-butylene glycol was substituted for purified water in Example 4, and squalane was substituted for Example 5.

In the use test, a group of 20 female panelists aged 20 to 40 was used as a group, and an appropriate amount of the sample was applied to the face in the blind twice a day after washing the face when rising and immediately before going to bed. . Before and after the use test, the panelists evaluated the condition of the stratum corneum, the elasticity of the skin using a cutometer, and the fine wrinkles evaluated by the naked eye and photographs. In addition,
For the evaluation of the condition of the stratum corneum, the condition 30 days after the start of the use test, and 6 for the evaluation of skin elasticity and fine wrinkles
The condition after 0 days was evaluated in comparison with that before use. [Evaluation of state of stratum corneum] A commercially available cellophane tape is applied to the cheek of a subject in a state of having a small amount of oil after washing the face, and after holding for a while, it is peeled off and attached to a slide glass to which an adhesive is applied in advance. Then, this slide glass is immersed in xylene for 1 hour, the tape is gently peeled off, and then again immersed in xylene for 1 hour. Then, the slide glass is taken out, air-dried, and then immersed in a 1% gentian violet B aqueous solution for 10 minutes. Then, the slide glass is taken out, washed with water, dried and enclosed in balsam to obtain a horny layer sample.

The obtained keratinous specimens were visually observed using a microscope, and the keratinocyte shape, detachment density, and number of nucleated cells were scored according to the criteria shown in Tables 4 to 6, respectively. Regarding the multiplicity of exfoliation of the stratum corneum, the obtained image of the stratum corneum was loaded into a computer and scored as follows using image analysis software.

The area S of the portion occupied by the corneocytes captured as an image and the area S _n of the overlapping portion of the n horny layers are determined using image analysis software. Based on this value, the stratum corneum detachment multiplicity was calculated using the following formula (2), and the value of the obtained stratum corneum detachment multiplicity was scored according to the criteria shown in Table 7. Exfoliation multiplicity = Σn · S _n / S (2)

[0041]

[Table 4]

[0042]

[Table 5]

[0043]

[Table 6]

[0044]

[Table 7] Evaluation of detachment multiplicity of keratinocytes

Compared with the total value of the state score of the stratum corneum prepared before the test, the evaluation was made in three grades of "improved", "slightly improved" and "no change". The change in skin elasticity and fine wrinkle state was also evaluated in three grades of "improvement", "slight improvement" and "no change". The results are summarized in Table 8 below.

[0046]

[Table 8]

From the above results, it was revealed that the external preparation for skin containing the extract of the genus Primrose significantly improved the condition of the epidermis and the stratum corneum and had high anti-aging properties. Furthermore, during this use test period, Examples 6 to 10
The effect of continuous administration of the above on the skin was observed, but none of the groups using any of the examples complained of skin irritation such as pain and itch, or skin disorders such as allergic reaction.

Further, various abuse tests were tried in order to confirm the stability of the preparation, but no deterioration of the quality of the cosmetic such as sedimentation, separation and alteration of the blended components was observed.

[0049]

INDUSTRIAL APPLICABILITY The present invention can provide an antioxidant and a cell activator having excellent effects. Furthermore, by adding this to an external preparation, it is possible to deal with various skin troubles such as skin aging symptoms such as wrinkles and spots caused by external stress such as aging and ultraviolet rays, deterioration of skin elasticity and rough skin, and anti-aging. It is possible to provide a skin external preparation excellent in the effect and the effect of restoring epidermal homeostasis.

─────────────────────────────────────────────────── ───

[Procedure amendment]

[Submission date] January 29, 2003 (2003.1.2
9)

[Procedure Amendment 1]

[Document name to be amended] Statement

[Name of item to be amended] Title of invention

[Correction method] Change

[Correction content]

Title : Antioxidant, dermal fibroblast activator and
Epidermal cell activator

[Procedure Amendment 2]

[Document name to be amended] Statement

[Name of item to be amended] Claims

[Correction method] Change

[Correction content]

[Claims]

[Procedure 3]

[Document name to be amended] Statement

[Correction target item name] 0008

[Correction method] Change

[Correction content]

That is, the present invention is directed to
Anti-acid for skin excluding scalp, which contains the extract of Narcissus as an active ingredient
Agent, dermal fibroblast activator, epidermal cell activator
It is a thing.

─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. ⁷ Identification code FI theme code (reference) A61P 43/00 107 A61P 43/00 107 (72) Inventor Ritsuko Koshimizu 6-chome, Nakajima-cho, Minatojima, Chuo-ku, Hyogo Prefecture No. 1 Noevir Kobe Head Office, 13 (1) Inventor Akinori Hanano 6, No. 6, Minatojima Nakamachi, Chuo-ku, Kobe, Hyogo Prefecture No. 1 Noevir Kobe Head Office, F-term (reference) 4C083 AA111 AA112 AA122 AB032 AC022 AC072 AC102 AC122 AC242 AC422 AC432 AC442 AC482 AC582 AD042 AD092 AD112 AD152 AD572 BB51 CC02 CC04 CC05 CC07 CC23 DD22 DD23 DD27 DD31 DD41 EE12 4C088 AB12 AC01 BA08 BA09 BA10 CA03 MA63 NA14 ZA89 ZB22 ZC21

Claims (4)

[Claims] 1. A Primula genus ( Primu)
la L. ) An external anti-aging agent for skin containing a plant extract. 2. A primrose genus ( Primu)
la L. ) A skin external preparation for restoring epidermal homeostasis, which contains an extract of a plant. 3. A primrose genus ( Primu)
la L. ) An antioxidant containing a plant extract as an active ingredient. 4. A primrose genus ( Primu)
la L. ) A cell activator comprising a plant extract as an active ingredient.