Enhanced anti-aging cosmetic composition

Abstract

To provide an enhanced anti-aging cosmetic composition.SOLUTION: An anti-aging cosmetic composition comprises (A) 18-98 wt.%, preferably 30-90 wt.%, based on the total weight of the cosmetic composition, of concentrated birch sap which has a concentration factor of 1.05-8 times, preferably 1.1-4 times, and further preferably 1.2-2 times, and (B) one or more materials selected from polypeptide, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and adenosine.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to an enhanced anti-aging cosmetic composition comprising (A) concentrated birch sap having a concentration of 1.05 to 8 times, preferably 1.1 to 4 times, more preferably 1.2 to 2 times, and (B) one or more substances selected from a polypeptide, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone, and adenosine. [Background technology]

[0002] Birch is a deciduous tree of the Betulaceae family. There are currently about 100 species in the world, mainly distributed in the northern temperate and cool temperate zones. Among them, there are about 29 species in China, mainly distributed in the northeast, northwest and southwest. Birch trees mainly grow in remote mountainous areas with little human interference and no industrial pollution. Birch sap (also called birch juice) is fresh sap from cut birch bark or drilled trunks. It is colorless or light yellow, without sediment or impurities, and has a light birch fragrance. Birch sap contains a large number of compounds such as sugars, amino acids, vitamins, biotin, cytokinins, trace mineral elements, aromatic oils, betulin and saponins, and has excellent skin care and anti-aging effects.

[0003] Skin aging refers to the decline of the skin's ability to protect and regulate the body, and therefore cannot adapt to changes in the internal and external environment, and shows some changes in the overall appearance, such as skin color and condition, resulting in reduced or lost skin elasticity, sagging skin, increased wrinkles, dry skin, thinning, easy desquamation, itching, dull skin color, lack of lustre, and the concomitant occurrence of dark spots and warts.With the aging of the population and the continuous improvement of living standards, consumers' awareness of anti-wrinkle continues to increase, and more and more consumers are willing to use cosmetics to maintain a youthful appearance.According to statistics, anti-aging cosmetics have become the fastest growing and most promising category in China's cosmetics market. Summary of the Invention

[0004] In one aspect, the present invention relates to the use of a combination of (A) concentrated birch sap and (B) one or more substances selected from polypeptides, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and adenosine in an enhanced anti-aging cosmetic composition, wherein the concentrated birch sap has a concentration of 1.05 to 8 times, preferably 1.1 to 4 times, more preferably 1.2 to 2 times.

[0005] In another aspect, the present invention provides an enhanced anti-aging cosmetic composition comprising (A) concentrated birch sap having a concentration of 1.05 to 8 times, preferably 1.1 to 4 times, more preferably 1.2 to 2 times, and (B) one or more substances selected from a polypeptide, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone, and adenosine.

[0006] The anti-aging cosmetic composition according to the present invention can promote the synthesis of types I, III, IV, VII, and XVII collagen, elastin, and laminin in the extracellular matrix, reduce the expression of matrix metalloproteinase MMP-1, promote the production of hyaluronic acid, strengthen the structural integrity and functionality of the epidermis, dermis, and the dermal-epidermal junction, improve skin elasticity, and reduce wrinkles, while at the same time improving the skin barrier, reducing transepidermal water loss, and having anti-inflammatory and soothing effects, thereby providing significant anti-aging, especially anti-wrinkle, effects.

[0007] The anti-aging cosmetic composition does not contain further added water, but does not exclude water inherently contained in each of the components of the composition.

[0008] In a preferred embodiment, the anti-aging cosmetic composition is free of chelating agents such as EDTA salts, sodium polyphosphate, sodium metaphosphate, gluconic acid, and the like.

[0009] The birch sap involved in the present invention is obtained from the genus Betula of the family Betulaceae, which includes four varieties: Betala alba, Betula pubescens, Betula Pendula, and Betula platyphylla. Birch sap is a colorless, transparent, and highly nutritious birch sap without sediment or impurities, which is obtained by artificially drilling a hole at the base of the trunk of a birch tree and collecting it from there from when the snow starts to melt until the tree leaves. Birch sap is commercially available and used as it is (in this case, it is also called non-concentrated birch sap or raw birch sap), and can be purchased, for example, from Daxinganling Chaoyue Wild Berry Development Co., Ltd.

[0010] The concentrated birch sap used in the present invention is obtained by concentrating the above-mentioned commercially available birch sap raw product. Concentration methods such as heat concentration, low-temperature and vacuum concentration, and membrane concentration, etc. are known in the art. In the present invention, concentration is preferably carried out by low-temperature freeze concentration or membrane concentration process. For example, the commercially available birch sap raw product is introduced into a low-temperature drying device, cooled to -40 to -70°C, and evacuated to 0.1 to 30 Pa for the low-temperature and vacuum concentration process to obtain concentrated birch sap with a concentration degree of 1.05 to 8 times.

[0011] The inventors have surprisingly found that the combination of birch sap concentrate with a concentration of 1.05-8 times, preferably 1.1-4 times, more preferably 1.2-2 times, compared to non-concentrated birch sap concentrate, and polypeptide, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and / or adenosine can significantly improve the anti-aging, especially anti-wrinkle, effect of the cosmetic composition. This indicates that the combination of concentrated birch sap with polypeptide, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and / or adenosine produces a synergistic effect.

[0012] The content of (A) concentrated birch sap is about 18 to 98% by weight, preferably about 20 to 95% by weight, more preferably about 22 to 92% by weight, and most preferably about 30 to 90% by weight, based on the total weight of the anti-aging cosmetic composition.

[0013] The polypeptides in component (B) are known in the art to be capable of promoting the synthesis of matrix proteins, particularly collagen, and may also increase the production of elastin, hyaluronic acid, glycosaminoglycans and fibronectin to provide an anti-wrinkle effect. Examples of polypeptides that may be used in the present invention include, but are not limited to, dipeptide-2, dipeptide-4, tripeptide-1, tetrapeptide-21, pentapeptide-3, hexapeptide-3, hexapeptide-8, hexapeptide-9, hexapeptide-10, palmitoyl dipeptide-5, palmitoyl dipeptide-7, palmitoyl tripeptide-1, palmitoyl tripeptide-5, palmitoyl tetrapeptide-3, palmitoyl tetrapeptide-7, palmitoyl pentapeptide-3, palmitoyl pentapeptide-4, palmitoyl hexapeptide-6, palmitoyl oligopeptide, acetyl tetrapeptide-3, acetyl tetrapeptide-4, acetyl tetrapeptide-5, acetyl tetrapeptide-6, acetyl tetrapeptide-7, acetyl tetrapeptide-8, acetyl tetrapeptide-9, acetyl tetrapeptide-10 ... The polypeptides include rapeptide-5, acetyl tetrapeptide-9, acetyl pentapeptide-3, acetyl hexapeptide-3, acetyl hexapeptide-8, acetyl octapeptide-1, carnosine, copper peptide, oligopeptide-1, myristoyl pentapeptide-11, dipeptide diaminobutyroyl benzylamide diacetate, decarboxycarnosine HCL, and any combination thereof, preferably palmitoyl tripeptide-5, palmitoyl tetrapeptide-7, acetyl hexapeptide-3, dipeptide diaminobutyroyl benzylamide diacetate, palmitoyl oligopeptide, hexapeptide-9, and any combination thereof. The polypeptides are preferably selected from palmitoyl tripeptide-5, palmitoyl tetrapeptide-7, acetyl hexapeptide-3, dipeptide diaminobutyroyl benzylamide diacetate, palmitoyl oligopeptide, hexapeptide-9, and any combination thereof. All of the above substances are commercially available.

[0014] Examples of sodium hyaluronate in component (B) include, but are not limited to, one or more of high molecular weight sodium hyaluronate (1800-2200KDa), medium molecular weight sodium hyaluronate (1000-1800KDa), low molecular weight sodium hyaluronate (10-1000KDa), hydrolyzed sodium hyaluronate (1-10KDa), and acetylated sodium hyaluronate. Sodium hyaluronate can be prepared by methods known in the art, for example, sodium hyaluronate is first prepared from a plant-derived medium (peptone, glucose, etc.) by fermentation. Sodium hyaluronate is also commercially available, for example from Huaxi Furuida Biomedical Co.,Ltd.

[0015] Retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and adenosine in component (B) are also components known in the art and are all commercially available.

[0016] The content of component (B) is about 0.005 to 10% by weight, preferably about 0.01 to 8% by weight, more preferably about 0.1 to 6% by weight, and most preferably about 0.5 to 5% by weight, based on the total weight of the anti-aging cosmetic composition.

[0017] In addition to the above-mentioned components (A) and (B), the anti-aging cosmetic composition may optionally contain (C) a component commonly used in skin care cosmetics. Examples include, but are not limited to, vehicles, active ingredients, and excipients. All of these components are known in the art, and those skilled in the art can select the type and amount of component (C) as needed. For example, the content of component (C) is typically about 0-70% by weight based on the total weight of the anti-aging cosmetic composition.

[0018] The vehicle is known in the art as a diluent, dispersant, and carrier. Examples include, but are not limited to, ethanol, dipropylene glycol, and butanediol. The content of the vehicle in the cosmetic composition is known in the art, and is typically, for example, 0.5-20% based on the total weight of component (C).

[0019] Active ingredients are those known in the art. Examples include, but are not limited to, emollients, moisturizers, and other anti-wrinkle active ingredients.

[0020] Examples of emollients include, but are not limited to, olive oil, macadamia nut oil, sweet almond oil, grapeseed oil, avocado oil, corn oil, sesame oil, soybean oil, peanut oil, meadowfoam seed oil, safflower seed oil, Rosa canina fruit oil, Argania spinosa kernel oil, Simmondsia chinensis seed oil, sunflower seed oil, Mauritius palm oil, and oleaginous linseed oil. flexuosa) fruit oil, squalane, ethylhexyl palmitate, isopropyl myristate, hydrogenated polyisobutylene, isocetane, isododecane, diethylhexyl carbonate, dioctyl carbonate, isopropyl lauroyl sarcosine, isononyl isononanoate, hydrogenated polydecene, triethylhexanoin, cetyl ethyl hexanoate, bis-diethoxydiglycol cyclohexane 1,4-dicarboxylate, caprylic / capric triglyceride, oleyl erucate, octyldodecanol myristate, octyldodecanol, polydimethylsiloxane, octylpolymethylsiloxane, cetyl dimethicone, cyclopentadimethylsiloxane. Examples of solid emollients include, but are not limited to, one or more of cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, squaryl alcohol, lauric acid, myristic acid, palmitic acid, stearic acid, beeswax, candelilla wax, carnauba wax, lanolin, ozokerite, jojoba seed wax, paraffin wax, microcrystalline wax, hydrogenated rice bran wax, hydrogenated cocoglycerides, glyceryl behenate / eicosandioate, myristyl myristate, bis-diglyceryl polyacyladipate-2, butyrospermum parkii (shea butter), and astrocaryum murumuru seed butter. The content of emollients in cosmetic compositions is known in the art, and is typically 1-50% by weight based on the total weight of component (C).

[0021] Examples of humectants include, but are not limited to, glycerol, diglycerol, propylene glycol, dipropylene glycol, 1,3-propanediol, 1,2-pentanediol, polyethylene glycol-8, polyethylene glycol-32, methyl gluceth-10, methyl gluceth-20, PEG / PPG-17 / 6 copolymer, glycereth-7, glycereth-26, glyceryl glucoside, PPG-10 methyl glucose ether, PPG-20 methyl glucose ether, PEG / PPG / polybutylene glycol-8 / 5 / 3 glycerol, sucrose, trehalose, rhamnose, mannose, raffinose, betaine, erythritol, xylitol, urea, glycereth-5 lactate, sodium hyaluronate, hydrolyzed sodium hyaluronate, acetylated sodium hyaluronate, sodium polyglutamate, hydrolyzed sclerotium gum, pullulan, tremellam, and tamarindus Indica (Citrus indica) seed polysaccharides. The content of the moisturizer in the cosmetic composition is known in the art, and is typically, for example, 1 to 30% based on the total weight of component (C).

[0022] Examples of other anti-wrinkle actives include, but are not limited to, hydrolyzed collagen, hydrolyzed elastin, yeast extract, oryzanol, tetrahydrocurcumin, ellagic acid, whey protein, salicyloyl phytosphingosine, silymarin, sericin, sodium tocopheryl phosphate, allantoin, ribonucleic acid (RNA), grape (Vitis vinifera) seed extract, Pterocarpus marsupium bark extract, tea (Camellia sinensis) polyphenols, wine extract, apple seed extract, European beech (Fagus sylvatica) bud extract, African baobab (Adansonia digitata) extract, Artemia extract, Iris florentina root extract, hesperidin, ginsenosides, Salvia miltiorrhiza extract, nicotinamide, ursolic acid, lycopene, Coffea arabica extract, lactic acid, superoxide dismutase (SOD), evening primrose (Oenothera biennis) oil, ceramide, dipalmitoyl hydroxyproline, hydroxystearic acid, salicylic acid, ergothioneine, lysolecithin, lipoic acid, glycogen, resveratrol, ferulic acid, bifidobacterium culture lysis buffer, and lactococcus culture lysis buffer. The content of other anti-wrinkle active ingredients in the cosmetic composition is known in the art, and is typically 0.01 to 10% based on the total weight of component (C).

[0023] Examples of excipients include, but are not limited to, emulsifiers, thickeners, preservatives, and flavoring agents.

[0024] Examples of emulsifiers include, but are not limited to, cetearyl olivate, sorbitan olivate, polysorbate-60, polysorbate-80, methyl glucose sesquistearate, PEG-20 methyl glucose sesquistearate, PEG-40 hydrogenated castor oil, PPG-26-buteth-26, PEG-4 polyglyceryl-2 stearate, PEG-60 hydrogenated castor oil, steareth-2, steareth-21, PPG-13-decyltetradeceth-24, cetearyl glucoside, PEG-100 stearate, glyceryl stearate, glyceryl stearate SE, cocosyl stearate, glycer ... Coglucoside, ceteareth-25, PEG-40 stearate, polyglyceryl-3 methylglucose distearate, glyceryl stearate citrate, polyglyceryl-10 stearate, polyglyceryl-10 myristate, polyglyceryl-10 dioleate, polyglyceryl-10 laurate, polyglyceryl-10 isostearate, polyglyceryl-10 oleate, polyglyceryl-10 diisostearate, polyglyceryl-6 laurate, polyglyceryl-6 myristate, sucrose stearate, and sucrose polystearate. The content of the emulsifier in the cosmetic composition is known in the art, and is typically 0.5 to 10% by weight based on the total weight of component (C).

[0025] Examples of thickeners include, but are not limited to, one or more of high molecular weight polymers such as carbomer, acrylates and their derivatives, xanthan gum, gum arabic, polyethylene glycol-14M, polyethylene glycol-90M, succinyl polysaccharides, hydroxyethyl cellulose, hydroxypropyl cellulose, and hydroxypropyl methyl cellulose. The content of the thickener in the cosmetic composition is known in the art, and is typically, for example, 0.1 to 10% based on the total weight of component (C).

[0026] Examples of preservatives include, but are not limited to, one or more of methyl hydroxybenzoate, propyl hydroxybenzoate, phenoxyethanol, benzyl alcohol, phenylethanol, bis(hydroxymethyl)imidazolidinyl urea, potassium sorbate, sodium benzoate, chlorophenesin, sodium dehydroacetate, caprylhydroxamic acid, 1,2-hexanediol, 1,2-pentanediol, p-hydroxyacetophenone, caprylyl glycol, glyceryl caprylate, glyceryl undecylenate, sorbitan caprylate, ethylhexylglycerol, and peony root extract. The content of preservatives in cosmetic compositions is known in the art, and is typically, for example, 0.01-2% based on the total weight of component (C).

[0027] The anti-aging cosmetic composition according to the present invention can be prepared by any suitable method known in the art. For example, the composition can be prepared using equipment commonly used in the field of cosmetics, such as dissolving tanks, emulsifying pots, dispersing machines, transfer pumps, etc. During preparation, the water-soluble material is charged into the water-phase dissolving kettle, the oil-soluble material is charged into the oil-phase dissolving kettle, and the two kettles are heated to about 80°C respectively; for agglomerated raw materials, a dispersing machine can be used to pre-disperse them. Once dissolution is complete, the oil and water phases are transferred to an emulsifying pot and homogenized and emulsified for about 5-15 minutes. Once emulsification is complete, the bulk is cooled to room temperature, fragrances, preservatives, etc. are optionally added, and the pH of the product is adjusted as necessary.

[0028] The above preparation methods can be modified or adjusted according to the requirements of the formulation. The anti-aging cosmetic composition can be prepared into various product forms, such as ointments, creams, lotions, essences, etc.

[0029] example The present invention will be further described in detail below with reference to examples. However, these examples and comparative examples are only used to specifically illustrate the present invention, and should not be understood as limiting the scope of the appended claims of the present invention in any way.

[0030] Example 1: Preparation of compositions A, A1, B, B1, B2, B3, B4, C, C1, C2, D, D1, D2, E, E1, E2, F, F1, F2, J The specific formulation of the above composition was as follows: [Table 1]

[0031] The above composition was prepared as follows: 1. Fresh birch sap (Betula Blba sap) stock solution purchased from Daxinganling Chaoyue Wild Berry Development Co., Ltd. was introduced into a low-temperature drying device, cooled to -65°C, evacuated to 0.1 Pa, and concentrated to the extent of 1.2 times, 4 times, and 9 times. 2. Raw materials 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 and / or 11 were mixed to obtain the corresponding composition.

[0032] Example 2: Effect of compositions A, A1, B, B1, B2, B3, B4, C, C1, C2, D, D1, D2, E, E1, E2, F, F1, F2, J on the expression of anti-aging related genes In this example, the effects of the above compositions A, A1, B, B1, B2, B3, B4, C, C1, C2, D, D1, D2, E, E1, E2, F, F1, F2, J on the expression of anti-aging related genes were tested and compared. Experimental equipment: fluorescent quantitative PCR (Roche), clean bench (Su Jing), CO2 incubator (Binder), microplate reader (BIO-TEK), microoscillator. Experimental reagents and materials: human primary fibroblasts, 6-well plate, culture medium for fibroblasts, RNA extraction kit, reverse transcription kit, Trizol lysis buffer, etc.

[0033] The steps of fibroblast-based gene expression analysis were as follows: (1) Seeding: Cells were seeded into 6-well culture plates at a density of 5E5 cells / well and incubated overnight at 37°C in an incubator containing 5% CO2; (2) Administration: When the cell seeding rate of the 6-well culture plate reached about 60%, each group of test substances was added, providing 6 replicate wells for each group of test substances; (3) Sample collection: After inoculation in an incubator containing 5% CO2 at 37°C for 24 hours, the culture medium was discarded, 1 mL of Trizol was added to each well to dissolve the cells, and then the samples were collected; (4) PCR detection: RNA was extracted, reverse transcribed into cDNA, and detected by fluorescent quantitative PCR; (5) Analysis:2 -ΔΔCT The results were calculated using the method, and the T-test method was used for statistical analysis.

[0034] The test results are shown in the table below. [Table 2]

[0035] The results showed that compared with the blank control J, all other compositions could improve the gene expression levels of collagen type I, III, IV, VII, elastin and laminin, and showed that the compositions containing birch sap, concentrated birch sap, palmitoyl tripeptide-5, sodium hyaluronate, retinol, tocopherol and / or ubiquinone had certain anti-wrinkle effects. However, by comparing the results of compositions B2, C2, D2, E2 and F2 with compositions A1, B, C, D, E and F respectively, it can be clearly seen that the combination of 1.2 times concentrated birch sap with palmitoyl tripeptide-5, sodium hyaluronate, retinol, tocopherol or ubiquinone significantly increases the gene expression level of each protein, fully showing that it brings about a synergistic effect; in particular, by comparing the results of compositions B2, B3, B4, C2, D2, E2 and F2 with compositions B1, C1, D1, E1 and F1, it can be clearly seen that compared with non-concentrated birch sap, the combination of concentrated birch sap with polypeptide, sodium hyaluronate, retinol, tocopherol or ubiquinone significantly improves the anti-wrinkle effect of the cosmetic composition, and the concentrated birch sap has a concentration of about 1.05 to 8 times, preferably about 1.1 to 4 times.

[0036] Example 3: Effect of Compositions G, G1 and G2 on the Expression of Anti-Aging Related Proteins In this example, the effects of compositions G, G1 and G2 on the expression of anti-aging related proteins were tested and compared. Experimental equipment: Clean bench (Su Jing), immunological microplate washer (BIO-RAD), microplate reader (BIO-TEK), CO2 incubator (Binder) Experimental reagents and materials: human primary fibroblasts, 12-well culture plates, culture medium for fibroblasts, ELISA kits for various indicators, etc.

[0037] Testing Method: (1) Seeding: Cells were seeded into 12-well culture plates at a density of 2E5 / well and incubated at 37°C in an incubator containing 5% CO2, with the medium replaced every 2 days; (2) Dosing: When cell fusion reached more than 60% again, each group of test substances was added, providing six replicate wells for each group of test substances; (3) Sample collection: After inoculation in an incubator containing 5% CO2 at 37°C for 48 hours, the culture medium was discarded, 1 mL of Trizol was added to each well to dissolve the cells, and then the samples were collected; (4) Detection: The indicators were determined according to the determination method of the ELISA kit. (5) Analysis: T-test method was used for statistical analysis.

[0038] The test results are shown in the table below. [Table 3]

[0039] The results show that, compared with adenosine alone, compositions G1 and G2 containing birch sap or 1.2 times concentrated birch sap and adenosine significantly increase the expression level of anti-aging related proteins in fibroblasts, indicating that birch sap or concentrated birch sap and adenosine have a synergistic effect.Furthermore, comparing G1 and G2, it can be seen that concentrated birch sap has a significantly higher synergistic effect on polypeptides than birch sap pure solution.

[0040] Example 4: Preparation of compositions H, H1, H2 and J1 H: Palmitoyl tripeptide-5 H1: Birch sap extract + palmitoyl tripeptide-5 H2: 1.2x concentrated birch sap + palmitoyl tripeptide-5 J1: Blank control (water-based, no birch sap, no peptides)

[0041] The formulation of the above composition is shown below: [Table 4]

[0042] The above composition was prepared as follows: 1. Oil Phase: Raw materials 6, 8, 9, 10, 11, 13, 14, 15 and 16 were added to the oil phase pot, heated to 80°C, dissolved and mixed well; 2. Raw materials 4, 17 and 19 were mixed thoroughly at room temperature; 3. Raw materials 12, 18 and 21 were mixed thoroughly at room temperature; 4. Water Phase: Ingredients 1, 2, 3, 5 and 7 were heated to 80°C, the mixture from step 2 was added, dissolved and mixed well; 5. Emulsification: Add the water phase and oil phase into the emulsification tank, keep at 80℃, homogenize and emulsify at 3000rpm for 5 minutes, add raw material 20 after the emulsification is completed; 6. When cooled to 40°C with stirring, raw material 22 and the mixture from step 3 were added, stirred well, and discharged to obtain each of the compositions.

[0043] Example 5: Effect of Compositions H, H1, H2 and J1 on a Photoaged 3D Full Thickness Skin Model In this example, the effects of face cream compositions H, H1, H2 and J1 described above on a photoaged 3D full thickness skin model were tested and compared. Experimental equipment: clean bench (Su Jing), CO2 incubator (Binder), UVA and UVB irradiator, microplate reader (BIO-TEK), freezing microtome (Leica). Experimental reagents and materials: 3D full thickness skin model (self-made in the lab), ELISA test kits for various indicators, MTT kits, etc.

[0044] The experimental procedure was as follows: (1) Construction of a 3D full-thickness skin model: A 3D full-thickness skin model was constructed using keratinocytes and fibroblasts; (2) Modeling and administration: When the model leaves the factory, that is, on day 0, it is irradiated with SSUV (UVA: 30 J / cm 2 ;UVB: 50mJ / cm2 ) was performed every day, and then a certain amount of sample was applied to the corresponding model surface; in the model control, only the model culture medium was applied, and six replicate wells were provided for each group of test substances, and application was performed once a day for a total of four days; (3) Sample collection and detection: After modeling and administration, the culture medium was collected and MMP1 was determined using an ELISA kit; three models were obtained from each group, and the model viability was determined using an MTT kit, and the remaining three models were subjected to tissue fixation and IHC staining to determine the type IV collagen content at the junction between the epidermis and dermis; (4) Analysis: T-test method was used for statistical analysis.

[0045] The test results are shown in the table below. [Table 5]

[0046] The results show that, compared with composition H, compositions H1 and H2 significantly increase the tissue vitality of FulKutis, promote the expression of type IV collagen at the junction between the epidermis and dermis, while significantly reducing the expression of MMP-1 in the extracellular matrix, fully indicating that the combination of birch sap or concentrated birch sap and polypeptide can significantly improve the anti-wrinkle effect, and they have a significant synergistic effect. Furthermore, when comparing H1 with H2, it can be seen that concentrated birch sap has a significantly higher synergistic effect on polypeptide than pure birch sap.

[0047] Example 6: Effect of Compositions H and H2 on Human Skin Morphology In this example, subjects with wrinkle grades 1-5 were selected to test the changes in the subjects' left and right crow's feet wrinkles, as well as the changes in cheek moisture and TEWL after 2 and 4 weeks of use of Compositions H and H2, thereby evaluating Compositions H and H2 for their anti-wrinkle effects, skin moisture content and improvement of skin barrier function.

[0048] Using a half-face controlled test method, subjects were tested prior to product application and after 2 and 4 weeks of product application as follows: 1) Primos was used to photograph the subjects' left and right corners of the eyes, and the software was used to calculate wrinkle parameters, including wrinkle volume, wrinkle area, wrinkle depth, etc.; 2) Skin moisture content of the left and right cheeks was tested using a Corneometer; 3) Transepidermal water loss (TEWL) values ​​were tested on the left and right cheeks using a Tewameter.

[0049] After cleansing in the morning and evening, and after using lotion, an appropriate amount of the test sample was applied to the left and right faces (including the area around the eyes). The original skin care routine was maintained throughout the study, and only the face cream that the subject had previously used was replaced with the test sample.

[0050] The test equipment used was: Primos (Canfield, USA) Skin moisture tester Corneometer (Courage & Khazaka, Germany) TEWL tester Tewameter (Courage & Khazaka, Germany)

[0051] Subjects: Select subjects who meet the following criteria: 1) According to the standard photos of wrinkle levels, pick up subjects with wrinkle grades 1-5, and the wrinkles were not caused by diseases; 2) the test sites were free of skin procedures, cosmetic and other tests that may affect the results; 3) Subjects who have not used hormone or immunosuppressant drugs in the past month; 4) Not currently participating in any other clinical trials at the study site or in the past 3 months;

[0052] Of these, those who meet any of the following criteria will be excluded: 1) Pregnant or breastfeeding women; 2) People with severe systemic disease, immunodeficiency or autoimmune disease; 3) Subjects who have used antihistamines in the past week or immunosuppressants in the past month; 4) those who used anti-inflammatory drugs at the study site in the past 2 months; 5) Patients with insulin-dependent diabetes mellitus; 6) Patients with ongoing respiratory disease; 7) Those with allergies, allergic dermatitis, or a history of skin diseases; 8) Subjects undergoing dermatological treatment; 9) Subjects with large areas of birthmarks, scars, vitiligo, pigmented nevi, keloids, or other skin characteristics that may affect testing in the test area.

[0053] Other requirements: 1) During the study, the use of other products that may affect the study is prohibited; 2) the same facial immobilization equipment and methods were used throughout the study; 3) The test environment, test time and test location are as follows: 1) The test areas included the corners of the eyes, forehead and cheeks; before the test, the subjects washed their faces with face cream and wiped them with cosmetic tissue; 2) sitting in a standard room for 20 minutes, without water or beverages, exposing the test area, relaxing, and not touching the test area; 3) The left and right eye corners were randomly divided into product application and blank control areas to ensure statistical balance; 4) During the test, the same facial fixation equipment and fixation method were used, and photos of the subject's left and right crow's feet were collected before use of the product and after 2 and 4 weeks of use of the product according to the Primos instructions, and the moisture and TEWL values ​​of both sides of the subject's cheeks were tested using a Corneometer and a Tewameter, respectively.

[0054] Number of subjects: 39 enrolled, 5 withdrew, for a total of 34 active subjects, mean age 45.5 ± 8.5 years. (1) Amount of wrinkles [Table 6]

[0055] The amount of wrinkles was used to characterize the amount of wrinkles at the crow's feet, with higher values ​​indicating more wrinkles and vice versa. After the use of H2, the amount of wrinkles gradually decreased, and the amount of wrinkles was significantly decreased at 4 weeks (p<0.01). Compared with before use, after 4 weeks of using H, there was no significant difference in the area of ​​wrinkles (P>0.05). After 4 weeks of use, the difference between H2 and H was highly significant (p<0.01), indicating that H2 has the effect of reducing skin wrinkles. (2) Depth of wrinkles [Table 7]

[0056] Wrinkle depth was used to characterize the depth of crow's feet wrinkles, the higher the value, the deeper the wrinkles, and vice versa. After the use of H2, the wrinkle depth gradually decreased, and the wrinkle depth was significantly decreased at 4 weeks (p<0.01). Compared with before use, there was no significant difference in wrinkle depth after 4 weeks of use of H (P>0.05). After 4 weeks of use, the difference between H2 and H was highly significant (p<0.01), indicating that H2 has the effect of reducing skin wrinkles. (2) Wrinkle area [Table 8]

[0057] The wrinkle area was used to characterize the total area of ​​crow's feet wrinkles, with higher values ​​indicating more wrinkles and vice versa. After the use of H2, the wrinkle area gradually decreased, and the wrinkle area was significantly decreased at 4 weeks (p<0.01). Compared with before use, there was no significant difference in the wrinkle area after using H for 4 weeks (P>0.05). After 4 weeks of use, the difference between H2 and H was highly significant (p<0.01), indicating that H2 has the effect of reducing skin wrinkles. 4) Moisture content [Table 9]

[0058] Moisture content was used to characterize the moisture content of the stratum corneum of the skin, the higher the value, the higher the skin moisture content, and vice versa. After the use of H2, the skin moisture content gradually increased, and the increase was highly significant at 4 weeks (p<0.01). Compared with before use, after 4 weeks of using H, there was no significant difference in skin moisture content (P>0.05). After 4 weeks of use, the difference between H2 and H was highly significant (p<0.01), indicating that H2 has the effect of increasing skin moisture content. (5) TEWL [Table 10]

[0059] TEWL was used to characterize the skin barrier function, the higher the value, the worse the skin barrier function and vice versa. After the use of H2, the TEWL value gradually decreased, and the decrease was significant at 4 weeks (p<0.05). Compared with before use, there was no significant difference in the TEWL value after using H for 4 weeks (P>0.05). After 4 weeks of use, the difference between H2 and H was highly significant (p<0.01), indicating that H2 has the effect of repairing the skin barrier function. [Table 11]

[0060] An anti-wrinkle eye cream composition was prepared as follows: 1. Oil phase: Raw materials 1, 3, 4 and 5 were added to the oil phase pot, heated to 80°C, dissolved and mixed well; 2. Raw materials 6, 7, 9, 10 and 11 were mixed thoroughly at room temperature; 3. Water Phase: Heat raw material 2 to 80℃, add the mixture from step 3, dissolve and mix well; 4. Emulsification: the water phase and oil phase were added to the emulsification tank, kept at 80℃, homogenized and emulsified at 3000 rpm for 5 minutes, and after the emulsification was completed, raw material 12 was added; 5. Add raw material 8, cool to 40℃ with stirring, add the mixture from step 2, stir well, and discharge to get the anti-wrinkle eye cream composition.

[0061] Using a half-face controlled test method, 20 subjects were tested before and after 4 weeks of product use as follows: 1) Primos was used to photograph the subjects' left and right corners of the eyes, and the software was used to calculate wrinkle parameters, including wrinkle volume, wrinkle area, wrinkle depth, etc.; 2) The skin moisture content of the left and right corners of the eyes was tested using a Corneometer;

[0062] The results showed that 18 out of 20 subjects had a significant increase in skin moisture content at the corners of the eyes, and 16 of these subjects had significantly shallower and lighter wrinkles, a reduction in the wrinkle area, and a reduction in the amount of wrinkles.

[0063] [Table 12]

[0064] An anti-wrinkle milk composition was prepared as follows: 1. Oil Phase: Raw materials 4, 5, 6, 7, 10, 12, 13 and 14 were added to the oil phase pot, heated to 80°C, dissolved and mixed well; 2. Raw materials 1, 2, 8, 9, 17 and 19 were mixed thoroughly at room temperature; 3. Raw materials 3, 18 and 20 were mixed thoroughly at room temperature; 4. Water Phase: Heat the mixture from step 2 to 80°C and add the mixture from step 3, dissolve and mix well; 5. Emulsification: the water phase and oil phase were added to the emulsification tank, kept at 80℃, homogenized and emulsified at 3000 rpm for 5 minutes, and after the emulsification was completed, raw material 16 was added; 6. Add raw material 8, cool to 40°C with stirring, add raw materials 11, 12 and 15, stir well, and discharge to obtain an anti-wrinkle emulsion composition.

[0065] Nineteen subjects were treated with the above lotion composition for four weeks and then made subjective evaluations of the use, among which 18 reported a significant increase in skin moisture and smooth, delicate and elastic skin; 15 reported a significant improvement in nasolabial folds and eye wrinkles.

Claims

1. 1. Use of a combination of (A) concentrated birch sap and (B) one or more substances selected from palmitoyl tripeptide-5, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone and adenosine in an anti-aging cosmetic composition, wherein the concentrated birch sap has a concentration of 1.2 to 4 times, the content of component (A) concentrated birch sap is 18 to 98 wt % based on the total weight of the cosmetic composition, and the content of component (B) is 0.005 to 10 wt % based on the total weight of the cosmetic composition.

2. 2. Use according to claim 1, wherein the concentrated birch sap has a concentration of 1.2 to 2 times.

3. An anti-aging cosmetic composition comprising: (A) concentrated birch sap having a concentration of 1.2 to 4 times; and (B) one or more substances selected from palmitoyl tripeptide-5, sodium hyaluronate, retinol, retinal, retinyl palmitate, tocopherol, ubiquinone, and adenosine. The content of component (A) concentrated birch sap is 18 to 98% by weight based on the total weight of the cosmetic composition, and the content of component (B) is 0.005 to 10% by weight based on the total weight of the cosmetic composition.

4. 4. The anti-aging cosmetic composition according to claim 3, wherein the concentrated birch sap has a concentration of 1.2 to 2 times.

5. 4. The anti-aging cosmetic composition according to claim 3, wherein the content of component (B) is 0.01 to 8% by weight based on the total weight of the cosmetic composition.

6. 6. The anti-aging cosmetic composition according to claim 5, wherein the content of component (B) is 0.1 to 6% by weight based on the total weight of the cosmetic composition.

7. 7. The anti-aging cosmetic composition according to claim 6, wherein the content of component (B) is 0.5 to 5% by weight based on the total weight of the cosmetic composition.

8. The anti-aging cosmetic composition according to any one of claims 3 to 7, which does not further contain added water.

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