CN113712858A - Preparation and application of antibacterial and anti-inflammatory plant extract composition - Google Patents

Preparation and application of antibacterial and anti-inflammatory plant extract composition Download PDF

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CN113712858A
CN113712858A CN202110771103.8A CN202110771103A CN113712858A CN 113712858 A CN113712858 A CN 113712858A CN 202110771103 A CN202110771103 A CN 202110771103A CN 113712858 A CN113712858 A CN 113712858A
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basil
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chlorogenic acid
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曹茜
周秋娜
金荣熙
姚清
申彦晟
金延埈
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Cosmax China Cosmetics Co Ltd
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Abstract

The invention discloses an antibacterial and anti-inflammatory plant extract composition and application thereof. According to the invention, the plant extract composition with low addition and strong antibacterial and anti-inflammatory effects is finally obtained by taking the compounding ratio of basil, chlorogenic acid and medicinal rhubarb as an entry point to carry out relevant tests on the antibacterial activity and the addition of the composition. Wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is (1-3) to (0.05-0.2) to (1-3). The composition can effectively inhibit the breeding of skin pathogenic bacteria, and can reduce inflammatory reaction by reducing active oxygen free radicals, eliminating inflammatory factors, improving stratum corneum water loss and the like.

Description

Preparation and application of antibacterial and anti-inflammatory plant extract composition
Technical Field
The invention belongs to the field of cosmetics, and relates to preparation and application of an antibacterial and anti-inflammatory plant extract composition.
Background
Due to the influence of the unapproved life style, the continuous change of living environment, the age, the psychological pressure, the environmental pollution, the change of four seasons, the abuse of chemicals and the like, the skin and the mucous membrane of the skin bring a plurality of damages, and the incidence rate of skin diseases shows a continuously rising trend. Modern medical research shows that dysbacteriosis and pathogenic bacteria breeding of a human body can cause endocrine dysfunction, sebum exuberance usually occurs on skin in reaction, and meanwhile, inflammation, acne redness, pimple on the top and the like are caused.
Ocimum basilicum (Ocimum basilicum) is a plant belonging to the genus Ocimum of the order Labiatae, and is called lavender, bird's-nest, cymbidium and West-cowherb, and is a medicinal and edible aromatic plant. The taste is similar to fennel, the whole plant is small and exquisite, the leaf color is emerald green, the flower color is bright, and the fragrance is diffused all around. Basil is one of the main aromatic oil plants, and the volatile oil mainly exists in stems, leaves and flower ears and generally contains 0.1-0.12% of oil. The whole basil herb can be used as a medicine, has warm and pungent properties, has various efficacies of dispelling wind and promoting qi circulation, activating blood circulation, eliminating dampness, promoting digestion, detoxifying and the like, and has nineteen percent of sterilization rate of pure basil essential oil.
Chlorogenic acid (Chlorogenic acid) is an ester formed by caffeic acid and quinic acid, is present in common Chinese herbal medicines such as oriental wormwood, honeysuckle and the like, has a strong broad-spectrum antibacterial effect, and the research on the biological activity of Chlorogenic acid by modern science is deeply carried out in a plurality of fields such as food, health care, medicine, daily chemical industry and the like. Chlorogenic acid is an important bioactive substance, and has antibacterial, antiviral, leukocyte increasing, liver protecting, gallbladder promoting, antitumor, blood pressure lowering, blood lipid reducing, free radical scavenging, and central nervous system exciting effects.
The radix et rhizoma Rhei is dry root and rhizome of Rheum palmatum L, Rheum officinale Baill, Rheum officinale Kitag et al, Rheum tanguticum Maxim. ex Balf. The main functional indications are as follows: purging heat-toxin, breaking stagnation and removing blood stasis. The anthraquinone compounds include emodin, physcion, aloe-emodin, rhein, chrysophanol, etc. The rhubarb has wide antibacterial spectrum and has an inhibiting effect on a plurality of gram-positive bacteria and gram-negative bacteria such as staphylococcus aureus, hemolytic streptococcus, typhoid bacillus, dysentery bacillus, helicobacter pylori and the like; has inhibitory effect on various fungi, influenza virus, hepatitis virus and human immunodeficiency virus.
At present, the application of basil, chlorogenic acid and rhubarb is mainly concentrated in the fields of medicines and food health products, and the application of the basil, the chlorogenic acid and the rhubarb in the field of cosmetics is not much. Singh S finds that the basil volatile oil has obvious inhibition effect on plantar swelling caused by rat carrageenan and edema caused by arachidonic acid and leukotriene, meanwhile, basil (whole plant) extract can reduce ear swelling degree of the rat, and has inhibition effect on leukocyte migration in a rat ballooning model caused by the carrageenan, so that NO and MDA contents in serum are reduced, and SOD activity is enhanced; in recent years, a new antibacterial mechanism of chlorogenic acid has been reported to play a role by reducing the hardness of bacterial cell walls, slowing the migration of bacteria, affecting the stability of bacterial cell membranes and inducing the generation of Reactive Oxygen Species (ROS); researches of Agarwal SK and the like show that the effective components in rhubarb, such as rhein, aloe-emodin, chrysophanol and physcion, have antibacterial effects on cryptococcus neoformans, Leptophyceae and Epsilon, Candida albicans and Aspergillus fumigatus. The rhein, emodin and aloe-emodin in the antibacterial effective components have the most obvious effect.
When the epidermal flora of a human body is disordered, the breeding of pathogenic bacteria can cause inflammatory reaction of the skin, and meanwhile, the generated inflammatory factors can stimulate the skin in turn, so that the increase of active oxygen free radicals is caused, more damage is generated, and the phenomena of acne redness, epidermal water loss and the like occur. Therefore, the invention reduces the risk of skin infection by regulating the biological activity of epidermal flora and inhibiting the breeding of harmful bacteria, and reduces inflammatory reaction by reducing active oxygen free radicals, eliminating inflammatory factors, improving stratum corneum water loss and the like.
The existing research almost rarely mentions the application of the compounding of basil, chlorogenic acid and medicinal rhubarb in the antibacterial activity of the field of cosmetics.
Disclosure of Invention
The invention aims to provide a bacteriostatic anti-inflammatory plant extract composition and application thereof, and solves the problems in the prior art. According to the invention, the plant extract composition with low addition and strong antibacterial and anti-inflammatory effects is finally obtained by taking the compounding ratio of basil, chlorogenic acid and medicinal rhubarb as an entry point to carry out relevant tests on the antibacterial activity and the addition of the composition.
In view of the problems existing in the technical background, the invention aims to provide a preparation method of an anti-inflammatory and bacteriostatic plant extract composition, which comprises the following steps:
1) pulverizing radix et rhizoma Rhei raw material, extracting with deionized water and cellulase, and filtering to obtain first primary filtrate;
2) cutting fresh basil into segments, and extracting with ethanol to obtain a second primary filtrate;
3) mixing the first primary filtrate and the second primary filtrate, concentrating, diluting with water, extracting with organic phase, mixing the organic phases, and concentrating to obtain fluid extract;
4) dissolving the fluid extract with ethanol, adding chlorogenic acid powder for dissolving, concentrating to obtain concentrated solution, and ultrafiltering to obtain the plant extract composition with antiinflammatory and antibacterial effects;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is (1-3) to (0.05-0.2) to (1-3).
Preferably, the preparation method comprises the following steps:
1) pulverizing radix et rhizoma Rhei; adding deionized water for extraction, wherein the mass ratio of the rhubarb raw material to the deionized water is 1:20-1:50, and soaking for 1-3 hours; adding cellulase in a water bath at the temperature of 40-50 ℃, wherein the total mass of the added cellulase is 10-20% of the mass of the rhubarb raw material, stirring for 20 minutes, heating to 40-60 ℃, performing microwave treatment for 5-15 minutes, performing ultrasonic water bath reflux extraction for 1-3 hours, cooling to 20-30 ℃, and filtering by using 100-mesh gauze of 200 meshes to obtain a first primary filtrate;
2) cutting fresh basil into 1-2cm sections according to mass ratio, soaking in 3-5 times of 95% ethanol solution for 1h, performing ultrasonic oscillation extraction at low temperature, filtering, and mixing filtrates to obtain second primary filtrate;
3) mixing the first primary filtrate and the second primary filtrate, concentrating under reduced pressure, adding distilled water with 1 volume of the concentrated solution, and sequentially extracting with petroleum ether, chloroform and ethyl acetate; repeating for 2-3 times until the extractive solution is colorless, mixing ethyl acetate layers, and concentrating under reduced pressure to obtain fluid extract;
4) dissolving the extract with 1-3 times volume of ethanol, adding chlorogenic acid powder according to mass ratio, and stirring to dissolve completely; filtering, adding clarifier, standing, centrifuging for 30-60 min, and filtering with microfiltration membrane to obtain filtrate. Concentrating under reduced pressure to recover ethanol to obtain concentrated solution; filtering with ultrafiltration membrane to obtain the plant extract composition with antiinflammatory and antibacterial effects;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is (1-3) to (0.05-0.2) to (1-3).
More preferably, the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is 1:0.2:2 or 1:0.1: 3.
Further preferably, the clarifying agent in the step 4) is one or more of a natural clarifying agent, chitosan, a fruit juice clarifying agent, gelatin and egg white.
Further preferably, the pore diameter of the microfiltration membrane in the step 4) is 0.1-1.0 μm; the pore diameter of the ultrafiltration membrane is 0.01-0.05 μm.
The invention also provides an anti-inflammatory and bacteriostatic plant extract composition, which is prepared by the preparation method;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is 1:0.2:2 or 1:0.1: 3.
In certain more specific embodiments, the preparation method is specifically:
(1) crushing a large xanthogen material according to a mass ratio;
(2) adding deionized water for extraction, wherein the mass ratio of the raw materials to the deionized water is 1:20, and soaking for 2 hours. Water bath, adding cellulase when the temperature is 48 ℃, stirring for 20 minutes, heating to 54 ℃, performing microwave treatment for 10 minutes, and performing ultrasonic water bath reflux extraction for 3 hours, wherein the total mass of the added cellulase accounts for 10 percent of the total mass of the raw materials;
(3) cooling the extracting solution obtained in the step (2) to room temperature, and filtering with 200-mesh gauze to obtain primary filtrate 1;
(4) cutting fresh basil into 1-2cm sections according to mass ratio, soaking in 3 times of 95% ethanol solution for 1h, extracting at low temperature by ultrasonic oscillation, filtering, and mixing filtrates to obtain primary filtrate 2;
(5) mixing the filtrates of steps (3) and (4), and concentrating under reduced pressure in a rotary evaporator at 55 deg.C to obtain fluid extract; dissolving the extract with 1 time of distilled water, sequentially extracting with petroleum ether, chloroform and ethyl acetate at a volume ratio of 1: 1; shaking for 3 hr, separating organic layer, extracting for 3 times until colorless, mixing ethyl acetate layers, concentrating under reduced pressure in a rotary evaporator, recovering ethyl acetate at 35 deg.C to obtain fluid extract;
(6) dissolving the extract with 3 times of ethanol, adding chlorogenic acid powder according to the mass ratio, stirring to fully dissolve, adding a clarifying agent, standing, centrifuging for 60 minutes, and filtering with a microfiltration membrane to obtain a filtrate. Filtering, concentrating under reduced pressure, and recovering ethanol to obtain concentrated solution.
(7) Characterized in that the rotating speed in the step (5) is 8000 rpm;
(8) and (4) filtering the solution obtained in the step (6) by using an ultrafiltration membrane, and collecting filtrate to obtain the plant extract composition with the effects of resisting inflammation and inhibiting bacteria.
The invention also provides an application of the composition in preparing cosmetics with anti-inflammatory and bacteriostatic effects.
The invention also provides a cosmetic comprising the composition and cosmetically acceptable adjuvants.
Preferably, the composition accounts for 0.5-5% of the cosmetic by mass.
Preferably, the cosmetic is a water, an emulsion, a spray, a cream, a gel or a mask.
The application has the following beneficial effects:
1) can effectively inhibit the breeding of skin pathogenic bacteria, and has no influence on normal flora of skin epidermis.
2) Can reduce inflammatory reaction by reducing active oxygen free radicals, eliminating inflammatory factor, improving horny layer water loss, etc.
3) Compared with the conventional bacteriostatic composition, the bacteriostatic composition disclosed by the invention uses natural products as raw materials, and is safer and non-irritant.
Drawings
FIG. 1 is a graph of the effect of different compositions on IL1- α secretion;
FIG. 2 is a graph of the effect of different compositions on IL-6 secretion;
FIG. 3 is a graph of the effect of different compositions on transdermal water loss;
figure 4 is a graph of the effect of different compositions on erythema.
Detailed Description
Embodiments of the present application will be described in detail by examples, so that how to apply technical means to solve technical problems and achieve technical effects of the present application can be fully understood and implemented.
The raw materials and equipment used in the present application are all common raw materials and equipment in the field, and are all from commercially available products, unless otherwise specified. The methods used in this application are conventional in the art unless otherwise indicated.
There are many other possible embodiments of the present invention, which are not listed here, and the embodiments claimed in the claims of the present invention can be implemented.
Example 1 preparation of a plant extract composition effective against inflammation and bacteria
In the following examples and comparative examples of the present invention, the plant extract composition effective in anti-inflammatory and bacteriostatic effects was prepared by the following process.
(1) Crushing a large xanthogen material according to a mass ratio;
(2) adding deionized water for extraction, wherein the mass ratio of the raw materials to the deionized water is 1:20-1:50, and soaking for 1-3 hours. Adding cellulase in water bath at 40-50 deg.C, stirring for 20 min, heating to 40-60 deg.C, performing microwave treatment for 5-15 min, and performing ultrasonic water bath reflux extraction for 1-3 hr;
(3) cooling the extracting solution obtained in the step (2) to 20-30 ℃, and filtering with 100-200-mesh gauze to obtain primary filtrate 1;
(4) cutting fresh basil into 1-2cm sections according to mass ratio, soaking in 3-5 times of 95% ethanol solution for 1h, performing ultrasonic oscillation extraction at low temperature, filtering, and mixing filtrates to obtain primary filtrate 2;
(5) mixing the filtrates of steps (3) and (4), and concentrating under reduced pressure in a rotary evaporator at 50-60 deg.C to obtain fluid extract; dissolving the extract with 1 time of distilled water, sequentially extracting with petroleum ether, chloroform and ethyl acetate at a volume ratio of 1: 1; shaking for 2-4 hr, separating organic layer, extracting for 2-3 times until colorless, mixing ethyl acetate layers, concentrating under reduced pressure in a rotary evaporator, recovering ethyl acetate at 35-50 deg.C to obtain fluid extract;
(6) dissolving the extract with 1-3 times of ethanol, adding clarifier, standing, centrifuging for 30-60 min, filtering with microfiltration membrane to obtain filtrate, and reflux-extracting with 1-3 times of solution for 3-5 hr. Adding chlorogenic acid powder according to the mass ratio, and stirring until the chlorogenic acid powder is fully dissolved. Filtering, concentrating under reduced pressure, and recovering ethanol to obtain concentrated solution.
(7) Characterized in that the rotating speed in the step (5) is 5000-10000 rpm;
(8) and (4) filtering the solution obtained in the step (6) by using an ultrafiltration membrane, and collecting filtrate to obtain the plant extract composition with the effects of resisting inflammation and inhibiting bacteria.
Example 2 evaluation of antioxidant efficacy of composition combinations of different proportions
(1) Crushing a large xanthogen material according to a mass ratio;
(2) adding deionized water for extraction, wherein the mass ratio of the raw materials to the deionized water is 1:20, and soaking for 2 hours. Water bath, adding cellulase when the temperature is 48 ℃, stirring for 20 minutes, heating to 54 ℃, performing microwave treatment for 10 minutes, and performing ultrasonic water bath reflux extraction for 3 hours, wherein the total mass of the added cellulase accounts for 10 percent of the total mass of the raw materials;
(3) cooling the extracting solution obtained in the step (2) to room temperature, and filtering with 200-mesh gauze to obtain primary filtrate 1;
(4) cutting fresh basil into 1-2cm sections according to mass ratio, soaking in 3 times of 95% ethanol solution for 1h, extracting at low temperature by ultrasonic oscillation, filtering, and mixing filtrates to obtain primary filtrate 2;
(5) mixing the filtrates of steps (3) and (4), and concentrating under reduced pressure in a rotary evaporator at 55 deg.C to obtain fluid extract; dissolving the extract with 1 time of distilled water, sequentially extracting with petroleum ether, chloroform and ethyl acetate at a volume ratio of 1: 1; shaking for 3 hr, separating organic layer, extracting for 3 times until colorless, mixing ethyl acetate layers, concentrating under reduced pressure in a rotary evaporator, recovering ethyl acetate at 35 deg.C to obtain fluid extract;
(6) dissolving the extract with 3 times of ethanol, adding chlorogenic acid powder according to the mass ratio, stirring to fully dissolve, adding a clarifying agent, standing, centrifuging for 60 minutes, and filtering with a microfiltration membrane to obtain a filtrate. Filtering, concentrating under reduced pressure, and recovering ethanol to obtain concentrated solution.
(7) Characterized in that the rotating speed in the step (5) is 8000 rpm;
(8) and (4) filtering the solution obtained in the step (6) by using an ultrafiltration membrane, and collecting filtrate to obtain the plant extract composition with the effects of resisting inflammation and inhibiting bacteria.
The three plant extracts were compounded according to the following ratio in table 1 to obtain compositions 1-15, comparative examples 1-3.
TABLE 1
Figure BDA0003152987070000081
In the composition and the comparative example of the invention, the method for testing the bacteriostasis and repair effect of the bacteriostatic and anti-inflammatory plant extract composition and the results are as follows:
detection of bacteriostatic effects
Selecting strains: staphylococcus aureus, pseudomonas aeruginosa, propionibacterium acnes; the preparation of the bacterial liquid selects pseudomonas aeruginosa, staphylococcus aureus and propionibacterium acnes as listed strains. Preparation: it was diluted to about 1.0x10 with sterile physiological saline5cfu/ml~1.0x106cfu/ml ofAnd (4) bacterial suspension. The prepared bacterial suspension can be used within 2h, or can be stored at 2-8 ℃ for no more than 24 h.
And (3) detecting the antibacterial effect: the plant composition obtained in step (8) of example 2 was taken, and 20. mu.L of the actual plant composition was dropped onto each of sterile dried filter paper sheets. Test bacterium inoculation: taking 1mL of each test bacterial suspension, and uniformly smearing the test bacterial suspension on the surface of a nutrient agar culture medium; the bacteriostatic test samples are attached, one bacterial staining flat plate is attached to each test, 4 filter paper sheets are attached to each dish, 3 filter paper sheets are test sample sheets, and 1 filter paper sheet is blank. A sample piece is attached to the surface of the flat plate by using a sterile forceps, the flat plate is placed in a constant temperature incubator at 36 +/-1 ℃, the result is observed after the flat plate is cultured for 18 hours, and the diameter of the antibacterial ring is measured by using a vernier caliper. The results are the average of 3 measurements.
The experimental results are as follows: results table 2 below, comparing compositions 1-15 with comparative examples 1-3, it was found that:
1) the bacteriostatic activity of the compounded and combined 3 raw materials is superior to that of a single plant;
2) the antibacterial activities corresponding to different proportions of the plant compound combination are different, preferably, the antibacterial activities are as follows: chlorogenic acid: rheum officinale (1-3): (0.05-0.2): 1-3), more preferably basil: chlorogenic acid: rhubarb is 1:0.2:2 or 1:0.1: 3.
TABLE 2
Figure BDA0003152987070000091
Figure BDA0003152987070000101
The test results show that the compositions in the test examples 1 to 15 have good bacteriostatic effects compared with the blank group, but the compositions have different proportions under the same condition and influence the bacteriostatic intensity of various bacteria, wherein the bacteriostatic effects of the compositions 6, 8 and 10 are relatively good.
Example 3 detection of cellular inflammation
(1) MTT cytotoxicity assay
In 96well Multi plate (corning)According to 1X104cells/well were seeded at a density of 100. mu.L each in DMEM medium containing 10% bovine serum and keratinocytes (HaCaT), and 24 hours later in culture were replaced with serum-free medium. The compositions 6, 8 and 10 of the above examples were added to serum-free medium, respectively, and the mixture was cultured for 24 hours after treatment. Thereafter, the medium was removed, treated with 20. mu.L of MTT solution, and allowed to react at 37 ℃ for 2 hours. 200 μ L of isopropanol was added to the cells from which the MTT solution was removed, gently shaken for 30min to completely dissolve the crystalline formazan, absorbance was measured at 570nm, and cell viability was calculated according to the following formula.
Figure BDA0003152987070000102
The control group was tested without the addition of sample. The cytotoxicity-related results are shown in table 3 below.
TABLE 3
Figure BDA0003152987070000111
(2) Inflammatory factor detection
IL 1-alpha and IL-6 are cell inflammatory factors and are detected by an ELISA method. HaCat cells without any treatment were used as a blank group, and HaCat cells induced by Lipopolysaccharide (LPS) were used as a model group. After stimulation of HaCat cells with 1. mu.g/ml LPS, 1% of the composition 6, 8, 10 was added to 12-well cell plates at 100. mu.l per well, at 37 ℃ in 5% CO2Incubate at constant temperature for 72h, 3 replicates per experimental group. And collecting cell culture supernatant, carrying out anti-inflammatory efficacy evaluation by an ELISA detection kit, and averaging results. The test is as follows, taking the content detected by blank group as the reference, namely 100%.
Specific results are shown in FIGS. 1 and 2, where FIG. 1 shows the effect of different compositions on IL1- α secretion; FIG. 2 is a graph showing the effect of different compositions on IL-6 secretion. The results show that the compositions 6, 8 and 10 can well inhibit the generation of IL 1-alpha and IL-6 inflammatory factors after being stimulated by LPS, have obvious anti-inflammatory effect and have the best effect of the composition 10.
Example 4.
In a specific embodiment, the invention provides a formula process of a mask muscle base solution capable of effectively resisting inflammation and inhibiting bacteria, and the specific formula is as follows:
TABLE 4
Figure BDA0003152987070000121
The extract of claim was added and compositions 6, 8, 10 were added to the mask muscle base formulation of table 5 below, using formulations commonly used in the art, at an add-on level of 1%, to make mask muscle base examples 1-3.
TABLE 5
Composition 6 Composition 8 Composition 10
Sample 1 Sample 2 Sample 3
1. Safety test (human skin patch test)
Selecting 15 healthy subjects with no allergic history of skin diseases between the ages of 20 and 50, and performing a spot pasting method: selecting a qualified spot tester, dropping about 15 mu L of samples 1-3 into the spot tester in a closed spot test mode, externally sticking a special adhesive tape on the back of a test subject, sticking 20 spot testers on each test subject, respectively sticking muscle base fluid samples of the samples 1-3, removing the test substances after 24 hours, observing skin reactions after 0.5, 6, 12, 24 and 48 hours after removal, and recording the results according to the skin reaction grade standard in skin care product sanitation standard.
And (3) test results: the results of the human skin patch test show that all the subjects pass the patch test, and the skin reaction is observed in 0.5, 6, 12, 24 and 48 hours, wherein 0 case has adverse reactions such as skin erythema, pimple and blister, which indicates that the product of the invention is safe and non-irritant.
2. Skin Water loss and erythema repair test
(1) The number of tested persons: a total of 45 persons; divided into 5 groups of 9 people each.
(2) The tested part: the skin of the forearm flexor side of the tested person;
(3) sterilizing the part to be tested with 70% ethanol, and measuring skin color ERYTHEMA value (ERYTHEMA) and TEWL value after the ethanol is completely evaporated; selecting 1x 1cm on weak skin of forearm of human subject2The areas of (a) are control (blank), model (0.075% capsaicin challenge), and the rest are test groups. Wherein the test groups were protected with the preferred compositions 6, 8, 10(20 μ L, 10mg/mL), stimulated with 0.075% capsaicin, and then skin color erythema and TEWL values were measured after 30min to evaluate the repair status.
Specific results are shown in fig. 3 and 4, fig. 3 being the effect of different compositions on transdermal water loss
The experimental results are as follows: the respective plant extract compositions are effective in relieving the rise of percutaneous water loss (TEWL) and the increase of ERYTHEMA (ERYTHEMA) due to capsaicin stimulation, while the comparative examples have limited relieving effects on TEWL and ERYTHEMA.
The details not described in the specification of the present application belong to the common general knowledge of those skilled in the art.
In the following description and in the claims, the terms "include" and "comprise" are used in an open-ended fashion, and thus should be interpreted to mean "include, but not limited to. "substantially" means within an acceptable error range, and a person skilled in the art can solve the technical problem within a certain error range to substantially achieve the technical effect.
It is also noted that the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a good or system that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such good or system. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other like elements in a commodity or system that includes the element.
The foregoing description shows and describes several preferred embodiments of the present application, but as aforementioned, it is to be understood that the application is not limited to the forms disclosed herein, but is not to be construed as excluding other embodiments and is capable of use in various other combinations, modifications, and environments and is capable of changes within the scope of the inventive concept as expressed herein, commensurate with the above teachings, or the skill or knowledge of the relevant art. And that modifications and variations may be effected by those skilled in the art without departing from the spirit and scope of the application, which is to be protected by the claims appended hereto.

Claims (10)

1. The preparation method of the plant extract composition with anti-inflammatory and bacteriostatic effects is characterized by comprising the following steps of:
1) pulverizing radix et rhizoma Rhei raw material, extracting with deionized water and cellulase, and filtering to obtain first primary filtrate;
2) cutting fresh basil into segments, and extracting with ethanol to obtain a second primary filtrate;
3) mixing the first primary filtrate and the second primary filtrate, concentrating, diluting with water, extracting with organic phase, mixing the organic phases, and concentrating to obtain fluid extract;
4) dissolving the fluid extract with ethanol, adding chlorogenic acid powder for dissolving, concentrating to obtain concentrated solution, and ultrafiltering to obtain the plant extract composition with antiinflammatory and antibacterial effects;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is (1-3) to (0.05-0.2) to (1-3).
2. The method of claim 1, comprising the steps of: 1) pulverizing radix et rhizoma Rhei; adding deionized water for extraction, wherein the mass ratio of the rhubarb raw material to the deionized water is 1:20-1:50, and soaking for 1-3 hours; adding cellulase in a water bath at the temperature of 40-50 ℃, wherein the total mass of the added cellulase is 10-20% of the mass of the rhubarb raw material, stirring for 20 minutes, heating to 40-60 ℃, performing microwave treatment for 5-15 minutes, performing ultrasonic water bath reflux extraction for 1-3 hours, cooling to 20-30 ℃, and filtering by using 100-mesh gauze of 200 meshes to obtain a first primary filtrate;
2) cutting fresh basil into 1-2cm sections according to mass ratio, soaking in 3-5 times of 95% ethanol solution for 1h, performing ultrasonic oscillation extraction at low temperature, filtering, and mixing filtrates to obtain second primary filtrate;
3) mixing the first primary filtrate and the second primary filtrate, concentrating under reduced pressure, adding distilled water with 1 volume of the concentrated solution, and sequentially extracting with petroleum ether, chloroform and ethyl acetate; repeating for 2-3 times until the extractive solution is colorless, mixing ethyl acetate layers, and concentrating under reduced pressure to obtain fluid extract;
4) dissolving the extract with 1-3 times volume of ethanol, adding chlorogenic acid powder according to mass ratio, stirring to dissolve completely, adding clarifier, standing, centrifuging for 30-60 min, and filtering with microfiltration membrane to obtain filtrate; filtering, concentrating under reduced pressure, and recovering ethanol to obtain concentrated solution; filtering with ultrafiltration membrane to obtain the plant extract composition with antiinflammatory and antibacterial effects;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is (1-3) to (0.05-0.2) to (1-3).
3. The method of claim 2, wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is 1:0.2:2 or 1:0.1: 3.
4. The preparation method of claim 3, wherein the clarifying agent in the step 4) is one or more of natural clarifying agent, chitosan, juice clarifying agent, gelatin and egg white.
5. The method according to claim 3, wherein the pore size of the microfiltration membrane in the step 4) is 0.1 to 1.0 μm; the pore diameter of the ultrafiltration membrane is 0.01-0.05 μm.
6. An anti-inflammatory bacteriostatic plant extract composition prepared by the preparation method of any one of claims 1 to 5;
wherein the basil: chlorogenic acid: the mass ratio of the rhubarb raw materials is 1:0.2:2 or 1:0.1: 3.
7. Use of a composition according to claim 6 for the preparation of a cosmetic product with anti-inflammatory and bacteriostatic effects.
8. A cosmetic comprising the composition of claim 6 and cosmetically acceptable adjuvants.
9. The cosmetic of claim 8, wherein the composition is present in an amount of 0.5 to 5% by weight of the cosmetic.
10. The cosmetic of claim 8, wherein the cosmetic is a lotion, emulsion, spray, cream, gel, or mask.
CN202110771103.8A 2021-07-07 2021-07-07 Preparation and application of antibacterial and anti-inflammatory plant extract composition Active CN113712858B (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101961376A (en) * 2010-07-23 2011-02-02 新疆医科大学 Method for refining sweet basil herb extract
CN108308203A (en) * 2018-01-31 2018-07-24 南京紫源康医药科技有限公司 A kind of preparation method of Chinese medicinal compound extract, extract and bacteria inhibiting composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101961376A (en) * 2010-07-23 2011-02-02 新疆医科大学 Method for refining sweet basil herb extract
CN108308203A (en) * 2018-01-31 2018-07-24 南京紫源康医药科技有限公司 A kind of preparation method of Chinese medicinal compound extract, extract and bacteria inhibiting composition

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Title
周秋丽等: "现代中药基础研究与临床", vol. 1, 天津科技翻译出版公司, pages: 107 - 21 *

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