阅读说明：本技术 石墨烯产品和其化妆品应用 (Graphene products and cosmetic applications thereof ) 是由 马丁·马丁内斯·罗维拉 约瑟·安东尼奥·马丁内斯·罗维拉 玛利亚·德·普拉多·拉维·洛佩兹 阿 于 2019-07-17 设计创作，主要内容包括：石墨烯产品来自石墨烯纳米纤维(GNFs),其具有改性的晶体结构和限定的粒径分布。所述产品为无毒的并且具有生物学特性,例如伤口愈合,改善皮肤外观。所述产品能够用于治疗。(The graphene products are derived from Graphene Nanofibers (GNFs) having a modified crystal structure and a defined particle size distribution. The product is non-toxic and has biological properties, such as wound healing, improving the appearance of the skin. The product can be used for therapy.)

1. A graphene nanomaterial selected from graphene nanofibers, wherein the graphene nanomaterial has a particle size distribution with a dn (90) of 0.60 μ ι η or less in number of particles and a particle volume dv (90) of 80.00 μ ι η or less in particles, the particle size distribution being measured by laser diffraction ion analysis.

2. The graphene nanomaterial according to claim 1, wherein the BET specific surface area of the graphene nanomaterial is 100 to 500m²Between/g.

3. The graphene nanomaterial as claimed in claim 2, wherein the BET specific surface area of the graphene nanomaterial is 300-350m²Between/g.

4. The graphene nanomaterial of claim 1, wherein the graphene nanomaterial has a pore volume of 0.35-0.40cm³Between/g.

5. The graphene nanomaterial of claim 1, wherein the stone is stoneThe BET specific surface area of the graphene nano material is 300-350m²Between/g, pore volume is 0.35-0.40cm³Between/g.

6. The graphene nanomaterial of any one of claims 1 to 5, wherein the weight percentage of impurities in the nanomaterial is less than 0.01%.

7. Use of the graphene nanomaterial of any of claims 1 to 6 for cosmetics.

8. Use of a cosmetic according to claim 7 for the treatment of skin.

9. Use of a cosmetic according to claim 7 or 8 for reducing adipose tissue of the skin, preferably for reducing fat in the subcutaneous space.

10. A cosmetic treatment method for preventing or reducing adipose tissue volume increase and/or fat mass formation, characterized in that the graphene nanomaterial according to any one of claims 1 to 6 or a composition comprising the same is applied to the skin.

11. A cosmetic treatment method according to claim 10 for reducing cellulitis, wrinkles and/or varicose veins.

12. Cosmetic use of the graphene nanomaterial or composition comprising the same according to any one of claims 1 to 6 for preventing or reducing adipose tissue volume increase and/or fat mass formation, wherein the nanomaterial or composition is applied to the skin.

13. The graphene nanomaterial or the composition comprising the same according to claim 12 for cosmetic use, wherein the use is to reduce cellulitis, wrinkles and/or varicose veins.

14. A cosmetic composition comprising the graphene nanomaterial product of any one of claims 1 to 6 and a cosmetically acceptable excipient.

15. The cosmetic composition of claim 14, suitable for topical use.

16. The cosmetic composition of claim 14 or 15, wherein the cosmetic composition is in a form selected from the group consisting of a cream, lotion, ointment, microemulsion, fatty ointment, gel, milky gel, paste, foam, tincture, patch, bandage, film, and transdermal delivery system.

17. The cosmetic composition of claim 16, wherein the cosmetic composition is selected from the form of a cream, a hydrogel, or a milky gel.

18. A method of making the product of any one of claims 1 to 6 from a graphene nanofiber feedstock, comprising the steps of:

a) purifying the graphene starting material, preferably using a strong acid, to remove any metals or impurities present in the graphene starting material,

b) reducing the particle size of the purified graphene nanomaterial, preferably by an exfoliation process, to a particle number dn (90) of 0.60 μm or less, to a particle volume dv (90) of 80.00 μm or less, the particle size distribution being measured by laser diffraction ion analysis,

c) optionally, the obtained product is subjected to a depyrogenation treatment.

Technical Field

The present invention relates to novel graphene products, compositions thereof and applications for cosmetics.

Background

After the 2010 nobel prize in physics, the graphene-based or graphene-related family of materials has gained increasing attention, and these materials have subsequently seen explosive growth in numerous applications in the energy, electronics, sensors, light processing, medical, and environmental fields. Graphene is the "founder" member of this family, consisting of sp²Two-dimensional materials made of hybridized carbon atoms arranged in a hexagonal honeycomb lattice.

An extended family of graphene-related materials includes graphene (single and multi-layered), graphite, polycyclic aromatic hydrocarbons, carbon nanotubes, fullerenes, various graphene nanostructures of different sizes (e.g., graphene nanofibers, graphene nanoparticles, graphene quantum dots, graphene nanoribbons, graphene nanogrids, graphene nanodiscs, graphene foams, graphene nanopillars), other graphene-related materials, any combination of substituted graphene-related materials (e.g., carbon atoms substituted with N, B, P, S, Si, or otherwise), and graphene-related materials functionalized with reactive functional groups (e.g., carboxyl, ester, amide, thiol, hydroxyl, diol groups, ketone groups, sulfonate groups, carbonyl, aryl, epoxy, phenol groups, phosphonic acids, amine groups, porphyrins, pyridine, polymers, and combinations thereof).

Various publications describe graphene for medical applications.

US2006/0134096 describes a composition comprising graphene-rich and a method for medical use, in particular non-porous carbon, which comprises graphene in addition to fullerenes or nanotubes. They are used topically on wounds, as adsorbents for toxins or in hemodialysis.

EP313353 discloses a graphene nanostructure-based pharmaceutical composition for the prevention or treatment of neurodegenerative diseases. The graphene nanostructures inhibit fibril formation caused by protein misfolding.

US2014/0120081 discloses the use of carbon nanomaterials for treating oxidative stress in a subject by reducing the level of reactive oxygen species. The carbon nanomaterial is selected from nanotubes, graphene nanoribbons, graphite oxide, and the like, which may be functionalized.

GB2532449 describes functionalized nanomaterials for use in the treatment, prevention or prophylaxis of cancer by inhibiting the proliferation of cancer stem cells, wherein the nanomaterials are single-layer graphene, multi-layer graphene, nanographite, single-or multi-walled carbon nanotubes, fullerenes, carbon nanohorns (nanohorns), carbon nanofibers or amorphous or partially amorphous nanocarbons or mixtures thereof. Graphene oxide is preferred.

Guratahan s. and Kim J-H, international journal of nanomedics, 2016: 11, 1927-1945, review the synthesis, toxicity, biocompatibility and biomedical applications of graphene and graphene-related materials. As discussed in this document, many of these products still suffer from related toxicity and biocompatibility issues. The toxic effects of graphene can be influenced by physicochemical properties (e.g., size and distribution, surface charge, surface area, number of layers, lateral dimension, surface chemistry, purity, particle state, surface functional groups, and shape). Anti-cancer therapy, photothermal therapy, drug delivery, gene transfection, biosensing, imaging and tissue engineering are biomedical applications mentioned herein.

There remains a need for new graphene-based materials that have low or no toxicity, good biocompatibility and can provide useful biological effects and applications in cosmetics.

Disclosure of Invention

We have now found a novel graphene product which has exceptional properties, low or no toxicity, and which can be used in cosmetics.

In a first aspect, the present invention relates to a graphene nanomaterial selected from graphene nanofibers, wherein the graphene nanomaterial has a particle size distribution with a particle number dn (90) of 0.60 μm or less and a volume particle dv (90) of 80.00 μm or less as measured by a laser diffraction particle analyzer.

Preferably, the BET specific surface area of the graphene nano material is between 100 and 500m²Between/g, more preferably between 300 and 350m²Between/g.

In another embodiment, the pore volume of the graphene nanomaterial is in the range of 0.35 to 0.40cm³Between/g.

Also preferably, the impurities in the graphene nanomaterial are less than 0.01% by weight.

In another aspect, the invention relates to the use of graphene nanomaterials defined as cosmetic products. Preferably, the cosmetic is for the treatment of the skin.

In another aspect, the present invention relates to the use of graphene nanomaterials as described above to improve the appearance of skin, preferably to reduce the adipose tissue of the skin, preferably to reduce subcutaneous fat.

In another aspect, the present invention relates to a cosmetic treatment method for preventing or reducing the volume increase and/or cellulite formation of subcutaneous adipose tissue, characterized in that graphene according to the invention, or a composition comprising the same, is applied to the skin. Preferably, the cosmetic treatment is for reducing cellulitis (cellulitis), wrinkles and/or varicose veins.

Preferably, the cosmetic is for topical treatment of the skin.

In another aspect, the present invention contemplates the graphene nanomaterial of the present invention or a composition comprising the same for cosmetic use, for preventing or reducing volume increase of adipose tissue and/or formation of fat mass, wherein the nanomaterial or the composition is applied to skin.

In another aspect, the present invention relates to a cosmetic composition comprising the graphene nanomaterial described above.

Drawings

FIG. 1 is a Raman spectrum of GMC-1;

FIG. 2 shows GMC-1 at N₂Adsorption-desorption in (1);

FIG. 3A is an X-ray diffraction of GNFs starting materials;

FIG. 3B is a ray diffraction of GMC-1;

FIG. 4A is a particle number size distribution comparison of GNFs feedstock and GMC-1;

figure 4B is a particle size distribution comparison of particle percentages by particle volume weight for GNFs feedstock and GMC-1.

FIG. 5 is a toxicity assay of cultured adipocytes (differentiated from the 3t3l1 cell line) treated with 2 XGMC-1 or vehicle (CT) for 24 hours. A) Viability as determined by trypan blue cell exclusion, and B) cellular metabolism as determined by MTT with vehicle and 10 XGMC-1 concentration. The values are expressed as mean +/-SEM.

FIG. 6 is the expression of adipose differentiation markers in a cultured adipose model. Cultured adipocytes (differentiated from the 3T3L1 cell line) or isolated visceral white adipose tissue explants from rodents (rattus norvegicus) were treated with 2 XGMC-1 or vehicle (CT) for 24 hours. Fold change in mRNA expression of differentiation markers PPAR γ (a, B) and C) inflammatory adipokine IL-6(C) and insulin sensitivity marker GLUT4(D) in visceral white adipose tissue was determined by RT-qPCR. The values are expressed as mean +/-SEM. P <0.05 vs control, which value was considered statistically significant.

Detailed Description

Graphene raw material

In the present invention, the term "graphene" refers to a material that forms a polycyclic aromatic molecule having a plurality of carbon atoms covalently bonded to each other. The covalently bonded carbon atoms form a six-membered ring as a repeating unit.

The term "graphene nanofibers" (GNFs) refers to cylindrical nanostructures in which graphene layers are arranged in stacked cones, cups, or plates. The graphene planar surface is tilted from the fiber axis, exposing planar edges present on the surface and outer surface of the carbon nanofibers.

The term "graphene nanotubes" (GNTs) refers to single-walled or multi-walled concentric cylinders of graphene, whose basal planes form a less reactive surface than graphene nanofibers, because they are cylindrical and hollow like tubes, but graphene nanofibers are rod-like and there is typically no internal empty space inside the rod.

The product of the present invention is a GNF-derived carbon-based nanomaterial that undergoes a series of purifications and treatments to obtain a medical grade material with unexpected biological properties.

The starting carbon nanomaterial is a graphene-based material (graphene nanofibers). In one embodiment, the graphene nanofibers used to make the products of the present invention have a particle size distribution dn (90) with a particle count of 4.0 μm or less and a volume particle of dv (90) of 105.00 μm or less. Preferably, they have a thickness of about 250-²Surface area in g.

The starting materials for obtaining the products of the invention can be synthesized by various methods, such as epitaxial growth on silicon carbide, chemical vapor deposition, micromechanical or mechanical exfoliation of graphite, chemical oxidation of graphite, oxidation of graphite by thermal reduction, etc., chemical or multi-step reduction, catalytic decomposition of hydrocarbons on metal catalysts, expanded carbon nanotubes, electrospinning, etc.

Epitaxial growth on silicon carbide is a method in which a monolayer detached from graphene can be synthesized on a single crystal silicon carbide crystal (SiC) used as a substrate. The method includes heating the SiC wafer to a high temperature (>1100 ℃) and a high vacuum. Under the conditions mentioned, the silicon atoms sublime, obtaining an epitaxial growth of graphene on the surface (rearrangement of the carbon atoms, formation of graphene) [ Sutter, p., epitaxial graphene: how the silicon leaves the field. Natural material, 2009.8 (3): p.171-172.

In the chemical vapor decomposition process, a carbon source is catalytically decomposed on a catalytic substrate. After thermal decomposition of the hydrocarbons, the catalytic surface leads to dissolution of the carbon atoms generated inside the metal [ jacoberger, r.m. et al, simple graphene synthesis by chemical vapour deposition. Journal of chemical education, 2015.92 (11): p is the same as the formula (I). 1903 year 1907, Lavin-Lopez, M.P. ]

The thickness of the graphene deposited on the polycrystalline nickel is controlled. Journal of new chemistry, 2015.39 (6): p.4414-4423 ].

Micromechanical exfoliation of graphite involves the separation of the outermost layer of the solid in a thin sheet by fine scraping using a solid surface object or tape [ geom, a.k. and k.s.novoselov, the rise of graphene natural material, 2007.6 (3): p.183-191 ]. Mechanical exfoliation allows flakes of suspended graphite to form in organic or aqueous solvents by ultrasonic separation. The obtained material is of high quality, but, due to its low yield and high production cost, it is not of great industrial value [ Lotya, m. Journal of the american chemical society, 2009. 131(10): p.3611-3620 ].

Graphene Nanofibers (GNFs) can also be synthesized using a variety of methods, which are particularly preferred for making the products of the present invention. For example, chemical vapor deposition for carbon nanofibers is a catalytic process in which a carbonaceous source is decomposed into growing GNFs in the presence of a catalyst. Transition metal catalytic particles such as iron, nickel, cobalt and copper are used as catalysts. The CVD process is carried out at temperatures between 500 and 1200 deg.c [ Martin-Gullon, i.e., et al, difference between carbon nanofibers produced using Fe and Ni catalysts in a floating catalyst reactor. Carbon, 2006.44 (8): p.1572-1580 ]. Electrospinning is another method of producing GNFs. In this method, a fine needle is required using the sol-gel process. To do this, a high voltage is applied to the droplets of the needle, causing the solution to flow from the needle to the target. When the surface tension of the solution is high enough to avoid entering fine droplets, the fibrous structure can be extracted and collected from the target [ Zhang, l., et al, Areview: carbon nanofiber of electrospun polyacrylonitrile and application thereof. Proceedings of materials science, 2014.49 (2): p.463-480 ].

The average diameter and length of the porous graphite material used to prepare the composite material of the present invention were measured by Transmission Electron Microscopy (TEM).

Purification and treatment

The graphene nanomaterials synthesized according to the methods reported above are used as raw materials for the synthesis of the graphene-based medical grade materials of the present invention. The crude graphene nanomaterial is then subjected to a purification process, preferably using a strong acid (H)₂SO₄、HCl、HF、HNO₃HBr, etc.) to remove any metals or impurities introduced into the graphene nanomaterial structure during synthesis. Any method capable of removing impurities without affecting the performance of the graphene material may be used. Among the acids, hydrochloric acid or hydrofluoric acid are particularly preferred, but the skilled person will choose the acid and the conditions according to the amount and type of impurities present. The purification process is preferably carried out at low temperature (20-50 ℃) for several hours (12-24 hours). If the solution is used in a purification process, the purified graphene nanomaterial can then be washed with Millipore water to neutral pH and then dried, for example, in vacuo.

The purified graphene nanomaterials are also treated to achieve a reduced particle size distribution, which makes the product suitable for medical and cosmetic use. The purified graphene nanomaterial is, for example, treated to reduce its size and alter its properties. In one embodiment, it is subjected to a stripping treatment at room temperature, for example by sonication, wet milling or mixing. Sonication is particularly preferred because of the simplicity of the process, and may also be monitored through the sample to check whether the desired particle size distribution is achieved. An optional delimitation procedure (delimitation) is then performed to control the particle size between 10-100 μm. The skilled person will readily determine the technique required to select the particle size distribution. This step can be achieved, for example, by filtration or centrifugation, preferably vacuum filtration, for example by means of a sintered glass filter. The delimiting step may advantageously form a particle count with dn (90) of 0.60 μm or less and a volume of particles with dv (90) of 80.00 μm or less.

Finally, in order to control the grade material from dragging traces of other toxic compounds, including bacterial contamination or endotoxins, and to maintain sterile and aseptic conditions, the material may also be subjected to a standard depyrogenation by heating (preferably at 200-.

The resulting particle size distribution may be determined by conventional means in the art, such as a particle size analyzer, e.g., Mastersizer 2000 from Malvern panalytical, used in the examples.

Therefore, another object of the present invention is a process for preparing the product of the invention from crude graphene nanofibers, comprising the steps of:

a) purifying the graphene starting material, preferably using a strong acid, to remove any metals or impurities present in the graphene starting material,

b) reducing the particle size of the purified graphene nanomaterial, preferably by an exfoliation process, to a particle number dn (90) of 0.60 μm or less, a particle volume of dv (90) of less than 80.00 μm or less, as measured by laser diffraction particle analyzer,

c) optionally, the product obtained is subjected to a depyrogenation process.

Step (b) may further comprise the step of delimiting the particles according to granularity prior to step (c). In one embodiment, the delimiting step is achieved by filtration or centrifugation, preferably vacuum filtration.

In the context of the present invention, a particle volume with a dn (90) of 0.60 μm or less and a dv (90) of 80.00 μm or less can be obtained by the following step (b), optionally including a further delimiting step, preferably a filtration step. Preferably, the filtration is a vacuum filtration with a sintered glass filter having a pore size between 1 and 20 μm, preferably between 4 and 20 μm, more preferably between 5 and 16 μm.

Product(s)

The product of the invention is a purified graphene nanomaterial having a particle size distribution with a dn (90) of about 0.60 μm or less in number of particles and a dv (90) of 80.00 μm or less, preferably 70.00 μm or less in particle size volume.

The particle size distribution was measured by a laser diffraction particle size analyzer. The particle size distribution D50 is a value of 50% of the particle sizes in the cumulative distribution. If D50 has a certain value, 50% of the particles in the sample are larger than this value, and 50% are smaller. The particle size distribution is the number of particles falling within each size range, as a percentage of the total number of all sizes in the target sample. The most widely used methods for describing the particle size distribution are the d-values (d10, d50 and d90), which are interpreted as 10%, 50% and 90% of the cumulative mass.

These values can be considered as the diameter of the material, which will divide the sample mass into the specified percentages when the particles are arranged in increasing mass. d10 is the diameter at which 10% of the sample mass consists of particles with a diameter smaller than this. d50 is the diameter of a particle for which 50% of the sample mass is less than this value and 50% of the mass is greater than this value. d90 is the diameter at which 90% of the sample mass consists of particles with a diameter smaller than this. These values may be applied to the number of particles (dn) and the volume of particles (dv).

A distribution with a particle number dn (90) refers to a point in the size distribution up to and including 90% of the total material in the sample.

The distribution of particle volumes having a dv (90) refers to the point in the size distribution up to and including which comprises 90% of the total volume of material in the sample.

The particle size distribution of the product of the invention was measured using a Mastersizer 3000 from Malvern Panalytical.

In the context of the present invention, the term "Specific Surface Area (SSA)" refers to the total surface area of a material per mass unit.

The properties of porosity and specific surface area described herein are measured using the Brunnauer-Emmet-Teller ("BET") method, which uses nitrogen as the adsorbent material in a physisorption technique, as is well known to those skilled in the art.

In one embodiment of the invention, the BET surface area of the product of the invention is 300-350m²/g。

In another embodiment, the inventionThe pore volume of the product is 0.35-0.40cm³Between/g.

In a preferred embodiment, the product of the invention has a thickness of 300-²BET surface area in g and 0.35-0.40cm³Pore volume per gram.

The product of the invention is in the form of graphene nanofibers.

Composition comprising a metal oxide and a metal oxide

In another aspect, the present invention relates to a cosmetic composition comprising the graphene product of the present invention and one or more cosmetically acceptable excipients.

As used herein, the term "cosmetic composition" refers to a composition intended to be applied to the skin of a consumer to regulate the condition of the skin and/or improve the appearance of the skin, including reducing subcutaneous fat.

In addition to the graphene product of the present invention as an active ingredient, the cosmetic composition of the present invention may further include conventional auxiliary excipients such as stabilizers, solubilizers, vitamins, pigments and perfumes.

The cosmetic composition may be prepared in any formulation conventionally used in the art. For example, the cosmetic composition may be prepared in the form of, for example, a suspension, an emulsion, a paste, a gel, a cream, an emulsion, a powder, an oil, a powder foundation, an emulsion foundation, a wax foundation, and a spray, but their formulation is not limited thereto. The cosmetic composition can be prepared in the form of sunscreen cream, softening lotion, astringent lotion, nourishing cream, massage cream, essential oil, eye cream, pack, spray or powder.

The term "excipient" refers to a vehicle, diluent or adjuvant with which the active ingredient is administered. Cosmetic excipients may be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like.

In a preferred embodiment, the cosmetic composition of the present invention is suitable for topical application to the skin, such as creams, lotions, ointments, microemulsions, fatty ointments, gels, milky gels, pastes, foams, tinctures, solutions, patches, bandages and transdermal delivery systems. Most preferred are creams, hydrogels or milky gels.

The cream or lotion is an oil-in-water emulsion. The oleyl radicals used are fatty alcohols, in particular those containing from 12 to 18 carbon atoms, such as lauryl, cetyl or stearyl alcohol; fatty acids, especially those containing from 10 to 18 carbon atoms, such as palmitic acid or stearic acid; fatty acid esters, such as tricaprin (neutral oil) or cetyl palmitate, liquid to solid waxes (such as isopropyl myristate, wool wax or beeswax) and/or hydrocarbons, especially liquid, semi-solid or solid substances or mixtures thereof, such as petroleum jelly (petrolatum, vaseline) or paraffin oil. Suitable emulsifiers are surface-active substances having predominantly hydrophilic properties, for example corresponding nonionic emulsifiers, for example fatty acid esters of polyhydric alcohols and/or ethylene oxide adducts thereof, in particular corresponding fatty acid esters with (poly) ethylene glycol, (poly) propylene glycol or sorbitol, in particular fatty acid groups having from 10 to 18 carbon atoms, in particular partial glycerol fatty acid esters or partial fatty acid esters of polyhydroxyethylene sorbitan, for example polyglycerol fatty acid esters or polyoxyethylene sorbitan fatty acid esters (T wens), and also polyoxyethylene fatty alcohol ethers or fatty acid esters, in particular fatty alcohol moieties having from 12 to 18 carbon atoms and in particular fatty acid moieties having from 10 to 18 carbon atoms, for example polyhydroxyethylene glycerol fatty acid esters (e.g. Tagat S), or corresponding ionic emulsifiers, for example alkali metal salts of fatty alcohol sulfates, especially those having from 12 to 18 carbon atoms in the fatty alcohol group, such as sodium lauryl, sodium cetyl or sodium stearyl sulphate, are usually used in the presence of fatty alcohols, such as cetyl or stearyl alcohol. Additives to the aqueous phase are, in particular, agents which prevent the cream from drying, such as humectants, for example polyols, such as glycerol, sorbitol, propylene glycol and/or polyethylene glycol, and also preservatives, fragrances, gelling agents, etc.

Ointments are water-in-oil emulsions which contain up to 70%, but preferably from about 20% to about 50% water or aqueous phase. Particularly suitable as the fatty phase are hydrocarbons, such as petroleum jelly, paraffin oil and/or hard paraffin, which preferably contain suitable hydroxy compounds for improving the water-binding capacity, such as fatty alcohols or esters thereof, for example cetyl alcohol or lanolin alcohol or wool wax or beeswax. Emulsifiers are the corresponding lipophilic substances, for example lipophilic substances of the type mentioned above, for example sorbitan fatty acid esters (Spans), for example sorbitan oleate and/or sorbitan isostearate. Additives to the aqueous phase are, in particular, humectants, such as polyols, for example glycerol, propylene glycol, sorbitol and/or polyethylene glycol, and also preservatives, fragrances and the like.

Microemulsions are isotropic systems based on four components: water, surfactants (e.g. tonicity active agents), lipids (e.g. apolar or polar oils, such as paraffin oil), natural oils (e.g. olive oil or corn oil) and alcohols or polyols containing lipophilic groups, such as 2-octyldodecanol or ethoxylated glycerol or polyglycerol esters. Other additives may be added to the microemulsion if desired. The microemulsion has colloidal particle or particle size less than 200nm, is transparent or semitransparent system, and is spontaneous and stable. Fatty ointments are anhydrous and comprise, in particular as a base, hydrocarbons, such as paraffin, petroleum jelly and/or liquid paraffin, and also natural or partially synthetic fats, such as fatty acid esters of glycerol, for example coconut fatty acid triglyceride, or preferably hardened oils, such as hydrogenated nut oil (ground nut oil), castor oil or waxes, and also fatty acid partial esters of glycerol, such as glycerol monostearate and glycerol distearate, and also, for example, fatty alcohols which increase the water absorption capacity, emulsifiers and/or ointment-related additives.

With regard to gels, a distinction is made between aqueous gels, anhydrous gels and gels with low water content, which gels consist of swellable, gel-forming materials. Transparent hydrogels based on inorganic or organic macromolecules are used in particular. The high molecular weight inorganic components having gel-forming properties are predominantly aqueous silicates, for example aluminum silicates, such as bentonite, magnesium aluminum silicate, such as Vegegum, or colloidal silicic acids, such as Aerosil. As high molecular weight organic substances, use is made, for example, of natural, semisynthetic or synthetic macromolecules. Such as natural and semi-synthetic polymers derived from polysaccharides containing various carbohydrate components, such as cellulose, starch, gum tragacanth (tragacanth), gum acacia and agar-agar, and also gelatin, alginic acid and its salts (e.g. sodium alginate), and derivatives thereof, such as lower alkyl celluloses, e.g. methyl or ethyl celluloses, carboxy or hydroxy lower alkyl celluloses, e.g. carboxymethyl or hydroxyethyl celluloses. The synthetic gel-forming macromolecular constituent is, for example, a suitably substituted unsaturated aliphatic compound such as vinyl alcohol, vinyl pyrrolidine, acrylic acid or methacrylic acid.

Emulsion-gels-also known as "latexes" -a composition that represents a heat gate that combines the properties of a gel with those of an oil-in-water Emulsion. Unlike gels, they comprise a lipid phase which, due to its fat recovery properties, enables the preparation to be massaged and used (massage), while also having pleasant properties of being absorbed directly into the skin. Furthermore, an increased solubility of lipophilic active ingredients can be observed. One advantage of milky gels over oil-in-water emulsions is the enhanced cooling effect due to the cold feel caused by evaporation of the additional alcohol component (if present).

Foams, for example, are administered from pressurized containers and are liquid oil-in-water emulsions in the form of aerosols. Unsubstituted hydrocarbons, such as alkanes, for example propane and/or n-butane, are used as propellants. As oil phase, in particular hydrocarbons are used, such as paraffin oil, fatty alcohols (e.g. cetyl alcohol), fatty acid esters (e.g. isopropyl myristate), and/or other waxes. As emulsifiers, use is made in particular of mixtures of emulsifiers having a hydrophilic character, such as polyoxyethylene sorbitan fatty acid esters (T wens) and emulsifiers having a lipophilic character, such as sorbitan fatty acid esters (Spans). Conventional additives such as preservatives and the like are also added. Tinctures and solvents usually have an ethanol base (base) to which water can be added and to which polyols, such as glycerol, ethylene glycol and/or polyethylene glycol, are added as moisturizers for reducing evaporation, as well as fat-repair substances, such as fatty acid esters with low molecular weight polyethylene glycol, propylene glycol or glycerol, i.e. lipophilic substances that are soluble in aqueous mixtures, in place of fatty substances removed from the skin by ethanol, and, if necessary, other auxiliaries and additives. Suitable tinctures or solvents can also be applied in the form of a spray by suitable means.

Transdermal delivery systems with (in particular) topical delivery of the graphene products of the invention contain an effective amount of the graphene product, optionally together with a carrier. Useful carriers include absorbable pharmacologically acceptable solvents to aid passage of the active ingredient through the skin. Transdermal delivery systems, for example in the form of patches, comprise (a) a matrix (═ backing layer or film), (b) a matrix containing the active ingredient, optionally a carrier and optionally (but preferably) a special adhesive for application of the system to the skin, and usually (c) a protective backing (═ release liner). The matrix (b) is usually present as a mixture of all components or may consist of individual layers.

Films and substrates comprising the graphene products described herein are also suitable for topical use by themselves or as part of more complex products (e.g., wound dressings, bandages, etc.). In such embodiments, such membranes or matrices are natural polymers such as polysaccharides (alginate, chitin, chitosan, heparin, chondroitin, carrageenan), proteoglycans, and proteins (collagen, gelatin, fibrin, keratin, silk fibroin, eggshell membrane); hydrogel based on polyglycolic acid, polylactic acid, polyacrylic acid, poly-epsilon-caprolactone, polyvinylpyrrolidone, polyvinyl alcohol, polyethylene glycol, or synthetic polymer such as biomimetic extracellular matrix micro/nanofibers.

All these systems are well known to the person skilled in the art. The manufacture of topically applicable pharmaceutical or cosmetic preparations is effected in a manner known per se, for example by suspending the graphene products of the invention in a substrate or, if necessary, in parts thereof.

The compositions according to the invention may also comprise the usual additives and adjuvants for dermatological applications, such as preservatives, in particular methyl, ethyl, propyl, butyl or quaternary ammonium parabens, such as benzalkonium chloride, or formaldehyde donors such as imidazolidinyl urea, or alcohols such as benzyl alcohol, phenoxyethanol or acids such as benzoic acid, sorbic acid; an acid or base for use as a pH buffering excipient; antioxidants, especially phenolic antioxidants such as hydroquinone, tocopherol and derivatives thereof, and flavonoids, or other antioxidants such as ascorbic acid, ascorbyl palmitate; a fragrance; fillers, such as kaolin or starch; a pigment or colorant; an ultraviolet screening agent; humectants, especially glycerol, butylene glycol, hexylene glycol, urea, hyaluronic acid or derivatives thereof; anti-radical agents, such as vitamin E or its derivatives; penetration enhancers, particularly propylene glycol; ethanol; isopropyl alcohol; dimethyl sulfoxide; n-methyl-2-pyrrolidone; fatty acids/alcohols, such as oleic acid, oleic alcohol; terpenes, such as limonene, menthol, 1-8 cineole; alkyl esters, such as ethyl acetate, butyl acetate; ion pairing agents, such as salicylic acid.

The composition can be made into facial mask, face cleaning, protecting, treating or caring cream, and is used for face or body (such as day cream, night cream, makeup removing cream, foundation cream or sunscreen cream), makeup removing milk or lotion, gel or foam for caring skin, such as cleaning milk.

For more details on suitable topical formulations, reference may be made to standard textbooks, such as "Harry's cosmetics" 9 th edition (2015), chemical publishing company.

In the formulation, the amount of the graphene nanomaterial product of the present invention may be in the range of 0.01% to 10% w/w, preferably 0.01% to 5% w/w, more preferably 0.1% to 3% w/w.

Advantageous effects and uses

As demonstrated in the examples below, the products of the invention are non-toxic, also in the case of topical use, and have good biocompatibility.

Furthermore, surprisingly, the product of the invention substantially alters the tissue phenotype of adipose tissue both in vitro and ex vivo culture and is therefore useful as a lipid-lowering agent in cosmetic application protocols.

Therefore, the graphene product and the composition thereof of the present invention can be used as cosmetics. The term "cosmetic product" is understood to mean intended to improve the aesthetic appearance of the skin or its appendages. It is non-therapeutic.

Obesity and/or being overweight are associated with phenotypic changes and responses of some cells called adipocytes, whose dynamic processes of accumulation or release of free fatty acids and glycerol to form triglycerides are unbalanced. [ Saponaro C et al, Nutrients, 2015, 79453-; tontonoz P. et al, Ann.A.Rev.Chat.Biochemical. 200877: 289-312)

Under the condition of over-rich diet or no physical exercise, the fat accumulated in the body is seriously unbalanced, and the problems including the increase of the area of fat tissue and the skin deformation caused by the thickening of subcutaneous fat tissue are gradually generated.

The graphene products described herein have been shown to be effective in phenotypic plastic modification of adipocytes and fat depots cultured in vitro and ex vivo.

Thus, the graphene product according to the present invention and the cosmetic composition comprising it can be used for the cosmetic treatment of fatty deposits in the skin and for reducing cellulitis and wrinkles.

According to the above, the present invention also relates to a cosmetic treatment method aimed at preventing or reducing the increase in adipose tissue volume and/or the formation of fat masses and/or a method of slimming comprising the systemic or topical application of a composition comprising the graphene product described herein. It can be applied to the affected part such as abdomen, thigh, or arm, or some part of face such as face bottom. The method improves the appearance of the human body and skin by altering adipocyte phenotype.

Thus, the graphene products of the present invention may be used for non-therapeutic (e.g. cosmetic) treatments ("non-therapeutic use"), for example to enhance fat distribution, for example of limbs, abdomen and/or buttocks, for aesthetic effect. Cosmetic uses of the graphene products described herein include the reduction of subcutaneous fat, which will improve cellulitis or other deformations due to subcutaneous fat accumulation, (e.g., the elimination of wrinkles, varicose veins and other skin imperfections or (other) easily improved appearance.

The subcutaneous cellulite is located in the dermis. Subcutaneously, the deep layers of the dermis, adipocytes or adipoblasts (adipocytes) come together to form leaflets separated by partitions (rows of collagen fibers) parallel to each other and perpendicular to the skin surface. An adipocyte is a large cell, 80% of whose volume consists of one or more lipid vacuoles. They are of different sizes. If the vacuole contains too much fat, the volume of fat cells increases and the dermal connective tissue thickens.

Another effect of fat accumulation in adipocytes is to reduce blood access to the tissue, which can lead to fluid accumulation, swelling, tissue damage and necrosis. This has a negative impact on the body and overall appearance, such as the formation of varicose veins. Thus, the products described herein, as well as compositions containing them, can be used to prevent or repair such damage. Preferably, the product of the invention is useful for the cosmetic treatment of varicose veins.

In another embodiment, the graphene products of the present invention and cosmetic compositions comprising the same may be used for cosmetic skin repair.

Mode of administration

Preferably, the composition used in this mode is applied topically.

The daily dose of the topical formulation comprising the graphene product of the present invention may depend on various factors, such as sex, age, weight and individual condition of the patient.

Examples

Example 1

Preparation of GMC-1 and research of physicochemical property thereof

Raw materials

The structural characteristics, graphitization degree, and main physico-chemical and thermal properties of the raw materials that can be used to prepare the graphene nanomaterials of the present invention are presented in table 1 below.

TABLE 1 physicochemical Properties of GNFs raw materials

a graphene face number in the crystal (npg ═ Lc/d); d is the interlayer range; lc is the average size of the crystals in the sample in the direction perpendicular to the graphene-based plane

^bID/IG is the quotient of the D and G band intensities in the Raman spectrum.

In this example, Graphene Nanofibers (GNFs) have been used to prepare the materials described in the present invention.

And (3) purifying the crude graphene-based carbon nanomaterials (GNFs) by using HF (hydrogen fluoride), so as to remove metals and impurities in the GNFs mixed in the synthesis process. The purification process is carried out at low temperature (20-50 ℃) for several hours (12-24 hours). Thereafter, the purified carbon nanomaterial was vacuum dried and washed with Millipore water to neutral pH.

The purified GNFs were stripped in water or other solvent solutions at room temperature for several hours (2-5 hours). Finally, the material is subjected to a standardized depyrogenation process by heating (200 ℃ C., 500 ℃ C., 10-60 minutes).

The properties of the product obtained (GMC-l) are as follows:

elemental analysis of GMC-1

The major difference between GMC-l and the feedstock was observed in its elemental analysis (table 2). In contrast to untreated GNFs, GMC-l consists only of carbon and oxygen. Toxicological experiments prove that the health-care food does not contain any impurities which can harm human health.

Table 2: elemental analysis of untreated GNFs and GMC-1

Element(s)	CNFs	GMC-1
			C	80-90	92-95
O	10-15	5-6
			Impurities (metals, catalyst supports, etc.)	0.5-1.5	0.0-0.01

Raman Spectroscopy of GMC-1

Raman spectra of GMC-l were acquired using a 512nm laser. Which shows (figure 1) the characteristic peaks of the carbon feedstock. D peak 1332cm^-1G peak 1580cm^-1. The G-band corresponds to the network of carbon atoms, i.e. the graphite structure in the ideal state, whereas the D-band is due to the presence of (in the actual case) basal planes and edge portions. The graphene nanofibers have a greater D band strength than the G band. If the graphite material contains a large number of edge portions, a large D peak appears as with the nanofibers. The fact that neither peak D nor peak G has too high a bandwidth also indicates that the nanofibers are crystalline.

GMC-1 adsorption denitrification analysis

The principle of measuring the total surface area of a solid by gas physisorption is to detect the number of gas molecules required to cover the surface of the solid. Once the area occupied by the molecules is known, the surface area of the solid can be measured by volume or weight methods (Brunauer, Emmett and Teller), estimated from the number of gas molecules absorbed.

Assuming the pores are subsequently filled with liquid adsorbate, the total specific surface area is calculated from the multipoint BET equation, while the total pore volume is calculated from the relative pressure P/P₀The amount of vapor adsorbed was determined at 0.99. The average pore diameter, assuming it is cylindrical, can be estimated from the total pore volume value and surface area, assuming that relative pressures less than 1, the unfilled pores have no effect on the volume and surface area of the pore sample.

Using QUANTACHROM model QUADRASORB-SI model, passing through N at 77K₂The adsorption-desorption of (A) was carried out for the analysis of the specific surface area, pore volume and pore area, the model having six degassing ports and three analysis ports, controlled by software (QUADRA-WIN) which collects N per volume₂Relative pressure value of (2). FIG. 2 shows the surface area, pore volume and pore diameter of GMC-1.

BET surface area: 300-350m²/g

Pore volume: 0,35-0,4cm³/g

Pore diameter: 5-6nm

X-ray diffraction analysis of GMC-1

The X-ray diffraction pattern corresponding to the GNFs sample was performed (fig. 3A). It was observed that it exhibited a peak around 25.9 °, which corresponds to the distance between the graphite planes 002, or the distance between the graphene sheets. In highly crystalline graphite, the interlayer spacing is 0.334 nm. In this case, the distance of the nanofibers is slightly larger, 0.343nm, which indicates that they have short-range crystallinity and exhibit turbo-layering. This fact can also be shown by the crystal size in the direction perpendicular to the plane 002(Lc) being 4.64 nm.

FIG. 3B shows a diffraction pattern corresponding to GMC-l, which is a material sample according to the present invention. GNFs and GMC-l exhibit the same peaks, but in GMC-l these peaks exhibit lower values 2 θ.

Table 3 shows the characteristic crystallographic parameters of GNFs and GMC-l:

interlayer space (d002)

Crystal stack height (Lc)

Inner crystallite size (La)

Number of layers of graphene in crystal (npg)

Wherein:

λ, wavelength of radiation (λ 015404nm)

Theta 1, diffraction Peak position (°)

Theta 2, diffraction Peak position (°)

k_lShape factor (k ═ 0,9)

k₂Wolon form factor constant (k ═ l, 84)

FWHM corresponding to full width at half maximum (rad) of diffraction peak

TABLE 3X-ray diffraction parameters of GNFs and GMC-l

	Lc(nm)	La(nm)	d(nm)	npg
					GNFs	2.19	2.99	0.341740	6.4
GMC-1	2.08	2.8	0.344338	6.05

When GNFs are converted to GMC-l, the crystal structure of the material changes. In this way, a reduction in the crystal stack height (Lc), in-plane crystallite size (La) and number of graphene layers in the crystal (Nc) was observed in GMC-l as the material goes through the purification, cleaning and exfoliation processes. The interlayer space in GMC-l increases due to the peeling process in the material test. The crystal stack height (Lc) and in-plane crystallite size (La) of experiment a decreased due to the purification and exfoliation process.

Particle size distribution

The particle size distributions of the starting GNFs and the product GMC-l described in the present invention were measured using a Mastersizer 3000 from Malvern Panalytical. Mastersizer 3000 uses laser diffraction techniques to measure particle size. The measurement is carried out by measuring the intensity of scattered light as the laser beam passes through the dispersed particle sample. These data are then analyzed to calculate the size of the particles that produce the scattering pattern.

FIG. 4A shows a comparison of particle size distributions (by particle number) of GNFs and GMC-1.

Figure 4B shows a comparison of particle volume percent versus particle size distribution based on GNFs and GMC-1.

The parameters d (0.1), d (0.5) and d (0.9) can be observed in the figure, dn referring to the number of particles and dv to the volume of particles.

For GNFs, the dn (l0) parameter indicates that 10% of the population is 1.121 μm or less in size, the dn (50) parameter indicates that 50% of the population is 1.573 μm or less in size, and the dn (90) parameter indicates that 90% of the population is 3.909 μm or less in size. For GNFs, the dv (l0) parameter means that 10% of the sample volume is occupied by particles of size 19.764 μm or less, the dv (50) parameter indicates that 50% of the sample volume is occupied by particles of size 57.711 μm or less, and the dv (90) parameter indicates that 90% of the sample volume is occupied by particles of size 103.114 μm or less.

In the case of GMC-l, the dn (l0) parameter indicates that 10% of the population has a size of 0.313 μm or less, the dn (50) parameter indicates that 50% of the population has a size of 0.394 μm or less, and the dn (90) parameter indicates that 90% of the population has a size of 0.577 μm or less. For GMC-l, the dv (l0) parameter indicates that 10% of the sample volume is occupied by particles having a particle size of 10.549 μm or less, the dv (50) parameter indicates that 50% of the sample volume is occupied by particles having a size of 39.693 μm or less, and the dv (90) parameter indicates that 90% of the sample volume is occupied by particles having a size of 69.576 μm or less.

A comparison of the particle size distributions of GNFs and GMC-l in number and volume indicates that GMC-l has a lower particle size distribution. In summary, the dn (90) number of GNFs is 3,909 μm or less, the dv (90) number of particle volumes is 103,114 μm or less, while the dn (90) number of GMC-l particles is 0.577 μm or less and the dv (90) number of particle volumes is 69.576 μm or less. FIGS. 4A and 4B clearly show the small number and volume of particles in GMC-l compared to the raw materials (GNFs) used.

Biological activity

Statistics of

Data shown are expressed as mean ± SEM of variable number experiments. Student's t tests were performed on 2 samples, one-or two-way analysis of variance (ANOVA) was performed on >2 samples, using either a paired or unpaired design, followed by multiple comparison tests. Values of P <0.05 were statistically significant.

Example 2 toxicity test of GMC-1 on adipocytes

Adipose tissue is distributed in different locations, from subcutaneous to abdominal (visceral fat). Tissues are formed from adipocytes or adipoblasts, and also preadipocytes and immune cells. The main functions of adipose tissue are to regulate and metabolize triglycerides and to produce regulatory hormones. Apart from the location of fat depots, adipose tissue has traditionally been classified as a) white adipose tissue, whose primary function is to accumulate lipid droplets as energy reserves, B) brown adipose tissue, whose primary function is to generate heat through a number of mitochondria, C) beige adipose tissue, which is present in WAT, but which has the morphological and functional characteristics of BAT. Considering the differentiation state of adipocytes from these different fat pools, their expression pattern is changeable from fully mature adipocytes to undifferentiated adipocytes, and thus these cells have important phenotypic plasticity [ Luo l., Liu m.; adipose tissue, a journal of endocrine, that controls metabolism. 2016 for 12 months; 23l (3): R77-R99.

Before studying the functional activity of GMC-L, we first tested the product viability and toxicity of adipocytes cultured under the culture condition of the adipocyte line 3T3L1 in suspension, as a model for in vitro differentiation of adipocytes in 6-well dishes, which cultured 300000 cells per well and allowed to grow in medium supplemented with 10% fetal bovine serum (DMEM, by default). Cells were incubated at 37 ℃ with 5% CO₂And humidity controlled incubator conditions. Once they reached the confluence point, the sera were removed for 16 hours. The product was dropped as a suspension into it under the same controlled maintenance conditions, and kept at the same final volume for 24 hours in different concentrations under the same controlled conditions. Thereafter, the cells were treated and tested for viability and toxicity in a complementary manner by two tests described in pharmacological and toxicological studies:

a) trypan blue exclusion, differentiation of live/dead cells, and

b) the metabolic activity is measured by MTT (3- (4, 5-dimethylthiazole-2) -2, 5-diphenyl tetrazolium bromide) cell staining method.

The results are shown in FIG. 5. The results show that GMC-l is non-toxic to cultured adipocytes.

Example 3In vitro functional assays of GMC-1 on adipocytes and fat pools.

Obesity and increased fat accumulation are associated with a variety of pathological conditions, such as type 2 diabetes and metabolic syndrome, because fat-accumulating adipocytes are associated with chronic inflammation, i.e., lower production of protective hormones (e.g., leptin, adiponectin) and increased production of pro-inflammatory hormones (or carnosine), such as interleukin-6 (IL-6). [ Luo L., Liu M.; adipose tissue for controlling metabolism. journal of endocrine 2016 month 12; 23l (3): R77-R99.]

Cosmetically, the increase in subcutaneous adipose tissue may gradually manifest as skin deformation due to thickening of the subcutaneous adipose tissue, which may cause undesirable skin appearance and cellulitis.

The expression of peroxisome proliferator-activated receptor g (PPAR γ), a lipogenic transcription factor, is important in view of the differentiation state of adipocytes. On the other hand, increased expression of insulin-dependent glucose transporter 4(GLUT4) correlates with improved insulin sensitivity.

Thus, an increase in PPAR γ expression in WAT implies an increase in the pro-obesity state, whereas an increase in GLUT4 expression in WAT implies a decrease in insulin resistance.

We investigated the ability of GMC-l to modify adipose tissue phenotype in vitro and ex vivo experiments.

As described in this section, functional studies are based on the phenotypic plasticity of adipocytes. Therefore, we examined the expression of genes such as interleukin-6 (IL-6), peroxisome proliferator-activated receptor gamma (PPAR γ), and interleukin-6 (IL-6), as well as glucose transporter 4(GLUT4) [ Jung, u.j. and Choi, m.s. obesity and its metabolic complications: the role of adipokines and the relationship between obesity, inflammation, insulin resistance, dyslipidemia, and nonalcoholic fatty liver disease. International journal of molecular science. 4 month 11 days 2014; 15(4): 6184-; (ii) a Armoni, m. Transcriptional regulation of the GLUT4 gene: from PPAR γ and FOXOl to FFA and inflammation. Endocrine metabolism trend. Month 4 in 2007; 18(3): 100-7.]

After treatment (24 hours), both solutions used a non-toxic concentration of 2 × GMC-l (20microG/ml) convenient suspension or common vehicle as a control. First, using confluent fully differentiated adipocytes, can be obtained by manipulating the culture conditions of the adipocyte cell line 3T3l 1. In the second step, the viscera (epididymal region) of rodents (brown rats) of similar weight, mechanically isolated normal weight, male or female, 3-8 months old, weighing between 300 and 500 (N18), are sectioned [ Gao, X, et al. Biochimerism and biophysics 1851(2015)152-162], reverse transcription quantitative polymerase chain reaction (RT-qPCR) was used to detect changes in expression. 100ng of DNA (cDNA) transformed from the original mRNA extracted from different samples was amplified using a commercial Gene expression assay (TaqMan, Life Technologies). The above values were normalized by molecular internal standards (. beta. -actin) and the fold change in expression was then visualized using the 2-deltadeltadeltaCt method.

The results are shown in FIG. 6. GMC-l alters the phenotypic plasticity of adipocytes, both in vitro and in ex vivo culture (in experiments).