CN113750005B - Ginseng paste-shaped mask and preparation method thereof - Google Patents

Ginseng paste-shaped mask and preparation method thereof Download PDF

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CN113750005B
CN113750005B CN202110991599.XA CN202110991599A CN113750005B CN 113750005 B CN113750005 B CN 113750005B CN 202110991599 A CN202110991599 A CN 202110991599A CN 113750005 B CN113750005 B CN 113750005B
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ginseng
glycerin
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CN113750005A (en
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何章
任晗堃
张单单
刘盼玉
曲召辉
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Zhiran Tiancheng Beijing Biotechnology 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8129Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers or esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers, e.g. polyvinylmethylether
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • 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
    • A61K8/9728Fungi, e.g. yeasts
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations
    • 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
    • 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 invention discloses a ginseng paste-shaped mask and a preparation method thereof, and belongs to the technical field of cosmetics. The ginseng paste mask comprises ginseng root powder, acryloyl dimethyl ammonium taurate/VP copolymer, polyvinyl alcohol, xanthan gum, ganoderma sinensis extract, snow lotus extract, ginseng root extract, peony extract, polyurethane-35 and conventional auxiliary materials in the field of cosmetics. The invention also discloses a preparation method of the ginseng paste mask. The ginseng paste mask disclosed by the invention is moist in skin feel, uniform in film forming and easy to wash; has no tension feeling after use, and has effects of moistening skin, reducing skin moisture loss, relieving fine wrinkles, tightening skin, and resisting aging.

Description

Ginseng paste-shaped mask and preparation method thereof
Technical Field
The invention relates to the technical field of cosmetics, and particularly relates to a ginseng paste mask and a preparation method thereof.
Background
With the progress of society, the development of economy and the continuous improvement of the living standard of people, the requirements of people on beauty and skin care cosmetics are higher and higher, and the beauty and skin care cosmetics are developed in the direction of naturalization, nutrition and efficacy. The skin is an organ in which the human body is easily aged. With the aging, human cells, especially skin cells, gradually age due to their own characteristics and the influence of external environment, and skin problems such as decrease in skin plumpness and elasticity, increase in wrinkles, loose and aged skin, color spots, dullness, and the like, are followed. Wrinkles, which are a sign of the appearance of skin aging, are called the "annual ring of youth". With the improvement of the life quality of people, the moisture retention and aging resistance become a hot topic of attention of the majority of cosmetic consumers. Skin aging is classified into intrinsic aging and extrinsic aging. The former is also called natural aging, which is a natural process of programmed aging. The latter is skin aging due to external environmental factors such as ultraviolet, smoking, blowing, exposure to chemicals. Ultraviolet radiation is the most dominant factor in extrinsic aging. When the skin is irradiated by ultraviolet, excessive active oxygen is generated in cells, so that aging-related genes are expressed, inflammation cascade reaction is induced, the expression quantity of elastin and collagen is reduced, and the skin has aging phenomena such as relaxation, wrinkles and the like.
Compared with a facial mask, the mud-shaped facial mask is one of facial masks, contains rich mineral substances and nutrient components, can strongly adsorb dirt in skin, helps the skin to remove the dirt, and helps the nutrition of subsequent skin care products to be effectively absorbed. The mud mask mainly comprises a wash-free mud mask and a wash-off mud mask, such as a cleaning mud mask. However, in the prior art, the washing-off type mud mask generally has the problems of difficult washing-off, too strong cleaning capability, easy skin sensitivity, poor skin feeling after use, lack of skin care effect and the like.
In order to solve the problems, the development of a mud mask which has good skin feel, uniform film formation, easy washing, no tight feeling after use and anti-aging effect is very necessary.
Disclosure of Invention
Based on the defects of the prior art, the invention aims to provide the ginseng paste mask which has the advantages of moist skin feel, uniform film forming, easy washing and no tight feeling after use;
the ginseng paste mask disclosed by the invention has the effects of moistening and moisturizing skin, reducing skin moisture loss, fading fine wrinkles, tightening skin, resisting aging and the like.
Therefore, the technical scheme provided by the invention is as follows:
the invention provides a ginseng paste mask in a first aspect.
According to the invention, the ginseng paste mask comprises the following components in percentage by mass: ginseng root powder 2.0wt% -10.0wt%, caprylic acid/capric triglyceride/hydrogenated polyisobutene/ganoderma sinensis extract/snow lotus herb extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% -5.0wt%, water/glycerin/dendrobium stem extract/aloe vera leaf extract/ginseng root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 2.0wt% -10.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxy ethanol/1,2-hexanediol 0.5wt% -5.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%.
According to the invention, the particle size of the ginseng root powder is 10-60 mu m.
According to some embodiments of the invention, the ginseng root powder has a particle size of 20 to 50 μm.
According to the invention, the ginseng paste-like mask further comprises the following components in percentage by mass: 6.0 to 15.0 weight percent of humectant, 0.08 to 0.12 weight percent of chelating agent, 0.3 to 1.0 weight percent of thickening agent, 2.0 to 4.5 weight percent of emulsifier, 2.0 to 6.0 weight percent of emollient, 10.0 to 15.0 weight percent of film forming agent and 0.3 to 0.8 weight percent of skin conditioner.
According to the invention, the humectant comprises one or more of glycerol, butanediol, propylene glycol, dipropylene glycol, pentanediol and sodium hyaluronate.
According to the invention, the chelating agent comprises one or more of disodium EDTA, trisodium EDTA, tetrasodium EDTA, and sodium glucoheptonate.
According to the invention, the thickening agent comprises one or more of acryloyl dimethyl ammonium taurate/VP copolymer, xanthan gum, carrageenan, hydroxyethyl cellulose, sodium polyacrylate grafted starch, polyvinyl alcohol, carbomer and acrylic acid (ester)/C10-30 alkanol acrylate cross-linked polymer.
According to the invention, the emulsifier comprises one or more of sucrose stearate, cetearyl glucoside, arachidol glucoside, coco glucoside, glyceryl stearate, PEG-100 stearate, ceteareth-20, methylglucamine sesquistearate.
According to the invention, the emollient comprises one or more of caprylic/capric triglyceride, shea butter, jojoba ester, isostearyl alcohol isostearate, isopropyl isostearate and polydimethylsiloxane.
According to the invention, the film forming agent comprises one or more of polyurethane-35, gum arabic and polyvinylpyrrolidone.
According to the invention, the skin conditioning agent comprises one or more of betaine, tocopherol acetate, panthenol, and glyceryl polyether-26.
According to the invention, the ginseng paste mask comprises the following components in percentage by mass:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glyceryl polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 10.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% -5.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3510.0 wt% -15.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/wolfberry fruit extract of lycium barbarum/1,2-hexanediol/echinacea purpurea extract 2.0wt% -10.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -5.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the present invention, the ginseng puree mask comprises, in mass percent:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 8.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% -4.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3510.0 wt% -14.0wt%, water/glycerin/dendrobium stem extract/aloe vera leaf extract/sophora flavescens root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the present invention, the ginseng puree mask comprises, in mass percent:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 6.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (di-tert-butyl hydroxyhydrocinnamate) 1.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -14.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/wolfberry fruit extract of lycium barbarum/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the present invention, the ginseng puree mask comprises, in mass percent:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 3.0 to 5.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 2.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -13.0wt%, water/glycerin/dendrobium stem extract/aloe vera) leaf extract/ginseng root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, and essence 0.01wt% -0.03wt%.
According to the invention, the hyaluronic acid has a molecular weight of 1.0X 10 6 ~1.8×10 6 Da。
According to the present invention, the ginseng puree mask may be prepared using a method that is conventional in the art.
According to some embodiments of the present invention, the ginseng mask is prepared by a preparation method comprising the steps of:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 80-85 deg.C, and mixing;
2) Weighing phase C, heating to 80-85 deg.C, and mixing;
3) Adding phase C into the mixed phase of phase A and phase B, homogenizing for 3-5min;
4) Cooling to 45 deg.C, adding phase D, and stirring;
5) Cooling to 38 deg.C, checking, filtering, and discharging.
In a second aspect, the present invention provides a method for preparing the ginseng paste mask of the first aspect.
According to the invention, the preparation method comprises the following steps:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 80-85 deg.C, and mixing;
2) Weighing phase C, heating to 80-85 deg.C, and mixing;
3) Adding phase C into the mixed phase of phase A and phase B, homogenizing for 3-5min;
4) Cooling to 45 deg.C, adding phase D, and stirring;
5) Cooling to below 38 ℃, filtering and discharging after passing inspection.
According to the invention, the ginseng paste mask comprises the following components in percentage by mass:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 10.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% to 4.0wt%, caprylic/capric triglyceride 1.0wt% to 3.0wt%, isostearyl isostearate 1.0wt% to 3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% to 5.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% to 1.2wt%;
phase D: polyurethane-3510.0 wt% -15.0wt%, water/glycerin/dendrobium stem extract/aloe barbadensis leaf extract/sophora flavescens root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 2.0wt% -10.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -5.0wt%, caprylyl hydroxamic acid/glyceryl caprylate/3536-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the present invention, the ginseng puree mask comprises, in mass percent:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 8.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (di-tert-butyl hydroxyhydrocinnamate) 1.0wt% -4.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3510.0 wt% -14.0wt%, water/glycerin/dendrobium stem extract/aloe barbadensis leaf extract/sophora flavescens root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylyl hydroxamic acid/glyceryl caprylate/3536-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the invention, the ginseng mud-like mask comprises, by mass:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 6.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (di-tert-butyl hydroxyhydrocinnamate) 1.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -14.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/wolfberry fruit extract of lycium barbarum/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%.
According to some embodiments of the present invention, the ginseng puree mask comprises, in mass percent:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 3.0 to 5.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 2.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -13.0wt%, water/glycerin/dendrobium stem extract/aloe vera) leaf extract/ginseng root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, and essence 0.01wt% -0.03wt%.
According to some embodiments of the invention, the ginseng root powder has a particle size of 10 to 60 μm.
According to still other embodiments of the present invention, the ginseng root powder has a particle size of 20 to 50 μm.
According to the invention, the hyaluronic acid has a molecular weight of 1.0X 10 6 ~1.8×10 6 Da。
The invention has the beneficial effects that:
the ginseng paste mask comprises ginseng root powder, acryloyl dimethyl ammonium taurate/VP copolymer, polyvinyl alcohol, xanthan gum, ganoderma sinensis extract, snow lotus extract, ginseng root extract, peony extract, polyurethane-35 and conventional auxiliary materials in the field of cosmetics. Natural plant powder ginseng root powder is used for replacing mineral powder such as kaolin, volcanic mud/rock and the like in the traditional mud mask, and the natural plant powder ginseng root powder and the plant extract have synergistic effect; has no tension feeling after use, and has effects of moistening skin, reducing skin moisture loss, relieving fine wrinkles, tightening skin, and resisting aging.
Drawings
FIG. 1 is a graph of relative cell viability of the ginseng mud mask of example 1;
FIG. 2 is the result of the cytomorphological observation of the ginseng paste mask of example 1;
FIG. 3 is the effect of example 1 on the results of COL-I expression assays.
Detailed Description
The invention is further illustrated below with reference to specific examples, to which, however, the invention is not restricted.
It should be appreciated by those skilled in the art that the present invention is not limited to the embodiments, and any changes and modifications to the present invention are within the protection scope of the present invention.
The experimental methods described in the following examples are all conventional methods unless otherwise specified; the experimental materials and reagents are commercially available, unless otherwise specified.
The raw materials of the invention can be purchased commercially, and the main raw materials and sources used in the invention are shown in table 1:
TABLE 1 raw materials and sources
Figure BDA0003232541270000061
Examples 1 to 3
Examples 1-3 ginseng mud mask components and ratios are shown in table 2.
Table 2 examples 1-3 ginseng mud mask compositions and proportions
Figure BDA0003232541270000071
Example 1 a method for preparing a ginseng paste mask includes the steps of:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 85 deg.C, and mixing uniformly;
2) Weighing phase C, heating to 85 deg.C, and mixing;
3) Adding phase C into mixed phase (A + B), and homogenizing for 5min;
4) Cooling to 45 deg.C under stirring, adding phase D, and stirring;
5) Cooling to 38 ℃, filtering and discharging after passing the inspection.
Example 2 a method for preparing a ginseng paste mask includes the steps of:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 80 deg.C, and mixing uniformly;
2) Weighing the phase C, heating to 80 ℃, and uniformly mixing;
3) Adding phase C into mixed phase (A + B), and homogenizing for 3min;
4) Cooling to below 40 deg.C under stirring, adding phase D, and stirring;
5) Cooling to 35 ℃, filtering and discharging after passing inspection.
Example 3 a method for preparing a ginseng paste mask comprises the steps of:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 83 deg.C, and mixing uniformly;
2) Weighing the phase C, heating to 83 ℃, and uniformly mixing;
3) Adding phase C into mixed phase (A + B), and homogenizing for 4min;
4) Cooling to 45 deg.C under stirring, adding phase D, and stirring;
5) Cooling to 35 ℃, filtering and discharging after passing inspection.
Comparative examples 1 to 4
Comparative examples 1-4 ginseng paste-like mask components and compounding ratios are shown in table 3.
Table 3 comparative examples 1-4 ginseng paste-like mask components and ratios
Figure BDA0003232541270000081
Figure BDA0003232541270000091
Comparative examples 1-4 a ginseng mud-like mask was prepared in the same manner as in example 1.
And (3) marketing competitive products: the main ingredients comprise glycerol, 1,2-pentanediol, butanediol, glycerol, sodium hyaluronate, adenosine, rice fermentation product filtrate, rosa damascena (ROSADAMASCENA) flower oil, folium Camelliae sinensis (CAMELLIA SINENSIS) extract, tocopherol (vitamin E), tocopherol acetate, betaine, sodium hyaluronate, blackberry (RUBUS FRUTICOSUS) leaf extract, yeast fermentation product filtrate, grape (VITIS VINIFERA) seed oil, hydrogenated lecithin, litchi (LITCHI CHINENSIS) seed extract, oat (AVENA SATIVA) kernel extract), etc.
Test example 1: skin moisturization test
The skin moisture content is measured based on the capacitance test principle, and at normal temperature, the dielectric constant of water is 81, the dielectric constant of other substances in the skin is usually less than 7, and the water is the substance with the largest dielectric constant in the skin. When the moisture content changes, the capacitance of the skin also changes, so the moisture content on the skin surface can be analyzed by measuring the capacitance of the skin. The larger the skin moisture content value is, the higher the skin moisture content is, and the better the moisturizing effect is.
The human body test of the moisture content of the skin comprises the following specific information:
volunteers: 48 persons (18-45 years old);
test sites: the forearm is bent, and the area of the test area is 3 multiplied by 4cm 2 The interval between the areas is 1.5cm.
Test samples: examples 1-3, comparative examples 1-4, and the competitors.
The use mode is as follows: applying corresponding test samples to the test areas, each test area (3X 4 cm) 2 ) The sample application amount is 0.5mL, the sample stays for 10min after being evenly applied, and then the test sample is washed off by clear water and is lightThe residual moisture was wiped dry with a paper towel.
And (3) testing environment: temperature: 20.0-21.5 ℃, relative humidity: 47 to 49 percent.
Testing an instrument: skin moisture content tester Corneometer (CM 825, courage and Khazaka, germany).
The test method comprises the following steps: and (3) measuring the moisture content of the skin before and after use (0 h, 0.5h, 1h, 2h and 4 h) by using a skin tester, and judging the moisturizing effect of the mask according to the change of the moisture value. The results and the mean change rates are shown in Table 4.
TABLE 4 moisture content of skin before, after 0h, 0.5h, 1h, 2h, and 4h
Figure BDA0003232541270000092
Figure BDA0003232541270000101
Note: the above average value is an average value of 6 persons of moisture content.
As shown in the test results in the table 4, compared with the comparative examples 1 to 4 and competitive products, the ginseng paste mask disclosed in the embodiments 1 to 3 of the invention can obviously improve the moisture content of the skin, and the instant moisture content of the skin after use is improved by 96.9 to 99.2 percent; after the ginseng paste mask is used for 2-4 hours, the skin can still keep higher moisture content, which shows that the ginseng paste mask has the moisturizing effect on the basis of supplementing the moisture content of the skin. The ginseng mud-shaped mask disclosed by the invention has better moisturizing effects through the synergistic effect of the ginseng powder and the plant extract. In conclusion, the ginseng paste mask disclosed by the invention can improve the moisture content of the skin and has a better moisturizing effect.
Test example 2: percutaneous moisture loss test
The skin moisture loss tester Aqua Flux (AF 200, BIOX, uk) was tested by collecting water vapor that has diffused through the skin in a closed condensation chamber. The water vapor diffused and frozen on the condensing plate at-7.65 ℃. The air humidity of the part close to the skin in the test cavity is high, the air humidity of the part close to the condenser plate is low, the humidity difference between the test cavity and the condenser plate enables water vapor to move from the surface of the skin to the condenser in a passive diffusion mode, and the water vapor flow density of the test area can be calculated by measuring the humidity gradient. In the instrument, a single silicon chip is used as a sensor for the temperature and humidity of water vapor, and the flow density of the water vapor is measured, so that the water dispersion of the skin is measured. The percutaneous water loss test has the following specific information:
volunteers: 48 persons (18-45 years old);
test sites: the forearm is bent, and the area of the test area is 3 multiplied by 4cm 2 And the regions are spaced 1.5cm apart.
Test samples: examples 1-3, comparative examples 1-4, and competitors.
The use method comprises the following steps: volunteers were used 2 times a week for 15min each time.
And (3) testing environment: temperature: 20.0-21.5 ℃, relative humidity: 47 to 49 percent.
Testing the instrument: skin moisture loss tester AquaFlux (AF 200, BIOX, uk).
The test method comprises the following steps: the skin water dispersion loss before and after use (0 h, 0.5h, 1h, 2h and 4 h) is measured by a skin water dispersion tester, and the higher the value of the percutaneous water dispersion TEWL is, the faster the percutaneous water dispersion is. The results and the mean change rates are shown in Table 5.
TABLE 5 Water Dispersion loss of skin before, after 0h, 0.5h, 1h, 2h, 4h of ginseng paste mask
Figure BDA0003232541270000102
Note: the above average value is an average of 6 persons' moisture content.
From the test results in table 5, it can be seen that the average TEWL values of all test areas are reduced compared to those before use (initial value); compared with a comparative example area and a competitive product area, the reduction range of the skin moisture loss in the areas of examples 1-3 is larger at the same test time point, which shows that the ginseng paste mask has better capability of inhibiting the skin moisture loss through the synergistic effect of the ginseng powder and the plant extract, and shows that the compounding of the components has obvious synergistic effect.
Test example 3: sensory evaluation
Volunteers: no allergic reaction occurs in 240 volunteers of 18-50 years old;
the using part: the face.
Test samples: examples 1-3, comparative examples 1-4, and the competitors.
The use and evaluation methods were: applying 10g of mask on the face for 15min, carrying out sensory evaluation on the mask, evaluating the result by 5 points, investigating the indexes such as smearing, film forming uniformity, washing-off, overall acceptance and the like after use, scoring between 0 and 10 points according to the use effect, wherein 8 to10 points are good, 6 to 8 points are good, 4 to 6 points are general, 2 to 4 points are poor, and 0 to 2 points are poor, and taking an average value; the stabbing pain and the tightening feeling after use are considered, the use effect is divided into 0-10 points, 8-10 points are poor, 6-8 points are poor, 4-6 points are general, 2-4 points are good, 0-2 points are good, and the average value is taken.
TABLE 6 evaluation and evaluation results of Ginseng radix paste facial mask
Figure BDA0003232541270000111
The sensory evaluation results of the ginseng paste mask are shown in table 6, compared with the comparative example, the ginseng paste mask disclosed by the invention has the advantages that the paste mask is easy to apply and wash off through the synergistic effect of the ginseng root powder and the plant extract, the film is uniform, the skin is moistened after the use, the tight feeling is avoided, and the overall acceptance is high. Meanwhile, volunteers showed no irritation of the ginseng mud mask. In conclusion, the ginseng paste mask disclosed by the invention is moist in skin feel, uniform in film forming, easy to wash off, free of tight feeling after being used and high in overall acceptance.
Test example 4: verification of anti-aging efficacy
Skin aging is classified into intrinsic aging and extrinsic aging. The former is also called natural aging, which is a natural process of programmed aging. The latter is skin aging due to external environmental factors such as ultraviolet, smoking, air blowing, exposure to chemicals. Ultraviolet radiation is the most dominant factor in extrinsic aging. When the skin is irradiated by ultraviolet, excessive active oxygen is generated in cells, so that aging-related genes are expressed, inflammation cascade reaction is induced, the expression quantity of elastin and collagen is reduced, and the skin is subjected to aging phenomena such as relaxation, wrinkles and the like.
During skin aging, intracellular MAPK signaling pathways are activated. This pathway inhibits the expression of transforming growth factor beta (TGF- β) while up-regulating the level of Matrix Metalloproteinases (MMP), ultimately leading to a decrease in the amount of type I collagen (COL-I) secretion in the cells, causing skin aging. The amount of COL-I secretion is the most intuitive indicator for skin aging.
The method is based on a human skin fibroblast (HFF-1) model, and the anti-photoaging efficacy of the product is evaluated by measuring the effect of the product on type I collagen after photodamage.
Test materials
Human skin fibroblasts (HFF-1) were purchased from the stem cell bank of the Chinese academy of sciences.
Fetal bovine serum (FBS, gibco), DMEM high-sugar medium (DMEM, gibco), dimethyl sulfoxide (DMSO, sigma), phosphate buffer (PBS, gibco), vitamin E (VE), thiazole blue (MTT, sigma), human COL-I ELISA kit (Shanghai Weiao).
Test apparatus
Super clean bench (Adata Kelong), inverted microscope (Leica), carbon dioxide incubator (Thermo), electric suction aid (Eppendorf), enzyme-labeling instrument (Tecan), ultraviolet irradiation box (Chinese Boda).
Test method
1. HFF-1 cell-based toxicity assays
The test adopts MTT method to detect cell activity and screen the maximum safe concentration of the given sample of cells. The assay was set up with a negative control (medium), a positive control (10% dmso in medium) and a zero-adjusted well (PBS), the sample concentration settings are shown in table 7, and 3 replicate wells were set for each concentration. The specific operation steps are as follows:
(1) Inoculation: taking cells in logarithmic growth phase for digestionThen inoculated into a 96-well plate, and the plate was placed at 37 ℃ in 5% CO 2 And incubating and culturing for 18-24h in the incubator.
(2) Preparing liquid: test substances were prepared at different concentrations according to the concentration settings in table 7.
TABLE 7 sample cytotoxic concentration settings
Sample name Sample concentration (m/v)
Example 1 0.008%、0.016%、0.031%、0.063%、0.125%、0.25%、0.5%、1%
(3) Sample feeding: removing supernatant after cell growth for 18-24 hr, adding culture medium containing different concentrations of test substance, and placing the culture plate at 37 deg.C and 5% CO 2 And incubating and culturing for 18-24h in the incubator.
(4) And (3) detection: after the cells were cultured for 18-24h, the supernatant was discarded, the prepared and filtered MTT (0.5 mg/mL) was added, mixed gently and incubated at 37 ℃ for 4h in the dark. Discarding supernatant after incubation, adding 150 μ L DMSO into each well, shaking for 20min, and reading OD with microplate reader 540nm The value is obtained.
(5) Relative cell viability calculation formula:
Figure BDA0003232541270000121
2. HFF-1 cell COL-I expression detection based on UVA irradiation
(1) Inoculation: seeding the cells into 6-well plates, 37 ℃,5% CO 2 The incubator is incubated for 18-24h.
(2) Preparing liquid: the test substances and positive controls were formulated according to table 8.
(3) Sample feeding: grouping and concentration setting according to the test of Table 8, after the cells in the 6-well plate are plated and grown for 18-24h, grouping and giving samples, and setting 3 multiple wells in each group. In group 1, the cell culture medium containing 0.1% DMSO was added to both the blank control and the negative control, and the cell culture medium containing 10. Mu.g/mL vitamin E was added to the positive control; in group 2, the blank control and the negative control were added with cell culture medium, and the sample group was added with cell culture medium containing the corresponding concentration of sample, at 37 ℃ and 5% CO 2 The incubator continues to culture for 24h.
Table 8 test groupings and concentration settings
Figure BDA0003232541270000131
(4) Irradiation: adding sample, culturing for 18-24 hr, removing culture medium, washing with pre-warmed 1mL PBS twice, removing washing solution, adding 1mL PBS, and setting the group to be irradiated at 30J/cm 2 Irradiation was performed at UVA dose. After the irradiation dose was reached, PBS was removed from the wells, washed once with 1mL of pre-warmed PBS, and added to DMEM medium for further incubation for 18-24h.
(5) Detecting the content of the type I collagen: the supernatant was collected and detected by ELISA kit.
(6) Data processing: each item of data obtained in the experiment was processed and plotted by Excel software. Statistical analysis was performed using SPSS 17.0 and comparisons between groups were judged to be significant when P <0.05 using one-way analysis of variance (ANOVA).
The cytotoxicity test results of the ginseng mud-like mask are shown in table 9, the relative cell viability change trend is shown in fig. 1, and the morphological observation results of the cells are shown in fig. 2.
TABLE 9 cytotoxicity test results of ginseng paste-like mask
Figure BDA0003232541270000132
Cell efficacy test concentration selection criteria:
(1) Relative cell viability ± SD > 85% (no significant difference (P > 0.05) compared to negative control group when mean relative cell viability is between 85-90% (excluding 90%));
(2) Cell morphology, no significant change compared to negative control group;
based on the cytotoxicity test results, the cell morphology, and customer requirements, the mask of example 1 was selected to be administered at concentrations of 0.125%, 0.25%, and 0.5% on HFF-1 cells.
TABLE 10 COL-I expression assay results
Figure BDA0003232541270000133
Figure BDA0003232541270000141
Remarking:
a tangle-solidup indicates a very significant difference compared to SC (UVA-, 0.1% dmso) group, P <0.01;
Δ means very significant difference compared to the BC (UVA-) group, P <0.01;
# indicates a significant difference compared to the SC (UVA +,0.1% DMSO) group, P <0.05;
* Indicating significant differences compared to the NC (UVA +) group, P <0.05.
The test results of table 10 show that the ginseng paste mask of example 1 can significantly improve the expression of COL-I secretion amount and has anti-aging effect when the concentration is 0.125% compared to NC (UVA +) group.

Claims (9)

1. The ginseng paste mask is characterized by comprising the following components in percentage by mass: ginseng root powder 2.0wt% -10.0wt%, caprylic acid/capric triglyceride/hydrogenated polyisobutene/ganoderma sinensis extract/snow lotus herb extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% -5.0wt%, water/glycerin/dendrobium stem extract/aloe vera leaf extract/ginseng root extract/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 2.0wt% -10.0wt%, water/glycerin/trehalose/opuntia ficus indica stem extract/tapioca starch/phenoxy ethanol/1,2-hexanediol 0.5wt% -5.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%;
the granularity of the ginseng root powder is 10-60 mu m;
the thickening agent comprises 0.3-0.8 wt% of acryloyl dimethyl ammonium taurate/VP copolymer and 0.08-0.12 wt% of xanthan gum;
the film forming agent comprises polyurethane with the weight percentage of 10.0 to 15.0 percent.
2. The ginseng mud mask as claimed in claim 1, wherein the ginseng root powder has a particle size of 20 to 50 μm.
3. The ginseng mud mask as claimed in claim 1, further comprising in mass percent: 6.0 to 15.0 weight percent of humectant, 0.08 to 0.12 weight percent of chelating agent, 0.3 to 1.0 weight percent of thickening agent, 2.0 to 4.5 weight percent of emulsifier, 2.0 to 6.0 weight percent of emollient, 10.0 to 15.0 weight percent of film forming agent and 0.3 to 0.8 weight percent of skin conditioner.
4. The ginseng mud mask as claimed in claim 3, wherein the moisturizer comprises one or more of glycerin, butylene glycol, propylene glycol, dipropylene glycol, pentylene glycol, and sodium hyaluronate, the chelating agent comprises one or more of disodium EDTA, trisodium EDTA, tetrasodium EDTA, and sodium glucoheptonate, the emulsifier comprises one or more of sucrose stearate, cetearyl glucoside, arachidyl glucoside, cocoyl glucoside, glyceryl stearate, PEG-100 stearate, ceteareth-20, and methyl glucosesquistearate, the emollient comprises one or more of caprylic/capric triglyceride, shea butter, jojoba esters, isostearyl isostearate, isopropyl isostearate, and polydimethylsiloxane, and the skin conditioner comprises one or more of betaine, tocopherol acetate, panthenol, and glyceryl polyether-26.
5. The ginseng mud-shaped mask is characterized by comprising the following components in percentage by mass:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 10.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 1.0wt% -5.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3510.0 wt% -15.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 2.0wt% -10.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -5.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%;
the particle size of the ginseng root powder is 10-60 mu m.
6. The ginseng mud-shaped mask is characterized by comprising the following components in percentage by mass:
phase A: 100 percent of water To, 0.3 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 0.8 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.08 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 8.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (di-tert-butyl hydroxyhydrocinnamate) 1.0wt% -4.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3510.0 wt% -14.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%;
the particle size of the ginseng root powder is 10-60 mu m.
7. The ginseng mud-shaped mask is characterized by comprising the following components in percentage by mass:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 2.0 to 6.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (di-tert-butyl hydroxyhydrocinnamate) 1.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -14.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe barbadensis leaf extract/root extract of sophora alopecuroides/1,2-pentanediol/lycium barbarum fruit extract/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0-0.03wt%;
the particle size of the ginseng root powder is 10-60 mu m.
8. The ginseng mud-shaped mask is characterized by comprising the following components in percentage by mass:
phase A: 100 percent of water To, 0.5 To 0.8 percent of acryloyl dimethyl ammonium taurate/VP copolymer, 1.0 To 1.2 percent of polyvinyl alcohol, 0.08 To 0.12 percent of EDTA disodium, 0.02 To 0.03 percent of sodium hyaluronate, 0.1 To 0.12 percent of xanthan gum, 0.3 To 0.8 percent of betaine, and 5363 To 2.5 percent of glycerol polyether-261.0;
phase B: 3.0 to 6.0 weight percent of glycerin, 3.0 to 5.0 weight percent of ginseng root powder and 2.0 to 6.0 weight percent of butanediol;
and C phase: cetearyl alcohol 2.0wt% -4.0wt%, caprylic/capric triglyceride 1.0wt% -3.0wt%, isostearyl isostearate 1.0wt% -3.0wt%, caprylic/capric triglyceride/hydrogenated polyisobutene/Ganoderma sinensis extract/snow lotus flower extract/ginseng root extract/peony extract/pentaerythritol tetrakis (bis-tert-butylhydroxyhydrocinnamate) 2.0wt% -3.0wt%, sucrose stearate/cetearyl glucoside/cetyl alcohol 0.5wt% -1.2wt%;
phase D: polyurethane-3512.0 wt% -13.0wt%, water/glycerin/stem extract of dendrobium nobile/aloe vera) leaf extract/extract of ginseng radix/1,2-pentanediol/extract of lycium barbarum/1,2-hexanediol/echinacea purpurea extract 3.0wt% -6.0wt%, water/glycerin/trehalose/stem extract of opuntia ficus indica/tapioca starch/phenoxyethanol/1,2-hexanediol 0.5wt% -2.0wt%, caprylhydroxamic acid/glyceryl caprylate/1,2-pentanediol 0.3wt% -0.8wt%, 1,2-hexanediol 0.1wt% -0.3wt%, essence 0.01wt% -0.03wt%;
the particle size of the ginseng root powder is 10-60 mu m.
9. A method for preparing a ginseng paste mask according to any one of claims 5 to 8, comprising the steps of:
1) Respectively dispersing phase A and phase B uniformly, adding phase B into phase A, heating to 80-85 deg.C, and mixing;
2) Weighing phase C, heating to 80-85 deg.C, and mixing;
3) Adding phase C into the mixed phase of phase A and phase B, homogenizing for 3-5min;
4) Cooling to 45 deg.C, adding phase D, and stirring;
5) Cooling to below 38 ℃, filtering and discharging after passing inspection.
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