KR20210066498A - Cosmetic composition for hair care with extraction of Stellaria media (L.) Vill. - Google Patents

Abstract

The present invention relates to a cosmetic composition for scalp and hair comprising an extract of Stellaria media (L.) Vill. containing polyamine. The cosmetic composition of the present invention exhibits anti-inflammatory, anti-allergic, moisturizing, hair damage inhibition or damaged hair recovery effects, and can be used as a hair care composition.

Description

Cosmetic composition for scalp and hair care comprising extract of star flower {Cosmetic composition for hair care with extraction of Stellaria media (L.) Vill.}

The present invention relates to a cosmetic composition for scalp and hair using an extract of Stellaria media (L.) Vill. containing polyamine.

The causes of hair damage can be divided into physiological, physical, chemical, and environmental factors, and in general, it has been reported that chemical treatments such as permanent wave or dyeing have a great influence. When a physical or chemical stimulus is applied to the hair, the anion group is exposed as the bond between the surface of the hair and the hair is broken, and the generated anions cause a repulsive force, which excites the cuticle layer.

In addition, as the number of chemical treatments increases, the number of times that the chemical components contained in hair products come into contact with the scalp also increase. Abnormal symptoms such as ringworm and atopic dermatitis appear.

Representative materials used in hair care products are mostly cationic lipids and polymers chemically synthesized with quaternary ammonium to facilitate adsorption to hair. As such, there is a limit to artificial synthesis in order to impart a cationic group to the material so far.

On the other hand, PPD (paraphenylenediamine), which is known as the main cause of allergic contact dermatitis caused by hair dyes, is used as a component of henna used in mascara and tattoos, and about 70% of countries using hair dyes It is used as the main ingredient in As PPD acts as a major antigen and causes side effects on the scalp, there is a need to simultaneously explore ways to secure the stability of ingredients and relieve irritation caused by chemical treatments.

Republic of Korea Patent No. 10-1553486 (September 2015) discloses a method for manufacturing a hair care composition. Korean Patent Application Laid-Open No. 10-2015-0109784 (2015.10.02) discloses a cosmetic composition for hair care containing a natural complex, a method for preparing the same, and a composition for hair care containing the same as an active ingredient.

The present invention is to develop and provide a novel cosmetic composition for scalp and hair care using natural materials as a kind of method for preventing the side effects of existing chemicals.

The present invention provides a cosmetic composition for scalp and hair comprising an extract of Starflower ( Stellaria media (L.) Vill.).

In the cosmetic composition for scalp and hair of the present invention, the extract of Starflower (( Stellaria media (L.) Vill.)) preferably contains polyamine.

The cosmetic composition for scalp and hair of the present invention preferably has anti-inflammatory, anti-allergic, moisturizing, hair damage suppression or damaged hair recovery effects.

The cosmetic composition for scalp and hair of the present invention may be, for example, hair shampoo, hair conditioner, hair pack, hair oil, hair treatment, and hair cream.

The cosmetic composition of the present invention can be used as a composition for hair care by exhibiting anti-inflammatory, anti-allergic, moisturizing, hair damage inhibition or damaged hair recovery effects.

1 is a result of qualitative and quantitative analysis of polyamine components using dansylation of a star flower extract.
2 is a cytotoxicity evaluation result of a star flower extract.
Figure 3 is a result of confirming the mRNA expression levels of TNF-alpha, IL-1a, IL-8 for the evaluation of the anti-inflammatory efficacy of the star flower extract.
4 is a result of evaluating the anti-allergic efficacy of the star flower extract.
5 is a result of evaluating the moisturizing effect of the star flower extract.
6 is a result of confirming the hair damage inhibitory effect of the star flower extract through microscopic observation.
7 is a result of confirming the hair damage inhibitory effect of the star flower extract through the methylene blue dyeing method.
8 is a result confirming the hair damage inhibitory effect of the star flower extract by measuring the degree of hair cuticle loss.
9 is a result of confirming the effect of recovering damaged hair of the star flower extract through microscopic observation.
10 is a result confirming the effect of recovering damaged hair of a star flower extract through methylene blue dyeing method.
11 is a result confirming the effect of recovering damaged hair of a star flower extract by measuring the degree of loss of hair cuticles.

Physiologically active substances of natural substances have various functions such as anticancer, anti-inflammatory, and anti-allergy, and they are recently used as raw materials for pharmaceuticals and cosmetics. Most of the raw materials for hair products are chemical raw materials, and as the trend of preference for natural cosmetics is spreading, the necessity of discovering natural materials in the future is increasing. Accordingly, the present invention provides a cosmetic composition for scalp and hair comprising an extract of Starflower (( Stellaria media (L.) Vill.)).

Starflower ( Stellaria media (L.) Vill.)) is a biennial weed that is commonly grown in fields and roadsides across the country, and is widely distributed around the world. The stem is branched a lot from the bottom, and it is 10-20cm long and the lower part is lying down. The leaves are opposite and egg-shaped. Flowers bloom in March-April on the end of a branch, and are white. The peduncle bends downward after the flower fades, and then rises again when the fruit ripens. There are 5 sepals. The petals are 5, deeply divided into two, and slightly shorter than the sepals. There are 1-7 stamens and 3 styles. The fruit is a capsule, divided into 6 parts. Fruits appear around August-September. Young plants use the herbs for medicinal purposes.

In the cosmetic composition for scalp and hair of the present invention, the extract of Starflower (( Stellaria media (L.) Vill.)) preferably contains polyamine.

Polyamine is an aliphatic hydrocarbon having two or more primary amino groups as a bioamine widely present in biological systems. There are more than 20 types of polyamines, but representative examples include diamines such as ptrecine, cataberine, triamines, spermidine, and tetraamines, spermine.

The physiological actions of polyamines include stabilization of nucleic acids, promotion of nucleic acid and protein synthesis, post-translational modification of proteins (acetylation, phosphorylation), activation of various enzymes, and stabilization of cell membranes. The polyamine synthesis system starts with the formation of prescine by decarboxylation of ortinine, followed by spermine and spermidine. Polyamine metabolism occurs by oxidation, acetylation, transaminotranslation, and carbamoylation.

The biodistribution is high in nucleic acid or protein-rich tissues such as the thymus, prostate, and pancreas, and low in heart and skeletal muscle. Also, the content changes according to physiological conditions. The metabolites are excreted as water-soluble polyamine derivatives in the urine. The following metabolites have been reported in urine. In particular, it is useful as a tumor marker because it is abundantly present in cancer tissues and also appears in blood or urine. Cancer, sarcoma, leukemia, multiple myeloma, malignant melanoma, pernicious anemia, hemolytic anemia, rheumatoid arthritis, alcoholic liver cirrhosis, psoriasis, and cystic fibrosis have.

On the other hand, in the cosmetic composition for preventing hair loss of the present invention, the star flower extract or polyamine may be contained in an amount of 0.001% to 30% by weight relative to the total weight of the composition, and more specifically, it may be contained in an amount of 0.01% to 10% by weight. . When the content of the star flower extract or polyamine is less than 0.001% by weight, the hair care effect (hair damage suppression or recovery of damaged hair) does not appear, and when it exceeds 30% by weight, the degree of increase in the hair care effect with respect to the content increase is insignificant And, there is a problem in the safety and stability of the formulation, and it is not economical.

The cosmetic composition for scalp and hair of the present invention preferably has anti-inflammatory, anti-allergic, moisturizing, hair damage suppression or damaged hair recovery effects, and the hair care effect of the star flower extract of the present invention was confirmed through the following experiment.

Meanwhile, the cosmetic composition for scalp and hair of the present invention may be, for example, hair shampoo, hair conditioner, hair pack, hair oil, hair treatment, and hair cream.

On the other hand, the components included in the cosmetic composition of the present invention may include components commonly used in cosmetic compositions in addition to the star flower extract or polyamine of the present invention as an active ingredient, for example, antioxidants, stabilizers, solubilizers, vitamins, pigments. and conventional adjuvants such as perfumes, and carriers.

The cosmetic composition of the present invention may be prepared in any formulation conventionally prepared in the art, for example, a solution, suspension, emulsion, paste, hair gel, hair cream, hair lotion, hair powder, soap, interface It may be formulated as an active agent-containing shampoo, a surfactant-free shampoo, hair oil, hair pack, hair essence, spray, and the like, but is not limited thereto.

When the formulation of the cosmetic composition of the present invention is a paste, cream or gel, animal oil, vegetable oil, wax, paraffin, starch, tracanth, cellulose derivative, polyethylene glycol, silicone, bentonite, silica, talc or zinc oxide, etc. This can be used.

When the formulation of the cosmetic composition of the present invention is a solution or emulsion, a solvent, solubilizer or emulsifier is used as a carrier component, for example, water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene fatty acid esters of glycol, 1,3-butylglycol oil, glycerol aliphatic esters, polyethylene glycol or sorbitan.

When the formulation of the cosmetic composition of the present invention is a suspension, as a carrier component, a liquid diluent such as water, ethanol or propylene glycol, ethoxylated isostearyl alcohol, a suspending agent such as polyoxyethylene sorbitol ester and polyoxyethylene sorbitan ester , microcrystalline cellulose, aluminum metahydroxide, bentonite, agar, or tracanth may be used.

When the formulation of the cosmetic composition of the present invention is a powder or a spray, lactose, talc, silica, aluminum hydroxide, calcium silicate or polyamide powder may be used as a carrier component, and in particular, in the case of a spray, additional chlorofluorohydro It may contain a propellant such as carbon, propane/butane or dimethyl ether.

When the formulation of the cosmetic composition of the present invention is a surfactant-containing shampoo, aliphatic alcohol sulfate, aliphatic alcohol ether sulfate, sulfosuccinic acid monoester, isethionate, imidazolinium derivative, methyl taurate, sarcosinate, Fatty acid amide ether sulfate, alkylamidobetaine, fatty alcohol, fatty acid glyceride, fatty acid diethanolamide, vegetable oil, lanolin derivative or ethoxylated glycerol fatty acid ester and the like can be used.

When the cosmetic composition of the present invention is a soap, surfactant-containing shampoo or surfactant-free shampoo formulation, it may be applied to the skin and then wiped off, removed, or washed off with water. As a specific example, the soap is liquid soap, powder soap, solid soap, and oil soap, but is not limited thereto.

Hereinafter, the configuration of the present invention will be described in detail through the following examples. However, the scope of the present invention is not limited only to the following examples, and includes modifications of technical ideas equivalent thereto.

[ Example 1: Preparation of star flower extract]

1. Preparation of star flower extract

The dried star flower was immersed in a solvent (70% ethanol) adjusted to pH 2 using hydrochloric acid, and stirred at room temperature for 3 hours. The extract obtained through this was filtered and concentrated under reduced pressure to prepare a star flower extract.

2. Analysis of polyamine components

end) single room reaction( dansylation ) polyamine component qualitative analysis (TLC) using

Standards Putrescine, spermidine, and spermine were dissolved and used as a standard solution. The standard solution and the star flower extract were mixed with dansyl chloride and pre-treated for one hour at 60° C. in dark conditions, and then poline was treated to remove unreacted dansyl chloride. After the reaction was completed, the sample was developed with a developing solvent and confirmed at UV 330 nm.

I) single room reaction( dansylation ) for quantitative analysis of polyamine components ( Flourometer )

After determining the significance of the fluorescence intensity for each concentration of the standard solution subjected to the dansylation pretreatment, the polyamine content of the candidate extract was analyzed (FIG. 1). 1 is a result of qualitative and quantitative analysis of polyamine components using dansylation of a star flower extract.

As a result of the experiment, it was confirmed that the polyamine content was 1,200.86 ppm in the star flower extract extracted with 70% ethanol, the pH was adjusted using hydrochloric acid (HCl) as a solvent.

[ Experimental example 1: Cytotoxicity evaluation]

The skin keratinocytes were inoculated into a 96-well plate at the ^{number of 1×10 5} cells, and then cultured at 37° C., 5% CO _{2 in an} incubator for 24 hours. Using a serum-free medium, samples diluted to an appropriate concentration were treated at 100 μl per well and cultured for 24 hours. After incubation for 24 hours, 20 μl of MTT reagent dissolved at a concentration of 5 mg/ml was added and incubated at 37° C. for 2 hours. Thereafter, all of the medium containing the MTT reagent and the sample was removed, isopropanol was added to each well, stirred for 30 minutes, and the absorbance value was measured at 570 nm using an ELISA reader, and then cell viability ) was confirmed (FIG. 2). 2 is a cytotoxicity evaluation result of a star flower extract.

As a result of the experiment, it was confirmed that the star flower extract did not significantly affect the cell viability.

[ Experimental example 2: anti-inflammatory and anti-allergy Efficacy evaluation]

1. real-time polymerase chain reaction (RT-) PCR ) to evaluate anti-inflammatory efficacy

^{The skin keratinocytes were inoculated in a 6} -well plate at a number of 2×10 6 cells, and then cultured for 24 hours. Thereafter, a sample diluted to an appropriate concentration in a serum-free medium was treated with the cultured cell line for 24 hours. Then, after the medium was completely removed, RNA was isolated using TriZol, and cDNA was synthesized to confirm the expression level of the inflammatory mediator.

When the MTT assay was performed to confirm the cytotoxicity of the embryonic extract, as shown in FIG. 2 , the cytotoxicity of the star flower extract was not at a significant level, but cytotoxicity was observed at 1000ppm of spermidine. (Fig. 3). 3 is a result of confirming the mRNA expression levels of TNF-alpha, IL-1a, IL-8 for the evaluation of the anti-inflammatory efficacy of the star flower extract.

To confirm the anti-inflammatory effect, the mRNA expression levels of TNF-alpha, IL-1a, and IL-8, which are known as representative anti-inflammatory molecules, were checked, and as a result, TNF-alpha, IL-1a, and It was confirmed that the IL-8 mRNA expression level decreased in a concentration-dependent manner.

2. anti-allergy Efficacy evaluation

RBL-2H3 cells were inoculated in a 24-well plate at a ^{number of 2×10 5} cells, and then cultured for 24 hours. After washing twice with Siraganian buffer, 1 ml of Siraganian buffer was added, and incubated at 37°C for 10 minutes. After 10 minutes, the prepared samples were incubated at 37° C. for 1 hour after treatment. After treatment with DNP-HSA at a concentration of 10 μg/ml, incubator at 37° C. for 1 hour, and then left on ice for 10 minutes to terminate the reaction. After putting the same amount (50 ul) of the supernatant and the substrate buffer, incubated for 1 hour at 37 ℃. After stopping the reaction by adding 200 μl of stop buffer, absorbance was measured. (Fig. 4). 4 is a result of evaluating the anti-allergic efficacy of the star flower extract.

As a result of performing the anti-allergic efficacy test by measuring the amount of beta-hexosaminidase secreted out of the cell, the anti-allergic efficacy was confirmed by the positive control group, and allergy to 50 and 100 µg/ml of Starflower extract It was confirmed that the alleviation effect appeared.

[ Experimental example 3: Evaluation of moisturizing effect]

In order to check the amount of hyaluronan secreted into the medium by promoting the synthesis by the star flower extract, the skin keratinocytes ^{were inoculated into a 24-well plate at the number of 1×10 6} cells and cultured for 24 hours. After culturing, a sample of an appropriate concentration was prepared using a serum-free medium and cultured in the cultured cells for 24 hours. Then, the culture medium was taken and the expression level of hyaluronan was confirmed using the Hyaluronan Quantikine ELISA kit (FIG. 5). 5 is a result of evaluating the moisturizing effect of the star flower extract.

As a result of the experiment, the synthesis of hyaluronan, which had been reduced by UVB, was increased in a concentration-dependent manner by the star flower extract.

[ Experimental example 4: Evaluation of hair damage inhibition efficacy]

1. Create damaged hair ( SEM )

In order to confirm the recovery efficacy of the star flower extract for damaged hair due to discoloration, this experiment was conducted in the same manner as using the existing OLPLEX, and the star flower extract of Example 1 and positive controls spermidine (SM), CETAB And the competitor product OLAPLEX's sample was mixed with a bleaching agent to evaluate the cuticle lifting effect. For this, the first agent (ammonium persulfate) and the second agent (35% hydrogen peroxide) of the bleaching agent (Sehwa Corporation) were mixed in a ratio of 1:3, and spermidine (SM), the star flower extract of Example 1, CETAB and OLAPLEX's samples were added for each concentration and mixed. 1.5 g of the mixed bleaching agent was applied to 1.5 g of virgin hair and bleached at room temperature for 30 minutes. Then, it was washed thoroughly with a weak acid shampoo and dried in a dry oven at 40° C. for 2 hours. After repeating this process twice, the degree of lifting of the cuticle was confirmed through a microscope (FIG. 6). 6 is a result of confirming the hair damage inhibitory effect of the star flower extract through microscopic observation.

As a result of the experiment, it was confirmed that the star flower extract had the effect of inhibiting hair damage in a concentration-dependent manner, and it was confirmed that the effect of inhibiting hair damage was superior compared to the samples of CETAB and OLAPLEX, a competitor product, used as a positive control.

2. Measurement of hair damage by methylene blue dyeing

6 strands of 3 cm of sample hair were immersed in an Eppendrof tube containing 1 ml of 1% methylene blue (methylene blue in DW), and then the sample hair was dyed in a dry oven at 50° C. for 30 minutes. After that, the hair was collected and excess methylene blue (MB) was removed with a paper towel, and 'ethanol : glacial acetic acid : water = 49% : 1% : 50%' to extract the methylene blue solution adsorbed to the damaged area. 1 ㎖ of NR desorv solution made with NR was re-extracted for 20 minutes. The absorbance of the re-extracted solution was measured at 600 nm using ELISA (FIG. 7). 7 is a result of confirming the hair damage inhibitory effect of the star flower extract through the methylene blue dyeing method.

This experiment is a method to measure the degree of damage by re-extracting the MB solution absorbed in the damaged hair tissue after MB dyeing. As a result of the experiment, when the star flower extract was treated, the absorption rate of the methylene blue solution was very low in a concentration-dependent manner. could check In addition, it was confirmed that the methylene blue solution absorption capacity was very low compared to the samples of CETAB and OLAPLEX, a competitor product, used as a positive control.

3. Hair of the cuticle dropout measurement

30 mg of hair sample and 1.5 ml of purified water were placed in an e-tube and sonicated for 3 hours. Then, after removing the hair, centrifugation was performed at 1,2000 rpm for 15 minutes. Thereafter, a reducing buffer (3M Urea, 1M NaOH, 0.06% CHAPS) was added to dissolve the pellet remaining after removing the supernatant and sonicated until dissolved. Thereafter, the degree of cuticle loss was measured through BCA quantification ( FIG. 8 ). 8 is a result confirming the hair damage inhibiting effect of the star flower extract by measuring the degree of hair cuticle loss.

As a result of the experiment, it was confirmed that the hair treated with the star flower extract had a higher level of relief from cuticle lift than the hair treated with OLAPLEX, a competitor's product.

[ Experimental example 5: Evaluation of damaged hair recovery efficacy]

1. Construction of hair damage suppression model

Virgin hair was bleached for 30 minutes with 4.5% hydrogen peroxide adjusted to a pH of about 10. Then, it was washed with a weak acid shampoo and dried in a dry oven at 40° C. for 2 hours. This operation was repeated three times to produce damaged hair. After that, the weakly acidic shampoo/hair lotion containing the sample (the star flower extract of Example 1 and the positive control CETAB and the competitor OLAPLEX sample) was alternately treated 5 times, and the degree of lifting of the cuticle was checked under a microscope ( Fig. 9). 9 is a result of confirming the effect of recovering damaged hair of the star flower extract through microscopic observation.

As a result of the experiment, it was confirmed that the milbea extract had the effect of restoring damaged hair in a concentration-dependent manner, and it was confirmed that the effect of restoring damaged hair was superior compared to the samples of CETAB and OLAPLEX, a competitor product, used as a positive control.

The compositions of the weakly acidic shampoo and hair lotion used to construct the damage suppression model are shown in Tables 1 and 2, respectively.

Weak Acid Shampoo Base (10%) phase ingredient % 1_1 water 51.1 cocamidopropyl betaine 15 glucamate 0.2 1_2 sodium benzoate 0.3 citric acid 0.2 2 SLES 15 Decyl glucoside 8 3 phemocy ethamol 0.2 4 sample 10 Total 100

Hair Lotion (10%) phase ingredient % A water 43.03 1,3-BG 2.00 phenoxy ethanol 0.50 sodium chloride 0.20 EDTA-2Na 0.05 citric acid 0.02 B water 24.75 natrosol 250HR 0.25 C MS-165 2.00 cetearyl alcohol 2.00 LP 10.00 GTCC 5.00 DC556 0.20 D sample 10.00 Total 100.00

2. Measurement of hair damage by methylene blue dyeing

6 strands of 3 cm of sample hair were immersed in an Eppendrof tube containing 1 ml of 1% methylene blue (methylene blue in DW), and then the sample hair was dyed in a dry oven at 50° C. for 30 minutes. After that, the hair was collected and excess methylene blue (MB) was removed with a paper towel, and 'ethanol : glacial acetic acid : water = 49% : 1% : 50%' to extract the methylene blue solution adsorbed to the damaged area. 1 ㎖ of NR desorv solution made with NR was re-extracted for 20 minutes. The absorbance of the re-extracted solution was measured at 600 nm using ELISA (FIG. 10). 10 is a result of confirming the effect of recovering damaged hair of a star flower extract through methylene blue dyeing method.

As a result of the experiment, it was confirmed that the absorption capacity of the methylene blue solution was similar to that of OLAPLEX, a competitive product.

3. Hair of the cuticle dropout measurement

30 mg of hair sample and 1.5 ml of purified water were placed in an e-tube and sonicated for 3 hours. Then, after removing the hair, centrifugation was performed at 1,2000 rpm for 15 minutes. Thereafter, a reducing buffer (3M Urea, 1M NaOH, 0.06% CHAPS) was added to dissolve the pellet remaining after removing the supernatant and sonicated until dissolved. Thereafter, the degree of cuticle loss was measured through BCA quantification ( FIG. 11 ). 11 is a result confirming the effect of recovering damaged hair of a star flower extract by measuring the degree of loss of hair cuticles.

As a result of the experiment, when the shampoo/lotion containing Starflower extract was treated on damaged hair, the shampoo/lotion treatment containing OLPALEX, a competitor product, had similar effects on hair damage and cuticle lifting.

[ Formulation example One: Example Contains 1, Starflower extract hair care manufacture of products]

A formulation was prepared with butylene glycol 50% (w/v), distilled water 49.95% (v/v), and 0.05% (w/v) dry cup of the star flower extract of Example 1.

Protein content was measured using the Pierce BCA Protein Assay Kit (Table 3). Protein can exhibit an alleviating effect on damaged hair, and when checking the protein concentration for the developed formulation containing the star flower extract, it was measured to be 425.536 μg/ml.

Name concentration (μg/ml) C.V. Stellaria ethanol extract 425.536 11.019

[ Experimental example 6: Formulation example 1 Stability evaluation]

1. Microbial testing

After dispensing 1 ml of Formulation Example 1 in the medium (TSA, SDA), plated so as to be impregnated in the medium, and then cultured in an incubator at 35°C. Bacteria were observed for 48 hours/fungi were observed for 120 hours and confirmed every 24 hours to confirm the growth of bacteria (Table 4). Upon microbial testing of the formulation, no bacteria and fungi were detected.

No. Microorganism-Bacteria (48 hours) Microorganism-Fungi (120 hours) 35℃(incobator) Stellaria ethanol extract Non detected Non detected

2. Stability test

A) pH stability test

Put 3 ml of Formulation Example 1 diluted to 5% in distilled water in a 151 ml Falcon tube, and adjust the pH to pH 2, 4, 6, 8, 10 using 0.1 M NaOH and 0.1 M HCl to obtain color, precipitation, and turbidity The presence or absence was checked. In order to confirm the stability of the prepared formulation according to various pH conditions, using purified water, 1%, 3%, and 5% diluted Formulation Example 1 was changed to 1M HCl, 1M NaOH, and the pH was changed to observe the change in properties (Table 5) .

As a result of the experiment, there was no change in turbidity or sedimentation, but a change in color can be confirmed. Under basic conditions (> pH8), it was confirmed that the color of the sample diluted with light yellow color became slightly darker, which was easier to confirm as the dilution concentration increased.

dilution concentration pH 2 4 6 8 10 One% + + + ± ± 2% + + + ± ± 3% + + + ± ±

* +: stable, ±: slightly unstable, -: unstable

b) Ethanol stability test

Ethanol is diluted in distilled water so that it becomes 10%, 30%, 50%, 70%, and 90%, and Formulation Example 1 is added to Ethanol so that the final dilution concentration of Formulation Example 1 is 5% for each concentration of color, precipitation, and turbidity. The presence or absence was confirmed (Table 6).

As a result of the experiment, there was no color change or precipitate formation.

dilution concentration Ethanol concentration (%) 0 (DW) 10 30 50 70 90 One% + + + + + ± 2% + + + + + ± 3% + + + + + ±

* +: stable, ±: slightly unstable, -: unstable

C) Temperature stability (high temperature stability test)

In order to confirm the stability at high temperature of the prepared Formulation Example 1, the formulation was diluted to 1%, 3%, 5% with purified water, and then in an oven at 40°C, 60°C, 80°C for a total of 2 hours (120 minutes). It was left and checked for color change, turbidity change, and precipitation at 30-minute intervals (Table 7).

As a result of the experiment, the turbidity and precipitation state did not change, but when the 3% and 5% solutions were left at 60° C. for 120 minutes, it was confirmed that the color became slightly darker than the control. This phenomenon was also observed in the sample left at 80° C. for 60 minutes. It is considered that the color of the yellow component in the natural extract is denatured by heat.

temperature/time 40℃ 60℃ 80℃ dilution concentration 30 minutes 60 minutes 90 minutes 120 minutes 30 minutes 60 minutes 90 minutes 120 minutes 30 minutes 60 minutes 90 minutes 120 minutes One% + + + + + + + + + + + ± 3% + + + + + + + ± + ± ± ± 5% + + + + + + ± ± + ± ± ±

* +: stable, ±: slightly unstable, -: unstable

D) Temperature stability (Stability test under freeze-thaw cross condition)

In order to check the stability under the freezing/thaw conditions, which are the storage conditions of the prepared Formulation Example 1, the prepared formulation stock solution is cross-stored at -20°C and room temperature (25-30°C), and color change, turbidity change, and presence or absence of precipitate formation was confirmed (Table 8).

Cross storage was performed a total of 3 times, and it was confirmed that there was no change in color change, turbidity change, and precipitation formation under all storage conditions.

Storage conditions and number of storage number of times Primary Secondary tertiary Frozen (-20℃) + + + Thaw (room temperature) + + +

* +: stable, ±: slightly unstable, -: unstable

hemp) change in appearance Confirm

The prepared Formulation Example 1 was stored at room temperature for a total of 1 month, and color change, turbidity change, and presence or absence of precipitation were checked. At the time of storage, the temperature was maintained at 25-30°C (Table 9). As a result of observation for one month, it was confirmed that there was no change in color change, turbidity change, and presence or absence of precipitation.

Storage conditions term 0 weeks 1 week 2 weeks 3 weeks 4 weeks room temperature + + + + +

* +: stable, ±: slightly unstable, -: unstable

3. Skin Stability Assessment

To evaluate the safety of skin in humans, skin irritation was confirmed in 5 healthy adults. The Finn chamber patch was applied for 24 hours, and skin irritation was checked after 1 hour and 24 hours after removal of the patch (Table 10). As a result of the test, no irritation was observed in most of the test subjects.

extract test subject Judgment result stimulus degree One% 2% 3% 1 hours 24 hours 1 hours 24 hours 1 hours 24 hours star flower extract One - - - - - - 0 2 - - - - - - 0 3 - - - - - - 0 4 - - - - - - 0 5 - - - - - - 0

Claims (4)

Star flower (( Stellaria media (L.) Vill.)) cosmetic composition for scalp and hair comprising an extract.
According to claim 1,
The star flower (( Stellaria media (L.) Vill.)) extract,
A cosmetic composition for scalp and hair, characterized in that it contains polyamine.
According to claim 1,
The cosmetic composition for the scalp and hair,
A cosmetic composition for scalp and hair, characterized in that it has anti-inflammatory, anti-allergic, moisturizing, hair damage inhibition or damaged hair recovery effects.
According to claim 1,
The cosmetic composition,
A cosmetic composition for scalp and hair, characterized in that it is a hair shampoo, hair conditioner, hair pack, hair oil, hair treatment, and hair cream.

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