CN115607490A - Skin care composition for inhibiting sebaceous gland inflammation and preparation method thereof - Google Patents

Skin care composition for inhibiting sebaceous gland inflammation and preparation method thereof Download PDF

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CN115607490A
CN115607490A CN202211245534.1A CN202211245534A CN115607490A CN 115607490 A CN115607490 A CN 115607490A CN 202211245534 A CN202211245534 A CN 202211245534A CN 115607490 A CN115607490 A CN 115607490A
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extract
skin care
care composition
eucalyptus globulus
powder
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CN115607490B (en
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田勇
申福澈
田云才
张金女
沈洁
袁菊懋
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Shanghai Zhenchen Cosmetics Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/005Antimicrobial preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/592Mixtures of compounds complementing their respective functions
    • A61K2800/5922At least two compounds being classified in the same subclass of A61K8/18

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Abstract

The application discloses a skin care composition for inhibiting sebaceous gland inflammation and a preparation method thereof, wherein the skin care composition comprises the following components in parts by weight: 10 parts of bighead atractylodes rhizome extract; 0.92-960 parts of a combination of Gleditsia sinensis extract, eucalyptus globulus extract and radix Inulae extract. The addition of Atractylodis rhizoma extract into Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract can improve the effects of the skin care composition on inhibiting the growth of sebaceous gland cells, inhibiting Acidobacterium acnes and inhibiting new vessels; has effects of inhibiting red tide or red blood streak, controlling oil and removing acne, and can inhibit sebaceous gland inflammation.

Description

Skin care composition for inhibiting sebaceous gland inflammation and preparation method thereof
Technical Field
The application belongs to the technical field of daily cosmetics, and particularly relates to a skin care composition for inhibiting sebaceous gland inflammation and a preparation method thereof.
Background
Acne is a chronic inflammatory disease caused by the intrinsic defect of the sebaceous glands of the fur, and the main causes of acne include: hyperproliferation of hair follicle keratinocytes, hypersecretion of sebum, proliferation of acne-inducing bacteria such as acidobacterium acnes (Propionibacterium acnes), inflammation caused by sebaceous glands, and the like. Acne on the face is caused by the interaction of the above factors, causing substances in the hair follicles to flow out of the dermis.
The existing treatment methods generally comprise using preparations containing chemical components such as steroid hormones, benzoyl peroxide, azelaic acid, isotretinoin and the like, but the components can cause other problems such as safety and antibiotic resistance. Meanwhile, inflammatory factors secreted from the skin surface under the long-term stimulation of microorganisms can stimulate the skin immune system, cause the expansion of capillaries on the skin surface, show the phenomena of facial redness or pigmentation and the like on the skin surface, not only cause the problems of skin health, but also cause psychological damage. Therefore, improvements in related care products are still needed.
Disclosure of Invention
In view of the above, the present application provides a skin care composition for inhibiting sebaceous gland inflammation and a preparation method thereof, and aims to provide a skin care composition for inhibiting sebaceous gland cell growth, inhibiting lactobacillus acnes and inhibiting neovascularization.
In a first aspect, the embodiments of the present application provide a skin care composition for inhibiting sebaceous gland inflammation, comprising the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
0.92-960 parts of a combination of Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract.
An embodiment according to one aspect of the application comprises the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
10-100 parts of a combination of a gleditsia sinensis extract, an eucalyptus globulus extract and an elecampane inula root extract.
An embodiment according to one aspect of the present application comprises the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
30-60 parts of a combination of a gleditsia sinensis extract, an eucalyptus globulus extract and an elecampane inula root extract.
According to an embodiment of one aspect of the present application, the mass ratio of the honey locust extract, the eucalyptus globulus labill extract and the elecampane inula root extract is: 1:0.92-960:0.92-960.
According to an embodiment of one aspect of the application, the skin care composition is in powder form and has an average particle size of 0.25 to 10 μm.
According to an embodiment of one aspect of the present application, the skin care composition has an ethanol content of 0.1ppm or less.
According to an embodiment of one aspect of the present application, the skin care composition further comprises a solvent selected from organic alcohols, water, vegetable fats or combinations thereof.
According to an embodiment of one aspect of the present application, the vegetable fat is selected from jojoba oil, sunflower seed oil, castor oil, coconut oil, grape seed oil, shea butter, meadowfoam seed oil, macadamia nut oil, olive oil, palm oil, squalane, cocoa butter, jojoba fat, glycolipids, octyldodecanol, caprylic/capric triglyceride, coco-caprylic/capric triglyceride, oleic/linoleic/linolenic polyglyceryl esters and dioctyldodecanol dimer linoleate or combinations thereof;
according to an embodiment of one aspect of the present application, the organic alcohol is selected from the group consisting of methyl propylene glycol, 1, 3-propanediol, 1, 3-butanediol, 1, 2-pentanediol, 1, 2-hexanediol, caprylyl glycol, ethyl hexyl glycerol, or combinations thereof.
According to an embodiment of one aspect of the present application, the skin care composition further comprises at least one of a moisturizer, a thickener, an emulsifier, a neutralizer and a preservative.
In a second aspect, the present application provides a method of making the skin care composition of the first aspect, comprising:
soaking Gleditsia sinensis powder, eucalyptus globulus Labill powder, radix Inulae powder and Atractylodis rhizoma powder in solvent respectively to obtain Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution;
stirring the Gleditsia sinensis extract, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution at 15-100 deg.C and 300-800rpm for 1-8 hr, filtering, and concentrating the filtrate to obtain Gleditsia sinensis extract, eucalyptus globulus Labill extract, radix Inulae extract and Atractylodis rhizoma extract;
mixing the Gleditsia sinensis extract, eucalyptus globulus extract, radix Inulae extract and Atractylodis rhizoma extract to obtain the skin care composition.
In a third aspect, the present application provides a method of making the skin care composition of the first aspect, comprising:
mixing and soaking gleditsia sinensis powder, eucalyptus globulus labill powder, elecampane powder and bighead atractylodes rhizome powder in a solvent to obtain a mixture;
stirring the mixture at the temperature of 15-100 ℃ and the rotating speed of 300-1000rpm for 1-24h, and then filtering to obtain a filtrate;
concentrating the filtrate to obtain the skin care composition.
According to an example of one aspect of the present application, the particle sizes of the honey locust powder, the eucalyptus globulus labill powder, the elecampane powder and the atractylodes macrocephala powder are 60-80 mesh, respectively.
According to an embodiment of one aspect of the application, the solvent is selected from water, ethanol or a combination thereof.
Compared with the prior art, the application has at least the following beneficial effects:
the present application provides a skin care composition for inhibiting sebaceous gland inflammation comprising: 10 parts of bighead atractylodes rhizome extract; 0.92-960 parts of a combination of Gleditsia sinensis extract, eucalyptus globulus extract and radix Inulae extract; the addition of Atractylodis rhizoma extract into Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract can improve the effects of the skin care composition on inhibiting the growth of sebaceous gland cells, inhibiting Acidobacterium acnes and inhibiting new vessels; has effects of inhibiting red tide or red blood streak, controlling oil and removing acne, and can inhibit sebaceous gland inflammation.
Drawings
FIG. 1 shows a graph of the results of the sebaceous gland cell inhibitory activity provided herein;
fig. 2 shows a microscopic observation of neovascularization as provided herein.
Detailed Description
In order to make the application purpose, technical solution and beneficial technical effects of the present application clearer, the present application is further described in detail with reference to the following embodiments. It should be understood that the embodiments described in this specification are only for explaining the present application and are not intended to limit the present application.
For the sake of brevity, only a few numerical ranges are explicitly disclosed herein. However, any lower limit may be combined with any upper limit to form ranges not explicitly recited; and any lower limit may be combined with any other lower limit to form a range not explicitly recited, and similarly any upper limit may be combined with any other upper limit to form a range not explicitly recited. Also, although not explicitly recited, each point or individual value between endpoints of a range is encompassed within the range. Thus, each point or individual value can form a range not explicitly recited as its own lower or upper limit in combination with any other point or individual value or in combination with other lower or upper limits.
In the description of the present application, it is to be noted that, unless otherwise specified, "above" and "below" are inclusive of the present number, and "plural" of "one or more" means two or more.
The above summary of the present application is not intended to describe each disclosed embodiment or every implementation of the present application. The following description more particularly exemplifies illustrative embodiments. At various points throughout this application, guidance is provided through lists of examples, which examples can be used in various combinations. In each instance, the list is provided only as a representative group and should not be construed as exhaustive.
Acne, a type of chronic inflammatory disease caused by the self-localization of the sebaceous glands of the fur, occurs mainly as a result: acne on the face surface generally occurs by the flux of substances in hair follicles out of the dermis layer accompanying the interaction of the above factors, such as hyperproliferation of hair follicle keratinocytes, hyperseborrhea, proliferation of acne-inducing bacteria such as acidobacterium acnes (Propionibacterium acnes), and inflammation around sebaceous glands.
In the treatment of acne, preparations containing chemical components such as steroid hormones, benzoyl peroxide, azelaic acid and isotretinoin are generally used, which have the problems of potential safety hazards, antibiotic resistance and the like, and meanwhile, inflammatory factors secreted by long-term stimulation of skin surface microorganisms stimulate the skin immune system to cause the dilation of skin surface capillaries, which are manifested as phenomena such as facial redness or pigmentation in the skin surface and are unpleasant in appearance.
However, most of the development ideas of acne treatment or acne removal products are mostly focused on the primary bacteriostatic and anti-inflammatory stage, which is beneficial to solving the skin redness, pigmentation and facial red tide phenomena caused by the chronic inflammation reaction in the early stage of acne.
The inventors have studied and found that it is desirable to provide a product which can improve the appearance of skin by inhibiting bacteria and diminishing inflammation in the early stage and which does not use the chemical components having the safety risk and the resistance to antibiotics. Surprisingly, the inventors found that the addition of the extract of white atractylodes rhizome to the extract of honey locust, the extract of eucalyptus globulus and the extract of elecampane inula root can improve the acne removing, oil controlling and red blood streak inhibiting effects of the plant composition.
Skin care compositions
In a first aspect, the embodiments of the present application provide a skin care composition for inhibiting sebaceous gland inflammation, comprising the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
0.92-960 parts of a combination of Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract.
Gleditsia sinensis (Gleditsia sinensis Lam.) also called Gleditsia sinensis Tree and fructus Gleditsiae Abnormalis, is a deciduous tree or small tree of Gleditsia of Leguminosae, has effects of eliminating phlegm, dredging orifice, relieving cough, inducing diuresis, relieving swelling, expelling pus, killing parasite, and treating tinea, and can be used for treating facial black nevus, small pimple, lump, miliaria and acne in folk, and can be used as topical preparation for inhibiting sebum secretion.
Eucalyptus globulus Labill, also known as "Eupatorium berry", is an arborvitae tree of Eucalyptus of Myrtaceae, and Eucalyptus globulus is due to its effective antibacterial, antioxidant, antiallergic and antiinflammatory pharmacological effects. In the application of skin care, the eucalyptus globulus labill extract is widely used as a raw material plant in the aspect of acne removing efficacy due to the strong antibacterial effect of the eucalyptus globulus labill extract on the acidobacillus acnes.
The elecampane inula root (Innula helenium L) is the root of elecampane inula root of the genus inula of the family Compositae, has warm, bitter and pungent properties, has the effects of strengthening the spleen and stomach, promoting the circulation of qi and removing blood stasis, regulating qi and resolving depression and the like, and has various effects of expelling parasites, resisting bacteria, reducing blood sugar and the like in physiological activity.
Atractylodis Rhizoma (Atractylodes rhizome, atractylodes japonica Koidz) is a perennial herb of Atractylodes of Compositae, has medicinal function of spleen-activating, bitter, warm, pungent and strong property, and has effects of eliminating dampness, eliminating turbid pathogen, and relieving pain.
According to the skin care composition provided by the embodiment of the application, the combination of 10 parts by weight of the bighead atractylodes rhizome extract and 0.92-960 parts by weight of the gleditsia sinensis lam extract, the eucalyptus globulus labill extract and the elecampane inula root extract has the effects of inhibiting the red tide and removing acnes, and the inhibition on the growth of sebaceous gland cells, the inhibition on the acnes caused by acidibacterium acnes and the inhibition on the new blood vessels are improved by adding the bighead atractylodes rhizome extract into the gleditsia sinensis lam, the eucalyptus globulus labill and the elecampane root extract. Can also be used for treating chronic inflammation such as acne.
In some embodiments, the following components are included in parts by weight:
10 parts of bighead atractylodes rhizome extract;
10-100 parts of a combination of a gleditsia sinensis extract, a eucalyptus globulus labill extract and an elecampane inula root extract.
In some embodiments, the following components are included in parts by weight:
10 parts of bighead atractylodes rhizome extract;
30-60 parts of a combination of a gleditsia sinensis extract, a eucalyptus globulus labill extract and an elecampane inula root extract. The combination of the atractylodes macrocephala koidz extract, the gleditsia sinensis lam extract, the eucalyptus globulus labill extract and the elecampane inula root extract in parts by weight can further improve the red tide inhibiting effect and the acne removing effect, and improve the sebaceous gland cell growth inhibiting effect, the acnes acidibacterium acnes inhibiting effect and the angiogenesis inhibiting effect.
In some embodiments, the weight ratio of the gleditsia sinensis extract, the eucalyptus globulus labill extract and the elecampane inula root extract is: 1:0.92-960:0.92-960. The mass ratio of the gleditsia sinensis extract to the eucalyptus globulus extractive to the elecampane inula root extract can be as follows: 1:1:1,1:32:1,1:32:32,1:20:1,1:1:20. Has effects in inhibiting red tide and removing acne.
According to an embodiment of one aspect of the application, the skin care composition is in powder form and has an average particle size of 0.25 to 10 μm. The powdered skin care composition has the effects of improving the stability and uniformity of the Atractylodis rhizoma extract, the Gleditsia sinensis extract, the Eucalyptus globulus Labill extract and the radix Inulae extract, further improving the effects of inhibiting red tide and removing acne, and further improving the effects of inhibiting the growth of sebaceous gland cells, inhibiting Acidobacterium acnes and inhibiting new vessels.
In some embodiments, the skin care composition has an ethanol content of 0.1ppm or less. In the skin care composition, the content of the ethanol is less than or equal to 0.1ppm, and the ethanol is little or not contained, so that the skin irritation, particularly the irritation to sensitive muscles, is avoided.
In some embodiments, the skin care composition further comprises a solvent selected from organic alcohols, water, vegetable fats, or combinations thereof. The skin care composition can be used in a water-soluble medium and an oil-soluble medium, has high compatibility and has a more common use scene.
In some embodiments, the vegetable oil is selected from jojoba oil, sunflower seed oil, castor oil, coconut oil, grape seed oil, shea butter, meadowfoam seed oil, macadamia nut oil, olive oil, palm oil, squalane, cocoa butter, jojoba fat, glycolipids, octyldodecanol, caprylic capric triglyceride, coco-caprylic capric triglyceride, oleic/linoleic/linolenic polyglycerides and dioctyldodecanol dimer linoleate, or a combination thereof. According to the embodiment of the present application, the vegetable oil or fat can ensure the safety, moisturizing property, fluidity and homogeneity of the skin care composition, and ensure the moisturizing effect. Wherein, the grape seed oil, the coconut oil and the sunflower seed oil also have antioxidant effect, can improve the repairing effect on the chapped skin and reduce the damage of ultraviolet rays.
In some embodiments, the organic alcohol is selected from methyl propylene glycol, 1, 3-propanediol, 1, 3-butanediol, 1, 2-pentanediol, 1, 2-hexanediol, octyl glycol, ethylhexyl glycerol, or a combination thereof. The skin care composition is dissolved in the organic alcohol, so that the skin care composition has good intersolubility and can improve the moisturizing effect of the composition.
In some embodiments, the skin care composition further comprises at least one of a humectant, a thickener, an emulsifier, a neutralizer, and a preservative. Any one or more additives can be added to the skin care composition, so that the skin care composition has corresponding functions and the use effect of the composition is improved.
In some embodiments, the humectant is selected from glycerin, butylene glycol, 1, 3-propanediol, 1, 2-pentanediol, caprylyl glycol, and sodium hyaluronate, or a combination thereof. The above moisturizer can enhance the moisturizing effect of the skin care composition for skin, and is well mixed with each component.
In some embodiments, the thickening agent is selected from carbomers, acrylic polymers crosslinked with C10-C30 alkanol acrylate, xanthan gum, or combinations thereof. The thickening agents described above have important effects on the thickening, stability and rheology of skin care compositions for the skin; by using thickeners in different weight ratios, the skin care composition for skin can be in a liquid state, a paste state, or a gel state to be suitable for different scenes. The skin care composition has good thickness and excellent spreadability and extensibility due to the adoption of the thickening agent in a proper proportion.
In some embodiments, the plant emulsifier is selected from polyglyceryl-3 diisostearate, polyglyceryl 2-dipolyhydroxystearate, polyglyceryl-2 isostearate, polyglyceryl 4-isostearate, polyglyceryl 3-polyricinoleate, polyglyceryl 6-polyricinoleate, glyceryl stearate, sorbitan isostearate, sorbitan oleate and sucrose cocoate or a combination thereof. The plant emulsifier is plant-derived, green and safe, has no stimulation to skin, is suitable for sensitive muscle user groups, and has good anti-allergy and relieving effects. The polyglycerol stearate can form a lamellar liquid crystal type colloid network structure in an emulsification system, so that the stability of the emulsification system is improved. The polyglycerol-3 diisostearate and the polyglycerol 2-dipolyhydroxystearate have stronger emulsifying capacity, can wrap more water phase by less oil phase, has good dispersibility and stability, and has better compatibility with various water-in-oil system emulsifiers.
In some embodiments, the neutralizing agent is selected from sodium hydroxide, potassium hydroxide, or a combination thereof. By adding the neutralizing agent, the pH of the skin care composition for skin can be controlled to be more suitable for the skin of different users.
In some embodiments, the preservative is selected from phenoxyethanol, p-hydroxyacetophenone, 1, 2-pentanediol, 1, 2-hexanediol, p-anisic acid, caprylyl glycol, ethylhexyl glycerin, benzoic acid, sodium benzoate, caprylyl hydroxamic acid, or combinations thereof. The preservative is well compatible with other substances, and the shelf life of the skin care composition for skin can be prolonged and shelf life of the skin care composition can be prolonged by adding the preservative.
The skin care composition according to the present application may further comprise a combination of one or more of a radical scavenger, a chelating agent, an antioxidant, a film former, a stabilizer, a fragrance, a pigment, preferably, the stabilizer comprises one or more of sodium chloride, magnesium chloride and magnesium sulfate, and the chelating agent comprises EDTA-2Na and/or EDTA-4Na.
In some embodiments, the skin care composition can further comprise a skin immune enhancer of natural origin, such as sodium hyaluronate, bisabolol, cucumis sativus fruit extract, bergamot extract, cornflower extract, or a combination thereof. The skin immunity promoter is safe and healthy, and can improve skin immunity. The carboxymethyl B-glucan salt may be sodium carboxymethyl B-glucan, potassium carboxymethyl B-glucan, or the like.
The invention also provides application of the skin care composition in skin care products, preferably the skin care products comprise water-type skin care products, gel-type skin care products, emulsion-type skin care products, essence-type skin care products or cream-type skin care products.
Method for preparing skin care composition
In a second aspect, the present application provides a method of making the skin care composition of the first aspect, comprising:
soaking Gleditsia sinensis powder, eucalyptus globulus Labill powder, radix Inulae powder and Atractylodis rhizoma powder in solvent respectively to obtain Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution;
stirring the Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution at 15-100 deg.C and 300-800rpm for 1-8 hr, respectively, filtering, and concentrating the filtrate to obtain Gleditsia sinensis extract, eucalyptus globulus Labill extract, radix Inulae extract and Atractylodis rhizoma extract;
mixing the Gleditsia sinensis extract, eucalyptus globulus extract, radix Inulae extract and Atractylodis rhizoma extract to obtain the skin care composition.
Stirring at 300-800rpm at 15-100 deg.C for 1-8 hr to further improve dissolution of effective active substances in Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution, and improve effective active components thereof.
According to the embodiment of the application, the gleditsia sinensis extract, the eucalyptus globulus labill extract, the elecampane inula root extract and the bighead atractylodes rhizome extract are prepared and then mixed, and the mixture can be mixed according to the required proportion, so that the specific mass ratio and the corresponding effect are further achieved.
In a third aspect, the present application provides a method of making the skin care composition of the first aspect, comprising:
mixing and soaking gleditsia sinensis powder, eucalyptus globulus labill powder, elecampane inula root powder and atractylodes macrocephala powder in a solvent to obtain a mixture;
stirring the mixture at the temperature of 15-100 ℃ and the rotating speed of 300-1000rpm for 1-24h, and then filtering to obtain filtrate;
concentrating the filtrate to obtain the skin care composition.
The mixture of the gleditsia sinensis extract, the eucalyptus globulus extract, the elecampane inula root extract and the bighead atractylodes rhizome extract is prepared, so that the steps of respective extraction can be reduced, and the efficiency can be improved.
In some embodiments, the gleditsia sinensis powder, eucalyptus globulus labill powder, elecampane powder and atractylodes macrocephala powder have a particle size of 60-80 mesh, respectively. The granularity of the gleditsia sinensis powder, the eucalyptus globulus labill powder, the elecampane powder and the atractylodes macrocephala powder is in the range, so that the effective active components in the gleditsia sinensis powder can be dissolved out at a proper temperature and at a proper stirring speed, the preparation efficiency is improved, and the content of the effective active components is improved.
In some embodiments, the solvent is selected from water, ethanol, or a combination thereof. The extract is extracted by water and ethanol, so that the loss of raw materials can be reduced, and the preparation cost can be saved.
In some embodiments, the weight ratio of the gleditsia sinensis powder, the eucalyptus globulus labill powder and the elecampane inula root powder is 1:0.92-960, the above-mentioned quality combination ratio can control oil and inhibit acne bacillus and skin red blood silk together with the white atractylodes rhizome extract.
The preparation method of the skin care composition can be used for preparing the skin care composition, the process is simple, the time consumption is short, the requirement on equipment is low, the prepared skin care composition system is stable, the harm to the body health of a user can not be caused, and the skin care composition has great large-scale application potential.
Examples
The present disclosure is more particularly described in the following examples that are intended as illustrative only, since various modifications and changes within the scope of the present disclosure will be apparent to those skilled in the art. Unless otherwise indicated, all parts, percentages, and ratios reported in the following examples are on a weight basis, and all reagents used in the examples are commercially available or synthesized according to conventional methods and can be used directly without further treatment, and the equipment used in the examples is commercially available.
Examples 1 to 4
This example provides a method of making a skin care composition comprising: crushing the gleditsia sinensis, the eucalyptus globulus, the elecampane and the bighead atractylodes rhizome into powder by using a wall breaking machine respectively, sieving the powder with a 80-mesh sieve for later use, and soaking crushed and filtered gleditsia sinensis, the eucalyptus globulus, the elecampane and the bighead atractylodes rhizome in mixed liquid of 70 parts of ethanol and 30 parts of distilled water respectively, wherein the volume of the mixed liquid is about 20 times of the mixed volume of each crushed and filtered substance. Stirring was carried out at 600rpm for 3h at 25. + -. 2 ℃ respectively. Filtering to remove solid residue, concentrating the filtrate under reduced pressure until ethanol is removed to obtain Gleditsia sinensis extract, eucalyptus globulus Labill extract, radix Inulae extract and Atractylodis rhizoma extract.
Mixing the obtained 4 extracts according to the mass ratio shown in the following table to obtain the skin care composition.
Table 1 weight ratio of the honey locust extract, the eucalyptus globulus labill extract, the elecampane inula root extract and the atractylodes macrocephala extract in examples 1-4 (unit: each part is kg).
Figure BDA0003886395310000101
Examples 5 to 10
This example provides a method of making a skin care composition comprising:
crushing the gleditsia sinensis, the eucalyptus globulus, the elecampane and the bighead atractylodes rhizome into powder by using a wall breaking machine, and sieving the powder by using a 60-80-mesh sieve for later use. Taking the gleditsia sinensis powder, the eucalyptus globulus labill powder, the elecampane powder and the atractylodes macrocephala powder according to the mass ratio for later use. Soaking the above powders in 1-20 times of the volume of the mixture. The components of the mixture are water and alcohol. Stirring at 300-1000rpm at 15-100 deg.C for 1-24 hr, and extracting the above raw materials under stirring. Filtering to remove solid residue, and concentrating the filtrate under reduced pressure until ethanol is removed to obtain skin care extract. The mass ratio of the gleditsia sinensis lam, the eucalyptus globulus, the elecampane powder and the atractylodes macrocephala powder is shown in table 2.
Table 2 weight ratio (unit, kg) of the honey locust powder, the eucalyptus globulus labill powder, the elecampane inula root powder and the atractylodes macrocephala powder in examples 5-10.
Figure BDA0003886395310000102
Figure BDA0003886395310000111
Comparative example 1
This comparative example provides a method of preparing a skin care composition comprising: crushing the gleditsia sinensis, the eucalyptus globulus and the elecampane into powder by using a wall breaking machine, sieving the powder with a 80-mesh sieve for later use, respectively soaking crushed and filtered gleditsia sinensis, the eucalyptus globulus and the elecampane into mixed liquor with the volume of 20 times, wherein the mixed liquor comprises 70 parts of ethanol and 30 parts of distilled water. Stirring was carried out at 600rpm for 3h at 25. + -. 2 ℃. Filtering to remove solid residue, and concentrating the filtrate under reduced pressure until ethanol is removed to obtain Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract. The obtained 3 extracts are mixed according to the weight proportion of 25 parts: 25 parts of: after mixing in a ratio of 25 parts, a skin care composition is obtained.
Comparative example 2
The comparative example provides a preparation method of a skin care composition, wherein bighead atractylodes rhizome is crushed into powder by a wall breaking machine, the powder is sieved by a 80-mesh sieve for later use, and the powder is soaked in a mixed solution with the volume 20 times that of the mixed solution, and the mixed solution comprises 70 parts of ethanol and 30 parts of distilled water. Stirring was carried out at 600rpm for 3h at 25. + -. 2 ℃. Filtering to remove solid residue, and vacuum concentrating the filtrate until no ethanol is contained to obtain Atractylodis rhizoma extract. I.e., the skin care composition of this comparative example.
Test section
1) Sebaceous gland cell growth rate test
After the sebaceous gland cells undergo a differentiation process for about one week, the cortical cells mature, and sebum is removed through the cortical tubes. The inhibitory effect of examples 1 to 10 and comparative example 1 on sebaceous gland cells was preliminarily evaluated by the sebaceous gland cell proliferation inhibitory potency test method.
Taking logarithmHuman sebaceous gland cells (SZ 95) in the growth phase, digested with 0.25% pancreatic enzyme, collected and counted in a 96-well plate at 5X10 4 cells/mL were seeded at a cell density of about 60-70% per well 48h after plating, in medium: DMEM +10% FBS +1% P/S, culture conditions: 37 ℃ C., 5% CO 2 The culture is carried out under the condition of content, and the activity meets the requirement. The experimental groups were divided into 12 groups, a control group, and examples 1 to 10 and comparative examples 1 to 2.DMEM is a medium containing various amino acids and glucose, FBS stands for fetal bovine serum, and P/S stands for penicillin/streptomycin. The control group was treated with serum-free medium for 1,3,5 days, respectively.
The samples of examples 1 to 10 and comparative examples 1 to 2 were prepared as aqueous solutions having mass concentrations of 10. Mu.g/mL, 50. Mu.g/mL, and 100. Mu.g/mL, respectively. And (3) dropwise adding 100ug of the sample aqueous solution into a cell culture dish, continuously and respectively culturing for 1,3 and 5 days, adding 20 mu L of CCK8 solution in the CCK8 kit into each hole, incubating for 2 hours, measuring the light absorption value at the position of 570nm of wavelength by using an ultraviolet spectrophotometer, performing 3 parallel experiments, and taking the average value. The absorbance was recorded and the calculated cell growth rate is shown in table 3 and fig. 1.
TABLE 3 test results for% sebaceous gland cell growth rate
Figure BDA0003886395310000121
Calculating the cell growth rate according to the obtained light absorption value, wherein the calculation mode is as follows:
Figure BDA0003886395310000131
tx: sample treatment time (1, 3,5 days)
Examples 1-4 and comparative example 1 the concentrations to be measured were 10. Mu.g/mL, 50. Mu.g/mL, 100. Mu.g/mL;
independent sample t-tests using SPSS22.0 software were significantly different with p < 0.05. Here, the experimental group Tx OD570 value represents the absorbance at 570nm wavelength.
As can be seen from the above table, the sebaceous gland cells cultured in the absence of serum had no inhibitory effect, and the extracts of the examples and comparative examples had inhibitory effects on the sebaceous gland cells with increasing concentrations.
Examples 1-8 showed significantly stronger inhibitory effects on sebaceous gland cells than comparative examples 1-2, due to the addition of Atractylodis rhizoma extract to Gleditsia sinensis extract, eucalyptus globulus Labill extract and Inula helenia extract.
Examples 9 and 10 in the more extreme case, the inhibition of sebaceous gland cells was observed compared to the control group, and the compositions used in high concentrations required appropriate dilution. In example 4, the inhibitory activity of the sebaceous gland cell growth at the first day treatment time at a concentration of 100. Mu.g/ml is preferable, and the sebaceous gland cell growth rate is 23%.
2) Propionibacterium acnes zone of inhibition test
Acidibacterium acnes (Propionibacterium acnes), which is one of the genus lactobacilli and causes acne, were subjected to zone of inhibition tests using the skin care compositions of example 1 and comparative example 1.
Inoculating the preserved Propionibacterium acnes (ATCC 6919) into BHI liquid culture medium under aseptic condition, culturing at 37 deg.C in anaerobic incubator for 48 hr, centrifuging, resuspending, and adjusting Propionibacterium acnes concentration to 1X10 6 CFU/ml, spare. Taking sterile culture dishes with the diameter of 90mm in a sterile environment, introducing 20mL of BHI melting culture medium into each culture dish, cooling and fixing, uniformly coating 100 mu l of resuspended Acidobacterium acnes solution on the culture medium, taking circular filter paper with the diameter of 7mm to dip test drugs, respectively diluting comparative example 1 and examples 1-4 into 0.5% concentration, respectively preparing a blank control group and a positive control group, uniformly placing the filter paper dipped with the test drugs on the BHI solid culture medium coated with the Acidobacterium acnes, respectively carrying out 3 parallels, sealing the culture dishes by using sealing films, horizontally inverting the culture dishes in an anaerobic incubator at 37 ℃ for 20 hours, measuring the diameter of a bacteriostatic ring, and calculating the average diameter of the bacteriostatic ring of each test drug. The results are shown in Table 4.
The skin care compositions of examples 1-4 and comparative example 1 were present at 0.5% in the BHI melt medium;
the blank control group is PBS solution;
the positive control group was 0.1% triclosan.
Table 4 results for the zone of inhibition of acidibacterium acnes.
Figure BDA0003886395310000141
The results are shown in Table 4, where the inhibition zone was not shown by the sterile PBS treatment, the diameter of the inhibition zone of 0.1% tris-hydroxydiphenyl ether in the positive control group was 40.3mm, the diameter of the inhibition zone of comparative example 1 was 15.9mm, the diameter of the inhibition zone of example 1 was 18.7mm, the diameter of the inhibition zone of example 2 was 20.1mm, the diameter of the inhibition zone of example 3 was directly 19.2mm, and the diameter of the inhibition zone of example 4 was 20.7mm. Comparative example 1 and examples 1 to 4 both showed inhibition zones against acnes, and examples 1 to 4 were larger in diameter than comparative example 1, wherein example 4 had a better inhibition effect.
3) Neovascularization assay
Continuous or excessive application of steroid hormone preparations to inflammatory reaction of acne patients, weakening of skin vessel wall, expansion of capillary, exposure of capillary to skin surface, or appearance of facial redness or flush, etc. can be evaluated for the inhibition of angiogenesis in comparative examples 1-2 and examples 1-4.
Matrigel was added to a pre-cooled 96-well plate and transferred to 37 ℃ for incubation for 30min to allow the matrigel to polymerize. Adding the sample to the polymerized matrigel, and removing CO at 37 deg.C and 5% of the total 2 Incubate for another 30min at ambient. Then, human Umbilical Vein Endothelial Cells (HUVEC) in logarithmic growth phase were taken, digested with 0.25% pancreatin, collected and cultured at 1.5X10 per well 4 Inoculating the cells at a cell/well inoculation rate of 5% CO at 37 ℃ with saturated humidity 2 After 8h incubation in the incubator, the formation of new vessels was collected microscopically and the number of new vessels formed was counted.
Examples 1-4 and comparative example 1 had a concentration of 50. Mu.g/mL in the mixture per well plate; the control group was the same volume of distilled water.
The neovasculature of the control group, comparative example 1 and examples 1-4 was observed under an electron microscope as shown in FIG. 2. After 8h incubation, the vessels generated in comparative example 1 and example 1 have looser distance between the vessels and incomplete linking degree compared with the control group, and the comparison of examples 1-4 shows that the phenomenon is more obvious in example 1, which indicates that example 4 has the best effect on inhibiting the neovascularization.
Table 5 number of neovessels per well in well plates (averaged).
Group of Number of formed tubes
Control group 68
Comparative example 1 53
Comparative example 2 51
Example 1 45
Example 2 32
Example 3 29
Example 4 26
The results of formation of new blood vessels in the control group, comparative examples 1-2 and examples 1-4 are shown in Table 5, and the numbers of formed vessels were 68, 53, 51, 45, 32, 29 and 26, respectively, indicating that the formation of new blood vessels was inhibited in comparative examples 1-2 and examples 1-4, and the neovascularization inhibitory ability of examples 1-4 was greater than that of comparative examples 1-2, in which the inhibitory effect of example 4 was more excellent.
In conclusion, the skin care composition of the present application has the effects of inhibiting red tide and removing acne, and the best effect of example 4 is obtained by evaluating the effects of sebaceous gland cell growth inhibition, acidibacterium acnes inhibition and neovascularization inhibition in different mixing ratios of 4 plants using the gleditsia sinensis, eucalyptus globulus, elecampane and atractylodes macrocephala as raw material plants.
The above description is only for the specific embodiments of the present application, but the scope of the present application is not limited thereto, and any person skilled in the art can easily think of various equivalent modifications or substitutions within the technical scope of the present application, and these modifications or substitutions should be covered within the scope of the present application. Therefore, the protection scope of the present application shall be subject to the protection scope of the claims.

Claims (10)

1. A skin care composition for inhibiting sebaceous gland inflammation comprises the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
0.92-960 parts of a combination of Gleditsia sinensis extract, eucalyptus globulus Labill extract and radix Inulae extract.
2. The skin care composition according to claim 1, comprising the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
10-100 parts of a combination of a gleditsia sinensis extract, an eucalyptus globulus extract and an elecampane inula root extract.
3. The skin care composition according to claim 1, comprising the following components in parts by weight:
10 parts of bighead atractylodes rhizome extract;
30-60 parts of a combination of a gleditsia sinensis extract, a eucalyptus globulus labill extract and an elecampane inula root extract.
4. The skin care composition according to claim 1, wherein the weight ratio of the gleditsia sinensis extract, the eucalyptus globulus labill extract and the elecampane inula root extract is: 1:0.92-960:0.92-960.
5. The skin care composition according to claim 1, wherein the skin care composition is in a powder form and has an average particle size of 0.25 to 10 μm.
6. The skin care composition according to any one of claims 1-5, wherein the amount of ethanol in the skin care composition is less than or equal to 0.1ppm.
7. The skin care composition of claim 6, further comprising a solvent selected from the group consisting of organic alcohols, water, vegetable fats and oils, and combinations thereof.
8. The skin care composition of claim 7, wherein the vegetable oil or fat is selected from jojoba oil, sunflower seed oil, castor oil, coconut oil, grape seed oil, shea butter, meadowfoam seed oil, macadamia nut oil, olive oil, palm oil, squalane, cocoa butter, jojoba fat, glycolipids, octyldodecanol, caprylic/capric triglyceride, coco-caprylic/capric triglyceride, oleic/linoleic/linolenic polyglyceryl esters, and dioctyldodecanol dimer linoleate, or combinations thereof;
the organic alcohol is selected from methyl propylene glycol, 1, 3-butylene glycol, 1, 2-pentanediol, 1, 2-hexanediol, octyl glycol, ethylhexyl glycerol or a combination thereof;
the skin care composition further comprises at least one of a humectant, a thickener, an emulsifier, a neutralizer, and a preservative.
9. A method of making a skin care composition according to any one of claims 1 to 8 comprising:
soaking Gleditsia sinensis powder, eucalyptus globulus Labill powder, radix Inulae powder and Atractylodis rhizoma powder in solvent respectively to obtain Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution;
stirring the Gleditsia sinensis solution, eucalyptus globulus Labill solution, radix Inulae solution and Atractylodis rhizoma solution at 15-100 deg.C and 300-800rpm for 1-8 hr, respectively, filtering, and concentrating the filtrate to obtain Gleditsia sinensis extract, eucalyptus globulus Labill extract, radix Inulae extract and Atractylodis rhizoma extract;
mixing the Gleditsia sinensis extract, eucalyptus globulus extract, radix Inulae extract and Atractylodis rhizoma extract to obtain the skin care composition.
10. A method of making a skin care composition according to any of claims 1-8 comprising:
mixing and soaking gleditsia sinensis powder, eucalyptus globulus labill powder, elecampane powder and bighead atractylodes rhizome powder in a solvent to obtain a mixture;
stirring the mixture at the temperature of 15-100 ℃ and the rotating speed of 300-1000rpm for 1-24h, and then filtering to obtain filtrate;
concentrating the filtrate to obtain the skin care composition.
CN202211245534.1A 2022-10-12 Skin care composition for inhibiting sebaceous gland inflammation and preparation method thereof Active CN115607490B (en)

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