COSMETIC COMPOSITION COMPRISING DEAD LACTIC ACID BACTERIA LACTOBACILLUS PLANTARUM MASS OR CULTURE OF LACTIC ACID BACTERIA FOR PREVENTING OR ALLEVIATING SKIN AGING

Abstract

The present invention relates to a cosmetic composition for preventing or improving aging that comprises a culture of one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798) isolated from Kimchi and Lactobacillus plantarum Wikim 126 (Access No. BP1910799) and the Lactobacillus plantarum Wikim 127 (Access No. BP1910800) that are isolated from Sauerkraut and may further comprise a dead cell of one or more lactic acid bacteria selected from the group. The cosmetic composition for preventing or improving aging of the present invention can promote skin aging improvement effects through antioxidation, inflammation relief, moisturizing enhancement, skin tone improvement, elasticity and wrinkle improvement, by using natural derived lactic acid bacteria that are skin-friendly, safe, and capable of improving skin functions and cultures using these lactic acid bacteria.

Claims

1. A cosmetic composition for preventing or improving skin aging that prevents or improves skin aging through antioxidation, anti-inflammation, moisturizing enhancement, wrinkle improvement and skin tone lightening, comprising: a culture of one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798), Lactobacillus plantarum Wikim 126 (Access No. BP1910799), and Lactobacillus plantarum Wikim 127 (Access No. BP1910800).

2. The cosmetic composition of claim 1, further comprising a dead cell of one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798), Lactobacillus plantarum Wikim 126 (Access No. BP1910799), and Lactobacillus plantarum Wikim 127 (Access No. BP1910800).

3. The cosmetic composition of claim 1, wherein the Lactobacillus plantarum Wikim 125 (Access No. BP1910798) is isolated from Kimchi.

4. The cosmetic composition of claim 1, wherein the Lactobacillus plantarum Wikim 126 (Access No. BP1910799) and the Lactobacillus plantarum Wikim 127 (Access No. BP1910800) are isolated from Sauerkraut manufactured from cabbage or brussels sprout.

5. The cosmetic composition of claim 1, wherein the culture of the lactic acid bacteria is formed by lyophilizing supernatant obtained by culturing the lactic acid bacteria in a lactic acid bacteria culture medium and performing centrifugation.

6. The cosmetic composition of claim 2, wherein the dead cells of the lactic acid bacteria are obtained by culturing the lactic acid bacteria in a lactic acid bacteria culture medium, performing centrifugation, and then heat-treating precipitated cells of the lactic acid bacteria.

7. The cosmetic composition of claim 2, wherein the Lactobacillus plantarum Wikim 125 (Access No. BP1910798) is isolated from Kimchi.

8. The cosmetic composition of claim 2, wherein the Lactobacillus plantarum Wikim 126 (Access No. BP1910799) and the Lactobacillus plantarum Wikim 127 (Access No. BP1910800) are isolated from Sauerkraut manufactured from cabbage or brussels sprout.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1a shows a confirmation result of cytotoxicity in Hs68 cells for a composition of Example 7 of the present invention, and FIG. 1b shows a confirmation result of an MMP expression inhibitory ability.

[0018] FIG. 2a shows a measurement result of cytotoxicity, cell viability, in B16F10 cells for a composition of Example 7 of the present invention, and FIG. 2b shows an amount of melanin production, melanin content, in B16F10 cells.

[0019] FIG. 3a shows a confirmation result of cytotoxicity, cell viability, in HaCaT cells for the composition of Example 7 of the present invention, and FIG. 3b shows an HAS-2 expression degree in HaCaT cells.

[0020] FIG. 4a shows a confirmation result of cytotoxicity, cell viability, in RAW 264.7 cells for a composition of Example 7 of the present invention, FIG. 4b shows a NO production inhibitory ability in RAW 264.7 cells, and FIG. 4c shows a confirmation result of an iNOS expression inhibitory activity.

[0021] FIG. 5 shows an evaluation result of skin moisturizing degree of cream cosmetics according to Example 21 of the present invention and Comparative Example 5.

BEST MODE FOR THE INVENTION

[0022] The present invention relates to a cosmetic composition for preventing or improving skin aging that comprises cultures of one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798), Lactobacillus plantarum Wikim 126 (Access No. BP1910799), and Lactobacillus plantarum Wikim 127 (Access No. BP1910800).

Modes for the Invention

[0023] In the present invention, the Lactobacillus plantarum Wikim 125 (Access No. BP1910798) may be isolated from Kimchi, and the Lactobacillus plantarum Wikim 126 (Access No. BP1910799) and the Lactobacillus plantarum Wikim 127 (Access No. BP1910800) may be isolated from Sauerkraut, for example, Sauerkraut manufactured from cabbage or brussels sprout.

[0024] In the present invention, the cultures of the lactic acid bacteria may be formed by lyophilizing supernatant obtained by culturing one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798), Lactobacillus plantarum Wikim 126 (Access No. BP1910799), and Lactobacillus plantarum Wikim 127 (Access No. BP1910800) in a lactic acid bacteria culture medium such as MRS agar medium and performing centrifugation.

[0025] The cosmetic composition for preventing or improving skin aging may further comprise dead cells of one or more lactic acid bacteria selected from a group consisting of Lactobacillus plantarum Wikim 125 (Access No. BP1910798), Lactobacillus plantarum Wikim 126 (Access No. BP1910799), and Lactobacillus plantarum Wikim 127 (Access No. BP1910800).

[0026] In the present invention, the dead cells of the lactic acid bacteria may be obtained by a method known in the field of the present invention, for example, by culturing the lactic acid bacteria a lactic acid bacteria culture medium such as MRS agar medium, performing centrifugation, and then heat-treating precipitated cells of the lactic acid bacteria.

[0027] The cosmetic composition for preventing or improving skin aging according to the present invention may further comprises additional ingredients commonly used in cosmetic compositions, including at least one component selected from a group consisting of a pH adjuster, surfactant, oil, fat, alcohol, humectant, sterilization preservative, a chelating agent, fragrance, pigment, a UV absorber, a UV scattering agent, and an antioxidant agent, if necessary but is not limited thereto. Specific types and amounts of these additional ingredients are well known in the field of the present invention.

[0028] The formulation of the cosmetic composition for preventing or improving skin aging according to the present invention is not limited to a particular form. For example, the formulation of the cosmetic composition of the present invention may be provided in a form of flexible lotion, astringent lotion, nourishing lotion, eye cream, nourishing cream, massage cream, cleansing cream, cleansing foam, cleansing water, powder, ampoule, essence, BB cream, sun cream, a pack, lip balm, or the like. In addition, each formulation of the cosmetic composition for preventing or improving skin aging according to the present invention is not particularly limited thereto and may be selected and mixed by a person skilled in the art without difficulties according to purposes of the compositions.

EXAMPLES

[0029] Hereinafter, the present invention will be described in more detail with reference to Examples. However, the following examples are only for illustrating the present invention, and the present invention is not limited to scopes of these examples.

Preparation Example 1: Preparation of Dead Cells of Lactic Acid Bacteria

[0030] Dead cells of Lactic acid bacteria were obtained by culturing Lactobacillus plantarum Wikim 125 isolated from kimchi (Access No.: BP1910798), Lactobacillus plantarum Wikim 126 isolated from sauerkraut prepared from brussels sprouts from Jeju, Korea (Access No.: BP1910799), Lactobacillus plantarum Wikim 127 (Access No.: BP1910800) isolated from sauerkraut prepared from cabbage from Jeju, Korea, for 24 hours at 30° C. in MRS agar medium, performing centrifugation, and then heat-treating the precipitated cells at 80° C. for 60 minutes.

TABLE-US-00001 TABLE 1 Example of production of lactic acid bacteria dead cells Example Lactobacillus Culture Example 1 (Dead Cell 1) Dead cells of Lactobacillus plantarum Wikim 125 (Access No.: BP1910798) Example 2 (Dead Cell 2) Dead cells of Lactobacillus plantarum Wikim 126 (Access No.: BP1910799), Example 3 (Dead Cell 3) Dead cells of Lactobacillus plantarum Wikim 127 (Access No.: BP1910800)

Preparation Example 2: Preparation of Cultures of Lactic Acid Bacteria

[0031] Cultures of Lactic acid bacteria dead cells were obtained by lyophilizing supernatant obtained by culturing Lactobacillus plantarum Wikim 125 isolated from kimchi (Access No.: BP1910798), Lactobacillus plantarum Wikim 126 isolated from sauerkraut prepared from brussels sprouts from Jeju, Korea (Access No.: BP1910799), Lactobacillus plantarum Wikim 127 (Access No.: BP1910800) isolated from sauerkraut prepared from cabbage from Jeju, Korea, for 24 hours at 30° C. in MRS agar medium and performing centrifugation.

TABLE-US-00002 TABLE 2 Example of production of lactic acid bacteria dead cells Example Lactobacillus Culture Example 4 (Culture 4) Cultures of Lactobacillus plantarum Wikim 125 (Access No.: BP1910798) Example 5 (Culture 5) Cultures of Lactobacillus plantarum Wikim 126 (Access No.: BP1910799), Example 6 (Culture 6) Cultures of Lactobacillus plantarum Wikim 127 (Access No.: BP1910800)

Preparation Example 3: Preparation of Mixed Composition of Dead Cells and Cultures of Lactic Acid Bacteria

[0032] The mixed composition was prepared by mixing the dead cells and the cultures of the lactic acid bacteria prepared in Preparation Examples 1 and 2 in a composition ratio, weight ratio, shown in Table 3 below.

TABLE-US-00003 TABLE 3 Composition Ratio of Mixed Compositions Example Example Example Example Example Example Example Example Example Example Example Composition 7 8 9 10 11 12 13 14 15 16 17 Dead Cell 1 20.0 25.0 50.0 20.0 40.0 25.0 75.0 67.0 50.0 60.0 0.0 Dead Cell 2 60.0 70.0 25.0 20.0 20.0 75.0 0.0 0.0 0.0 0.0 33.0 Dead Cell 3 10.0 5.0 25.0 40.0 60.0 0.0 25.0 33.0 50.0 40.0 67.0 Culture 4 4.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 Culture 5 50.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 Culture6 1.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 Total 100.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0

Experimental Example 1: Evaluation of In Vitro Efficacy

[0033] In order to verify overall effectiveness of skin aging improvement for each of the lactic acid bacteria dead cells, lactic acid bacteria cultures, and the mixed composition of the lactic acid bacteria dead cells and cultures prepared in Preparation Examples 1 to 3, Antioxidation (active oxygen (ABTs) scavenging ability), anti-inflammation (NO inhibition), anti-inflammation and moisturizing enhancement (hyaluronidase inhibition), lightening (tyrosinase inhibition), and elasticity improvement (collagenase inhibition) were evaluated. In the case of Examples 1 and 2, the evaluation result was excellent in all the evaluation criteria and accordingly, it was confirmed that the compositions are useful for improving skin aging. The experimental procedures and evaluation results are as follows.

Experimental Example 1-1: Evaluation of Antioxidant Effect (Active Oxygen (ABTs) Scavenging Ability

[0034] The ABTS+[2,2′-Azino-bis(3-ethyl benzothiazoline-6-sulfonic acid)] radical scavenging activity, which is part of measurement of an antioxidant activity, can measure both hydrogen-donating antioxidants and chain breaking antioxidants, and it is a measurement method applicable to both aqueous phase and organic phase.

[0035] In the present invention, an ABTS radical solution formed by mixing 2.45 mM potassium persulfate in a 7 mM ABTS solution at a ratio of 1:1 (v/v) to be reacted in a dark room for about 24 hours, was mixed with the sample and heated for 10 minutes in a dark room, and then, absorbance was measured at 734 nm. The ABTS radical scavenging ability (%) was calculated using the following formula and shown in [Table 4].

ABTs Radical Scavenging Ability (%)=(Absorbance of Test Group/Absorbance of Untreated Group)×100

TABLE-US-00004 TABLE 4 Antioxidant Effect (Active Oxygen (ABTs) Scavenging Ability) Evaluation Result Test Active Oxygen (ABTs) Sample Concentration Scavenging Ability (%) Example 1 50 mg/mL 98.69 Example 2 50 mg/mL 99.42 Example 3 50 mg/mL 97.08 Example 4 1 mg/mL 36.37 Example 5 1 mg/mL 52.02 Example 6 1 mg/mL 41.05 Example 7 1 mg/mL 55.29 Example 8 1 mg/mL 51.00 Example 9 1 mg/mL 42.53 Example 10 1 mg/mL 45.68 Example 12 1 mg/mL 47.81 Example 13 1 mg/mL 39.30

[0036] In addition, a minimum inhibitory concentration (IC 50, mg/ml) that inhibits the activity of ABTS radicals by 50% was evaluated for Examples 4 to 6 (Cultures 1 to 3). As shown in [Table 5] to [Table 7], the ABTS radical scavenging effect was excellent even at low concentrations of 1.47 mg/ml, 0.96 mg/ml, and 1.35 mg/ml in Examples 4 to 6, respectively.

TABLE-US-00005 TABLE 5 Evaluation Result of Antioxidant Effect by Concentration of Culture 1 Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.56 0.561 0.556 0.553 — — treated Group Exam- 0.1 0.536 0.531 0.537 0.535 0.58 4.35 ple 4 0.2 0.532 0.527 0.525 0.528 0.65 5.55 0.4 0.494 0.492 0.493 0.493 0.18 11.81 0.6 0.458 0.454 0.452 0.454 0.72 18.78 1.0 0.358 0.358 0.351 0.356 0.72 36.37 2.0 0.198 0.195 0.138 0.194 0.92 65.35 5.0 0.012 0.011 0.019 0.014 0.78 97.5

TABLE-US-00006 TABLE 6 Evaluation Result of Antioxidant Effect by Concentration of Culture 2 Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.608 0.609 0.611 0.609 — — treated Group Exam- 0.1 0.575 0.578 0.577 0.577 0.25 5.36 ple 5 0.2 0.561 0.554 0.555 0.557 0.62 8.64 0.4 0.505 0.513 0.502 0.507 0.93 16.85 0.6 0.459 0.455 0.451 0.455 0.66 25.33 1 0.289 0.298 0.29 0.292 0.81 52.02 2 0.217 0.184 0.195 0.199 2.76 67.4 5 0.002 0.003 0.004 0.003 0.34 99.62

TABLE-US-00007 TABLE 7 Evaluation Result of Antioxidant Effect by Concentration of Culture 3 Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.595 0.595 0.593 0.594 — — treated Group Exam- 0.1 0.571 0.567 0.563 0.567 0.67 4.6 ple 5 0.2 0.547 0.544 0.543 0.545 0.35 8.36 0.4 0.494 0.497 0.498 0.496 0.35 16.49 0.6 0.445 0.453 0.443 0.447 0.89 24.79 1 0.357 0.344 0.35 0.35 1.09 41.05 2 0.208 0.195 0.195 0.199 1.26 66.46 5 0.018 0.01 0.009 0.012 0.73 98.82

Experimental Example 1-2: Evaluation of Anti-Inflammatory Effect (No Inhibitory Ability)

[0037] When mammals receive an inflammatory stimulus, they synthesize NO (nitric oxide) by macrophages, which is a neurotransmitter that dilates blood vessels and suppresses inflammation.

[0038] Therefore, in order to check an effect of inhibiting NO radicals, the sample was mixed with 10 mM sodium nitroferricyanide dihydrate and reacted at 25° C. for 150 minutes. After aliquoting 0.5 mL each, 1 mL of 1% sulfanylamine was added, and the mixture reacted at room temperature for 10 minutes. After the reaction, 2 mL of 0.1% N-(1-naphthyl) ethylenediamine dihydrochloride was mixed, and the mixture was reacted at room temperature for 30 minutes. Then, absorbance was measured at 540 nm. A NO radical scavenging ability (%) was calculated using the following formula, and the results are shown in [Table 8].

NO Radical Scavenging Ability (%)=(Absorbance of Test Group/Absorbance of Untreated Group)×100

TABLE-US-00008 TABLE 8 Evaluation result of anti-inflammatory effect (inhibition rate of NO production) Test Inhibition rate of Sample Concentration NO production (%) Example 1 50 mg/mL 44.59 Example 2 50 mg/mL 32.09 Example 3 50 mg/mL 80.22 Example 4 1 mg/mL 53.01 Example 5 1 mg/mL 30.24 Example 6 1 mg/mL 43.58 Example 7 1 mg/mL 74.18 Example 8 1 mg/mL 59.85 Example 9 1 mg/mL 53.44 Example 14 1 mg/mL 54.35 Example 15 1 mg/mL 59.33 Example 16 1 mg/mL 66.67

[0039] In addition, the minimum inhibitory concentration (IC 50, mg/ml) that inhibits the activity of NO radicals by 50% for Examples 4 to 6 (Cultures 1 to 3) was evaluated. As shown in [Table 9] to [Table 11], NO radical scavenging effects were excellent even at low concentrations of 0.80 mg/ml, 3.19 mg/ml and 1.41 mg/ml in Examples 4 to 6, respectively.

TABLE-US-00009 TABLE 9 Evaluation Result of Anti-inflammatory Effect by Concentration of Culture 1 (Example 4) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.113 0.116 0.12 0.116 — — treated Group Exam- 0.1 0.036 0.098 0.089 0.094 4.06 18.91 ple 4 0.2 0.081 0.078 0.078 0.079 1.49 32.09 0.4 0.071 0.068 0.071 0.07 1.49 39.83 0.6 0.058 0.049 0.068 0.058 8.17 49.86 1 0.05 0.06 0.054 0.055 4.33 53.01 2 0.057 0.046 0.047 0.05 5.23 57.02 5 0.036 0.043 0.036 0.038 3.47 67.05

TABLE-US-00010 TABLE 10 Evaluation Result of Anti-inflammatory Effect by Concentration of Culture 2 (Example 5) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.193 0.191 0.198 0.194 — — treated Group Exam- 0.1 0.178 0.181 0.172 0.177 2.36 8.76 ple 5 0.2 0.171 0.175 0.174 0.173 1.07 10.65 0.4 0.161 0.155 0.164 0.16 2.36 17.53 0.6 0.15 0.145 0.153 0.149 2.08 23.02 1 0.138 0.135 0.133 0.135 1.3 30.24 2 0.118 0.115 0.106 0.113 3.22 41.75 5 0.078 0.077 0.063 0.073 4.32 62.54

TABLE-US-00011 TABLE 11 Evaluation Result of Anti-inflammatory Effect by Concentration of Culture 3 (Example 6) Standard Concen- Devia- Inhib- tration Aver- tion ition Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.182 0.173 0.175 0.176 — — treated Group Exam- 0.1 0.14 0.145 0.147 0.144 2.04 18.49 ple 5 0.2 0.126 0.129 0.119 0.125 2.9 29.43 0.4 0.115 0.121 0.114 0.117 2.14 33.96 0.6 0.102 0.107 0.112 0.107 2.83 39.43 1 0.1 0.101 0.098 0.1 0.86 43.58 2 0.077 0.068 0.073 0.073 2.55 58.87 5 0.058 0.057 0.057 0.057 0.33 67.55

Experimental Example 1-3: Evaluation of Anti-inflammatory And Moisturizing Effect (Hyaluronidase Inhibition)

[0040] Hyaluronidase is an enzyme that hydrolyzes hyaluronic acid, which is a skin moisturizing factor, and has a function of causing inflammation. An anti-inflammatory effect was evaluated using a method of measuring the anti-inflammatory effect by confirming a degree of inhibition of an activity of hyaluronidase (Y Kakegawa, et al., Japanese J. Inflammation, 4: 437-438, 1984).

[0041] The sample was added to 0.1 ml of a hyaluronidase solution (10 mg/m1) dissolved in 1M acetic acid buffer solution (pH 3.5) and reacted at 37° C. for 20 minutes. After 12.5 mM CaCl 2 0.1 ml was added, the mixture was reacted for 20 minutes at 37° C. again. After the reaction, a hyaluronic acid solution (6 mg/ml) dissolved in 0.25 ml of 0.1M acetic acid buffer solution (pH 3.5) was added and reacted for 40 minutes at 37° C., and 0.1 ml of 0.4N NaOH and 0.1 ml of 0.4M potassium tetraborate were added, reacted for 3 minutes at 100° C., and cooled. Then, 2.5 ml of ρ-dimethylaminobenzaldehyde solution was added, and reacted for 20 minutes at 37° C. again to develop color, and absorbance was measured at 540 nm. A hyaluronidase inhibitory ability was calculated using the following formula, and the results are shown in [Table 12].

Hyaluronidase Inhibitory Ability (%)=(Absorbance of Test Group/Absorbance of Untreated Group)×100

TABLE-US-00012 TABLE 12 Anti-inflammatory And Moisturizing Effect (Hyaluronidase Inhibition) Evaluation Result Test Active Oxygen (ABTs) Sample Concentration Scavenging Ability (%) Example 1 50 mg/mL 51.19 Example 2 50 mg/mL 52.1 Example 3 50 mg/mL 90.49 Example 4 1 mg/mL 36.13 Example 5 1 mg/mL 44.06 Example 6 1 mg/mL 33.55 Example 7 1 mg/mL 52.85 Example 8 1 mg/mL 33.33 Example 9 1 mg/mL 62.2 Example 10 1 mg/mL 47.32 Example 12 1 mg/mL 55.64 Example 13 1 mg/mL 55.6

[0042] In addition, a minimum inhibitory concentration (IC 50, mg/ml) that inhibits the activity of hyaluronidase by 50% was evaluated for Examples 4 to 6 (Cultures 1 to 3). As shown in [Table 13] to [Table 15], the hyaluronidase inhibitory effects were excellent even at low concentrations of 1.36 mg/ml, 2.09 mg/ml and 3.99 mg/ml in Examples 4 to 6, respectively.

TABLE-US-00013 TABLE 13 Evaluation Result of Hyaluronidase Inhibitory Ability by Concentration of Culture 1 (Example 4) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.255 0.243 0.236 0.246 — — treated Group Exam- 0.1 0.242 0.239 0.244 0.241 1.02 1.89 ple 4 0.2 0.237 0.241 0.241 0.239 0.94 2.71 0.4 0.194 0.212 0.202 0.203 3.66 17.73 0.6 0.163 0.174 0.179 0.169 3.32 30.18 1 0.158 0.169 0.145 0.164 4.88 36.13 2 0.136 0.131 0.127 0.134 1.83 46.68 5 0.106 0.112 0.108 0.109 1.24 55.89

TABLE-US-00014 TABLE 14 Evaluation Result of Hyaluronidase Inhibitory Ability by Concentration of Culture 2 (Example 5) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.148 0.163 0.152 0.154 — — treated Group Exam- 0.1 0.144 0.148 0.139 0.144 2.92 6.91 ple 5 0.2 0.134 0.128 0.122 0.128 3.89 17.06 0.4 0.121 0.129 0.116 0.122 4.25 20.95 0.6 0.105 0.111 0.107 0.108 1.98 30.24 1 0.078 0.097 0.084 0.086 6.29 44.06 2 0.073 0.079 0.081 0.078 2.7 49.68 5 0.054 0.061 0.069 0.061 4.86 60.26

TABLE-US-00015 TABLE 15 Evaluation Result of Hyaluronidase Inhibitory Ability by Concentration of Culture 3 (Example 6) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.145 0.157 0.151 0.151 — — treated Group Exam- 0.1 0.153 0.149 0.15 0.151 1.38 0.22 ple 5 0.2 0.142 0.148 0.139 0.143 3.03 5.3 0.4 0.132 0.141 0.128 0.134 4.41 11.48 0.6 0.119 0.108 0.121 0.116 4.64 23.18 1 0.098 0.103 0.1 0.1 1.67 33.55 2 0.088 0.097 0.084 0.09 4.41 40.62 5 0.071 0.063 0.071 0.068 3.06 54.75

Experimental Example 1-4: Evaluation of Lightening Effect (Tyrosinase Inhibition)

[0043] Tyrosinase is an enzyme that promotes oxidation of tyrosine in the living body and helps to produce melanin. A lightening effect was evaluated by applying a method of measuring a degree of inhibition of forming of a black polymer called melanin, which is caused by tyrosine oxidation by inhibiting the function of this enzyme (Pomerantz S. H.: J. Biochem., 24: 161 - 168, 1996). A tyrosinase inhibitory activity was measured by modifying a method, such as vagi, of measuring DOPA chrome produced as a result of the action of tyrosinase by a colorimetric method. Specifically, in 2.3 mL of 50 mM sodium phosphate buffer solution (pH 6.8), 0.5 mL of 10 mM L-DOPA, 0.5 mL of 110 unit/ml mushroom tyrosinase, and 20 μl of the sample solution were added, and then reacted at 25° C. for 10 minutes. The absorbance was measured at 475 nm, and a tyrosinase inhibitory ability (%) was calculated using the following formula and shown in [Table 16].

Tyrosinase Inhibitory Ability (%)=(Absorbance of Test Group/Absorbance of Untreated Group)×100

TABLE-US-00016 TABLE 16 Evaluation Result of Lightening Effect (Tyrosinase Inhibitory Ability) Test Tyrosinase Inhibitory Sample Concentration Ability (%) Example 1 50 mg/mL 85.68 Example 3 50 mg/mL 79.61 Example 4 1 mg/mL 44.13 Example 6 1 mg/mL 32.62 Example 7 1 mg/mL 34.13 Example 8 1 mg/mL 24.19 Example 14 1 mg/mL 47.89 Example 15 1 mg/mL 35.04

[0044] In addition, the minimum inhibitory concentration (IC.sub.50, mg/ml) that inhibits the activity of tyrosinase by 50% for Examples 4 and 6 (Cultures 1 and 3) was evaluated. As shown in [Table 17] and [Table 18], a tyrosinase inhibitory ability was excellent even at low concentrations of 2.03 mg/ml and 4.16 mg/ml in Examples 4 and 6, respectively.

TABLE-US-00017 TABLE 17 Evaluation Result of Tyrosinase Inhibitory Ability by Concentration of Culture 1 (Example 4) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.283 0.288 0.285 — — treated Group Exam- 0.1 0.267 0.279 0.273 2.97 4.38 ple 4 0.2 0.238 0.248 0.243 2.48 14.89 0.4 0.231 0.228 0.23 0.74 19.61 0.6 0.201 0.198 0.2 0.74 30.12 1 0.156 0.163 0.16 1.73 44.13 2 0.142 0.144 0.143 0.5 49.91 5 0.111 0.126 0.119 3.72 58.49

TABLE-US-00018 TABLE 18 Evaluation Result of Tyrosinase Inhibitory Ability by Concentration of Culture 3 (Example 6) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.451 0.461 0.443 0.451 — — treated Group Exam- 0.1 0.437 0.444 0.451 0.444 1.55 1.7 ple 5 0.2 0.422 0.417 0.423 0.421 0.71 6.86 0.4 0.377 0.383 0.384 0.381 0.84 15.57 0.6 0.334 0.34 0.349 0.341 1.67 24.5 1 0.317 0.299 0.297 0.304 2.44 32.62 2 0.268 0.279 0.259 0.269 2.22 40.52 5 0.196 0.222 0.21 0.209 2.88 53.65

Experimental Example 1-5: Evaluation of Elasticity and Wrinkle Improvement Effect (Collagenase Inhibition)

[0045] Collagenase is known to be an enzyme that decomposes collagen, and its expression is greatly increased by irradiation with ultraviolet rays. Collagenase is a major cause of reduction and degeneration of collagen by ultraviolet rays and is a major cause of skin wrinkle formation. Using the fact that collagenase is the main factor of skin problems, a collagenase inhibitory effect was measured for the test group, and elasticity and wrinkle improvement effects were evaluated.

[0046] The collagenase enzyme activity inhibition experiment was performed using the azochol method using azocoll, which is a dye for collagen. In order to measure the enzyme inhibitory activity, 4 mM CaCl.sub.2 was added to 0.25 mL of 0.1M Tris-HCl buffer solution (pH 7.5) in 0.1 mL of the sample. After adding a substrate solution dissolved with 4-phenylazobenzyloxycarbonyl-Pro-Leu-Gly-Pro-Arg (0.3 mg/ml) and 0.15 mL of collagenase (0.2 mg/ml) enzyme solution, the mixture was reacted at room temperature for 20 minutes. Then, 0.5 mL of 6% citric acid and 2.5 mL of ethyl acetate were added in order, and absorbance was measured at 320 nm. The collagenase inhibitory ability (%) was calculated using the following formula, and the results are shown in [Table 19].

Collagenase Inhibitory Ability (%)=(Absorbance of Test Group/Absorbance of Untreated Group)×100

TABLE-US-00019 TABLE 19 Evaluation Result of Elasticity and Wrinkle Improvement Effect (Collagenase Inhibition Ability) (Example 4) Test Collagenase Inhibitory Sample Concentration Ability (%) Example 1 50 mg/mL 79.33 Example 3 50 mg/mL 93.44 Example 4 1 mg/mL 36.73 Example 6 1 mg/mL 25.95 Example 7 1 mg/mL 33.36 Example 8 1 mg/mL 31.75 Example 14 1 mg/mL 25.36 Example 15 1 mg/mL 21.7

[0047] In addition, the minimum inhibitory concentration (IC 50, mg/ml) that inhibits the activity of collagenase by 50% for Examples 4 and 6 (Cultures 1 and 3) was evaluated. As shown in [Table 20] to [Table 21], elasticity and wrinkle improvement effect were excellent even at low concentrations of 3.12 mg/ml and 4.78 mg/ml in Examples 4 and 6, respectively.

TABLE-US-00020 TABLE 20 Evaluation Result of Elasticity and Wrinkle Improvement Effect by Concentration of Culture 1 (Collagenase Inhibition Ability) (Example 4) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.283 0.288 0.285 — — treated Group Exam- 0.1 0.267 0.279 0.273 2.97 4.38 ple 4 0.2 0.238 0.248 0.243 2.48 14.89 0.4 0.231 0.228 0.23 0.74 19.61 0.6 0.201 0.198 0.2 0.74 30.12 1 0.156 0.163 0.16 1.73 44.13 2 0.142 0.144 0.143 0.5 49.91 5 0.111 0.126 0.119 3.72 58.49

TABLE-US-00021 TABLE 21 Evaluation Result of Elasticity and Wrinkle Improvement Effect by Concentration of Culture 3 (Collagenase Inhibition Ability) (Example 6) Standard Inhib- Concen- Devia- ition tration Aver- tion Rate Sample (mg/mL) O.D. 734 nm age (%) (%) Un- — 0.287 0.292 0.288 0.289 — — treated Group Exam- 0.1 0.274 0.282 0.288 0.281 2.43 2.65 ple 5 0.2 0.269 0.274 0.279 0.274 1.73 5.19 0.4 0.258 0.263 0.253 0.258 1.73 10.73 0.6 0.224 0.232 0.248 0.235 4.23 18.8 1 0.219 0.214 0.209 0.214 1.73 25.95 2 0.178 0.183 0.181 0.181 0.87 37.49 5 0.147 0.135 0.143 0.142 2.11 50.98

Experimental Example 2: Evaluation of Efficacy in Cells In Vitro

[0048] In order to verify an overall effectiveness of a composition of Example 7 on skin aging improvement at a cellular level, cytotoxicity, wrinkle improvement (mRNA expression of MMP-1 using Hs68 cells, ATCC, and real-time PCR), lightening improvement (B16F10 cells, Korean Cell Line Bank, melanin content confirmation), moisturizing improvement (HAS-2 expression confirmation using HaCaT cells, ATCC, and real-time PCR), and anti-inflammatory improvement (mRNA expression of iNOS using RAW264.7 cells, Korean Cell Line Bank, NO Production inhibition ability, and real-time PCR) were evaluated. As a result, at a concentration of 1,000 μg/ml or less, cytotoxicity was not observed, and it was confirmed that the effect of improving skin aging was excellent through inhibiting MMP-1 mRNA expression, reducing melanin production, promoting HAS-2 expression, inhibiting NO production, and inhibiting iNOS mRNA expression. Significance was verified with an independent sample student t-test, and when the p-value was less than 0.05, it was determined that there was a statistically significant difference. The experimental procedure and evaluation results are as follows.

Experimental Example 2-1: Evaluation of Wrinkle Improvement Effect (Inhibition of MMP1 Expression)

[0049] Skin aging is caused by a structural change in the extracellular matrix existing in the dermal layer of skin. Specifically, skin aging is caused by a decrease in collagen, a protein that is a skin elasticity component in the dermal tissue of the skin. Extracellular matrix degradation occurs by matrix-metalloproteinases (MMPs), and collagen degradation occurs by MMP-1, thereby causing wrinkles. As a result of evaluating an efficacy through MMP-1 expression inhibition ability, cytotoxicity was not observed at the concentration of 1,000 μg/ml and less, and it significantly decreases at the concentration of 600 to 1,000 μg/ml, and 52.63% MMP-1 mRNA expression was inhibited at the concentration of 1,000 μg/ml.

1-1) Cell Culture

[0050] Hs68 cells used in the experiment were purchased from ATCC. The 10% FBS and 1% Penicillin/streptomycin were added to DMEM medium and cultured in an incubator at 37° C. under 90% of relative humidity and 5% of CO.sub.2.

1-2) Cell Viability

[0051] Hs68 cells were cultured in 96-well plates at a concentration of 5×10.sup.3 cells/well for 24 hours. The samples were treated by each concentration and cultured for 24 hours. The 10 μl of MTT solution (5 mg/ml) was added for each sample and further incubated for 4 hours. After removing supernatant, 100 μl of dimethyl sulfoxide (DMSO) was added, and absorbance were measured at 570 nm. Cell viability was calculated according to the following formula.

Cell Viability (%)=(Absorbance in Sample Added Group/Absorbance in Sample Not Added Group)×100

1-3) Real-time PCR

[0052] Real-time PCR was performed to confirm mRNA expression of MMP-1 in Hs68 cells. Hs68 cells were aliquoted to a volume of 5×10.sup.5 cells/well in a 60 mm plate and cultured for 24 hours in an incubator at 37° C. under 5% of CO.sub.2. Example 1 was treated for 45 minutes by concentration, treated with TNF-α (20 ng/ml, and reacted for 24 hours, and then, supernatant was removed. Cells were dissolved using Trizol reagent (Ambion, USA). cDNA was synthesized according to manufacturing instructions of Revertra ACE-α- (Toyobo, Japan). The real-time PCR for synthesized cDNA was conducted using GAPDH (Hs02786624_g1), MMP1 (Hs00899658_m1) primers, and Taqman master mix (Thermo fisher, USA).

[0053] FIG. 1a shows a confirmation result of cytotoxicity in Hs68 cells, and FIG. 1b shows a confirmation result of an MMP expression inhibitory ability.

Experimental Example 2-2 Evaluation of Lightening Effect (Inhibition of Melanin Production)

[0054] Skin darkening is caused by increased melanogenesis in melanocytes present in the skin. Through external stimuli such as UV exposure, melanin forming cells synthesize melanin from L-tyrosine, and several enzymes are involved in this process. In order to promote melanin synthesis in B16F10 cells, α-MSH (200 nM), which is a melanogenesis stimulating hormone, was treated, and a lightening effect was evaluated by confirming a decrease in melanin content. Cytotoxicity was not observed at a concentration of 1,000 μg/ml or less, and the melanin content significantly decreased at a concentration of 600 to 1,000 μg/ml, and melanin production was inhibited by 46.69% at a concentration of 1,000 μg/ml.

1-1) Cell Culture

[0055] B16F10 cells used in the experiment were purchased from the Korean Cell Line Bank. The 10% FBS and 1% Penicillin/streptomycin were added to DMEM medium and cultured in an incubator at 37° C. under 90% of relative humidity and 5% of CO.sub.2.

1-2) Cell Viability

[0056] *B16F10 cells were aliquoted in a 96-well plate at a concentration of 4×10.sup.3 cells/well and cultured for 24 hours. After incubation for 24 hours, α-MSH (200 nM) and samples were treated for each concentration and cultured for 72 hours. MTT solution (5 mg/ml) was added for each 10 μl and further incubated for 4 hours. Then, the medium was removed, 100 μl of dimethyl sulfoxide (DMSO) was added, and the absorbance was measured at 570 nm. Cell viability was calculated according to the following formula.

Cell Viability (%)=(Absorbance in Sample Added Group/Absorbance in Sample Not Added Group)×100

1-3) Melanin Content

[0057] B16F10 cells were aliquoted in a 6-well plate at a concentration of 4×10.sup.4 cells/well and cultured for 24 hours. α-MSH at a concentration of 200 nM was co-treated with the sample, and melanin synthesis was promoted for 72 hours. After 72 hours, the cultured cells were treated with trypsin/EDTA and centrifuged. After reacting at 80° C. for 1 hour using 1N of NaOH, absorbance was measured at 405 nm.

[0058] FIG. 2a shows a measurement result of cytotoxicity (cell viability) in B16F10 cells, and FIG. 2b shows an amount of melanin production (melanin content) in B16F10 cells.

Experimental Example 2-3: Evaluation of Moisturizing Effect (Increase in Has-2 Expression)

[0059] *In order for skin barrier to work smoothly, various types of lipids, sugars, and proteins are involved and interact with each other. Among them, hyaluronic acid (HA) is a high molecular weight glycosaminoglycan present in the extracellular connective tissue and acts as a barrier to prevent water evaporation. It is known that the content of HA decreases with age, and the decrease in the content of HA due to these intrinsic or extrinsic factors causes factors of a decrease in skin elasticity, rough skin, wrinkles, and the like. Using the fact that HA content is controlled by continuous synthesis by hyaluronic acid synthase (HAS) and degradation by hyaluronidase (HYAL), the moisturizing effect was evaluated through increased HAS-2 expression. As a result, it was confirmed that cytotoxicity was not observed at a concentration of 1,000 μg/ml or less, HAS-2 expression significantly increased at a concentration of 600 to 1,000 μg/ml, and HAS-2 mRNA expression increased by 54% at a concentration of 1,000 μg/ml.

1-1) Cell Culture

[0060] HaCaT cells used in the experiment were purchased from ATCC. The 10% FBS and 1% Penicillin/streptomycin were added to DMEM medium and cultured in an incubator at 37° C. under 90% of relative humidity and 5% of CO.sub.2.

1-2) Cell Viability

[0061] HaCaT cells were aliquoted in a 96-well plate at a concentration of 1×10.sup.5 cells/well and cultured for 24 hours. Samples were treated for each concentration and incubated for 24 hours. The 10 μl of MTT solution (5 mg/ml) was added for each sameple and further incubated for 4 hours. After removing the medium, 100 μl of Dimethyl Sulfoxide (DMSO) was added, and absorbance was measured at 570 nm. Cell viability was calculated according to the following formula.

Cell Viability (%)=(Absorbance in Sample Added Group/Absorbance in Sample Not Added Group)×100

1-3) Real-time PCR

[0062] Real-time PCR was performed to confirm an mRNA expression of HAS-2 in HaCaT cells. HaCaT cells were aliquoted in a 60 mm plate to be a 6×10.sup.5 cells/well and cultured for 24 hours in an incubator at 37° C. under 5% of CO.sub.2. After the samples were treated for 24 hours at each concentration, the supernatant was removed. The treated cells were dissolved using Trizol reagent (Ambion, USA). cDNA was synthesized according to the manufacturing instructions of Revertra ACE-α- (Toyobo, Japan). Real-time PCR for synthesized cDNA was conducted using GAPDH (Hs02786624_g1), HAS-2 (Hs00193435_m1) primers, and Taqman master mix (Thermo fisher, USA). As a result, cytotoxicity was not observed at a concentration of 1,000 μg/ml or less, and an increase in HAS-2 mRNA expression was confirmed to be 1.54% at a concentration of 1,000 μg/ml, and a production increase rate of 54% was observed.

[0063] FIG. 3a shows a confirmation result of cytotoxicity (cell viability) in HaCaT cells, and FIG. 3b shows an HAS-2 expression degree in HaCaT cells.

Experimental Example 2-4: Evaluation of Anti-inflammatory Effect (Inhibition of No Production and Inhibition of iNOS Expression)

[0064] In order to evaluate an ability to inhibit NO production leading to autoimmune diseases and inflammatory diseases, RAW 264.7 cells were treated with LPS, which is an inflammatory mediator, to significantly increase NO production, and an anti-inflammatory efficacy through inhibition of NO production and iNOS expression of samples was evaluated. As a result, cytotoxicity was not observed at a concentration of 1,000 μg/ml or less, NO production was significantly reduced at a concentration of 400 μg/ml to 1,000 μg/ml, and NO production was reduced by 61.57% at a concentration of 1,000 μg/ml. In addition, iNOS mRNA expression was significantly decreased at a concentration of 600 μg/ml to 1,000 μg/ml, and iNOS mRNA expression was reduced by 50.40% at a concentration of 1,000 μg/ml.

1-1) Cell Culture

[0065] RAW 264.7 cells used in the experiment were purchased from the Korean Cell Line Bank and used by adding 10% FBS and 1% Penicillin/streptomycin to DMEM medium.

1-2) Cell Viability

[0066] RAW 264.7 cells were cultured in 96-well plates at a concentration of 5×10.sup.4 cells/well for 24 hours. Samples were treated by concentration and incubated for 24 hours. 10 μl of MTT solution (5 mg/ml) was added for each and further incubated for 4 hours. After removing the supernatant, 100 μl of dimethyl sulfoxide (DMSO) was added, and the absorbance was measured at 570 nm. Cell viability was calculated according to the following formula.

Cell Viability (%)=(Absorbance in Sample Added Group/Absorbance in Sample Not Added Group)×100

1-3) Inhibition of NO Production

[0067] RAW 264.7 cells were aliquoted in a 96-well plate at a concentration of 5×10.sup.4 cells/well and cultured in DMEM medium containing 10% of FBS for 24 hours. The medium was removed, and LPS was treated at a concentration of 1 μg/ml together with samples diluted by each concentration in DMEM (serum free) medium and cultured for 24 hours again. Griess reagent of the same amount as 100 ml of the culture supernatant was added, and the absorbance was measured at 540 nm after reaction for 10 minutes.

NO Production Inhibitory Ability (%)=(Absorbance of Sample Added Group/Absorbance of Sample Not Added Group)×100

1-4) Real-time PCR

[0068] Real-time PCR was performed to confirm the mRNA expression of iNOS in RAW 264.7 cells. RAW 264.7 cells were aliquoted to 5×10.sup.5 cells/well in a 6-well plate and cultured in an incubator at 37° C. under 5% of CO.sub.2 for 24 hours. After the samples were treated for 24 hours at different concentrations, the supernatant was removed. Cells were dissolved using Trizol reagent (Ambion, USA). cDNA was synthesized according to the manufacturing instructions of Revertra ACE-α- (Toyobo, Japan). Real-time PCR for the synthesized cDNA was conducted using GAPDH (Mm99999915_g1), iNOS (Mm00440502_m1), primers, and Taqman master mix (Thermo fisher, USA).

[0069] FIG. 4a shows a confirmation result of cytotoxicity, cell viability, in RAW 264.7 cells for a composition of Example 7 of the present invention, FIG. 4b shows a NO production inhibitory ability in RAW 264.7 cells, and FIG. 4c shows a confirmation result of an iNOS expression inhibitory activity.

Preparation Example 4: Preparation of Solid Powder of Mixed Composition of Dead Cells and Cultures of Lactic Acid Bacteria

[0070] The mixed compositions of Examples 7 and 8 prepared in Preparation Example 3 were spray-dried with a spray dryer (Buchi Co. B-290, Swiss, Inlet 160° C., Outlet 100° C., Pump 10%, Aspirator 100%)), respectively, and solid powder of a mixture composition of lactic acid bacteria dead cells and cultures was obtained. The composition (weight ratio) is shown in [Table 22] below.

TABLE-US-00022 TABLE 22 Solid Powder Composition of Mixed Composition of Lactic Acid Bacteria Dead Cells and Cultures Example Comparative Comparative Component Example 18 Example 18 Example 1 Example 2 Maltodextrin 25.00 0.00 15.00 0.00 Isomalt 0.00 15.00 0 25.00 Phospholipid 0.25 0.15 0 0.00 Example 7 0.25 0.00 1.50 0.00 Example 8 0.00 0.85 0.00 0.50 Purified 74.5 84.00 83.5 74.5 water Total 100.00 100.00 100.00 100.00

Preparation Example 5: Preparation of Liquid Polymersome Composition of Dead Cells and Cultures of Lactic Acid Bacteria

[0071] A probiotic liquid polymersome material was obtained from the mixed composition of Example 7 prepared in Preparation Example 3 by a high-pressure dispersion process using a high-pressure disperser (Suflux, NLM 100, 10000 bar, 60° C.). The composition (weight ratio) of liquid polymersome is shown in Table 23 below.

TABLE-US-00023 TABLE 23 Composition of Liquid Polymersome Composition Comparative Comparative Component Example 20 Example 3 Example 4 Purified water 88.95 88.95 89.95 Tamarindus Indica 0.05 0.00 0.05 Seed Polysaccharide Xanthan Gum 0.00 0.05 0.00 Butylene Glycol 6.00 6.00 6.00 1,2-Hexanediol 3.00 3.00 3.00 Phospholipid 0.50 0.50 0.00 Polyglyceryl-6 0.5.00 0.50 0.00 oleate Example 7 1.00 1.00 1.00 Total 100.00 100.00 100.00

Experimental Example 3: Evaluation of Stability

[0072] Phase stability (discoloration, discoloration, phase separation, and others) according to temperature conditions was evaluated for the solid powder composition prepared in Preparation Example 4 and the liquid polymersome composition prepared in Preparation Example 5, and the results are shown in Table 24 below.

[0073] As shown in [Table 24], the solid powder composition was confirmed to be stable when it contained maltodextrin and isomalt as excipients and phospholipids as stabilizers, and the liquid polymersome composition was confirmed to be stable when it contained tamarind seed polysaccharide and phospholipids and polyglyceryl-6 oleate as stabilizers.

TABLE-US-00024 TABLE 24 Stability Evaluation Result of Solid Powder and Liquid Polymersome Compositions After After After After Example 1 Day 1 Week 2 Week 4 Week Example 18 Room ⊚ ⊚ ⊚ ⊚ Temperature 50° C. ⊚ ⊚ ⊚ ⊚ 4° C. ⊚ ⊚ ⊚ ⊚ Example 19 Room ⊚ ⊚ ⊚ ⊚ Temperature 50° C. ⊚ ⊚ ⊚ ◯ 4° C. ⊚ ⊚ ⊚ ⊚ Comparative Room ⊚ ◯ ◯ .box-tangle-solidup. Example 1 Temperature 50° C. ◯ .box-tangle-solidup. .box-tangle-solidup. .box-tangle-solidup. 4° C. ⊚ ◯ ◯ ◯ Comparative Room ◯ ◯ .box-tangle-solidup. .box-tangle-solidup. Example 2 Temperature 50° C. ◯ .box-tangle-solidup. .box-tangle-solidup. .box-tangle-solidup. 4° C. ⊚ ◯ ◯ .box-tangle-solidup. Example 20 Room ⊚ ⊚ ⊚ ⊚ Temperature 50° C. ⊚ ⊚ ⊚ ⊚ 4° C. ⊚ ⊚ ⊚ ⊚ Comparative Room ⊚ ◯ .box-tangle-solidup. .box-tangle-solidup. Example 3 Temperature 50° C. ⊚ .star-solid. .star-solid. .star-solid. 4° C. ⊚ ◯ .box-tangle-solidup. .box-tangle-solidup. Comparative Room ⊚ ◯ .box-tangle-solidup. .star-solid. Example 4 Temperature 50° C. ⊚ .star-solid. .star-solid. .star-solid..star-solid. 4° C. ⊚ ◯ .box-tangle-solidup. .box-tangle-solidup.

[0074] Stability evaluation criteria ⊚: No discoloration, ◯: Light yellow discoloration, .box-tangle-solidup.: Yellow discoloration and odor, .star-solid.: Phase separation, .star-solid..star-solid.: Phase separation, discoloration, and odor

Preparation Example 6: Preparation of Cream Cosmetic Containing Dead Cells and Cultures of Lactic Acid Bacteria

[0075] Cream cosmetics were prepared from the solid powder material of Example 18 prepared in Preparation Example 4 by an emulsion emulsification process using an emulsifier (T.K. Homo Mixer Markll, Model 2.5, 3,000 rpm, 75° C.). The composition (weight ratio) is shown in [Table 25] below.

TABLE-US-00025 TABLE 25 Composition of Cream Cosmetic Comparative Example 21 Example 5 Type Component (%) (%) Aqueous 1. Purified water To 100 To 100 Phase 2. EDTA-2Na 0.05 0.05 3. Glycerin 10.00  10.00 4. 1,3-butylene glycol 10.00  10.00 5. Niacinamide 2.00 2.00 6. Carbomer 0.20 0.20 7. Xanthan Gum 0.05 0.05 Oil 8. Cetostearyl alcohol 2.50 2.5 Phase 9. Arachidyl Alcohol, 2.00 2.00 Behenyl Alcohol, Arachidyl Glucoside 10. Self-emulsifying 1.00 1.00 glycerin momostearate 11. Hydrogenated 5.00 5.00 Polydecene 12. Ethylhexyl- 5.00 5.00 isononanoate 13. Cyclomethicone 5.00 5.00 Addition 12. Neutralizing Appropriate Appropriate Agent Amount Amount 13. Fragrance and Appropriate Appropriate sterilization Amount Amount preservative 14. Example 18 3.00 3.00

Experimental Example 4: Evaluation of Skin Moisturizing Power of Cream Cosmetic

[0076] A moisturizing ability of the cream cosmetic prepared in Preparation Example 6 was evaluated as follows. After washing the forearm of a tester with water, 10 μl of cream cosmetic was applied to an area of 2 cm×2 cm and spread well using a latex glove, the moisture content in the stratum corneum was measured immediately after application, after 1 hour, and after 2 hours, respectively, by using a moisture meter of Janus Premium (Pie, Korea), which uses the principle that resistance decreases when alternating current is applied if water is contained. The results are shown in FIG. 5. As shown in FIG. 5, the cream cosmetic (Example 21) containing the mixed composition of the dead cells and the cultures of lactic acid bacteria shows a superior moisture content increase and a moisturizing ability compared to the cream cosmetic (Comparative Example 5) that does not contain the mixed composition of the dead cells and the cultures of lactic acid bacteria.