Preparation method and application of a quick long-acting soothing repair composition suitable for sensitive skin

By combining golden camellia honey, oat extract, myrothamnus flabellifolia extract, and schisandra chinensis extract, a protective film is built on the skin surface and deep moisturizes and locks in moisture, blocking inflammatory pathways. This solves the problems of slow onset and strong irritation of existing soothing and repairing products, providing immediate soothing and long-lasting repair effects.

CN120899610BActive Publication Date: 2026-03-27N O D TOPIA (GUANGZHOU) BIOTECHNOLOGY CO LTD
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2025-08-07
Publication Date
2026-03-27

AI Technical Summary

Technical Problem

Existing soothing and repairing products are slow to take effect, have a single pathway of action, and are highly irritating, failing to meet the immediate soothing needs of sensitive skin.

Method used

Using a combination of golden camellia honey, oat extract, myrothamnus flabellifolia extract, and schisandra chinensis extract, it achieves rapid soothing and long-lasting repair by building a protective film on the skin surface, deeply moisturizing and locking in moisture, and blocking inflammatory pathways.

Benefits of technology

It instantly soothes skin redness and repairs the skin barrier, providing a fast and long-lasting safe solution suitable for sensitive skin, and is free of hormones, alcohol, and sensitizing preservatives.

✦ Generated by Eureka AI based on patent content.

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Abstract

The application belongs to the technical field of cosmetics, and particularly relates to a preparation method of a quick long-acting soothing and repairing composition suitable for sensitive skin and application thereof. The application provides a soothing and repairing composition, which is compounded by camellia chrysantha honey, oat extract, myrobalan extract and schisandra chinensis extract. The composition not only realizes quick redness fading, but also synchronously constructs a tough barrier against external stimulation. The composition is free of hormones, alcohol and sensitizing preservatives throughout the whole process, and provides a safe solution with first-aid and long-term repairing force for sensitive skin, filling the market gap of mild and quick-acting repairing products. The composition provided by the application has the advantages of simple preparation method, suitability for industrial production and the like, and can be applied to the preparation of soothing and repairing products, and has good market application value.
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Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of cosmetics, in particular to a preparation method of a quick and long-acting soothing and repairing composition suitable for sensitive skin and application thereof. BACKGROUND

[0002] Skin, as the largest organ of the human body, has functions of barrier protection, sensory conduction, body temperature regulation and aesthetic display. The skin barrier protects the body from external environmental hazards, helps maintain skin moisture, prevents excessive water loss, and thus maintains the softness and elasticity of the skin. However, irregular lifestyle phenomena such as staying up late, overeating, and excessive ultraviolet radiation, as well as excessive skin cleansing, can easily cause skin problems such as sensitive skin.

[0003] The soothing and repairing products on the current market generally have three limitations: traditional anti-sensitivity ingredients have a slow effect, which cannot meet the immediate soothing needs of sudden redness and pain of the skin; barrier repair ingredients mostly focus on physical moisturizing, lacking synergistic regulation of inflammatory pathways and photodamage; and some fast-acting anti-inflammatory products rely on hormones or strong ingredients, which may pose a risk of irritation and dependence.

[0004] Camellia chrysantha is a plant of the Theaceae family, and is known as the "Queen of Tea" and "Giant Panda of the Plant World" due to its unique golden yellow flowers. The flowers and leaves are rich in proanthocyanidins, flavonoid glycosides (such as quercetin glycoside and myricetin), tea polyphenols and various trace elements, which endow them with significant antioxidant, anti-inflammatory and moisturizing effects. However, the stability of Camellia chrysantha extract restricts its application breakthrough, and the honey produced by bees from the nectar of Camellia chrysantha flowers not only retains the inherent sugar moisturizing matrix and enzyme activity of honey, but also contains unique active ingredients of Camellia chrysantha, and has better stability than Camellia chrysantha extract, showing significant potential in skin care applications. Therefore, it is of great significance to study a soothing and repairing composition. SUMMARY

[0005] In view of the above defects or improvement needs of the prior art, the present application provides a preparation method of a quick and long-acting soothing and repairing composition suitable for sensitive skin and application thereof. The soothing and repairing composition forms a protective film on the skin surface, deeply moisturizes and locks in water, and blocks inflammatory pathways, thereby soothing redness and repairing the skin barrier, and the effect can be immediately realized and continuously maintained, which is suitable for sensitive skin and solves the problems of slow effect, single action pathway and strong irritation of existing soothing and repairing products.

[0006] The object of the present application can be achieved by the following technical solutions:

[0007] In a first aspect, the present application provides a soothing repair composition comprising the following components: camellia japonica honey, oat extract, myrobalan extract and schisandra chinensis extract, wherein the weight ratio of the camellia japonica honey, the oat extract, the myrobalan extract and the schisandra chinensis extract is (0.1-10):(0.01-2):(0.01-5):(0.01-2).

[0008] The camellia japonica honey is honey produced by bees collecting camellia japonica nectar, which not only has typical sugar and protein components of honey, but also contains active substances such as tea polyphenols and flavonoids. The sugar components form a moisturizing and water-locking film on the skin surface, and the polyphenols and flavonoids have a high antioxidant effect, which significantly enhances the skin's water-locking ability and soothes redness.

[0009] The oat extract is rich in dihydro-oat alkaloids, which have multiple functions such as anti-histamine, antioxidant, anti-irritation, anti-inflammatory and improvement of erythema.

[0010] The myrobalan extract is rich in glycerol glucoside and trehalose, which can activate the synthesis of AQP3 water channel protein to achieve deep skin moisturizing and barrier repair.

[0011] The schisandra chinensis extract is rich in schisandrin and lignans, which have a strong anti-inflammatory effect and can effectively soothe skin redness and tingling.

[0012] Preferably, the weight ratio of the camellia japonica honey, the oat extract, the myrobalan extract and the schisandra chinensis extract is (1-5):(0.05-0.5):(0.1-3):(0.05-0.5).

[0013] Preferably, the weight ratio of the camellia japonica honey, the oat extract, the myrobalan extract and the schisandra chinensis extract is (2-3):(0.1-0.2):(0.5-1):(0.1-0.2).

[0014] In a second aspect, the present application provides the use of the soothing repair composition of the first aspect in the preparation of a cosmetic product having moisturizing, soothing and repairing effects and suitable for sensitive skin.

[0015] Preferably, the cosmetic product is a cosmetic water, an emulsion, a cream, a mask, a serum or a spray.

[0016] In a third aspect, the present application provides an emulsion comprising the following raw materials by weight percentage: 2%-6% of the soothing repair composition of the first aspect, 0.05%-0.3% of a thickening agent, 0.5%-3% of a humectant, 0.01%-0.3% of a pH adjuster, 0.5%-5% of an emulsifier and 0.5%-3% of a preservative, and the balance is deionized water.

[0017] Preferably, the thickener comprises at least one of the following: polyacrylate crosspolymer-6, carbomer, carrageenan, gellan gum, xanthan gum, microcrystalline cellulose, cellulose gum, ethyl cellulose, sclerotium taurate gum, guar gum, ammonium acryloyl dimethyl taurate / VP copolymer, acrylate copolymers, and sclerotium taurate gum.

[0018] Preferably, the moisturizer comprises at least one of glycerin, D-panthenol, vitamin B5, 1,2-butanediol, 1,3-butanediol, 1,2-hexanediol, 1,3-propanediol, caprylyl glycol, dipropylene glycol, sodium hyaluronate, tremella polysaccharide, trehalose, betaine, allantoin, sodium hyaluronate, β-glucan, budding stalk polysaccharide, and ceramide.

[0019] Preferably, the pH adjuster includes at least one of arginine, tromethamine, and disodium EDTA.

[0020] Preferably, the emulsifier comprises at least one of the following: caprylic / capric triglyceride, C14-22 alcohol, C12-20 alkyl glucoside, sodium polyacrylate, hydrogenated lecithin, cetearyl glucoside, isononyl isononanoate, pentaerythritol tetraester, polydimethylsiloxane, stearyl alcohol, hydroxystearic acid, polymethylsilsesquioxane, pentaerythritol distearate, and sucrose stearate.

[0021] Preferably, the preservative includes at least one of p-hydroxyacetophenone and 1,2-hexanediol.

[0022] A fourth aspect of the present invention provides a method for preparing the emulsion described in the third aspect, comprising the following steps:

[0023] S1. Mix the humectant, thickener, part of the pH adjuster and deionized water, heat to 80-90℃, and homogenize at 1200-1400 rpm for 3-5 minutes. After homogenization, keep warm for later use to obtain the pre-prepared phase A.

[0024] S2. Mix the emulsifier, heat to 70-80℃, and homogenize at 1200-1400 rpm for 3-5 minutes. After homogenization, keep warm for later use to obtain the pre-prepared phase B.

[0025] S3. Mix the preservatives and heat to 55-65℃ to melt them, to obtain the pre-prepared C phase;

[0026] S4, the pre-preparation A phase temperature is adjusted to 75-85 DEG C, the pre-preparation B phase is added at the rotation speed of 250-350 rpm, stirring and mixing, cooling to 55-65 DEG C, the pre-preparation C phase is added at the rotation speed of 250-350 rpm, stirring and mixing, cooling to 40-50 DEG C, the soothing repair composition is added, continuing to stir at the rotation speed of 250-350 rpm for 7-9 min, the remaining pH regulator is added, stirring uniformly, discharging, and the emulsion is obtained.

[0027] Compared with the prior art, the beneficial effects of the present application are:

[0028] The present application provides a soothing repair composition. Among them, the golden tea honey forms a breathable water-retaining film quickly through fructose oligosaccharide, and the high-permeability flavonoid component directly attacks the source of inflammation; the oat extract precisely blocks the nerve ending stimulation signal at a trace concentration, immediately relieving the burning discomfort; the myrobalan extract activates the synthesis of deep water channel proteins, realizing long-term hydration and barrier reconstruction of the dermis; and the schisandra chinensis extract effectively suppresses the inflammatory cascade reaction, cutting off the vicious cycle of repeated redness. The composition realizes rapid redness subsidence through the four-dimensional linkage mechanism of "surface film water locking-nerve desensitization-inflammation interruption-deep water delivery", not only realizes rapid redness subsidence, but also synchronously constructs a resilient barrier against external stimuli, and the whole process does not contain hormones, alcohol and allergenic preservatives, providing a safe solution with first-aid and long-term repair force for sensitive skin, filling the market gap of mild and rapid repair products. BRIEF DESCRIPTION OF DRAWINGS

[0029] Figure 1 The skin redness comparison chart of the subjects using the serum of application example 1 and blank application example before use, 30 min after use and 7 days after use. DETAILED DESCRIPTION

[0030] In order to further illustrate the technical means and effects adopted by the present application to achieve the predetermined purpose, the specific embodiments, structures, features and effects according to the present application are described in detail as follows.

[0031] The experimental methods not specified in the following examples are usually carried out according to the conventional conditions or the conditions recommended by the manufacturers. The materials, reagents, etc. used, unless otherwise specified, can be obtained from commercial channels.

[0032] The golden tea honey is purchased from Beihai Jinlai Biotechnology Co., Ltd.;

[0033] The oat extract is purchased from Xi'an Jihe Biotechnology Co., Ltd.;

[0034] The myrobalan extract is purchased from Boseng Biotechnology (Shanxi) Co., Ltd.;

[0035] Schisandra chinensis extract was purchased from Draco Natural Products, USA;

[0036] Camellia sinensis extract was purchased from Shenzhen Weiqi Technology Co., Ltd.;

[0037] Portulaca oleracea extract was purchased from Xi'an Yousuo Biological Technology Co., Ltd.;

[0038] Scutellaria baicalensis extract was purchased from Shaanxi Xintianyu Biological Technology Co., Ltd.

[0039] The component composition (parts by weight) of the soothing repair composition of Examples 1-6 in the present application is shown in Table 1 below.

[0040] Table 1 Component and its parts by weight of soothing repair composition of Examples 1-6

[0041] Group Camellia sinensis honey (parts by weight) Oat extract (parts by weight) Myrobalan extract (parts by weight) Schisandra chinensis extract (parts by weight) Example 1 3 0.1 0.5 0.20 Example 2 2 0.2 1 0.10 Example 3 5 0.5 0.1 0.05 Example 4 1 0.05 3 0.50 Example 5 10 2 0.01 0.01 Example 6 0.1 0.01 5 2.00

[0042] Comparative Example 1: Compared with Example 1, the difference lies in that the weight ratio of Camellia sinensis honey, oat extract, Myrobalan extract and Schisandra chinensis extract in Comparative Example 1 is 15:0.001:10:0.001, and the total weight parts remain unchanged.

[0043] Comparative Example 2: Compared with Example 1, the difference lies in that the weight ratio of Camellia sinensis honey, oat extract, Myrobalan extract and Schisandra chinensis extract in Comparative Example 2 is 0.01:10:0.001:5.00, and the total weight parts remain unchanged.

[0044] Comparative Example 3: Compared with Example 1, the difference lies in that no Camellia sinensis honey is added in Comparative Example 3, and the missing amount is supplemented by oat extract, Myrobalan extract and Schisandra chinensis extract with a weight ratio of 0.1:0.5:0.20, and other conditions are consistent with Example 1.

[0045] Comparative Example 4: Compared with Example 1, the difference lies in that no oat extract is added in Comparative Example 4, and the missing amount is supplemented by Camellia sinensis honey, Myrobalan extract and Schisandra chinensis extract with a weight ratio of 3:0.5:0.20, and other conditions are consistent with Example 1.

[0046] Comparative Example 5: Compared with Example 1, the difference lies in that no Myrobalan extract is added in Comparative Example 5, and the missing amount is supplemented by Camellia sinensis honey, oat extract and Schisandra chinensis extract with a weight ratio of 3:0.1:0.20, and other conditions are consistent with Example 1.

[0047] Comparative Example 6: Compared with Example 1, the difference lies in that no Schisandra chinensis extract is added in Comparative Example 6, and the missing amount is supplemented by Camellia sinensis honey, oat extract and Myrobalan extract with a weight ratio of 3:0.1:0.5, and other conditions are consistent with Example 1.

[0048] Comparative Example 7: Compared with Example 1, the difference lies in that no Flos Lonicerae Japonicae nectar is added in Comparative Example 7, and the missing amount is made up with an equal amount of Myrobalan extract.

[0049] Comparative Example 8: Compared with Example 1, the difference lies in that no Avena extract is added in Comparative Example 8, and the missing amount is made up with an equal amount of Schisandra extract.

[0050] Comparative Example 9: Compared with Example 1, the difference lies in that no Flos Lonicerae Japonicae nectar is added in Comparative Example 9, and is replaced with an equal amount of Flos Lonicerae Japonicae extract.

[0051] Comparative Example 10: Compared with Example 1, the difference lies in that no Avena extract is added in Comparative Example 10, and is replaced with an equal amount of panthenol.

[0052] Comparative Example 11: Compared with Example 1, the difference lies in that no Myrobalan extract is added in Comparative Example 11, and is replaced with an equal amount of Portulaca oleracea extract.

[0053] Comparative Example 12: Compared with Example 1, the difference lies in that no Schisandra extract is added in Comparative Example 12, and is replaced with an equal amount of Scutellaria extract.

[0054] Performance test

[0055] Test Example 1: Verification of soothing and repairing effect of the composition

[0056] This test example investigates the soothing and repairing effect of the compositions prepared in Examples 1-6 and Comparative Examples 1-12.

[0057] The cell line used is human keratinocyte HaCaT (BeNa Biotech), and the test conditions are: incubator temperature 37±1℃, humidity 90±5%, carbon dioxide 5±1%; the cells are cultured and treated according to the grouping, and then tested, and the specific test is the detection of inflammatory factors IL-6 and filaggrin FLG content, and the test method is as follows:

[0058] (1) The cell suspension was inoculated in a 96-well cell culture plate, with a density of 2000 cells per well, and 100 μL of DMEM medium (2105341, Gibco) was added to each well, and cultured for 24 h;

[0059] (2) Discard the supernatant, add 100 μL of PBS buffer to each well, and expose the cells to UVB irradiation for 10 minutes, with a dose of 100 mJ / cm 2 ;

[0060] (3) Discard the supernatant, add 100 μL of DMEM medium to the blank control group, and add 100 μL of DMEM medium containing 0.01% of the corresponding sample (compositions prepared in Examples 1-7 and Comparative Examples 1-12) to the test groups, and set 6 parallel repeats for each group;

[0061] (4) After 48 h of incubation, the culture solution and cells were collected, respectively;

[0062] (5) Inflammatory factor IL-6 content detection: the human IL-6 ELISA kit (EHC007.96, Shenzhen Xingboshen Biological Technology Co., Ltd.) was used to detect the content of the inflammatory factor IL-6 released by the cells in the culture solution.

[0063] (6) Filaggrin FLG content detection: the collected cells were lysed with RIPA cell lysis solution containing protease inhibitors, the lysed samples were centrifuged at 12000 g for 5 minutes, the supernatant was taken, and the human filaggrin (FLG) ELISA kit (item number BLL107115E, Bailile Biological) was used to detect the filaggrin FLG content of the supernatant of each group of tissues;

[0064] Inflammatory response can affect the stability of skin structure through pathways such as destroying skin barrier function, degrading collagen, and triggering pigmentation. Long-term or excessive inflammatory response can lead to decreased skin defense and accelerate the aging process. Interleukin-6 (IL-6) is a marker of inflammatory response, and its elevated level represents the presence of inflammatory response in the body.

[0065] Filaggrin (FLG) is an important molecule that connects keratin fibers in the stratum corneum of human skin. Under the assistance of FLG monomers, keratin fibers regularly aggregate to form a solid physical barrier in the outermost layer of the epidermis, playing a role in strengthening the skin.

[0066] The soothing ability of the composition is represented by the improvement of the inflammatory factor IL-6, and the skin barrier repair ability is represented by the improvement of the filaggrin FLG content. The IL-6 improvement rate and the FLG improvement rate are calculated according to the following formula:

[0067] IL-6 improvement rate = (1-IL-6 content 样品处理 / IL-6 content 空白对照 ) x 100%;

[0068] FLG improvement rate = (FLG content 样品处理 / FLG content 空白对照 -1) x 100%;

[0069] The data is presented as an average value. As can be seen from the data of Example 1 and Comparative Examples 3-12 in Table 2, the IL-6 improvement rate and the FLG improvement rate of the composition of Example 1, which is prepared by compounding the four components of tea honey, oat extract, myrobalan extract and schisandra extract, are significantly increased, indicating that the four components of tea honey, oat extract, myrobalan extract and schisandra extract have a synergistic effect, and the prepared composition has excellent soothing and repairing effect.

[0070] As can be seen from the data of Examples 1-6 and Comparative Examples 1-2, when the weight ratio of tea honey, oat extract, myrobalan extract and schisandra extract is (2-3):(0.1-0.2):(0.5-1):(0.1-0.2), the soothing and repairing effect of the composition is better.

[0071] Table 2: Data of soothing and repairing effect of each group

[0072] Group IL-6 improvement rate (%) FLG improvement rate (%) Example 1 68.42 43.21 Example 2 67.19 45.03 Example 3 62.13 40.32 Example 4 64.05 38.87 Example 5 58.82 35.15 Example 6 55.34 33.59 Comparative Example 1 25.39 17.92 Comparative Example 2 28.27 19.73 Comparative Example 3 7.23 3.37 Comparative Example 4 7.59 10.08 Comparative Example 5 14.56 3.12 Comparative Example 6 4.21 9.46 Comparative Example 7 23.36 24.78 Comparative Example 8 24.83 23.22 Comparative Example 9 21.58 18.34 Comparative Example 10 22.04 22.16 Comparative Example 11 25.36 19.08 Comparative Example 12 18.83 21.57

[0073] Application Examples 1-8 and Comparative Application Examples 1-13

[0074] The compositions of Examples 1-6 and Comparative Examples 1-12 are added to the emulsion at a concentration of 4wt%, to obtain the emulsions of Application Examples 1-6 and Comparative Application Examples 1-12, and the formulations are shown in Table 3.

[0075] The preparation method of the emulsions of Application Examples 1-6 and Comparative Application Examples 1-12 specifically includes the following steps:

[0076] S1, mix the humectant, thickening agent, part of the pH adjuster with deionized water, heat to 85℃, then homogenize at a speed of 1300 rpm for 4 min, after homogenization, keep warm for standby, get pre-made A phase;

[0077] S2, mix the emulsifier, heat to 75℃, then homogenize at a speed of 1300 rpm for 4 min, after homogenization, keep warm for standby, get pre-made B phase;

[0078] S3, mix the preservative, melt at 60℃, get pre-made C phase;

[0079] S4, adjust the temperature of pre-made A phase to 80℃, add pre-made B phase at a speed of 300 rpm, stir evenly, cool to 60℃, then add pre-made C phase at a speed of 300 rpm, stir evenly, cool to 45℃, add the soothing and repairing composition, continue to stir at a speed of 300 rpm for 8 min, add the remaining pH adjuster, stir evenly, discharge, to obtain the emulsion.

[0080] Table 3: Formulation of emulsion of Application Examples 1-6 and Comparative Application Examples 1-12

[0081]

[0082] Application Example 7: Compared with Application Example 1, the difference is that the soothing repair composition is added into the emulsion at a concentration of 2 wt% in Application Example 7, and the preparation method is the same as that in Application Example 1.

[0083] Application Example 8: Compared with Application Example 1, the difference is that the soothing repair composition is added into the emulsion at a concentration of 6 wt% in Application Example 8, and the preparation method is the same as that in Application Example 1.

[0084] Comparative Application Example 13 (blank application example): Compared with Application Example 1, the difference is that the emulsion of Comparative Application Example 12 does not add the soothing repair composition, and an equal amount of deionized water is used instead of the composition, and the preparation method is the same as that in Application Example 1.

[0085] Test Example 2: Human skin patch test

[0086] Thirty volunteers, 15 males and 15 females, aged 20-50 years old, were recruited, and a closed patch test method was used. 0.025 mL of the test sample (emulsion prepared by Application Examples 1-8, Comparative Application Examples 1-12, and the blank application example) was placed in a specific patch tester, which was attached to the volunteer's arm with a low-sensitization tape, and was lightly pressed to evenly attach to the skin, and was left for 24 h; the blank control group was distilled water, and the blank application example was the emulsion without the soothing repair composition. After 24 h, the patch tester was removed, and the skin reaction was observed after 0.5 h, 24 h, and 48 h, and the results were recorded. The skin adverse reaction grade is shown in Table 4 below.

[0087] The results of the human skin patch test show that the Application Examples 1-8, Comparative Application Examples 1-12, and the blank application example of the present application have no skin adverse reactions after 0.5 h, 24 h, and 48 h of observation, and all are negative reactions, indicating that the emulsion prepared by the composition provided by the present application is safe, and it is safe and non-irritating to human skin.

[0088] Table 4 Skin adverse reaction grade

[0089] Score level Skin reaction 0 Negative reaction 1 Suspected reaction, only weak erythema 2 Weak positive reaction (erythema reaction): erythema, infiltration, edema, possibly papules 3 Strong positive reaction (vesicle reaction): erythema, infiltration, edema, papules; reaction can exceed the test area 4 Very strong positive reaction (fusion vesicle reaction): obvious erythema, severe infiltration, edema, fusion vesicles; reaction exceeds the test area

[0090] Test Example 3: Human efficacy test

[0091] Experimental method: 126 Asian adult test subjects aged 18-60 years who self-identified as having sensitive skin were selected and randomly divided into 21 groups, with 6 people in each group. The volunteers applied 1 g of sample to the whole face once in the morning and once in the evening (the sample was the emulsion prepared according to application examples 1-8, comparative application example 1-12, and the blank application example) each day. Data were collected before use (T0), 30 min after use (T30 min), and at 7 days after use (T7). After the volunteers washed their faces with facial cleanser and sat in an air-conditioned room with a temperature of 21 ± 1 °C and a humidity of 50 ± 10% for 30 min, the researchers measured the skin moisture content of the cheekbones using a skin moisture test probe (Corneometer); photographed the faces of the volunteers using Visia-7, and performed image analysis on the red region images to obtain the a* value; and measured the trans-epidermal water loss (TEWL) value of the cheekbones using a skin moisture loss test probe (TewaMeter®TM Hex). At the first visit, the volunteers were first measured for the initial value before use, then applied the sample to the whole face, and after sitting for 30 min, the values after 30 min of sample use were measured.

[0092] The skin moisturizing ability was represented by the improvement in skin moisture content, the skin soothing ability was represented by the improvement in a* value, and the skin barrier repair ability was represented by the improvement in TEWL value, which were calculated according to the following formulas, respectively:

[0093] The skin moisture content improvement rate = [(sample Tx - sample T0 ) / sample T0 - (blank application example Tx - blank application example T0 ) / blank application example T0 ] x 100%;

[0094] The a* value improvement rate = [(sample T0 - sample Tx ) / sample T0 - (blank application example T0 - blank application example Tx ) / blank application example T0 ] x 100%;

[0095] The TEWL value improvement rate = [(sample T0 - sample Tx ) / sample T0 - (blank application example T0 - blank application example Tx ) / blank application example T0 ] x 100%;

[0096] In the formula, sample T0 is the data of each index before use (T0) of the sample group; sample TxThe data of each index of the sample group using 30 min (T30min) or using 7 days (T7) are used; blank application example T0 The data of each index of the blank application example before use (T0) are used; blank application example Tx The data of each index of the blank application example on the Xth day are used;

[0097] The calculation results are averaged, and Table 5 is specifically shown.

[0098] Table 5: Human efficacy test data of each group of emulsions

[0099]

[0100] As can be seen from the data of application example 1 and comparative application examples 3-12 in Table 5, the skin moisture content improvement rate, a* value improvement rate and TEWL value improvement rate of the emulsion of application example 1 using four components of honey of camellia japonica, oat extract, myrobalan extract and schisandra chinensis extract are all significantly increased, indicating that the four components of honey of camellia japonica, oat extract, myrobalan extract and schisandra chinensis extract have a synergistic effect, and the prepared emulsion has excellent soothing and repairing effect.

[0101] It can be seen from the data of application examples 1-6 and comparative application examples 1-2 that when the weight ratio of honey of camellia japonica, oat extract, myrobalan extract and schisandra chinensis extract is (2-3):(0.1-0.2):(0.5-1):(0.1-0.2), the soothing and repairing effect of the emulsion is better.

[0102] It can be seen from the data of application example 1 and application examples 7-8 that when the soothing and repairing composition is added to the emulsion at a concentration of 2-6 wt%, the skin moisture content improvement rate, a* value improvement rate and TEWL value improvement rate are all higher, indicating that the soothing and repairing effect of the emulsion is better.

[0103] The above is only a preferred embodiment of the present application, and does not limit the present application in any form. Although the present application has been disclosed as above with a preferred embodiment, it is not intended to limit the present application. Any person skilled in the art can make some changes or modifications to the above disclosed technical content to obtain equivalent embodiments with equivalent changes, without departing from the technical solution of the present application. Any modification, change, equivalent change and modification of the above embodiments made according to the technical essence of the present application, without departing from the technical solution of the present application, are still within the scope of the technical solution of the present application.

Claims

1. A soothing and repairing composition, characterized in that, It includes the following components: Camellia chrysantha honey, oat extract, Myrothamnus flabellifolia extract and Schisandra chinensis extract, wherein the weight ratio of Camellia chrysantha honey, oat extract, Myrothamnus flabellifolia extract and Schisandra chinensis extract is (0.1-10):(0.01-2):(0.01-5):(0.01-2).

2. The soothing and repairing composition as described in claim 1, characterized in that, The weight ratio of the golden camellia honey, oat extract, myrothamnus flabellifolia extract and schisandra chinensis extract is (1-5):(0.05-0.5):(0.1-3):(0.05-0.5).

3. The soothing and repairing composition as described in claim 1, characterized in that, The weight ratio of the golden camellia honey, oat extract, myrothamnus flabellifolia extract and schisandra chinensis extract is (2-3):(0.1-0.2):(0.5-1):(0.1-0.2).

4. The use of the soothing and repairing composition according to any one of claims 1-3 in the preparation of cosmetics having moisturizing, soothing, and repairing effects and suitable for sensitive skin.

5. The use of the soothing and repairing composition as described in claim 4 in the preparation of cosmetics with moisturizing, soothing, and repairing effects suitable for sensitive skin, characterized in that... The cosmetics mentioned are toners, lotions, creams, masks, serums, or sprays.

6. An emulsion, characterized in that, The ingredients comprise the following ingredients by weight percentage: 2%-6% of the soothing and repairing composition according to any one of claims 1-3, 0.05%-0.3% of thickener, 0.5%-3% of moisturizer, 0.01%-0.3% of pH adjuster, 0.5%-5% of emulsifier, and 0.5%-3% of preservative, with the balance being deionized water.

7. The emulsion as described in claim 6, characterized in that, The raw material is selected from at least one of (a)-(e): (a) The thickener comprises at least one of the following: polyacrylate crosspolymer-6, carbomer, carrageenan, gellan gum, xanthan gum, microcrystalline cellulose, cellulose gum, ethyl cellulose, sclerotium taurate gum, guar gum, ammonium acryloyl dimethyl taurate / VP copolymer, acrylate copolymer, and sclerotium taurate gum; (b) The moisturizer comprises at least one of the following: glycerin, D-panthenol, vitamin B5, 1,2-butanediol, 1,3-butanediol, 1,2-hexanediol, 1,3-propanediol, caprylyl glycol, dipropylene glycol, sodium hyaluronate, tremella polysaccharide, trehalose, betaine, allantoin, sodium hyaluronate, β-glucan, budding stalk polysaccharide, and ceramide; (c) The pH adjuster includes at least one of arginine, tromethamine, and disodium EDTA; (d) The emulsifier comprises at least one of the following: caprylic / capric triglyceride, C14-22 alcohol, C12-20 alkyl glucoside, sodium polyacrylate, hydrogenated lecithin, cetearyl glucoside, isononyl isononanoate, pentaerythritol tetraester, polydimethylsiloxane, stearyl alcohol, hydroxystearic acid, polymethylsilsesquioxane, pentaerythritol distearate, and sucrose stearate; (e) The preservatives include at least one of p-hydroxyacetophenone and 1,2-hexanediol.

8. The method for preparing the emulsion according to claim 7, characterized in that, Includes the following steps: S1. Mix the humectant, thickener, part of the pH adjuster and deionized water, heat to 80-90℃, and homogenize at 1200-1400 rpm for 3-5 minutes. After homogenization, keep warm for later use to obtain the pre-prepared phase A. S2. Mix the emulsifier, heat to 70-80℃, and homogenize at 1200-1400 rpm for 3-5 minutes. After homogenization, keep warm for later use to obtain the pre-prepared phase B. S3. Mix the preservatives and heat to 55-65℃ to melt them, to obtain the pre-prepared C phase; S4. Adjust the temperature of the pre-prepared phase A to 75-85℃, add the pre-prepared phase B at 250-350 rpm, stir and mix well, cool down to 55-65℃, add the pre-prepared phase C at 250-350 rpm, stir and mix well, cool down to 40-50℃, add the soothing and repairing composition, continue stirring at 250-350 rpm for 7-9 minutes, add the remaining pH adjuster, stir evenly, and discharge to obtain the emulsion.

Citation Information

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