Preparation method of astaxanthin nano-liposome and application of astaxanthin nano-liposome in cosmetics
Technical Field
The invention relates to the technical field of cosmetics, in particular to a high-content astaxanthin nano-lipid plasmid prepared by using astaxanthin oil as an active ingredient, a preparation method thereof and application of the astaxanthin nano-lipid plasmid in cosmetics.
Background
Astaxanthin (Astaxanthin) is purple crystal with molecular formula of C40H5204The relative molecular weight is 596.86, is fat-soluble ketocarotenoid, is a terpene unsaturated compound, and belongs to xanthophyll-beta-carotene family. Astaxanthin is the strongest natural antioxidant found in nature so far, and has the antioxidant capacity of 1000 times that of natural VE, 10 times that of beta-carotene, 17 times that of grape seed oil, 150 times that of anthocyanin OPC and 60 times that of coenzyme Q10. More and more research results show that the medicine can effectively eliminate free radicals in vivo and maintain the organismAstaxanthin has attracted much attention in the cosmetic field because of its body balance, slowing down skin aging and protecting skin health.
However, astaxanthin has poor solubility in water and is easily isomerized and degraded under light, oxygen, heat, acid and alkali conditions due to its high degree of unsaturation in the molecule, resulting in a number of limitations and challenges in the application development process, such as: (1) the natural astaxanthin extract is mainly oil, is insoluble in a system taking water as a solvent, has single dosage form and limited application range; (2) astaxanthin is unstable in property, is easy to be oxidized and degraded in the processing and storage processes, and is not beneficial to commodity production and storage; (3) astaxanthin has low bioavailability, serious resource waste and difficult achievement of effective absorption dosage, and various challenges greatly limit the application and popularization of astaxanthin. Therefore, how to change the form of the natural astaxanthin dosage form and how to improve the water dispersibility, stability and bioavailability of the natural astaxanthin becomes a key technical problem in the application and popularization process of the astaxanthin.
The nanometer lipid plasmid technology (NLC) is a passive targeting drug delivery technology which is developed on the basis of solid lipid plasmid (SLN) and has wide application. The nano lipid particle can select proper liquid and solid lipid to completely seal the active substance (medicine) in the lipid inner cavity, and the liquid lipid can change the regular lattice of the solid lipid to increase the proportion of irregular crystals in the nano lipid structure, increase the space capacity of the active substance and have higher coating content.
The nano-encapsulation technology can improve the solubility and stability of the astaxanthin in water and improve the compatibility of the astaxanthin in a formula. In the invention, the astaxanthin oil is prepared into the nano-liposome, so that the fishy smell of the astaxanthin can be reduced, the astaxanthin can be conveniently dissolved in water and conveniently applied in the field of cosmetics, and the astaxanthin can be favorably permeated into the deep layer of the skin to fully play the roles of oxidation resistance and aging resistance.
The patent about astaxanthin nanocrystallization disclosed by the Chinese intellectual property office mainly comprises the following steps: CN 104257632A, disclose an astaxanthin solid lipid nanoparticle and its preparation method, is prepared from lipid material and aqueous phase according to the mass ratio of 1:11, have provided the beneficial effects of increasing astaxanthin solubility and releasing medicine in vitro; CN 109985008A discloses a method for preparing astaxanthin solid self-microemulsion by physically mixing astaxanthin, grease, emulsifier, co-emulsifier and solid adsorbent for adsorption and preparing astaxanthin solid self-microemulsion at normal temperature; ③ CN 109381447A discloses astaxanthin phospholipid nanoparticles which are obtained by mixing an organic phase dissolved with high molecular polymer and astaxanthin and a water phase dissolved with phospholipid, ultrasonically emulsifying and volatilizing the organic phase and are used as inner ear medicaments; CN 106214501A discloses an astaxanthin lipid nanocapsule and a preparation method thereof, the components of the astaxanthin lipid nanocapsule comprise astaxanthin oil, phospholipid, dipropylene glycol, glycerol and deionized water, and the astaxanthin lipid nanocapsule with the particle size of less than 250nm is obtained by high-pressure homogenization treatment. CN 107307403A discloses a method for preparing a cold water dispersible astaxanthin micro-nano solid stable preparation by using a natural astaxanthin extract as a raw material through processes of low-temperature treatment, low-energy self-micro-emulsification, microencapsulation, drying, twice granulation embedding and the like; and CN 104042568A and CN 108403666A, which respectively disclose two preparation methods of astaxanthin microcapsules prepared by high-pressure microjet and freeze drying. The disclosed astaxanthin nanocrystallization preparation is mainly a solid system, does not use an organic solvent, does not use high-pressure microjet, and has good solubility and high-efficiency bioavailability.
Disclosure of Invention
The main purpose of the present invention is to provide an astaxanthin liposome and a preparation method thereof, so as to solve the problems of low solubility and poor stability of astaxanthin in water.
In order to achieve the purpose, the technical scheme adopted by the invention is as follows:
an astaxanthin nano lipid plasmid comprises the following components in percentage by mass:
the astaxanthin raw material comprises esterified astaxanthin and free astaxanthin, and is extracted from the raw material by a solvent extraction method or a supercritical fluid extraction method, wherein the esterified astaxanthin comprises monoester and diester;
the base oil is one or more of squalane, coconut oil, corn oil, caprylic/capric triglyceride, grape seed oil, evening primrose oil, jojoba oil, olive oil, etc.;
the high astaxanthin-containing nano-lipid plasmid according to claim 1, wherein: the emulsifier is any one or more of Tween 60, Tween 80, Tween 20, polyglycerol-10 monolaurate, polyglycerol-6 caprylate, polyglycerol-10 stearate, sorbitan olive oleate, sorbitan stearate, olive oil PEG-7 esters, poloxamer 407, poloxamer 188, PEG-8 caprylic/capric glycerides, PEG-40 stearate and the like.
The high astaxanthin-containing nano-lipid plasmid according to claim 1, wherein: the coemulsifier is any one or combination of more than one of polyglycerol-3 cocoate, polyglycerol-3 diisostearate, PEG-30 dipolyhydroxystearate, cetyl PEG/PPG-10/1 dimethyl siloxane, polyglycerol-4 decanoate, cetostearyl alcohol, polyglycerol-6 ricinoleate, etc.
The humectant of claim 1 is any one or more of glycerin, butylene glycol, propylene glycol, dipropylene glycol, glyceryl polyether-7, glyceryl polyether-26, polyethylene glycol-400, glyceryl glucosyl polyether-20, etc.
The preservative according to claim 1 is one or more of phenoxyethanol, caprylyl glycol, ethylhexyl glycerin, p-hydroxyacetophenone, pentanediol, hexanediol, chlorphenesin, and the like.
The particle size range of the astaxanthin nano lipid particles is 20-200 nm;
the preparation method of the astaxanthin nano lipid plasmid comprises the following steps:
(1) preparing the following components in percentage by weight: 1-10% of astaxanthin, 1-20% of grease, 10-30% of emulsifier, 5-20% of co-emulsifier, 5-20% of humectant, 10-40% of water and 0-1% of preservative;
(2) stirring and dissolving the emulsifier and the co-emulsifier in a constant-temperature water bath at 50-80 ℃, and adding the mixture into an oil phase system for mixing;
(3) adding humectant, water and antiseptic at 50-80 deg.C, high-speed shearing to obtain astaxanthin primary emulsion, and homogenizing at 500-1000bar under high pressure for 1-5 times;
(4) stirring, cooling to normal temperature to obtain translucent to transparent orange red astaxanthin nano lipid particles
As an improvement of the invention, the preparation of the high-content astaxanthin nano lipid plasmid and the application thereof in cosmetics.
The carrier is loaded with astaxanthin, and the carrier has high astaxanthin loading amount.
The astaxanthin nano lipid particle has good stability and water solubility, the preparation method is simple and controllable, the repeatability is good, and the astaxanthin nano lipid particle can be applied to the preparation of cosmetics containing astaxanthin.
Compared with the prior art, the invention has the following beneficial effects because the technology is adopted:
(1) the astaxanthin nano lipid plasmid system has good stability;
(2) the astaxanthin-containing nano lipid plasmid has high astaxanthin load;
(3) the solubility of astaxanthin which is difficult to dissolve in water is improved, so that the bioavailability of the astaxanthin is improved;
(4) each component in the formula has high safety, no irritation to organisms and no toxicity, can be used as an intermediate type to be compounded with a cosmetic formula, has good compatibility, and can be widely used in the field of cosmetics;
drawings
FIG. 1 flow chart of preparation method of astaxanthin nano lipid plasmid
FIG. 2 particle size diagram of astaxanthin phospholipid nanoplatelets
Detailed Description
The present invention is further described below with reference to examples. These examples are intended to illustrate the invention and are not intended to limit the scope of the invention. The implementation conditions used in the examples can be further adjusted according to the conditions of the specific manufacturer.
Example 1:
weighing 0.1g of astaxanthin and 2.0g of corn oil, mixing the astaxanthin and the corn oil, and stirring at room temperature until most of the astaxanthin is dissolved in the corn oil to form an oil phase of a system; weighing 3g of Tween 80, 0.8g of cetyl PEG/PPG-10/1 dimethyl siloxane and 0.2g of cetostearyl alcohol, stirring in a constant-temperature water bath at 78 ℃, adding into the oil phase, and fully mixing to form a uniform phase; adding 1.8g of water, 2.0g of polyethylene glycol-400 and 0.1g of phenoxyethanol into the mixture of the oil phase, the emulsifier and the co-emulsifier in a constant-temperature water bath at 78 ℃, shearing at 5000rpm for 2min, and homogenizing at 800bar under high pressure for 3 times; and cooling to normal temperature to finally obtain the astaxanthin nano lipid particles.
Adding 1.0g of the astaxanthin nano lipid particle system into 100g of deionized water, uniformly dispersing, measuring by using a particle size analyzer that the average particle size of the astaxanthin nano lipid particle system after water dispersion is 61.2 +/-1.6 nm, standing at 25 ℃ for 1 month at room temperature, and then obtaining the astaxanthin nano lipid particle system with the average particle size of 70.7 +/-2.3 nm, wherein the particle size change has no obvious difference, and the stability is good.
Example 2:
weighing 2g of astaxanthin and 15g of squalane, mixing the astaxanthin and the squalane, stirring the astaxanthin and the squalane at room temperature, and dispersing and dissolving the astaxanthin into the squalane to form an oil phase of a system; weighing 30g of tween 20, 7g of polyglycerol polyricinoleate and 10g of polyglycerol-3 diisostearate, stirring in a constant-temperature water bath at 60 ℃, adding into the oil phase, and fully mixing to form a uniform phase; adding 10g glycerol, 25g water, 0.9g phenoxyethanol and 0.1g ethylhexyl glycerol into the mixture of oil phase, emulsifier and auxiliary emulsifier in a thermostatic water bath at 50 ℃, shearing at 3000rpm for 3min, and homogenizing at 600bar for 2 times; and cooling to normal temperature to finally obtain the astaxanthin nano lipid particles.
Adding 1.0g of astaxanthin liposome system into 100g of deionized water, uniformly dispersing, measuring by using a particle size analyzer that the average particle size of the astaxanthin liposome system after water dispersion is 67.5 +/-2.3 nm, standing at 25 ℃ for 1 month at room temperature, and then obtaining the astaxanthin liposome system with the average particle size of 74.7 +/-3.8 nm, wherein the particle size change has no obvious difference, and the stability is good.
Example 3:
weighing 0.5g of astaxanthin and 5.0g of caprylic/capric triglyceride, and mixing and stirring the astaxanthin and the caprylic/capric triglyceride uniformly to form an oil phase of a system; weighing 6.0g of polyglycerol-10 stearate, 1g of sorbitan olivetoleate and 2.5g of cetyl polyethylene glycol/polypropylene glycol-10/1 dimethyl siloxane, stirring in a constant temperature water bath at 50 ℃, adding into the oil phase, and fully mixing to form a uniform phase; adding 3.0g dipropylene glycol, 6.8g water and 0.2g phenoxyethanol into the mixture of the oil phase, the emulsifier and the co-emulsifier in a constant-temperature water bath at 50 ℃, shearing at 3500rpm for 1min, and homogenizing at 500bar for 1 time; and cooling to normal temperature to finally obtain the astaxanthin nano lipid particles.
Adding 1.0g of astaxanthin liposome system into 100g of deionized water, uniformly dispersing, measuring by using a particle size analyzer that the average particle size of the astaxanthin liposome system after water dispersion is 65.2 +/-3.1 nm, standing at 25 ℃ for 1 month at room temperature, and then the average particle size is 70.5 +/-2.4 nm, wherein the particle size change has no obvious difference, and the stability is good.
The astaxanthin nano lipid plasmid is applied to cosmetics, and the examples are as follows.
Example 1:
astaxanthin antioxidant essence
Composition (I)
|
Mass percent (%)
|
Deionized water
|
81.92
|
EDTA-disodium salt
|
0.05
|
PEG/PPG-17/6 copolymer
|
5
|
Butanediol
|
6.0
|
Hyaluronic acid sodium salt
|
0.05
|
Hydroxyethyl cellulose
|
0.18
|
Astaxanthin nano lipid plasmid
|
5
|
Phenoxyethanol
|
0.8
|
Saccharide isomerate
|
1 |
Accurately weighing deionized water (1% of the copolymer for dispersing astaxanthin nano lipid particles), EDTA-disodium, PEG/PPG-17/6 copolymer, butanediol, sodium hyaluronate and hydroxyethyl cellulose, stirring, mixing uniformly, heating to dissolve until the copolymer is transparent, adding the astaxanthin nano lipid particles dispersed uniformly by a small amount of deionized water in advance at 50 ℃, stirring uniformly, adding phenoxyethanol and saccharide isomerous body, cooling to room temperature, detecting and discharging.
Example 2:
astaxanthin antioxidation face mask
Composition (I)
|
Mass percent (%)
|
Deionized water
|
81.92
|
EDTA-disodium salt
|
0.05
|
Polyacrylamide sodium salt
|
0.1
|
PEG/PPG-17/6 copolymer
|
2
|
Glycerol
|
5.0
|
Hyaluronic acid sodium salt
|
0.02
|
Hydroxyethyl cellulose
|
0.03
|
Astaxanthin nano lipid plasmid
|
3
|
P-hydroxyacetophenone
|
0.4
|
Pentanediol
|
2 |
Accurately weighing deionized water (1% of which is reserved for dispersing astaxanthin nano lipid particles), EDTA-disodium, PEG/PPG-17/6 copolymer, glycerol, p-hydroxyacetophenone, sodium polyacrylate, sodium hyaluronate and hydroxyethyl cellulose, stirring, mixing uniformly, heating to dissolve until the mixture is transparent, adding the astaxanthin nano lipid particles which are dispersed uniformly by a small amount of deionized water in advance into the mixture at 50 ℃, stirring uniformly, adding pentanediol, cooling to room temperature, detecting and discharging qualified products.
Example 3:
astaxanthin antioxidation emulsion
Accurately weighing phase A, stirring, mixing uniformly, heating to 80-85 ℃ for uniform dissolution, heating phase B to 80-85 ℃ for complete dissolution, adding phase B into phase A, homogenizing at 3000rpm for 2-5min, stirring, cooling to 65 ℃, adding phase C, stirring uniformly, cooling to 45 ℃, adding astaxanthin nano lipid particles uniformly dispersed by a small amount of deionized water, stirring uniformly, adding phase E, stirring uniformly, cooling to room temperature, detecting, and discharging.
The above examples are only for illustrating the technical idea and features of the present invention, and the purpose of the present invention is to enable those skilled in the art to understand the content of the present invention and implement the present invention, and not to limit the protection scope of the present invention. All changes, modifications, substitutions, combinations, and simplifications that may be made in accordance with the spirit of the invention are to be regarded as being equivalent and are intended to be included within the scope of the invention.