阅读说明：本技术 一种珍珠亮白肽的制备方法及在美白化妆品中的应用 (Preparation method of pearl bright white peptide and application of pearl bright white peptide in whitening cosmetics ) 是由 盘学平 于 2021-01-20 设计创作，主要内容包括：本发明提供了一种贝类活性肽的制备方法,包括如下步骤：将贝壳去除角质层和棱柱层,得到珍珠母；用木瓜蛋白酶液处理珍珠母,干燥、粉碎,得到珍珠母粉；用中性蛋白酶或碱性蛋白酶将珍珠母粉和外套膜一起酶解,将酶解产物离心,去除沉淀,超滤,取过膜物,得到贝类活性肽。本发明还提供了一种组合物,包括：前述的贝类活性肽,脂质体形成材料和石榴籽精华、牛奶精华、甘油和维生素E。该贝类活性肽和组合物能够有效地抗氧化,清除DPPH,·OH和ABTS等自由基。(The invention provides a preparation method of shellfish active peptide, which comprises the following steps: removing horny layer and prismatic layer from shell to obtain Concha Margaritifera; processing Concha Margaritifera with papain, drying, and pulverizing to obtain Concha Margaritifera powder; performing enzymolysis on the nacre powder and the mantle with neutral protease or alkaline protease, centrifuging the enzymolysis product, removing precipitate, performing ultrafiltration, and collecting the membrane-passing substance to obtain the shellfish active peptide. The present invention also provides a composition comprising: the shellfish active peptide, the liposome forming material, pomegranate seed essence, milk essence, glycerol and vitamin E are described above. The shellfish active peptide and the composition can effectively resist oxidation and remove DPPH, OH, ABTS and other free radicals.)

1. A preparation method of shellfish active peptide comprises the following steps:

s1: mixing protease and Concha Margarit powder to form an enzymolysis reaction system, and performing enzymolysis to obtain enzymolysis Concha Margarit powder mixed solution;

s2: centrifuging the enzymolysis mother-of-pearl powder mixed solution, and removing precipitates to obtain a crude shellfish active peptide solution;

s3: and (3) carrying out ultrafiltration on the crude shellfish active peptide solution, and taking a membrane substance to obtain a refined shellfish active peptide solution.

2. The method of claim 1, wherein in step S1, the protease, the nacre powder and the mantle are mixed to form an enzymatic reaction system and the enzymatic reaction is performed to obtain a mixture of enzymatic nacre powder and mantle; in step S2, the mixed solution of the enzymolytic mother-of-pearl powder and the mantle is centrifuged to remove the precipitate, and the crude shellfish active peptide solution is obtained.

3. The method according to claim 1 or 2, wherein the mother-of-pearl powder is from a shell of one of hyriopsis cumingii, crista plicata, pinctada martensii, penguia penguin, Pinctada maxima and Pinctada maxima or a combination thereof;

preferably, in step S1, the protease is a neutral protease or an alkaline protease;

preferably, in step S1, the protease includes one or more of pepsin, trypsin, and subtilisin;

preferably, in step S1, the protease activity is 5-30 ten thousand U/g;

preferably, in step S1, the protease activity is 20 ten thousand U/g;

preferably, in step S1, the dry weight percentage of the protease in the enzymatic hydrolysis reaction system is 1-5 wt%;

preferably, in step S1, the amount of the nacre powder in the enzymatic hydrolysis reaction system is 15-60 g/L;

preferably, in the step S1, the total time of enzymolysis is 0.5 to 7 hours;

preferably, in step S1, enzyme deactivation is performed after the enzymatic hydrolysis is completed;

preferably, in step S1, the enzyme deactivation treatment is performed at 85-95 ℃;

preferably, in step S1, the enzyme deactivation processing time is 20-40 min;

preferably, in step S2, the centrifugation condition is 2000-5000 rpm;

preferably, in step S2, the time for centrifugation is 5-15 min;

preferably, in step S3, the pressure of ultrafiltration is 0.02-0.25 MPa;

preferably, in step S3, the pressure of ultrafiltration is 0.12 MPa;

preferably, in step S3, the ultrafiltration treatment employs an ultrafiltration membrane having a molecular cut-off of 3000Da or less;

preferably, in step S3, the ultrafiltration treatment employs an ultrafiltration membrane with a molecular cut-off of 2500-3000 Da;

preferably, the preparation method of the shellfish active peptide further comprises the following steps:

s4: drying the refined shellfish active peptide solution to obtain dried shellfish active peptide powder;

preferably, in step S4, the drying is vacuum drying;

preferably, in step S4, the vacuum drying is performed at a vacuum degree of 80 to 90 KPa;

preferably, in the step S4, the vacuum drying time is 10-15 min.

4. The method according to claim 1 or 2, characterized in that said nacre powder is prepared by the steps of:

sa: removing viscera from shellfish, and cleaning to obtain shell;

sb: removing stratum corneum and prismatic layer to obtain Concha Margaritifera;

and (C) Sc: treating the nacre with papain to obtain an enzymolyzed nacre;

sd: drying and crushing the enzymolyzed nacre to obtain nacre powder;

preferably, in step Sb, the horny layer and prismatic layer are polished off to obtain the mother-of-pearl;

preferably, in the step Sb, the mother-of-pearl is subjected to coarse pulverization and fine pulverization in sequence to have a final particle size of 80 to 100 mesh.

Preferably, in the step Sc, spraying papain solution into the inner layer of the mother-of-pearl, wherein the treatment time is 0.5-1.5 h;

preferably, in the step Sc, the activity of the papain for preparing the papain liquid is 3-18 ten thousand units/g, and the solvent of the papain liquid is lactic acid liquid with the concentration of 10-60 mg/mL;

in some embodiments, the concentration of papain in the aqueous lactic acid solution is 0.03-0.07 mg/mL.

Preferably, in step Sc, the ratio of the dry weight of papain to the mass of mother-of-pearl is 10^-3～3.4*10^-3：1；

Preferably, in the step Sd, the nacre powder is sieved by a 60-100 mesh sieve, and undersize products are taken for standby.

5. A shellfish active peptide produced by the production method according to any one of claims 1 to 4.

6. A composition comprising, as starting materials:

shellfish active peptide, liposome forming material and nutrient as described in claim 5.

7. The composition of claim 6, wherein the shellfish active peptide, the liposome forming material and the nutrient are present in a mass ratio of: (20-28): (130-480): (21-32);

preferably, the weight percentage of the shellfish active peptide in the composition is 5-15 wt%;

preferably, the composition is in the form of a liposome cosmetic;

preferably, the liposome-forming material comprises: phospholipids, sterols, and surfactants;

preferably, the mass ratio of the phospholipid, the sterol and the surfactant is: (100-300): (20-90): (10-90);

preferably, the phospholipid is selected from soy lecithin;

preferably, the sterol is selected from cholesterol;

preferably, the surfactant is selected from polyoxyethylene sorbitan monooleate;

preferably, the nutrients include: any one or combination of pomegranate seed essence, milk essence, glycerin and vitamin E;

preferably, the pomegranate seed essence is a pomegranate seed extract having a pomegranate seed polyphenol content of 7.55 to 8.05 wt%;

preferably, the mass ratio of the pomegranate seed essence, the milk essence, the glycerin and the vitamin E is as follows: (7-10): (6-10): (4-6): (4-6).

8. A method of preparing a composition, the method comprising the steps of:

si: preparing the liposome-forming material into a blank liposome solution;

sii: adding the shellfish active peptide and the nutrient substances into the blank liposome solution to obtain a mixture a;

siii: and (c) carrying out ultrasonic treatment on the mixture a to obtain the composition.

9. The preparation method according to claim 8, wherein in the step Si, the step of preparing the liposome-forming material into a blank liposome solution is:

mixing the liposome forming materials and then adding the mixture into an organic solvent to obtain a mixture b;

carrying out reduced pressure rotary evaporation on the mixture b to remove the organic solvent to obtain a mixture c;

adding the mixture c into a citric acid-sodium citrate buffer solution to obtain a mixture d;

carrying out rotary evaporation on the mixture d to obtain the blank liposome solution;

preferably, the mass to volume ratio g/ml of the liposome forming material to the organic solvent is 2:1 to 5: 1;

preferably, the citric acid-sodium citrate buffer solution is 0.2-0.4mol/L citric acid-sodium citrate buffer solution;

preferably, the citric acid-sodium citrate buffer has a pH of 1-4.

Preferably, the volume ratio of the organic solvent to the citric acid-sodium citrate buffer solution is 1:1 to 5: 1;

preferably, the volume ratio of the organic solvent to the citric acid-sodium citrate buffer solution is 2: 1;

preferably, the organic solvent is diethyl ether;

preferably, the pH of the mixture d is adjusted to 1-4 and then the water is subjected to rotary evaporation;

preferably, the reduced-pressure rotary evaporation is carried out at 45-55 ℃;

preferably, the blank liposome solution is filtered through a 0.45 micron filter membrane before being used in step Sii, and the filtrate is taken for standby;

preferably, in step Sii, saturated Na is used₂HPO₄Adjusting the pH value of the solution to 2.5-6.5 for use;

preferably, in step Siii, the power of the sonication is: 4000-;

preferably, in step Siii, the sonication time is: 5-10 min.

10. Use of the preparation process of any one of claims 1 to 4, the mussel active peptide of claim 5, the composition of claim 6 or 7 or the preparation process of claim 8 or 9 in the preparation of a preparation for use in preventing, treating, slowing and/or controlling the progression of oxidative damage in vivo, alone or in combination with other preparations;

preferably, the formulation is a skin care or cosmetic;

preferably, the formulation is in a dosage form selected from: liposome cosmetics, creams, lotions, powders, gels, sprays and masks.

Technical Field

The invention belongs to the field of marine biological resource utilization, relates to a preparation method of shellfish antioxidant peptide and application of shellfish antioxidant peptide in whitening cosmetics, and particularly relates to application of small peptide with antioxidant activity as an effective component in preparation of medicines, skin care products or/and cosmetics.

Background

The mother-of-pearl is generally considered as a by-product produced in the production process, and is lack of effective processing treatment, and the added value of the product is low, so that resources are wasted and environmental pollution is caused. Therefore, the development of deep processing utilization research on mother-of-pearl is urgently needed. And the prepared active small peptide of the mother-of-pearl has excellent biocompatibility as a natural marine biological resource, so the effective utilization of the components of the mother-of-pearl has wide application prospect and further generates great commercial value.

The effective elimination of the excessive free radicals in the human body is the most urgent scientific problem for solving the current human aging and cancer risks, so the application of the antioxidant peptide in the skin care product is considered as the most promising new field, and the antioxidant peptide has the functions of capturing the free radicals with high activity generated by various reactions, regulating the balance of the free radicals in the body and further achieving the process of effectively slowing down the skin aging.

The chinese patent application CN104470489A discloses a cosmetic composition comprising a scattering filler and nacres, the present invention relates to a cosmetic composition for caring for and/or making up keratin materials, in particular the facial skin, comprising, in a physiologically acceptable medium: (a) at least one scattering filler having a particle size of less than 35 microns, preferably from 2 microns to 35 microns, more preferably from 11 microns to 17 microns, (b) at least red or pink nacres, and (c) at least one blue nacre.

Chinese patent CN102698053A application discloses a nacre traditional Chinese medicine preparation for relieving depression, which is prepared from the following traditional Chinese medicine raw materials in parts by weight: the traditional Chinese medicine preparation has a remarkable treatment effect on patients with yin deficiency and fire excess type depression, and can rapidly relieve symptoms of dizziness, palpitation, insomnia, vexation, irritability or spermatorrhea and waist soreness, and the preparation has no toxic or side effect and a remarkable treatment effect, and fundamentally relieves the pain of the patients.

Chinese patent CN105821099A discloses a process for preparing antioxidant polypeptide of pinctada martensii by a fermentation method. Firstly, preprocessing the pinctada martensii into dry powder, inoculating a microbial strain for fermentation culture, and concentrating and spray-drying supernatant of fermentation liquor to obtain the antioxidant peptide product of the pinctada martensii. The invention adopts a microbial fermentation method to prepare the Pinctada martensii antioxidant polypeptide, overcomes the problem of high cost of the traditional enzyme method, and has the characteristics of easily controlled preparation conditions, low cost and good flavor of a fermentation product. The pinctada martensii is deeply processed to prepare the antioxidant polypeptide, so that the method has important significance for developing and improving the additional value of the pinctada martensii in the aquatic product industry; meanwhile, the obtained antioxidant polypeptide is nutritious and health-care, and plays a certain role in promoting the health of social residents.

The processing process of the active peptide prepared by the method has the defects of low extraction efficiency, damaged functional components, residual organic solvent and the like, and has the defects of difficult acquisition of raw materials, high cost, complex preparation process and the like, does not relate to actual application process technology and formula, and has no report on the application of the small antioxidant peptide of the mother-of-pearl in whitening cosmetics. Therefore, there is a need in research and practice to develop a novel method for preparing pearl bright white peptide with antioxidant activity, and the active extract is used as an antioxidant ingredient in skin care products or cosmetics.

Disclosure of Invention

The invention aims to solve the problems in the prior art, provides a preparation method of pearl bright white peptide and application of the pearl bright white peptide in whitening cosmetics, and particularly provides a preparation method of a shellfish active peptide liposome complex with excellent antioxidant activity and application of the shellfish active peptide liposome complex as an active ingredient in preparing cosmetics. The preparation method has the advantages of low cost, few byproducts, high activity, simple preparation process and the like, obtains the optimal process condition for preparing the high-activity small peptide with the antioxidant activity of the nacre by taking the scavenging rate of free radicals such as DPPH, OH, ABTS and the like in vitro and human body test data as evaluation indexes, can be used as an additional material to be directly applied to the field of whitening cosmetics, provides a new thought for developing novel antioxidant products, and has important guiding significance for the value-added utilization of marine biomass.

The invention provides a preparation method of shellfish active peptide, which comprises the following steps:

s1: mixing protease and Concha Margarit powder to form an enzymolysis reaction system, and performing enzymolysis to obtain enzymolysis Concha Margarit powder mixed solution;

s2: centrifuging the enzymolysis mother-of-pearl powder mixed solution, and removing precipitates to obtain a crude shellfish active peptide solution;

s3: and (3) carrying out ultrafiltration on the crude shellfish active peptide solution, and taking a membrane substance to obtain a refined shellfish active peptide solution.

In some embodiments, in step S1, mixing protease, nacre powder and mantle to form an enzymatic hydrolysis reaction system and performing enzymatic hydrolysis to obtain an enzymatic hydrolysis nacre powder and mantle mixed solution; in step S2, the mixed solution of the enzymolytic mother-of-pearl powder and the mantle is centrifuged to remove the precipitate, and the crude shellfish active peptide solution is obtained.

In some embodiments, the nacre powder is from a shell of one of hyriopsis cumingii, crista plicata, pinctada martensii, penguin shell, pteria alba and pteria thunbergii, or a combination thereof.

In some embodiments, in step S1, the protease is a neutral protease or an alkaline protease.

In some embodiments, in step S1, the protease includes one or more of pepsin, trypsin, and subtilisin.

In some embodiments, in step S1, the protease activity is 5-30 ten thousand U/g (e.g., 10 ten thousand U/g, 15 ten thousand U/g, 20 ten thousand U/g, 25 ten thousand U/g).

In some embodiments, in step S1, the protease activity is 20 ten thousand U/g.

In some embodiments, in step S1, the dry weight of the protease in the enzymatic reaction system is 1-5 wt% (e.g., 2 wt%, 3 wt%, 4 wt%).

In some embodiments, in step S1, the amount of the nacre powder in the enzymatic hydrolysis reaction system is 15-60g/L (e.g., 20g/L, 25g/L, 30g/L, 35g/L, 40g/L, 45g/L, 50g/L, 55 g/L).

In some embodiments, in step S1, the total time for enzymolysis is 0.5 to 7 hours (e.g., 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours).

In some embodiments, in step S1, enzyme deactivation is performed after the enzymatic hydrolysis is completed.

In some embodiments, in step S1, the enzyme deactivation process is performed at 85-95 deg.C (e.g., 86 deg.C, 87 deg.C, 88 deg.C, 89 deg.C, 90 deg.C, 91 deg.C, 92 deg.C, 93 deg.C, 94 deg.C).

In some embodiments, in step S1, the enzyme deactivation time is 20-40min (e.g., 25min, 30min, 35 min).

In some embodiments, in step S2, the centrifugation conditions are 2000-5000rpm (e.g., 2500rpm, 3000rpm, 3500rpm, 4000rpm, 4500 rpm).

In some embodiments, in step S2, the centrifugation time is 5-15min (e.g., 7min, 9min, 11min, 13 min).

In some embodiments, in step S3, the pressure of the ultrafiltration is 0.02 to 0.25MPa (e.g., 0.04Pa, 0.06Pa, 0.08Pa, 0.10Pa, 0.12Pa, 0.14Pa, 0.16Pa, 0.18Pa, 0.20Pa, 0.22Pa, 0.24 Pa).

In some embodiments, in step S3, the pressure of the ultrafiltration is 0.12 MPa.

In some embodiments, in step S3, the ultrafiltration process employs an ultrafiltration membrane having a molecular cut-off of 3000Da or less (e.g., 2600Da, 2700Da, 2800Da, 2900 Da).

In some embodiments, in step S3, the ultrafiltration treatment employs an ultrafiltration membrane having a molecular cut-off of 2500-3000 Da.

In some embodiments, the method for preparing the shellfish active peptide further comprises the steps of:

s4: and drying the refined shellfish active peptide solution to obtain dried shellfish active peptide powder.

In some embodiments, in step S4, the drying is vacuum drying.

In some embodiments, in step S4, the vacuum drying is performed at a vacuum degree of 80 to 90KPa (e.g., 82KPa, 84KPa, 86KPa, 88 KPa).

In some embodiments, in step S4, the vacuum drying time is 10 to 15min, such as 11min, 12min, 13min, 14 min).

In some embodiments, the preparation of the nacre powder comprises the steps of:

sa: removing viscera from shellfish, and cleaning to obtain shell;

sb: removing stratum corneum and prismatic layer to obtain Concha Margaritifera;

and (C) Sc: treating the nacre with papain to obtain an enzymolyzed nacre;

sd: drying and crushing the enzymolyzed nacre to obtain nacre powder.

In some embodiments, in step Sb, polishing removes the stratum corneum and prismatic layers, resulting in the mother-of-pearl.

In some embodiments, in step Sb, the mother-of-pearl is subjected to coarse pulverization and fine pulverization treatment in order to have a final particle size of 80 to 100 mesh.

In some embodiments, in step Sc, the papain solution is sprayed into the inner layer of nacres for a treatment time of 0.5 to 1.5h (e.g., 0.6h, 0.8h, 1.0h, 1.2h, 1.4 h).

In some embodiments, in step Sc, the papain solution is prepared with a papain activity of 3 to 18 ten thousand units/g (e.g., 5 ten thousand U/g, 7 ten thousand U/g, 9 ten thousand U/g, 11 ten thousand U/g, 13 ten thousand U/g, 15 ten thousand U/g, 17 ten thousand U/g), and the papain solution is prepared with a solvent of 10 to 60mg/mL (e.g., 15mg/mL, 20mg/mL, 25mg/mL, 30mg/mL, 35mg/mL, 40mg/mL, 45mg/mL, 50mg/mL, 55mg/mL) of lactic acid solution.

In some embodiments, the concentration of papain in the aqueous lactic acid solution is 0.03-0.07mg/mL (e.g., 0.04mg/mL, 0.05mg/mL, 0.06 mg/mL).

In some embodiments, in step Sc, the ratio of dry papain weight to mother-of-pearl mass is 10^-3～3.4*10^-3:1 (e.g. 1.5 x 10)^-3：1、2.0*10^-3：1、2.5*10^-3：1、3.0*10^-3：1)。

In some embodiments, in step Sd, the nacre powder is sieved through a 60-100 mesh sieve, and the undersize is taken for use.

In a second aspect, the present invention provides a shellfish active peptide prepared according to the preparation method of the first aspect of the present invention.

In a third aspect, the present invention provides a composition comprising, as starting materials:

the shellfish active peptide, liposome-forming material and nutrient according to the second aspect of the present invention.

In some embodiments, the shellfish active peptide, the liposome forming material and the nutrient are in a mass ratio of: (20-28): (130-480): (21-32) (e.g., (22, 24, 26): 150, 200, 250, 300, 350, 400, 450): 23, 25, 27, 29, 31)).

In some embodiments, the shellfish active peptide is 5 to 15 wt% (e.g., 7 wt%, 9 wt%, 11 wt%, 13 wt%) of the composition.

In some embodiments, the composition is in the form of a liposome cosmetic.

In some embodiments, the liposome-forming material comprises: phospholipids, sterols, and surfactants.

In some embodiments, the mass ratio of the phospholipid, the sterol, and the surfactant is: (100-300): (20-90): (10-90) (e.g., (150, 200, 250): 30, 40, 50, 60, 70, 80): 20, 30, 40, 50, 60, 70, 80)).

In some embodiments, the phospholipid is selected from soy lecithin.

In some embodiments, the sterol is selected from cholesterol.

In some embodiments, the surfactant is selected from polyoxyethylene sorbitan monooleate.

Soy lecithin, cholesterol and polyoxyethylene sorbitan monooleate are used to form empty liposomes.

In some embodiments, the nutrients comprise: pomegranate seed essence, milk essence, glycerin and vitamin E or their combination.

In some embodiments, the pomegranate seed essence is a pomegranate seed extract having a pomegranate seed polyphenol content of 7.55 to 8.05 wt%.

In some embodiments, the mass ratio of the pomegranate seed essence, the milk essence, the glycerin, and the vitamin E is: (7-10): (6-10): (4-6): (4-6) (e.g., (8, 9): 7, 8, 9): 5: 5).

The essence of pomegranate seeds has the main function of resisting oxidation.

The main function of the milk essence is whitening.

The main function of glycerol is to moisturize.

The main functions of vitamin E are whitening and antioxidation.

In a fourth aspect, the present invention provides a process for the preparation of a composition, said process comprising the steps of:

si: preparing the liposome-forming material into a blank liposome solution;

sii: adding the shellfish active peptide and the nutrient substances into the blank liposome solution to obtain a mixture a;

siii: and (c) carrying out ultrasonic treatment on the mixture a to obtain the composition.

In some embodiments, in step Si, the step of preparing the liposome-forming material into a blank liposome solution is:

mixing the liposome forming materials and then adding the mixture into an organic solvent to obtain a mixture b;

carrying out reduced pressure rotary evaporation on the mixture b to remove the organic solvent to obtain a mixture c;

adding the mixture c into a citric acid-sodium citrate buffer solution to obtain a mixture d;

and (4) performing rotary evaporation on the mixture d to obtain the blank liposome solution.

In some embodiments, the mass to volume ratio g/ml of the liposome forming material to the organic solvent is: 2:1 to 5:1 (e.g., 3:1, 4: 1). Namely: the unit of the liposome-forming material mass is g, and the volume of the organic solvent is ml.

In some embodiments, the citric acid-sodium citrate buffer is 0.2-0.4mol/L citric acid-sodium citrate buffer.

In some embodiments, the citric acid-sodium citrate buffer has a pH of 1-4 (e.g., 2, 3).

In some embodiments, the volume ratio of the organic solvent to the citric acid-sodium citrate buffer is 1:1 to 5:1 (e.g., 2:1, 3:1, 4: 1).

In some embodiments, the volume ratio of the organic solvent to the citric acid-sodium citrate buffer is 2: 1.

In some embodiments, the organic solvent is diethyl ether.

In some embodiments, the pH of mixture d is adjusted to a pH of 1-4 before rotary evaporation of water.

In some embodiments, the reduced pressure rotary evaporation is at 45-55 degrees C (e.g., 46 degrees C, 47 degrees C, 48 degrees C, 49 degrees C, 50 degrees C, 51 degrees C, 52 degrees C, 53 degrees C, 54 degrees C) under conditions.

In some embodiments, the blank liposome solution is filtered through a 0.45 micron filter before being used in step Sii, and the filtrate is taken for use.

In some embodiments, in step Sii, saturated Na is used₂HPO₄The solution is adjusted to pH 2.5-6.5 (e.g., 3, 3.5, 4, 4.5, 5, 5.5, 6) for use.

In some embodiments, in step Siii, the power of the sonication is: 4000-.

In some embodiments, in step Siii, the sonication time is: 5-10min (e.g., 6min, 7min, 8min, 9 min).

In a fifth aspect, the invention provides the use of a method of preparation according to the first aspect of the invention, a mussel active peptide according to the second aspect of the invention, a composition according to the third aspect of the invention or a method of preparation according to the fourth aspect of the invention in the preparation of a formulation for use alone or in combination with other formulations in the prevention, treatment, slowing and/or control of the progression of oxidative damage in a living body.

In some embodiments, the formulation is a skin care or cosmetic.

In some embodiments, the formulation is in a dosage form selected from: liposome cosmetics, creams, lotions, powders, gels, sprays and masks.

The product of the invention has the following advantages:

(1) the raw material adopts shellfish active small peptide with good antioxidant activity;

(2) encapsulating the shellfish active small peptide and nutrient substances in the liposome;

(3) technological process and preparation technical advantages;

(4) the reasonability of the formula and the excellent performance of the composition.

Drawings

FIG. 1 is a bar chart of the effect of shellfish active peptide liposome complex on mouse myocardial cell MDA content.

FIG. 2 is a bar chart showing the effect of shellfish bioactive peptide liposome complex on mouse myocardial cell SOD activity.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, embodiments of the present invention will be described in detail with reference to the accompanying drawings.

Material

Pomegranate seed essence: the main active component is pomegranate seed polyphenol with the content of 8 wt%. Purchased from Shanxi Hao Chen Biotech Co., Ltd.

The creamers are produced by SymriseContains 3 major proteins, including casein in a maximum amount of about 83% of the total protein, lactalbumin in an amount of about 13%, lactoglobulin and a small amount of lipocorm protein in an amount of about 4%; various enzymes exist, such as peroxidases, reductases, lipolytic enzymes, lactases.

Example 1

A pretreatment step: removing viscera from fresh shellfish (hyriopsis cumingii), cleaning with ice water, removing impurities and viscera to obtain shell and mantle.

Adding the cleaned shell into a grinding wheel dust remover, and grinding off the horny layer and the middle prismatic layer on the outer surface of the mother-of-pearl to obtain the mother-of-pearl. The mother-of-pearl is subjected to coarse crushing and micro-crushing treatment in turn, and the final granularity is about 80-100 meshes.

And performing primary chitin enzymolysis on the coarsely crushed and finely crushed mother-of-pearl by using an enzymolysis solution, specifically, spraying the enzymolysis solution into the inner layer of the mother-of-pearl, wherein the activity of papain used in the enzymolysis solution is 10 ten thousand units/g, a solvent is a lactic acid aqueous solution with the concentration of 40mg/mL, the concentration of the papain in the lactic acid aqueous solution is 0.05mg/mL, and the mass ratio of the dry weight of the papain to the mother-of-pearl is 10^-3～3.4*10^-3:1, treating for 1 hour to obtain the enzymolysis nacre.

And (3) fully reacting unpeeled variegated substances in the inner layer of the mother-of-pearl by using hydrolase (papain) under the action of an activating solution (lactic acid solution with the concentration of 1-6%), so that the unpeeled variegated substances in the inner layer of the mother-of-pearl are completely peeled off from the inner layer of the mother-of-pearl.

Cleaning the enzymolyzed mother-of-pearl and the mantle with clear water, draining, and drying in an oven to obtain a dry mixture of the mother-of-pearl and the mantle.

Preparing the dried mixture of the mother-of-pearl and the mantle into powder by a pounding machine, sieving the powder with a 60-mesh sieve, and taking undersize products to obtain the dry powder of the mixture of the mother-of-pearl and the mantle for later use.

Directional enzymolysis: performing directional protease enzymolysis treatment on the dried powder of the mixture of the nacre and the mantle, wherein the protease is 20 ten thousand U/g pepsin, the weight percentage of the dry enzyme weight to the enzymolysis reaction system (the enzyme, the buffer solution and the mixture of the nacre and the mantle) is 3%, the buffer solution is 25mM ammonium bicarbonate buffer solution, the using amount of the dried powder of the mixture of the nacre and the mantle is 20g/L, the treatment time is 4h, the enzyme deactivation treatment is performed at 90 ℃ for 30min, the centrifugal treatment is performed at 3000rpm for 10min, the precipitate is removed to obtain nacre enzymatic hydrolysate, performing ultrafiltration treatment on the nacre enzymatic hydrolysate, selecting an ultrafiltration membrane with the molecular interception amount of 3000Da, the ultrafiltration pressure is 0.12MPa, obtaining filtered nacre ultrafiltrate, and drying the filtrate to obtain shellfish active peptide powder (containing nacre endoproteolytic substances and mantle zymolytic proteins). The drying steps are as follows: under the vacuum degree of 80-90 KPa, the ultrafiltrate is polymerized into 10-200 mesh mist particles through an atomizer, the mist particles are directly contacted with hot air for heat exchange, drying is completed in a short time, and the drying time is 10-15 min.

The preparation process of the liposome comprises the following steps: dissolving 200g of soybean lecithin, 55g of cholesterol and 50g of polyoxyethylene sorbitan monooleate in 100ml of ether solvent, carrying out rotary evaporation at constant temperature of 50 ℃ under reduced pressure to remove the ether solvent, so that the soybean lecithin forms a layer of film at the bottom of an evaporation container, adding 0.3mol/L citric acid-sodium citrate buffer solution (pH2.5) with the volume of the ether of 1/3, adjusting the pH to 2.5 with hydrochloric acid, continuously carrying out rotary evaporation for 30 minutes, and filtering with a 0.45-micron filter membrane to obtain a blank liposome solution.

And (3) liposome encapsulation process: adding 24g shellfish active peptide powder into the blank liposome solution, adding 8.5g semen Granati essence, 8g milk essence, 5ml edible glycerol and 5g vitamin E, mixing, and adding saturated Na₂HPO₄Adjusting pH of the solution to 4.5, controlling power to 6000W, performing ultrasonic treatment for 7min to obtain shellfish active peptide liposome complex A1, and storing at low temperature.

Example 2

A pretreatment step: removing viscera from fresh shellfish (hyriopsis cumingii), cleaning with ice water, removing impurities and viscera to obtain shell and mantle.

Adding the cleaned shell into a grinding wheel dust remover, and grinding off the horny layer and the middle prismatic layer on the outer surface of the mother-of-pearl to obtain the mother-of-pearl. The mother-of-pearl is subjected to coarse crushing and micro-crushing treatment in turn, and the final granularity is about 80-100 meshes.

And performing primary chitin enzymolysis on the coarsely crushed and finely crushed mother-of-pearl by using an enzymolysis solution, specifically, spraying the enzymolysis solution into the inner layer of the mother-of-pearl, wherein the enzymolysis solution uses a lactic acid aqueous solution with the papain activity of 10 ten thousand units/g and the solvent concentration of 40mg/mL, the concentration of the papain in the lactic acid aqueous solution is 0.05mg/mL, and the mass ratio of the dry weight of the protease to the mother-of-pearl is 10^-3～3.4*10^-3:1, treating for 1 hour to obtain the enzymolysis nacre.

And (3) fully reacting unpeeled variegated substances in the inner layer of the mother-of-pearl by using hydrolase (papain) under the action of an activating solution (lactic acid solution with the concentration of 1-6%), so that the unpeeled variegated substances in the inner layer of the mother-of-pearl are completely peeled off from the inner layer of the mother-of-pearl.

Cleaning the enzymolyzed mother-of-pearl and the mantle with clear water, draining, and drying in an oven to obtain a dry mixture of the mother-of-pearl and the mantle.

Preparing the dried mixture of the mother-of-pearl and the mantle into powder by a pounding machine, sieving the powder with a 100-mesh sieve, and taking undersize products to obtain the dry powder of the mixture of the mother-of-pearl and the mantle for later use.

Directional enzymolysis: performing directional protease enzymolysis treatment on the dried powder of the mixture of the mother-of-pearl and the mantle, wherein the protease is trypsin of 20 ten thousand U/g, the mass percentage of the dry enzyme weight in an enzymolysis reaction system (enzyme, buffer solution and the mixture of the mother-of-pearl and the mantle) is 3 percent, the enzyme reverse buffer solution is ammonium bicarbonate buffer solution of 25mM, the using amount of the dried powder of the mixture of the mother-of-pearl and the mantle in the reaction system is 50g/L, the treatment time is 4h, the enzyme deactivation treatment is carried out at 90 ℃ for 30min, the centrifugal treatment is carried out for 10min under the condition of 3000rpm, the precipitate is removed, and the mother-of, and ultrafiltering with ultrafiltration membrane with molecular interception of 3000Da at ultrafiltration pressure of 0.12MPa to obtain filtered Concha Margaritifera ultrafiltrate, and drying the filtrate to obtain shellfish active peptide powder (containing Concha Margaritifera inner layer protein zymolyte and mantle protein zymolyte). The drying steps are as follows: under the vacuum degree of 80-90 KPa, the ultrafiltrate is polymerized into 10-200 mesh mist particles through an atomizer, the mist particles are directly contacted with hot air for heat exchange, drying is completed in a short time, and the drying time is 10-15 min.

The preparation process of the liposome comprises the following steps: dissolving 200g of soybean lecithin, 55g of cholesterol and 50g of polyoxyethylene sorbitan monooleate in 100ml of ether solvent, carrying out rotary evaporation at constant temperature of 50 ℃ under reduced pressure to remove the ether solvent, so that the soybean lecithin forms a layer of film at the bottom of an evaporation container, adding 0.3mol/L citric acid-sodium citrate buffer solution (pH2.5) with the volume of the ether of 1/3, adjusting the pH to 2.5 with hydrochloric acid, continuously carrying out rotary evaporation for 30 minutes, and filtering with a 0.45-micron filter membrane to obtain a blank liposome solution.

And (3) liposome encapsulation process: adding 24g shellfish active peptide powder into the blank liposome solution, adding 8.5g semen Granati essence, 8g milk essence, 5ml edible glycerol and 5g vitamin E, mixing, and adding saturated Na₂HPO₄Adjusting pH of the solution to 4.5, controlling power to 6000W, performing ultrasonic treatment for 7min to obtain shellfish active peptide liposome complex A2, and storing at low temperature.

Example 3

A pretreatment step: removing viscera from fresh shellfish (hyriopsis cumingii), cleaning with ice water, removing impurities and viscera to obtain shell and mantle.

Adding the cleaned shell into a grinding wheel dust remover, and grinding off the horny layer and the middle prismatic layer on the outer surface of the mother-of-pearl to obtain the mother-of-pearl. The mother-of-pearl is subjected to coarse crushing and micro-crushing treatment in turn, and the final granularity is about 80-100 meshes.

And performing primary chitin enzymolysis on the coarsely crushed and finely crushed mother-of-pearl by using an enzymolysis solution, specifically, spraying the enzymolysis solution into the inner layer of the mother-of-pearl, wherein the activity of papain in the enzymolysis solution is 10 ten thousand units/g, a solvent is a lactic acid aqueous solution with the concentration of 40mg/mL, the concentration of the papain in the lactic acid aqueous solution is 0.05mg/mL, and the mass ratio of the dry weight of the protease to the mother-of-pearl is 10^-3～3.4*10^-3:1, treating for 1 hour to obtain the enzymolysis nacre.

And (3) fully reacting unpeeled variegated substances in the inner layer of the mother-of-pearl by using hydrolase (papain) under the action of an activating solution (lactic acid solution with the concentration of 1-6%), so that the unpeeled variegated substances in the inner layer of the mother-of-pearl are completely peeled off from the inner layer of the mother-of-pearl.

Cleaning the enzymolyzed mother-of-pearl and the mantle with clear water, draining, and drying in an oven to obtain a dry mixture of the mother-of-pearl and the mantle.

Preparing the dried mixture of the mother-of-pearl and the mantle into powder by a pounding machine, sieving the powder with a 60-mesh sieve, and taking undersize products to obtain the dry powder of the mixture of the mother-of-pearl and the mantle for later use.

Directional enzymolysis: performing directional protease enzymolysis treatment on the dried powder of the mixture of the mother-of-pearl and the mantle, wherein the protease is subtilisin with 20 ten thousand U/g, the mass ratio of the dry weight of the protease to an enzymolysis reaction system (the enzyme, a buffer solution and the mixture of the mother-of-pearl and the mantle) is 3 percent, the enzyme reaction solution is 0.02mol/L, the pH value is 7.5 phosphoric acid buffer solution, the using amount of the dried powder of the mixture of the mother-of-pearl and the mantle in the reaction system is 20g/L, the treatment time is 4h, the enzyme deactivation treatment is carried out at 90 ℃ for 30min, the centrifugal treatment is carried out for 10min under the condition of 3000rpm, the precipitate is removed, and ultrafiltering with ultrafiltration membrane with molecular interception of 3000Da at ultrafiltration pressure of 0.12MPa to obtain filtered Concha Margaritifera ultrafiltrate, and drying the filtrate to obtain shellfish active peptide powder (containing Concha Margaritifera inner layer protein zymolyte and mantle protein zymolyte). The drying steps are as follows: under the vacuum degree of 80-90 KPa, the ultrafiltrate is polymerized into 10-200 mesh mist particles through an atomizer, the mist particles are directly contacted with hot air for heat exchange, drying is completed in a short time, and the drying time is 10-15 min.

The preparation process of the liposome comprises the following steps: dissolving 200g of soybean lecithin, 55g of cholesterol and 50g of polyoxyethylene sorbitan monooleate in 100ml of ether solvent, carrying out rotary evaporation at constant temperature of 50 ℃ under reduced pressure to remove the ether solvent, so that the soybean lecithin forms a layer of film at the bottom of an evaporation container, adding 0.3mol/L citric acid-sodium citrate buffer solution (pH2.5) with the volume of the ether of 1/3, adjusting the pH to 2.5 with hydrochloric acid, continuously carrying out rotary evaporation for 30 minutes, and filtering with a 0.45-micron filter membrane to obtain a blank liposome solution.

And (3) liposome encapsulation process: adding 24g shellfish active peptide powder into the blank liposome solution, adding 8.5g semen Granati essence, 8g milk essence, 5ml edible glycerol and 5g vitamin E, mixing, and adding saturated Na₂HPO₄Adjusting pH of the solution to 4.5, controlling power to 6000W, performing ultrasonic treatment for 7min to obtain shellfish active peptide liposome complex A1, and storing at low temperature.

Comparative example 1:

the other conditions and operations were the same as in example 2, and the enzymatic hydrolysis step was omitted from the pretreatment step, to obtain product B1.

Because the pearl inner protein can not be fully exposed, the content of the active small peptide of the mother-of-pearl is less, and the oxidation resistance of B1 is obviously lower than that of A2.

Comparative example 2:

the other conditions and operations are the same as those in the example 2, the directional enzymolysis step is omitted, and the liposome is prepared directly by using the pearl shell dry powder to obtain a product B2.

Because the pearl protein can not be decomposed into small peptide, the antioxidant capacity of B2 is obviously lower than that of A2.

Comparative example 3:

other conditions and operations were the same as in example 2, and the material edible glycerin was omitted in the liposome treatment step, to obtain product B3.

The whitening and moisturizing effects of B3 are obviously lower than those of A2.

Comparative example 4:

other conditions and operations were the same as in example 2, and vitamin E as a material was omitted in the liposome treatment step, to obtain B4 as a product.

The oxidation resistance of B4 is obviously lower than that of A2.

Test example 1: in vitro antioxidation experiment of shellfish active peptide liposome complex

(1) Measurement of DPPH.radical scavenging rate:

according to the method described in the literature, "research on enzymatic extraction process of chicken-derived collagen peptide and its radical scavenging ability" (mussajous et al, food industry, vol. 35, 2, p. 144-119, 2014), 0.3g of shellfish-derived bioactive peptide liposome complex A2 was placed in 50ml of absolute ethanol and stirred at room temperature for 12 hours to obtain a sample solution.

Taking 2ml of sample solution and DPPH solution as Ai (sample inhibition absorption value); the sample solution and absolute ethanol were Ac (sample control); DPPH solution and absolute ethanol are Aj (no absorption inhibition value); absolute ethanol is a control for uninhibited absorbance. The mixture was shaken well and mixed, and after standing at room temperature for 30min, the absorbance was measured at a wavelength of 517nm using a 1cm cuvette (two tubes were measured for each value at the same time).

DPPH.radical scavenging ratio was calculated according to the following formula by the method described in the above-mentioned document, and the results are shown in Table 1.

Wherein A is₀Represents the absorbance at 0 min. A. the₁Represents the absorption value at 30 min.

Hydroxyl radical scavenging rate:

the samples were respectively dissolved in water according to the method described in the literature, "spectrophotometry for the determination of hydroxy radical clearance in Chinese medicine" (Chenguanhua et al, Spectroscopy and Spectroscopy, 2002,22(4), p. 634-Preparing solutions with certain mass concentration (the concentration is 6mg/mL respectively), taking 1.0mL respectively, adding 1.4mL crystal violet solution (2X 10) into a series of 10mL color comparison tubes with covers^-5mol·L^-1)、1.0mLFe²⁺Solution (5X 10)^-3mol·L^-1)、0.4mLH₂O₂(1%) solution, 1.0mL of Tris-HCl solution (pH5.5), diluted to 10mL with redistilled water and shaken, left for 5min, and then the absorbance at 588nm was measured. To add no H₂O₂The sample solution of (2) is used as a background tube. VC was used as a positive control.

The hydroxyl radical scavenging ratio was calculated according to the method described in the above-mentioned document by the following formula, and the results are shown in Table 1. Represents:

D＝[(A_S-A₀)/(A-A₀)×100％]

d represents: hydroxyl radical scavenging rate.

A_SRepresents: adding the system absorbance of the shellfish active peptide liposome complex;

a represents: the system absorbance of the Fenton reagent and the shellfish active peptide liposome complex is not added;

A₀represents: the absorbance of the system without adding the shellfish active peptide liposome complex.

③ superoxide anion radical (ABTS)⁺) Clearance rate:

the superoxide anion radical scavenging rate was measured by the pyrogallol method according to the method described in the literature "research on enzymatic extraction process of chicken collagen peptide and its radical scavenging ability" (mussajous de et al, food industry, vol. 35, 2, p. 144-119 in 2014). The corresponding absorbance was measured at 325nm, and VC was used as a positive control.

Calculated as described in the above literature, superoxide anion radical scavenging was obtained, and the results are shown in Table 1.

TABLE 1 scavenging ability of active pearl leucin against free radicals

Free radical species	Time (min)	A1 clearance (%)	A2 clearance (%)	A3 clearance (%)
					DPPH	30	83	95	76
OH	30	75	98	73
					ABTS+	30	79	97	69

It can be seen that A2 has strong ability to scavenge the three aforementioned radicals.

Test example 2: in vivo test of antioxidant and free radical scavenging activity of shellfish active peptide liposome complex

Healthy adult male Kunming mice with the weight of 20-22g are selected and randomly divided into a shellfish bioactive peptide liposome complex A2 group (positive) and a tap water control group (black). The intervention is carried out once a day according to the dosage of 50mg/kg mouse body weight, the stomach is continuously drenched for 7 days, and the change of SOD activity and MDA content in serum is measured.

The method for measuring the SOD activity in the serum comprises the following steps: the test was carried out using a kit from Beijing Baiolaibo technologies, Inc.

The method for measuring the MDA content in the serum comprises the following steps: the test was carried out using a kit from Beijing Baiolaibo technologies, Inc.

The effect of shellfish bioactive peptide liposome complex on mouse cardiomyocyte MDA content is shown in figure 1.

The effect of shellfish bioactive peptide liposome complex on mouse myocardial cell SOD activity is shown in figure 2.

As can be seen from fig. 1, a2 can significantly reduce mouse cardiomyocyte MDA content, and thus can alleviate or repair oxidative damage. The ordinate is the MDA number in nmol/mg.

As shown in fig. 2, a2 significantly increased the mouse cardiomyocyte SOD activity, and thus reduced oxidative damage such as oxygen radicals in vivo. The ordinate is the SOD value in U/mg.

In conclusion, the invention adopts the mother-of-pearl as the main raw material, prepares the directional enzymolysis product with stronger antioxidant activity by optimizing the enzymolysis process, further separates and purifies to obtain the antioxidant component with the strongest activity, and obtains the antioxidant small peptide product, and the pearl antioxidant activity bright white peptide as the effective component has wide application prospect and great commercial value when being applied to the preparation of the whitening cosmetics.

It will be appreciated by those skilled in the art that the invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The embodiments disclosed above are therefore to be considered in all respects as illustrative and not restrictive. All changes which come within the scope of or equivalence to the invention are intended to be embraced therein.