CN113952288A

CN113952288A - Mother solution for repairing and beautifying muscle base and preparation method thereof

Info

Publication number: CN113952288A
Application number: CN202111339502.3A
Authority: CN
Inventors: 郑丽琼
Original assignee: Individual
Current assignee: Individual
Priority date: 2021-11-12
Filing date: 2021-11-12
Publication date: 2022-01-21

Abstract

The invention discloses a mother solution for repairing and beautifying muscle base and a preparation method thereof. The mother liquor for repairing and beautifying the skin bottom provided by the invention is prepared from multiple raw materials such as a secondary fission yeast fermentation product filtrate, schizophyllan, a secondary fission yeast fermentation product lysate, a leukocyte extract, a hydrolyzed placenta extract, a polypeptide freeze-dried powder and a composite extract, and the polypeptide repairing components can help the maintenance and growth of skin collagen and elastin, promote the self-repair of skin, lighten skin fine lines, and enable the skin to be full, smooth and compact and have high elasticity; active ingredients such as the secondary split yeast fermentation product filtrate, the secondarysplit yeast fermentation product lysate, the leucocyte extract, the hydrolyzed placenta extract and the composite extract can effectively moisten the skin and provide sufficient nutrition for the skin, and the active ingredients and the polypeptide ingredients have the synergistic effect of nourishing the skin, improving the water-deficient and dry state of the skin, and have the effects of resisting inflammation, fading fine wrinkles and repairing damaged skin.

Description

Mother solution for repairing and beautifying muscle base and preparation method thereof

Technical Field

The invention relates to the technical field of cosmetics, and particularly relates to a mother solution for repairing and beautifying muscle bases and a preparation method thereof.

Background

With the progress of the times, people pay more and more attention to their skin. Skin care is not available from various cosmetics, while the traditional cosmetics mostly use polyhydric alcohols and some saccharide humectants for moisturizing, but the moisturizers contained in the cosmetics cannot achieve the moisturizing effect of deep skin and long-acting moisturizing, and due to the lack of skin moisture and the influence of the environment on the skin, the barrier effect of the skin is damaged for a long time, so that the problem of more serious skin is caused.

In recent years, after growth factor polypeptides, collagen polypeptides and the like related to skin tissue cells are developed and successfully applied to skin beautifying repair cosmetics, people find that part of active peptides can directly activate skin cells to synthesize collagen, so that the collagen content is most effectively promoted and supplemented, the activity of the skin is fundamentally improved, the skin cells are activated to synthesize collagen, the skin repair is promoted, and the skin aging is resisted. However, the repair effect of a simple active peptide component on the skin is not obvious, so that a skin care product containing other active components is very necessary to be researched, and the skin repair is promoted and the cosmetic effect is improved through the synergistic effect between the other active components and the active peptide component.

Disclosure of Invention

The invention aims to provide a mother solution for repairing and beautifying muscle bases and a preparation method thereof, and aims to solve the technical problems.

In order to solve the technical problems, the technical scheme of the invention is as follows:

in a first aspect, the repair and beauty foundation mother solution provided by the invention comprises the following raw materials in percentage by weight: 0.1-10% of a schizosaccharomyces cerevisiae fermentation product filtrate, 0.1-3% of palmatine, 0.1-2% of a schizosaccharomyces cerevisiae fermentation product lysate, 0.1-2% of a leukocyte extract, 0.1-2.5% of a hydrolyzed placenta extract, 0.5-3% of a PEG/PPG-17/6 copolymer, 2-5% of butanediol, 2-8% of glycerol, 0.5-2% of jojoba wax PEG-120 esters, 5-25% of a composite extract, 0.5-2% of an ammonium acryloyldimethyl taurate/VP copolymer, 0.01-1% of a preservative, 0.1-1% of 1, 2-hexanediol, 1-3% of sodium hyaluronate, 0.1-0.5% of sodium polyglutamate, 1-10% of a lyophilized polypeptide powder, and the balance of water, wherein the composite extract is selected from a truffle extract, a ganoderma extract, a membrana astragali radix extract, a tripterygium wilfordii extract, a crocodile flower extract, a gardenia extract, a dendrobe extract, a dendrobium extract, a mangnolicina officinalis extract, a mangostin officinalis extract, a mangostin extract, and a officinalis extract, At least three of radix Saposhnikoviae extract, herba Sidae Rhombifoliae extract, and flos Albizziae extract; the polypeptide freeze-dried powder comprises the following raw materials in parts by weight: 2-10% of mannitol, 2-5% of trehalose, 11-5% of oligopeptide, 0.5-5% of glutathione, 10.1-1% of acetyl tripeptide, 50.1-1% of acetyl tetrapeptide, 0.1-1% of retinol/zymophyte polypeptide and the balance of water.

Preferably, the polypeptide freeze-dried powder is prepared by adopting the following method: heating water to 40-60 ℃, adding mannitol, trehalose, oligopeptide-1, glutathione, acetyl tripeptide-1, acetyl tetrapeptide-5 and retinol/zymophyte polypeptide, uniformly stirring, performing membrane filtration and centrifugation to obtain a mixed solution, and freeze-drying the obtained mixed solution to obtain the polypeptide freeze-dried powder.

Further preferably, the stirring conditions are as follows: the rotation speed is 1000-1500 r/min, and the time is 10-30 min.

Further preferably, the step of freeze-drying specifically comprises: filling the mixed solution into a container bottle, then putting the container bottle filled with the mixed solution into a vacuum freeze dryer, keeping a vacuum environment, cooling to-10 to-5 ℃, preserving heat, pre-freeze drying for 10-12 h, heating to-20 to-15 ℃, preserving heat, freeze drying for 10-15 h, heating to-1 to 2 ℃, preserving heat, sublimation drying for 4-8 h, finally heating to 40-45 ℃, preserving heat, desorbing and drying for 4-8 h.

Preferably, the polypeptide freeze-dried powder comprises the following raw materials in percentage by weight: 3-5% of mannitol, 2-3% of trehalose, 12.5-3% of oligopeptide, 1-2% of glutathione, 10.2-0.5% of acetyl tripeptide, 50.2-0.5% of acetyl tetrapeptide, 0.4-0.8% of retinol/zymophyte polypeptide and the balance of water.

Preferably, the repair beauty muscle base mother solution comprises the following raw materials in percentage by weight: 5-10% of a secondary split yeast fermentation product filtrate, 2-3% of palmatine, 1-2% of a secondary split yeast fermentation product lysate, 1-2% of a leukocyte extract, 1.5-2.5% of a hydrolyzed placenta extract, 1-2% of a PEG/PPG-17/6 copolymer, 2-4% of butanediol, 3.5-6% of glycerol, 1-2% of jojoba wax PEG-120 esters, 8-16% of a composite extract, 1-2% of an ammonium acryloyldimethyl taurate/VP copolymer, 0.2-0.5% of a preservative, 0.2-0.5% of 1, 2-hexanediol, 2-3% of sodium hyaluronate, 0.2-0.3% of sodium polyglutamate, 3-6% of polypeptide freeze-dried powder and the balance of water.

Preferably, the compound extract comprises truffle extract, astragalus membranaceus root extract, thunder god vine extract, gardenia extract and dendrobium officinale extract.

Further preferably, the weight ratio of the truffle extract, the astragalus membranaceus root extract, the tripterygium wilfordii extract, the gardenia extract and the dendrobium officinale extract is 1-2: 0.5-1: 1-2.

More preferably, the truffle extract is any one of truffle extract, tuber melanosporum and tuber albium.

Preferably, the preservative is selected from any one of p-hydroxyacetophenone and phenoxyethanol.

In a second aspect, the present invention provides a method for preparing a mother solution for repairing and beautifying muscle base according to the first aspect, comprising the following steps:

(1) mixing and stirring water, butanediol, glycerol, sodium hyaluronate and sodium polyglutamate uniformly, stirring and heating to 75-85 ℃, preserving heat for 10-30 min, and then cooling to 50 ℃ to obtain a mixture A;

(2) sequentially adding the secondary fission yeast fermentation product filtrate, schizophyllan, secondary fission yeast fermentation product lysate, leukocyte extract, hydrolyzed placenta extract, PEG/PPG-17/6 copolymer, jojoba wax PEG-120 esters, composite extract, acryloyl dimethyl ammonium taurate/VP copolymer, preservative and 1, 2-hexanediol into the obtained mixture A, and stirring for 10-30 min to obtain a mixture B;

(3) and adding the polypeptide freeze-dried powder into the mixture B, and uniformly stirring to obtain a finished product.

Compared with the prior art, the invention has the beneficial effects that:

the mother liquor for repairing and beautifying the skin bottom provided by the invention is prepared from multiple raw materials such as a secondary fission yeast fermentation product filtrate, schizophyllan, a secondary fission yeast fermentation product lysate, a leukocyte extract, a hydrolyzed placenta extract, a polypeptide freeze-dried powder and a composite extract, and the polypeptide repairing components can help the maintenance and growth of skin collagen and elastin, promote the self-repair of skin, lighten skin fine lines, and enable the skin to be full, smooth and compact and have high elasticity; active ingredients such as the secondary split yeast fermentation product filtrate, the secondarysplit yeast fermentation product lysate, the leucocyte extract, the hydrolyzed placenta extract and the composite extract can effectively moisten the skin and provide sufficient nutrition for the skin, and the active ingredients and the polypeptide ingredients have the synergistic effect of nourishing the skin, improving the water-deficient and dry state of the skin, and have the effects of resisting inflammation, fading fine wrinkles and repairing damaged skin.

Drawings

FIG. 1 is a graph showing the results of a test for the moisture content of the stratum corneum provided by the present invention;

FIG. 2 is a graph showing the results of the cell tissue viability assay provided by the present invention.

Detailed Description

The following further describes embodiments of the present invention with reference to the drawings. It should be noted that the description of the embodiments is provided to help understanding of the present invention, but the present invention is not limited thereto. In addition, the technical features involved in the embodiments of the present invention described below may be combined with each other as long as they do not conflict with each other.

Example 1

The preparation method of the mother solution for repairing and beautifying muscle base provided by the embodiment comprises the following steps:

(1) weighing the following raw materials in percentage by weight: mannitol 4%, trehalose 2.4%, oligopeptide-12.8%, glutathione 1.6%, acetyl tripeptide-10.4%, acetyl tetrapeptide-50.4%, retinol/zymophyte polypeptide 0.5%, and sterile water in balance; heating sterile water to 40-60 ℃, adding mannitol, trehalose, oligopeptide-1, glutathione, acetyl tripeptide-1, acetyl tetrapeptide-5 and retinol/zymophyte polypeptide, stirring for 20min under the condition of the rotation speed of 1200r/min, filtering by using a filter membrane with the pore diameter of not more than 0.1 mu m, centrifuging to remove impurities, filling the centrifuged solution into a container bottle, putting the container bottle filled with the mixed solution into a vacuum freeze dryer, keeping the vacuum environment, cooling to-10 to-5 ℃, preserving heat, pre-freeze drying for 12h, heating to-20 to-15 ℃, preserving heat, freeze drying for 14h, heating to-1-2 ℃, preserving heat, sublimation drying for 6h, finally heating to 40-45 ℃, preserving heat, desorbing and drying for 6h to obtain polypeptide freeze-dried powder;

(2) weighing the following raw materials in percentage by weight: 8% of a schizosaccharomyces cerevisiae fermentation product filtrate, 5% of rapamitocin, 1.6% of a schizosaccharomyces cerevisiae fermentation product lysate, 1.5% of a leukocyte extract, 2% of a hydrolyzed placenta extract, 1.5% of a PEG/PPG-17/6 copolymer, 3% of butanediol, 5% of glycerol, 1.2% of a Jojoba wax PEG-120 ester, 3% of a white truffle extract, 3% of a radix astragali extract, 1.5% of a thunder god vine extract, 1.5% of a gardenia extract, 3% of a dendrobium officinale extract, 1.4% of an acryloyl dimethyl ammonium taurate/VP copolymer, 0.4% of p-hydroxyacetophenone, 0.4% of 1, 2-hexanediol, 2.5% of sodium hyaluronate, 0.2% of sodium polyglutamate, 5% of polypeptide lyophilized powder, and the balance of sterile water;

mixing water, butanediol, glycerol, sodium hyaluronate and sodium polyglutamate, stirring and heating to 80 ℃, preserving heat for 20min, then cooling to 50 ℃ to obtain a mixture, sequentially adding the secondary fission yeast fermentation product filtrate, rapamicin, secondary fission yeast fermentation product lysate, leukocyte extract, hydrolyzed placenta extract, PEG/PPG-17/6 copolymer, Jojoba wax PEG-120 esters, truffle extract, astragalus membranaceus root extract, thunder god vine extract, gardenia extract, dendrobium officinale extract, ammonium acryloyldimethyl taurate/VP copolymer, p-hydroxyacetophenone and 1, 2-hexanediol into the obtained mixture, stirring for 20min, adding polypeptide freeze-dried powder, and stirring uniformly to obtain a finished product.

Example 2

(1) weighing the following raw materials in percentage by weight: mannitol 3%, trehalose 3%, oligopeptide-12.5%, glutathione 2%, acetyl tripeptide-10.5%, acetyl tetrapeptide-50.2%, retinol/zymophyte polypeptide 0.4%, and sterile water in balance, and then preparing polypeptide lyophilized powder according to the step (1) of example 1;

(2) weighing the following raw materials in percentage by weight: 10% of a schizosaccharomyces cerevisiae fermentation product filtrate, 3% of rapamitocin, 1% of a schizosaccharomyces cerevisiae fermentation product lysate, 1% of a leukocyte extract, 2.5% of a hydrolyzed placenta extract, 1% of a PEG/PPG-17/6 copolymer, 4% of butanediol, 3.5% of glycerol, 2% of a Jojoba wax PEG-120 ester, 2% of a truffle extract, 4% of a radix astragali extract, 1% of a thunder god vine extract, 2% of a gardenia extract, 4% of a dendrobium officinale extract, 2% of an acryloyl dimethyl ammonium taurate/VP copolymer, 0.5% of p-hydroxyacetophenone, 0.5% of 1, 2-hexanediol, 2% of sodium hyaluronate, 0.3% of sodium polyglutamate, 1-6% of a polypeptide lyophilized powder, and the balance of sterile water, and then preparing a finished product according to the step (2) of the example 1.

Example 3

(1) weighing the following raw materials in percentage by weight: mannitol 5%, trehalose 2%, oligopeptide-13%, glutathione 1%, acetyl tripeptide-10.2%, acetyl tetrapeptide-50.5%, retinol/zymophyte polypeptide 0.8%, and sterile water in balance, and then preparing polypeptide lyophilized powder according to the step (1) of example 1;

(2) weighing the following raw materials in percentage by weight: 5% of a schizosaccharomyces cerevisiae fermentation product filtrate, 2% of rapamitocin, 2% of a schizosaccharomyces cerevisiae fermentation product lysate, 2% of a leukocyte extract, 1.5% of a hydrolyzed placenta extract, 2% of a PEG/PPG-17/6 copolymer, 2% of butanediol, 6% of glycerol, 1% of a jojoba PEG-120 ester, 4% of a truffle extract, 2% of a astragalus membranaceus root extract, 2% of a tripterygium wilfordii extract, 1% of a gardenia extract, 2% of a dendrobium officinale extract, 1% of an ammonium acryloyldimethyltaurate/VP copolymer, 0.2% of p-hydroxyacetophenone, 0.2% of 1, 2-hexanediol, 3% of sodium hyaluronate, 0.3% of sodium polyglutamate, 3% of a polypeptide lyophilized powder and the balance of sterile water, and then preparing a finished product according to the step (2) of example 1.

Example 4

(1) preparing polypeptide freeze-dried powder according to the step (1) of the embodiment 1;

(2) weighing the following raw materials in percentage by weight: 0.1% of a schizosaccharomyces cerevisiae fermentation product filtrate, 0.1% of rapamitocin, 0.1% of a schizosaccharomyces cerevisiae fermentation product lysate, 0.1% of a leukocyte extract, 0.1% of a hydrolyzed placenta extract, 1.5% of a PEG/PPG-17/6 copolymer, 3% of butanediol, 5% of glycerol, 1.2% of a Hojoba wax PEG-120 ester, 3% of a white truffle extract, 3% of a radix astragali extract, 1.5% of a Tripterygium wilfordii hook.

Example 5

(2) weighing the following raw materials in percentage by weight: 15% of a schizosaccharomyces cerevisiae fermentation product filtrate, 5% of rapamitocin, 1.6% of a schizosaccharomyces cerevisiae fermentation product lysate, 1.5% of a leukocyte extract, 2% of a hydrolyzed placenta extract, 1.5% of a PEG/PPG-17/6 copolymer, 3% of butylene glycol, 5% of glycerol, 1.2% of jojoba wax PEG-120 esters, 3% of a white truffle extract, 3% of a radix astragali extract, 1.5% of a thunder god vine extract, 1.5% of a gardenia extract, 3% of a dendrobium officinale extract, 1.4% of an acryloyldimethyl ammonium taurate/VP copolymer, 0.4% of p-hydroxyacetophenone, 0.4% of 1, 2-hexanediol, 2.5% of sodium hyaluronate, 0.2% of sodium polyglutamate, 10% of a polypeptide lyophilized powder, and the balance of sterile water, and then preparing a finished product according to the step (2) of example 1.

Example 6

(1) weighing the following raw materials in percentage by weight: mannitol 2%, trehalose 5%, oligopeptide-15%, glutathione 0.5%, acetyl tripeptide-10.1%, acetyl tetrapeptide-50.1%, retinol/zymophyte polypeptide 0.1%, and water in balance, and then preparing polypeptide lyophilized powder according to the step (1) of example 1;

(2) the final product was obtained in step (2) of example 1.

Example 7

(1) weighing the following raw materials in percentage by weight: 10% of mannitol, 2% of trehalose, 11% of oligopeptide, 5% of glutathione, 11% of acetyl tripeptide, 51% of acetyl tetrapeptide, 1% of retinol/zymophyte polypeptide and the balance of water, and then preparing polypeptide freeze-dried powder according to the step (1) of the example 1;

(2) the step (2) of example 1 was repeated to obtain a finished product.

Example 8

The step (1) of the example 1 is repeated to prepare the polypeptide freeze-dried powder, the 'tuber melanosporum extract' is adopted to replace the 'tuber alba extract' in the step (2) of the example 1, and then the finished product is prepared according to the step (2) of the example 1.

Example 9

The step (1) of the example 1 is repeated to prepare the polypeptide freeze-dried powder, the 'summer truffle extract' is adopted to replace the 'white truffle extract' in the step (2) of the example 1, and then the finished product is prepared according to the step (2) of the example 1.

Example 10

Repeating the step (1) of the example 1 to prepare the polypeptide freeze-dried powder, replacing the tripterygium wilfordii extract in the step (2) of the example 1 with the calendula extract, replacing the gardenia extract in the step (2) of the example 1 with the albizia extract, and then preparing the finished product according to the step (2) of the example 1.

Effect example 1

To further illustrate the beneficial effects of the present invention, the present invention tests the moisturizing and hydrating effects of the products obtained in the above examples:

(1) marked 4X 4cm on the subject's arm²The area (2) was used as a test area, 0.4g of the obtained intramuscular stock solution of examples 1 to 10 was added dropwise to the test area of the subject once a day, the moisture content of the horny layer of the skin in the test area was measured by a skin moisture meter at 0.5h, 1h, 2h, and 6h before and after use, and the average value was obtained by repeating the test three times for each area. The test results are shown in fig. 1.

As can be seen from FIG. 1, the moisture content of the stratum corneum of the skin of the subjects remained high after 6 hours of application with the products of examples 1-3 and 5-10, while the moisture content of the stratum corneum of the subjects after 0.5 hours of application with the product of example 4 was increased, but the increase was significantly lower than that of the products of the other examples.

Effect example 2

In order to further illustrate the beneficial effects of the present invention, the present invention also tests the repairing effect of the product obtained in the above embodiment:

constructing a skin injury model by utilizing sodium dodecyl sulfate stimulation through a conventional means, taking the muscle base mother liquor obtained in examples 1-10 as samples to be tested, and uniformly coating the samples to be tested on the surfaces of 10 injured skin models in a surface administration manner to obtain the skin injury model10 test groups, the skin model without sample as a control group, and the skin models of the test group and the control group were placed in CO₂Incubate for 24h in an incubator (37. + -. 1 ℃, 5. + -. 1% CO2, 95% relative humidity). After the incubation, the washing procedure was started and the cell tissue viability was tested using the MTT assay, the results of which are shown in fig. 2.

The test results show that the tissue viability of the examples 1-10 is significantly higher than that of the control group, which indicates that the skin barrier of the skin barrier is effectively prevented from penetrating the skin barrier after the example 3 is used, wherein the tissue viability of the examples 1-3 is significantly higher than that of the other groups, which indicates that the barrier repair effect of the examples 1-3 is significantly better than that of the other groups.

The embodiments of the present invention have been described in detail with reference to the accompanying drawings, but the present invention is not limited to the described embodiments. It will be apparent to those skilled in the art that various changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, and the scope of protection is still within the scope of the invention.

Claims

1. The repair and beauty foundation mother solution is characterized by comprising the following raw materials in percentage by weight: 0.1-10% of a schizosaccharomyces cerevisiae fermentation product filtrate, 0.1-3% of palmatine, 0.1-2% of a schizosaccharomyces cerevisiae fermentation product lysate, 0.1-2% of a leukocyte extract, 0.1-2.5% of a hydrolyzed placenta extract, 0.5-3% of a PEG/PPG-17/6 copolymer, 2-5% of butanediol, 2-8% of glycerol, 0.5-2% of jojoba wax PEG-120 esters, 5-25% of a composite extract, 0.5-2% of an ammonium acryloyldimethyl taurate/VP copolymer, 0.01-1% of a preservative, 0.1-1% of 1, 2-hexanediol, 1-3% of sodium hyaluronate, 0.1-0.5% of sodium polyglutamate, 1-10% of a lyophilized polypeptide powder, and the balance of water, wherein the composite extract is selected from a truffle extract, a ganoderma extract, a membrana astragali radix extract, a tripterygium wilfordii extract, a crocodile flower extract, a gardenia extract, a dendrobe extract, a dendrobium extract, a mangnolicina officinalis extract, a mangostin officinalis extract, a mangostin extract, and a officinalis extract, At least three of radix Saposhnikoviae extract, herba Sidae Rhombifoliae extract, and flos Albizziae extract; the polypeptide freeze-dried powder comprises the following raw materials in parts by weight: 2-10% of mannitol, 2-5% of trehalose, 11-5% of oligopeptide, 0.5-5% of glutathione, 10.1-1% of acetyl tripeptide, 50.1-1% of acetyl tetrapeptide, 0.1-1% of retinol/zymophyte polypeptide and the balance of water.

2. The repair and beauty foundation myocyte mother solution of claim 1, wherein the polypeptide lyophilized powder is prepared by the following method: heating water to 40-60 ℃, adding mannitol, trehalose, oligopeptide-1, glutathione, acetyl tripeptide-1, acetyl tetrapeptide-5 and retinol/zymophyte polypeptide, uniformly stirring, performing membrane filtration and centrifugation to obtain a mixed solution, and freeze-drying the obtained mixed solution to obtain the polypeptide freeze-dried powder.

3. The cosmetic underpan repair solution as claimed in claim 2, wherein said step of freeze-drying comprises in particular: filling the mixed solution into a container bottle, then putting the container bottle filled with the mixed solution into a vacuum freeze dryer, keeping a vacuum environment, cooling to-10 to-5 ℃, preserving heat, pre-freeze drying for 10-12 h, heating to-20 to-15 ℃, preserving heat, freeze drying for 10-15 h, heating to-1 to 2 ℃, preserving heat, sublimation drying for 4-8 h, finally heating to 40-45 ℃, preserving heat, desorbing and drying for 4-8 h.

4. The repair and beauty foundation myocyte mother solution as claimed in claim 1, wherein the raw materials of the polypeptide lyophilized powder comprise, by weight: 3-5% of mannitol, 2-3% of trehalose, 12.5-3% of oligopeptide, 1-2% of glutathione, 10.2-0.5% of acetyl tripeptide, 50.2-0.5% of acetyl tetrapeptide, 0.4-0.8% of retinol/zymophyte polypeptide and the balance of water.

5. The repair and beauty foundation mother liquor as claimed in claim 1, which comprises the following raw materials by weight percent: 5-10% of a secondary split yeast fermentation product filtrate, 2-3% of palmatine, 1-2% of a secondary split yeast fermentation product lysate, 1-2% of a leukocyte extract, 1.5-2.5% of a hydrolyzed placenta extract, 1-2% of a PEG/PPG-17/6 copolymer, 2-4% of butanediol, 3.5-6% of glycerol, 1-2% of jojoba wax PEG-120 esters, 8-16% of a composite extract, 1-2% of an ammonium acryloyldimethyl taurate/VP copolymer, 0.2-0.5% of a preservative, 0.2-0.5% of 1, 2-hexanediol, 2-3% of sodium hyaluronate, 0.2-0.3% of sodium polyglutamate, 3-6% of polypeptide freeze-dried powder and the balance of water.

6. The mother liquor for repairing and beautifying muscle base according to claim 1, wherein the composite extract comprises truffle extract, astragalus membranaceus root extract, thunder god vine extract, gardenia extract and dendrobium officinale extract.

7. The mother liquor for repairing and beautifying muscle base according to claim 6, wherein the weight ratio of the truffle extract, the astragalus membranaceus root extract, the tripterygium wilfordii extract, the gardenia extract and the dendrobium officinale extract is 1-2: 0.5-1: 1-2.

8. The repair and beauty foundation mother liquor as claimed in claim 6, wherein the truffle extract is any one of truffle extract, tuber melanosporum and tuber albium.

9. The repair and beauty foundation mother liquor as claimed in claim 1, wherein the preservative is selected from any one of p-hydroxyacetophenone and phenoxyethanol.

10. A method for preparing a mother liquor for repairing and beautifying muscle base according to any one of claims 1 to 9, which comprises the following steps: