Disclosure of Invention
In order to solve the technical problems, the invention provides a skin care composition with the functions of moisturizing, whitening and resisting aging and an application thereof.
The method is realized according to the following technical scheme:
a skin care composition with moisture retention, whitening and anti-aging functions comprises 11-25 parts of a component A, 0.1-1.4 parts of a component B and 0.1-3 parts of a component C in parts by weight; the component A is bletilla striata extract, ampelopsis japonica extract and poria cocos extract; the component B is palmitoyl tripeptide-1 and acetyl hexapeptide-8; the component C is polyglutamic acid.
Further, the skin care composition with the functions of moisturizing, whitening and resisting aging also comprises the following components in parts by weight: 8-15 parts of component D, wherein the component D is a cosmetic auxiliary material or a cosmetic matrix.
1. Further, the cosmetic auxiliary materials comprise the following components in parts by weight: 27.3-65.7 parts of purified water, 15-28 parts of glycerol and 0.1-0.3 part of sodium lauryl sulfate.
Further, the cosmetic matrix is one or more of glyceryl stearate, cetyl alcohol, stearyl alcohol, isopropyl palmitate, polydimethylsiloxane, tocopherol, essence, methyl hydroxybenzoate and propyl hydroxybenzoate.
Further, the component A comprises the following components in parts by weight: 5-10 parts of bletilla striata extract, 1-5 parts of ampelopsis japonica extract and 5-10 parts of poria cocos extract.
Further, the component B comprises the following components in parts by weight: 0.05-1.2 parts of palmitoyl tripeptide-1 and 0.05-0.2 parts of acetyl hexapeptide-8.
The component A and the preparation method thereof are as follows: cleaning rhizoma Bletillae, radix Ampelopsis, and Poria, respectively, oven drying at 77-82 deg.C, pulverizing, adding 10-20 times of water by weight of the above raw materials, soaking for no less than 25min, heating to 90-100 deg.C, decocting for 1.0-2.0h, filtering to obtain medicinal liquid, vacuum concentrating the medicinal liquid to 3-5 times of the weight of the raw materials, standing, filtering, collecting filtrate as rhizoma Bletillae extract, radix Ampelopsis extract, and Poria extract, respectively, and mixing the extracts.
And (3) crushing, wherein the granularity of the crushed material is 10 meshes.
The skin care composition with the functions of moisturizing, whitening and resisting aging is applied to the production of masks, eye creams, face creams, essences, face cleaning lotions, skin toning water, emulsions, hydrolat and sun screen.
The production method of any one of essence, toner, hydrolat and facial mask comprises the following steps: placing cosmetic adjuvants in component D in a stirring container, heating to 65-70 deg.C at a speed of 3-4 deg.C/min, stirring, keeping the temperature for more than 5min, cooling to 35-40 deg.C at a speed of 3-5 deg.C/min, adding component A, stirring for 10-15min to mix the materials uniformly, adding essence, component B and component C, stirring for 10-15min, discharging, and standing.
The production method of any one of face cream, eye cream, face cleaning cream, emulsion and makeup base comprises the following steps:
pre-dissolution of the aqueous phase of S1: putting the glycerol and the purified water in the component D into a water phase jacketed kettle of a vacuum emulsifying machine, heating to 85-90 ℃ at the speed of 3-4 ℃/min, starting stirring at the rotation speed of 85 r/min, stirring and mixing for 5-10min, and adding sodium lauryl sulfate to disperse uniformly;
pre-dissolving of the oil phase of S2: placing the cosmetic matrix except essence in oil phase jacketed pan of vacuum emulsifying machine, heating to 85-90 deg.C at 3-4 deg.C/min, stirring at 85 rpm, stirring for mixing and dissolving;
s3 emulsification: feeding the water phase and oil phase materials into an emulsifying pot, emulsifying at the rotation speed of 2500-0.04 MPa and the temperature of 70-80 ℃ for 5-10min under the conditions of the vacuum degree of-0.03-0.04 MPa, cooling to 35-40 ℃ at the speed of 3-5 ℃/min, adding the component A, stirring for 10-15min to uniformly mix the materials, then adding the essence, the component B and the component C, stirring for 10-15min, discharging and standing.
The bletilla striata polysaccharide is fully dissolved out, the polysaccharide activity and the bletilla striata dissolving-out structure are improved by reasonably extracting the bletilla striata, so that the bletilla striata extract has the effects of promoting growth and resisting aging on skin cells and can delay cell aging. According to the invention, the Ampelopsis japonica is reasonably extracted, so that the naturalness of the extract is ensured to the maximum extent, the whitening components are fully dissolved out, the activity of tyrosinase is controlled, and the formation of melanin is reduced. The invention extracts tuckahoe reasonably, fully dissolves pachymaran, lecithin, trace protease, various inorganic elements and the like, and enhances the immunity of the organism.
On the basis of traditional Chinese medicine monarch, minister, guide, adjuvant and five-element health preservation, the effective components in the plants are extracted, and mainly comprise tannin, protein, amino acid, alkaloid, polysaccharide, volatile oil and the like, so that the effective components are mutually cooperated and promoted; the amino acid has high safety to environment and organisms, mild skin effect, small irritation, good foaming and emulsifying properties, strong dirt-removing power, good biodegradability, and good antibacterial and bactericidal properties. The polysaccharides have film forming property, adsorbability, water retention property and excellent lubricity, and can help the moisturizing factor to form a film and adhere to the surface of skin to form a water film, effectively remove dead cells on the surface of the skin and deeply clean the skin. The protein is hydrolyzed to form polypeptide, and the peptide has strong activity and diversity, and can promote active ingredients such as tannin, alkaloid, volatile oil, etc. to permeate into epidermis and be absorbed, promote collagen production, resist inflammation and resist oxidation. The alkaloid and volatile oil can prevent external environmental pollution or wrinkle, tarnish, dryness, and lack of luster caused by computer radiation. The volatile oil can inhibit tyrosinase activity and active oxygen generation.
The polyglutamic acid used in the invention is the main component of the viscous colloid in the natto, contains a large amount of free carboxyl on the main chain, can generate reactions such as cross linking, chelating, derivatization and the like, has strong water solubility, biocompatibility and biodegradability, has high water absorption capacity and slow release capacity, can effectively reduce the loss of skin moisture, and enables skin tissues to have increased elasticity, tenderness and smoothness and luster.
The palmitoyl tripeptide-1 and the acetyl hexapeptide-8 used in the invention have extremely strong activity and diversity, can promote active ingredients such as tannin, alkaloid, volatile oil and the like to permeate into the epidermis to be absorbed, can promote the generation of collagen, and can help to resist inflammation and resist oxidation.
The invention has the beneficial effects that:
the skin care composition provided by the invention is scientific in compatibility, can quickly control skin oil spilling, astringe pores, whiten skin, lock skin moisture, promote skin metabolism, enhance skin activity and antibacterial power, enhance free radical scavenging capacity and immunity, reduce pigmentation and prevent skin relaxation. The skin care composition does not contain western medicine components, is safe and non-irritant to skin, does not have side effects, has the advantages of wide raw material source, low cost and the like, and has a long-acting function.
The invention organically combines the traditional Chinese medicine whitening conditioning components, the antioxidant components, the polyglutamic acid which can be used as a high-efficiency moisturizing factor and a transportation carrier, and the like, is balanced in function, makes up for deficiencies of the components, and achieves the effects of long-acting whitening, moisturizing and anti-aging on the basis of ensuring the safety.
At present, the traditional Chinese medicinal materials with moisturizing, whitening and anti-aging effects are more, such as: chinese angelica, ginseng, lucid ganoderma, pearl, ginkgo leaf, dendrobium, coix seed, cordyceps sinensis, lithospermum, poria cocos, tree peony bark and the like, but traditional Chinese medicinal materials are directly used as auxiliary materials of cosmetics and a matrix to prepare a skin care product, so that the defects of the traditional Chinese medicine skin care product can be overcome by adding high moisturizing factors polyglutamic acid with different molecular weights and active peptide in the further optimization process, in order to improve the moisturizing, whitening and antioxidation performances, ten kinds of medicinal materials such as bletilla striata, poria cocos, Japanese ampelopsis, coix seed, dendrobe, angelica sinensis, ginseng and the like are tried to be added, the matching of primary and secondary medicines is carried out, and the effects can be better achieved by primarily determining that the bletilla striata is used as a monarch medicine, the poria cocos is used as a ministerial medicine, and the Japanese ampelopsis used as an adjuvant through multiple prescription screening.
The invention verifies the raw material collocation and the process control in the invention from three aspects of whitening, anti-aging and safety.
Firstly, screening raw materials
The invention obtains the following formulas (shown in table 1) by screening a plurality of traditional Chinese medicine raw materials and effective components with moisturizing, whitening and antioxidation functions:
TABLE 1
The emulsion is produced from the above composition according to the process disclosed in the present invention.
1.1 whitening efficacy
Assay to inhibit melanin synthesis in mouse melanocytes:
b16 mouse melanoma cells at 1X 105The cells/ml were plated on a 9cm diameter petri dish at 37 deg.C in 5% CO2Culturing for 2 days, discarding the supernatant, adding 18-22ml of sample solution after filtration and sterilization, culturing for 3 days, discarding the supernatant, washing with PBS, adding 0.5ml of pancreatin solution with the mass percent of 0.2% into each hole for digesting cells for 3min, adding 2ml of maintenance solution into each dish for terminating digestion, uniformly blowing, taking out 0.5ml of each concentration for counting cells, centrifuging the rest cell suspension for 5min at 2500r/min, discarding the supernatant, adding a NaoH solution into the precipitate, heating to dissolve melanin, and selecting an enzyme-linked immunosorbent assay instrument with the wavelength of 490nm for measuring the absorbance value.
Melanin synthesis inhibition rate ═ 1- (drug well absorbance + drug well cell density) + (control well absorbance + control well cell density) × 100%.
The results of the experiment for inhibiting melanin synthesis in mouse melanocytes are shown in Table 2
TABLE 2
|
Inhibition ratio (%)
|
Formulation group 1
|
92.3
|
Formulation group 2
|
72.5
|
Formulation group 3
|
84.1
|
Formulation group 4
|
77.6
|
Formulation group 5
|
65.7
|
Formulation group 6
|
63.8
|
Formulation group 7
|
87.7
|
Formulation group 8
|
70.2
|
Formulation group 9
|
81.4
|
Formulation group 10
|
73.9 |
1.2 anti-aging efficacy
1.2.1 Experimental materials
Taking the emulsion prepared by the formula groups 1-10
Experimental animals: kunming mouse, 18-22g in weight, half in sex, provided by animal research laboratory of Guiyang medical college.
1.2.2 Experimental methods
1.2.2.1 establishing 60 Kunming mice of an aging animal model, each half of the mice is divided into 12 groups randomly, each group comprises 5 mice, and the groups respectively comprise a normal control group, a model group and a formula group 1-10. Except for the normal control group, 120mg/kg of D-galactose aqueous solution is injected subcutaneously every day for 28 days continuously, and 0.2ml of normal saline is injected subcutaneously at the back of the neck every day. Each group of animals was modeled while gavage the corresponding receiving agent daily. The formula groups 1-10 mice were applied to the epidermis of the body once a day in an amount of 0.5 ml/time for 4 weeks (the normal control group and the aging model group were gazed with an equal amount of physiological saline). The mice are cut off and blood is taken out 30min after the last administration, and the content or activity of serum SOD and GSH-Px is determined.
1.2.2.2GSH-Px Activity measurements were calculated from GSH standard curves using the 2-nitrobenzoic acid method (DTNB method). Considering GSH, H2O2Since the above reaction can be carried out without enzymes, the activity of GSH-Px must be calculated at the end, except for the reduction of GSH caused by the enzyme reaction. GSH standard curves were prepared according to literature methods.
1.2.2.3SOD determination by xanthine oxidase-hydroxylamine method, adding serum to be tested (with dH)2Diluted 50 times with O) 0.5ml, dH20.1ml of O, 0.1ml of matrix solution, 0.1ml of nitroso generator and 0.2ml of enzyme solution, and keeping the temperature at 37 ℃ for 30 min. Then adding 2ml of color developing agent, standing at room temperature for 10min, and standing at 550nmThe absorbance was measured at the length. Control tube with 0.5ml dH2O replaced serum samples. The enzyme activity unit (NU) is defined as the amount of enzyme required to inhibit 50% of xanthine oxidase from catalyzing the oxidation of a substrate within 30min, and the serum SOD activity is expressed as the number of enzyme activity units per ml of serum.
The test results are shown in Table 3.
TABLE 3 Effect on mouse serum SOD and GSH-Px content
Group of
|
n
|
SOD(U/ml)
|
GSH-Px(U/ml)
|
Normal control group
|
5
|
1638.5±125.8
|
15.83±2.26
|
Aging model group
|
5
|
1391.7±424.3*
|
12.22±1.78*
|
Formulation group 1
|
5
|
1723.2±265.1**
|
16.48±2.71**
|
Formulation group 2
|
5
|
1706.4±132.6**
|
15.38±2.34**
|
Formulation group 3
|
5
|
1677.5±262.7**
|
14.66±2.08**
|
Formulation group 4
|
5
|
1543.8±312.5**
|
14.92±1.95**
|
Formulation group 5
|
5
|
1603.9±176.5**
|
15.19±2.11**
|
Formulation group 6
|
5
|
1667.1±89.3**
|
16.02±1.73**
|
Formulation group 7
|
5
|
1589.3±108.1**
|
15.48±1.07**
|
Formulation group 8
|
5
|
1645.5±117.6**
|
15.36±2.25**
|
Formulation group 9
|
5
|
1632.7±254.8**
|
15.67±3.01**
|
Formulation group 10
|
5
|
1590.5±223.9**
|
14.84±2.94** |
Note: comparison with normal control group: p < 0.01; p < 0.05 in comparison with aging model group
The results in table 3 show that the skin care composition of the present invention significantly increases the level of SOD in blood and the activity of GSH-Px, indicating that the skin care composition of the present invention can inhibit lipid peroxidation caused by D-galactose, and has anti-aging activity.
1.3 safety test
1.3.1 acute toxicity test on skin
Selecting 10 Wistar rats with male and female halves, weight of 200g, sampling at a dosage of 5000mg/kg body weight, and smearing on depilated area (range of 30-40 cm)2) Covering with two layers of parchment paper, and sealing and fixing with non-irritant adhesive plaster for 24 h. After 24h, the animals were removed from the test and observed for signs of intoxication for a period of 7 days. The results show that: none of the rats in the formula group died.
1.3.2 multiple skin irritation tests
Wistar rats were selected at 10 rats and weighed 200 g. Sampling at a dosage of 5000mg/kg body weight, and applying to depilated area (range of 30-40 cm)2) Sealing and fixing with non-irritant adhesive plaster for 1h, and taking the left depilatory area as control, 1 time per day for 20 days. The test article was washed with distilled water each time before being applied to the test article from day 2, and the skin irritation reaction results were observed after 1 hour. The results show that: the formula groups 1-5 have no irritation, and the formula groups 6-10 have skin allergy, red swelling and other phenomena.
1.4 moisture Retention test
1.4.1 Experimental materials
Taking the emulsion prepared by the formula groups 1-10.
1.4.2 Experimental methods
Weighing 30g of sample on a watch glass, drying the sample for 24 hours at the temperature of 85 ℃, weighing the sample again, and calculating the water loss rate according to the following formula: the water loss rate is (M1-M2)/M1 multiplied by 100 percent, and M1 and M2 are the total weight of the product and the watch glass respectively before and after the experiment.
The results are shown in Table 4.
TABLE 4
Second, process screening
The raw material components are as follows: the component A comprises: 5g of bletilla striata extract, 1g of ampelopsis japonica extract, 5g of poria cocos extract, and the component B: palmitoyl tripeptide-11 g, acetyl hexapeptide-80.1 g, and a component C: 1.5g of polyglutamic acid, component D: on the basis of 8g of essence auxiliary materials, the essence is prepared by adopting the following processes respectively:
2.1 moisturizing and whitening effects
Assay to inhibit melanin synthesis in mouse melanocytes:
b16 mouse melanoma cells at 1X 105The cells/ml were plated on a 9cm diameter petri dish at 37 deg.C in 5% CO2Culturing for 2 days, discarding the supernatant, adding 18-22ml of sample solution after filtration and sterilization, culturing for 3 days, discarding the supernatant, washing with PBS, adding 0.5ml of pancreatin solution with the mass percent of 0.2% into each hole for digesting cells for 3min, adding 2ml of maintenance solution into each dish for terminating digestion, uniformly blowing, taking out 0.5ml of each concentration for counting cells, centrifuging the rest cell suspension for 5min at 2500r/min, discarding the supernatant, adding a NaoH solution into the precipitate, heating to dissolve melanin, and selecting an enzyme-linked immunosorbent assay instrument with the wavelength of 490nm for measuring the absorbance value.
Melanin synthesis inhibition rate ═ 1- (drug well absorbance + drug well cell density) + (control well absorbance + control well cell density) × 100%.
Results of the experiment for inhibiting melanin synthesis in mouse melanocytes are shown in Table 5
TABLE 5
|
Inhibition ratio (%)
|
Process group 1
|
92.3
|
Process group 2
|
85.6
|
Process group 3
|
86.3
|
Process group 4
|
81.2
|
Process group 5
|
79.0
|
Process group 6
|
81.9
|
Process group 7
|
82.1
|
Process group 8
|
84.7 |
2.2 anti-aging efficacy
2.2.1 Experimental materials
Taking the emulsion prepared by the formula groups 1-10
Experimental animals: kunming mouse, 18-22g in weight, half in sex, provided by animal research laboratory of Guiyang medical college.
2.2.2 Experimental methods
2.2.2.1 establishing 60 Kunming mice of the aging animal model, each half of the mice is divided into 12 groups randomly, each group comprises 5 mice, and the groups are respectively a normal control group, a model group and a formula group 1-10. Except for the normal control group, 120mg/kg of D-galactose aqueous solution is injected subcutaneously every day for 28 days continuously, and 0.2ml of normal saline is injected subcutaneously at the back of the neck every day. Each group of animals was modeled while gavage the corresponding receiving agent daily. The mice of the technical groups 1 to 8 are coated on the epidermis of the body once a day according to the amount of 0.5 ml/time, and are continuously coated for 4 weeks (the normal control group and the aging model group are irrigated with the same amount of normal saline). The mice are cut off and blood is taken out 30min after the last administration, and the content or activity of serum SOD and GSH-Px is determined.
2.2.2.2 measurement of GSH-Px Activity calculated from the GSH standard curve using the 2-nitrobenzoic acid method (DTNB method). Considering GSH, H2O2Since the above reaction can be carried out without enzymes, the activity of GSH-Px must be calculated at the end, except for the reduction of GSH caused by the enzyme reaction. GSH standard curve according toThe method is prepared by a literature method.
2.2.2.3SOD determination is carried out by adding to-be-tested serum (by dH) sequentially by xanthine oxidase-hydroxylamine method2Diluted 50 times with O) 0.5ml, dH20.1ml of O, 0.1ml of matrix solution, 0.1ml of nitroso generator and 0.2ml of enzyme solution, and keeping the temperature at 37 ℃ for 30 min. Then, 2ml of a color developing agent was added thereto, and the mixture was left at room temperature for 10min, and the absorbance was measured at a wavelength of 550 nm. Control tube with 0.5ml dH2O replaced serum samples. The enzyme activity unit (NU) is defined as the amount of enzyme required to inhibit 50% of xanthine oxidase from catalyzing the oxidation of a substrate within 30min, and the serum SOD activity is expressed as the number of enzyme activity units per ml of serum.
The results are shown in Table 6.
TABLE 6 Effect on mouse serum SOD and GSH-Px content
Group of
|
n
|
SOD(U/ml)
|
GSH-Px(U/ml)
|
Normal control group
|
5
|
1638.5±125.8
|
15.83±2.26
|
Aging model group
|
5
|
1391.7±424.3*
|
12.22±1.78*
|
Process group 1
|
5
|
1722.6±266.3**
|
16.98±2.11**
|
Process group 2
|
5
|
1639.1±201.3**
|
16.37±1.92**
|
Process group 3
|
5
|
1617.8±177.5**
|
15.22±1.85**
|
Process group 4
|
5
|
1645.5±98.4**
|
15.71±2.03**
|
Process group 5
|
5
|
1892.7±104.5**
|
16.19±2.13**
|
Process group 6
|
5
|
1611.9±76.8**
|
15.32±1.76**
|
Process group 7
|
5
|
1557.9±213.5**
|
14.85±2.01**
|
Process group 8
|
5
|
1582.4±186.2**
|
16.12±1.55** |
Note: comparison with normal control group: p < 0.01; p < 0.05 in comparison with aging model group
2.3 safety test
2.3.1 acute toxicity test on skin
Selecting 10 Wistar rats with male and female halves, weight of 200g, sampling at a dosage of 5000mg/kg body weight, and smearing on depilated area (range of 30-40 cm)2) Covering with two layers of parchment paper, and sealing and fixing with non-irritant adhesive plaster for 24 h. After 24h, the animals were removed from the test and observed for signs of intoxication for a period of 7 days. The results show that: none of the rats in the technical group died.
2.3.2 multiple skin irritation tests
Wistar rats were selected at 10 rats and weighed 200 g. Sampling at a dosage of 5000mg/kg body weight, and applying to depilated area (range of 30-40 cm)2) Sealing and fixing with non-irritant adhesive plaster for 1h, and taking the left depilatory area as control, 1 time per day for 20 days. The test article was washed with distilled water each time before being applied to the test article from day 2, and the skin irritation reaction results were observed after 1 hour. The results show that: no irritation occurred in the process group.
2.4 moisture Retention test
2.4.1 Experimental materials
Samples prepared in Process groups 1-8 were taken.
2.4.2 Experimental methods
Weighing 30g of sample on a watch glass, drying the sample for 24 hours at the temperature of 85 ℃, weighing the sample again, and calculating the water loss rate according to the following formula: the water loss rate is (M1-M2)/M1 multiplied by 100 percent, and M1 and M2 are the total weight of the product and the watch glass respectively before and after the experiment.
The results are shown in Table 7.
TABLE 7
Detailed Description
The following is a detailed description of the embodiments of the present invention, but the present invention is not limited to these embodiments, and any modifications or substitutions in the basic spirit of the embodiments are included in the scope of the present invention as claimed in the claims.
Example 1
A skin care composition with moisturizing, whitening and anti-aging functions comprises:
the component A comprises: 7g of bletilla striata extract, 3g of ampelopsis japonica extract and 8g of poria cocos extract;
and B component: 0.52g palmitoyl tripeptide-1, 0.12g acetyl hexapeptide-8;
and C, component C: 1.8g of polyglutamic acid;
the preparation method of the component A comprises the following steps: cleaning rhizoma Bletillae, radix Ampelopsis, and Poria, respectively, oven drying at 82 deg.C, pulverizing to 10 mesh, adding 20 times of water, soaking for 28min, heating to 100 deg.C, decocting for 2.0h, filtering to obtain medicinal liquid, vacuum concentrating to 5 times of the weight of the raw materials, standing, filtering, collecting filtrate as rhizoma Bletillae extract, radix Ampelopsis extract, and Poria extract, and mixing the extracts;
the skin care composition with the functions of moisturizing, whitening and resisting aging is applied to the production of masks, eye creams, face creams, essences, face cleaning lotions, skin toning water, emulsions, hydrolat and sun screen.
Example 2
A skin care composition with moisturizing, whitening and anti-aging functions comprises:
the component A comprises: 10g bletilla striata extract, 5g ampelopsis japonica extract and 10g poria cocos extract;
and B component: 1.2g palmitoyl tripeptide-1, 0.2g acetyl hexapeptide-8;
and C, component C: 3g of polyglutamic acid;
the preparation method of the component A comprises the following steps: cleaning rhizoma Bletillae, radix Ampelopsis, and Poria, respectively, oven drying at 77 deg.C, pulverizing to 10 mesh, adding 10 times of water, soaking for 25min, heating to 90 deg.C, decocting for 1.0h, filtering to obtain medicinal liquid, vacuum concentrating to 3 times of the weight of the raw materials, standing, filtering, collecting filtrate as rhizoma Bletillae extract, radix Ampelopsis extract, and Poria extract, and mixing the extracts;
the skin care composition with the functions of moisturizing, whitening and resisting aging is applied to the production of masks, eye creams, face creams, essences, face cleaning lotions, skin toning water, emulsions, hydrolat and sun screen.
Example 3
A skin care composition with moisturizing, whitening and anti-aging functions comprises:
the component A comprises: 5g bletilla striata extract, 1g ampelopsis japonica extract and 5g poria cocos extract;
and B component: 0.05g palmitoyl tripeptide-1, 0.05g acetyl hexapeptide-8;
and C, component C: 0.1g of polyglutamic acid;
the preparation method of the component A comprises the following steps: cleaning rhizoma Bletillae, radix Ampelopsis, and Poria, respectively, oven drying at 80 deg.C, pulverizing to 10 mesh, adding 15 times of water, soaking for 30min, heating to 95 deg.C, decocting for 1.5h, filtering to obtain medicinal liquid, vacuum concentrating to 4 times of the weight of the raw materials, standing, filtering, collecting filtrate as rhizoma Bletillae extract, radix Ampelopsis extract, and Poria extract, and mixing the extracts;
the skin care composition is applied to the production of facial masks, eye creams, face creams, essences, face cleansers, skin lotions, hydrolat and sun screens.
Example 4
On the basis of any one of the embodiments 1 to 3, the skin care composition with the functions of moisturizing, whitening and resisting aging further comprises a component D of 10g, and is applied to the production of any one of essence, toner, hydrolat and facial mask, and the production method comprises the following steps:
placing cosmetic adjuvants in component D in a stirring container, heating to 65-70 deg.C at a speed of 3-4 deg.C/min, stirring, keeping the temperature for more than 5min, cooling to 35-40 deg.C at a speed of 3-5 deg.C/min, adding component A, stirring for 10-15min to mix the materials uniformly, adding essence, component B and component C, stirring for 10-15min, discharging, and standing;
the component D comprises: 35g of purified water, 22g of glycerol and 0.1g of sodium lauryl sulfate.
Example 5
On the basis of any one of the embodiments 1-3, the skin care composition with the functions of moisturizing, whitening and resisting aging also comprises a component D of 15g, and is applied to the production of any one of face cream, eye cream, facial cleanser, emulsion and sun screen, and the production method comprises the following steps:
pre-dissolution of the aqueous phase of S1: putting the glycerol and the purified water in the component D into a water phase jacketed kettle of a vacuum emulsifying machine, heating to 85-90 ℃ at the speed of 3-4 ℃/min, starting stirring at the rotation speed of 85 r/min, stirring and mixing for 5-10min, and adding sodium lauryl sulfate to disperse uniformly;
pre-dissolving of the oil phase of S2: placing the cosmetic matrix except essence in oil phase jacketed pan of vacuum emulsifying machine, heating to 85-90 deg.C at 3-4 deg.C/min, stirring at 85 rpm, stirring for mixing and dissolving;
s3 emulsification: feeding the water phase and oil phase materials into an emulsifying pot, emulsifying at the rotation speed of 2500-2800 r/min and the vacuum degree of-0.03-0.04 MPa at 70-80 ℃ for 5-10min, cooling to 35-40 ℃ at the speed of 3-5 ℃/min, adding the component A, stirring for 10-15min to uniformly mix the materials, adding the essence, the component B and the component C, stirring for 10-15min, discharging and standing;
the cosmetic auxiliary materials comprise: 43g of purified water, 24g of glycerol, 0.2g of sodium lauryl sulfate;
the cosmetic matrix is a composition of glyceryl stearate, cetyl alcohol, stearyl alcohol, isopropyl palmitate, polydimethylsiloxane, tocopherol, essence, methyl hydroxybenzoate and propyl hydroxybenzoate.