EP2892503A2 - Composition antivieillissement de la peau - Google Patents
Composition antivieillissement de la peauInfo
- Publication number
- EP2892503A2 EP2892503A2 EP13763016.6A EP13763016A EP2892503A2 EP 2892503 A2 EP2892503 A2 EP 2892503A2 EP 13763016 A EP13763016 A EP 13763016A EP 2892503 A2 EP2892503 A2 EP 2892503A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- skin
- combination
- amino acid
- peptide
- cells
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
- A61K8/645—Proteins of vegetable origin; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/61—Surface treated
- A61K2800/62—Coated
- A61K2800/624—Coated by macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/65—Characterized by the composition of the particulate/core
- A61K2800/654—The particulate/core comprising macromolecular material
Definitions
- the present invention relates to the field of pharmacy and cosmetics, in particular, it relates to a combination of active ingredients, to compositions containing them, to their pharmaceutical use for the prevention and/or treatment of cutaneous signs of aging, including photoaging caused by solar radiation, as well as to their cosmetical use as a skin care agent.
- ROS Reactive Oxygen Species
- mitochondrial function has been invoked as a major determinant of aging.
- the mitochondrial theory of aging predicts that, over the lifespan of an organism, increasing damage (predominantly oxidative damage) occurs in the mitochondrial genome and/or mitochondrial proteins, and ROS
- Mitochondrial DNA is particularly vulnerable because it is devoid of histone-type proteins, and physically close to the main source of ROS. It has been calculated that each molecule of DNA is subject to 10000 of free radicals attacks per day. As a consequence of repeated damage in
- mitrochondrial DNA the mitochondria become increasingly unable to produce energy, the ATP production is decreased and the production of oxygen radicals is increased leading to a vicious cycle of respiratory impairment.
- DNA has a repair intrinsic function to compensate the damage caused by these toxic agents.
- the repair activity becomes inefficient, the ability to respond to toxic agents is decreased.
- a series of gradual deterioration processes of cells takes place, which leads to deterioration of organs (including skin) and their associated functions.
- organs including skin
- Accumulation of ROS may, in turn, damage neighboring mitochondrial complexes, membranes and mtDNA and further accelerate the aging process in a kind of feedback loop. Once the damage of macromolecules has reached the level of mtDNA, leading to mutations, the energetic age of a mitochondrial, and thus of a cell, is carved in stone.
- a change in the composition of the macromolecules causes a progressive loss of physiological capacity and adaptation to environmental changes. Therefore, to obtain an optimal therapeutic response to pharmacological or cosmetic ingredient, it is necessary to regulate, balance and/or improve the energy status of the cell delaying or limiting these changes in biomolecules caused by free radicals.
- the aging process is the result of the accumulated damage on the
- Sirtuins are a family of enzymes involved in the regulation of gene expression, cellular apoptosis, fatty acid metabolism, and the regulation of cell longevity.
- SIRT1 -7 human Sirtuins
- SIRT3, SIRT4, and SIRT5 human skin, sirtuins are found both in the fibroblasts and keratinocytes.
- SIRT3 gene plays an important role in the energy metabolism. It decreases the membrane potential and ROS production and stimulates the production and regeneration of mitochondrial antioxidants, thereby preserving cellular and skin vitality and longevity. In addition to changes associated to chronological aging, the skin is damaged by various environmental stressors, especially by solar ultraviolet radiation (UVR). Stress responses induced by UVR elicit premature skin aging
- UV radiation in particular UVB
- UVB plays a central role in photodamage, such as clinical sunburn, hyperpigmentation, erythema, plaque-like thickening, loss of skin tone, deep furrowing, and fine wrinkle formation.
- photodamage such as clinical sunburn, hyperpigmentation, erythema, plaque-like thickening, loss of skin tone, deep furrowing, and fine wrinkle formation.
- photo- carcinogenesis both involve epidermal damage (such as induction of apoptosis),
- HSPs Heat shock proteins
- HSP70 expression is considered an early repair mechanism which limits the appearance of irreversible cell injury.
- An anti-aging composition acting at the level of mitochondrial DNA has been described in WO 201 1/1 13785.
- This document discloses a complex comprising at least one active ingredient showing activity at the level of mitochondrial DNA, such as a pentapeptide including serine, cysteine, isoleucine, asparagine, threonine amino acids; and hydrolized soy protein; and at least one active ingredient showing activity at the level of nuclear DNA, such as teprenone and Myrtus communis extract.
- the pentapeptide referred to as pentapeptide-28 in the examples is solely defined by amino acid content and not by an amino acid sequence, so that it is not clear what is the structure of the pentapetide.
- the inventors have developed a peptide comprising an amino acid sequence of formula (I) which can be useful in the prevention and/or treatment of cutaneous signs of aging, wherein aging comprises chronological aging and/or photoaging.
- the peptide of the invention is capable of reducing stress levels, e.g, caused by UV radiation, (HSP70 assay) and also reducing the DNA degradation under stress conditions, e.g, caused by hydrogen peroxide or UV radiation.
- the peptide comprising an amino acid sequence of formula (I) can be conveniently combined with a compound able to activate the synthesis of SIRT3 ptotein.
- this combination of actives increases the ATP production in human dermal fibroblasts and prevents cell overoxidation (especially in mitochondria).
- ROS radicals
- an aspect of the invention relates to a combination comprising a compound able to activate endogenous synthesis of SIRT3 protein in skin cells and a peptide comprising the amino acid sequence of formula (I)
- AA is an amino acid or a derivative thereof, n is 0, 1 , 2 or 3, and at least one of the lysine residues is acetylated.
- the combination of actives of the invention can be administered in the form of a microcapsule.
- a microcapsule comprising the combination comprising a compound able to activate endogenous synthesis of SIRT3 protein in skin cells and a peptide comprising the amino acid sequence of formula (I) as defined above.
- microcapsules allows to decrease the amounts nedded of the active ingredients with the consequence that potential side-effects are also reduced. Further, the microcapsules have also the advantage that are capable of penetrating skin and show a uniformly distribution on the entire epidermis.
- the combination of actives of the invention may be formulated as pharmaceutical or cosmetic compositions.
- a pharmaceutical or cosmetic composition comprising the combination comprising a compound able to activate endogenous synthesis of SIRT3 protein in skin cells and a peptide comprising the amino acid sequence of formula (I) as defined above and pharmaceutically or cosmetically acceptable excipients or carriers.
- the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above is useful as skin anti-aging agent.
- the invention also relates to the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above for use in the prevention and/or treatment of cutaneous signs of aging, wherein aging comprises chronological aging and/or photoaging.
- This aspect can also be formulated as the use of the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above for the preparation of a medicament for the prevention and/or treatment of cutaneous signs of aging, wherein aging comprises chronological aging and/or photoaging. It also relates to a method for the prevention and/or treatment of cutaneous signs of aging in a mammal, including a human, wherein aging comprises chronological aging and/or photoaging, the method comprising administering to said mammal an effective amount of the combination as defined above together with pharmaceutically acceptable carriers or excipients.
- another aspect of the present invention refers to the use of the combination of actives as defined above, as a skin care agent. It also forms part of the invention a cosmetic method for skin care of a mammal, including a human, said method comprising the administration to said mammal, including a human, of an effective amount of the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above, together with acceptable excipients or carriers.
- the present invention relates to a combination comprising a compound able to activate endogenous synthesis of SIRT3 protein in skin cells (herein also referred to as SIRT3 activating compound) and a peptide comprising the amino acid sequence of formula (I) (herein also referred to as peptide of formula (I)).
- the aminoacid sequence is written from N-terminus (N(t)) to C-terminus (C(t)), being the he N-terminus placed on the left.
- the peptide of formula (I) refers the peptide comprising the amino acid sequence: N(t)-(AA) n -Arg-His-Lys 1 -Lys 2 -Gln-(AA) n -C(t).
- the peptide of the combination above consists of the amino acid sequence (AA) n -Arg-His-Lys 1 -Lys 2 -Gln-(AA) n .
- each AA is independently an amino acid or a derivative thereof.
- amino acid derivative refers to a non- natural or modified amino acid which contains one or more modifications to backbone and/or side chain(s). These modifications can be introduced by incorporation of amino acid mimetics that show similarity to the natural amino acids.
- mimetics of amino acids include, but are not limited to, [beta]2- and [beta]3-amino acids, [beta]2,2-, [beta]2,3, and [beta]3,3-disubstituted amino acids, [alpha], [alpha]-disubstituted amino acids, statine derivatives of amino acids, D-amino acids, [alpha]- hydroxyacids, [alpha]-aminonitriles, N-alkylamino acids and the like.
- derivatives include amino acids with a modified amino acid side chain (referring to the side chain of the corresponding natural amino acid), such as 4-fluorophenylalanine, 4-hydroxylysine, 3-aminoproline, 2- nitrotyrosine, N-alkylhistidine or [beta]-branched amino acids or [beta]- branched amino acid mimetics with chirality at the [beta]-side chain carbon atom opposed to the natural chirality (e.g. allo-threonine, allo-isoleucine and derivatives).
- derivatives also include those amino acids wherein the amino group present in the amino acid side chain is modified, e.g. is acetylated.
- modified and unusual amino acids include without limitation: 2-aminoadipic acid, 3-aminoadipic acid, beta-alanine, beta- aminopropionic acid, 2-aminobutyric acid, 4-aminobutyric acid, piperidinic acid, 6-aminocaproic acid, 2-aminoheptanoic acid, 2-aminoisobutyric acid, 3- aminoisobutyric acid, 2-aminopimelic acid, 2,4 diaminobutyric acid, desmosine, 2,2'-diaminopimelic acid, 2,3-diaminopropionic acid, N- ethylglycine, N-ethylasparagine, hydroxylysine, allo-hydroxylysine, 3- hydroxyproline, 4-hydroxyproline, isodesmosine, allo-isoleucine, N- methylglycine, sarcosine, N-methylisoleucine, 6-N-methyllysine, N- methylvaline, norva
- the amino acid derivative is selected from a) a natural amino acid in which one or more hydrogen atoms of its side chain is replaced by a substituent selected from the group consisting of halogen, -NO 2 , -NH 2 , -NH(CrC 4 )alkyl, -OH, -SH and -NHCOCH 3 ; and/or one or more methylene groups (-CH 2 -) of its side chain is replaced by a substituent selected from the group consisting of a bond or (Ci-C 4 )alkyl, and b) a natural amino acid with chirality at the [beta]-side chain carbon atom opposed to the natural chirality.
- the amino acid derivative is selected from 4-fluorophenylalanine, 4-hydroxylysine, 3-aminoproline, 2-nitrotyrosine, N- alkylhistidine, allo-threonine, allo-isoleucine, 2-aminoadipic acid, 2- aminobutyric acid, 2-aminoheptanoic acid, 2-aminoisobutyric acid, 2- aminopimelic acid, 2,4 diaminobutyric acid, 2,3-diaminopropionic acid, N- ethylglycine, N-ethylasparagine, allo-hydroxylysine, 3-hydroxyproline, 4- hydroxyproline, allo-isoleucine, N-methylglycine, N-methylisoleucine, 6-N- methyllysine, N-methylvaline, norvaline, norleucine, and ornithine.
- each AA is independently selected from natural L- amino acids, such as Alanine (Ala), Arginine (Arg), Asparagine (Asn), Aspartic Acid (Asp), Cysteine (Cys), Glutamic Acid (Glu), Glutamine (Gin), Glycine (Gly), Histidine (His), Isoleucine (lie), Leucine (Leu), Lysine (Lys), Methionine (Met), Phenylalanine (Phe), Proline (Pro), Serine (Ser), Threonine (Thr), Tryptophan (Trp), Tyrosine (Tyr) and Valine (Val).
- L- amino acids such as Alanine (Ala), Arginine (Arg), Asparagine (Asn), Aspartic Acid (Asp), Cysteine (Cys), Glutamic Acid (Glu), Glutamine (Gin), Glycine (Gly), Histidine (His), Isoleucine (lie), Leucine (Leu), Ly
- above mentioned group of peptides may contain close structural analogues of amino acid or amino acids mimetics, for instance ornithine instead of lysine, homophenylalanine or phenylglycine instead of phenylalanine, [beta]-alanine instead of glycine, pyroglutamic acid instead of glutamic acid, norleucine instead of leucine or the sulfur-oxidized versions of methionine and/or cysteine.
- variants of peptides of formula (I) subject to additions or substitutions also form part of the present invention.
- a "variant" of the peptide of formula (I) refers herein to a peptide of formula (I) wherein from one to three amino acids, preferably one amino acid, of the amino acid sequence of formula (I) is substituted with any other natural amino acid or derivative thereof as defined above.
- the amino acid substitution may be conservative (i.e. one or more amino acids are are replaced by one or more amino acids with similar chemical properties; e.g.
- the C-terminus may be carboxamide, or other resulting from incorporation of one of the above mentioned amino acid mimetics.
- the peptide may contain one or more replacements of native peptide bonds with groups including, but not limited to, sulfonamide, retroamide, aminooxy-containing bond, ester, alkylketone, [alpha], [alpha]- difluoroketone, [alpha]-fluoroketone, peptoid bond (N-alkylated glycyl amide bond).
- groups including, but not limited to, sulfonamide, retroamide, aminooxy-containing bond, ester, alkylketone, [alpha], [alpha]- difluoroketone, [alpha]-fluoroketone, peptoid bond (N-alkylated glycyl amide bond).
- the linear and cyclized forms of the peptides mentioned above are covered by this invention, as well as their retro, inverso and/or retroinverso analogues.
- Such variants should not affect the properties of the peptides described herein.
- all amino acids constituting the peptide of the combination above are L-amino acids.
- the peptide of formula (I) comprises or consists of the amino acid sequence: Arg-His-Lys-Lys(Ac)-Gln, more preferably, the peptide of formula (I) comprises or consists of the amino acid sequence SEQ ID NO. 1 :
- the peptides described herein can be prepared by any known methods including, without limitation, solid phase synthesis, solution synthesis, expression of protein by a transformed host, cleavage from a synthetic or semisynthetic polypeptide, or a combination of these techniques.
- the peptides according to the present invention can also be obtained by methods known in the art in the form of pharmaceutically or cosmetically acceptable salts thereof, such as the sodium salt, potassium salt, calcium salt, magnesium salt and addition salts with acids.
- salts include salts of inorganic acids (e.g. hydrochloric acid, sulfuric acid and phosphoric acid) and organic acids (e.g. acetic acid, propionic acid, citric acid, tartaric acid, malic acid and methanesulfonic acid).
- the peptide of the combination is capable to decrease the DNA degradation in skin cells such as fibroblasts and
- keratinocytes when exposed to exogenous stressors such as UV radiation and H 2 O 2 .
- SIRT3 activating compound refers to an agent that increases the level of SIRT3 protein.
- a SIRT3 activating compound may increase the production of SIRT3 protein by at least 5%, 10%, 15%, 25% or 30% with respect to control (untreated cells).
- the identification of SIRT3 activating compounds may be generally carried out by cellular assay which comprises treating the cells with the test compound, lysing them and separating SIRT3 protein by electrophoresis as described in more detail in the examples.
- the SIRT3 activating compound comprises one or more peptides that have biomimetic activity to mitochondrial respiratory chain proteins.
- the compound able to activate endogenous synthesis of SIRT3 is hydrolyzed soy protein.
- hydrolyzed soy protein refers to a soy protein which has been hydrolyzed and typically has a reduced molecular weight in comparison to the protein in its non-hydrolyzed (unhydrolyzed) state. It refers to a protein hydrolyzate of soybean, i.e. to the product obtained by acidic, alkaline, or enzymatic hydrolysis of non-hydrolyzed soy protein, i.e. the soy protein that has not lost any quaternary, tertiary, and/or secondary structures present in the original unaltered protein.
- the hydrolyzed soy protein is composed primarily of amino acids, peptides, and proteins. It may contain impurities consisting chiefly of carbohydrates and lipids along with smaller quantities of miscellaneous organic substances of biological origin.
- the hydrolyzed soy protein is typically rich in bio-mimetic peptides against the respiratory chain proteins.
- si protein refers to any protein that may be derived from soy beans, whether or not the protein is actually derived from soy beans.
- the hydrolyzed soy protein is commercially available as Dynachondrine ISR (ISP Personal Care).
- a microcapsule comprising the combination comprising a SIRT3 activating compound and a peptide comprising the amino acid sequence of formula (I) as defined above.
- particular embodiments of the combination comprising the SIRT3 activating compound and the peptide of formula (I) above are also particular embodiments of the microcapsules.
- the microcapsules of the invention are generally made of one or more biodegradable polymers.
- the microcapsules of the invention are bilayered microcapsules which comprise a core polymer and an outer shell polymer.
- the core polymer and the outer shell polymer are different.
- the core polymer is poly(D,L-lactide-co-glycolide) (PLGA) and the outer shell polymer is polyvinyl alcohol (PVA).
- PLGA has a lactide/glycolide molar ratio from 40:60 to 60:40, more preferably 50:50.
- the bilayered microcapsules of the invention can be used as a highly efficient delivery system with sustained and controlled release of the encapsulated active ingredient at the target cells (fibroblasts and keratinocytes).
- the microcapsules escape from the endosomal and lysosomal compartment, so that the encapsulated active ingredient is released directly in the cytoplasm and can reach the target quickly, optimizing the application and the bioavailability of the encapsulated active agents.
- the microcapsules of the invention have the advantage that they show higher migration and penetration into the skin when compared with conventional microcapsules. By using these microcapsules lower concentrations of the active ingredient are needed to achieve same performance, and, as a consequence side effects are reduced.
- the microcapsule comprises from 15 to 30%, preferably from 20 to 25% of SIRT3 activating compound and from 0.05 to 10%, preferably from 0.05 to 5%, preferably from 0.1 to 3% of the peptide of formula (I) in relation to the total weight of the microcapsule.
- the SIRT3 activating compound is encapsulated within the core polymer, and the peptide of formula (I) is attached to the outer shell polymer on the surface of the microcapsule. More particularly, the peptide of fornnula (I) is attached to the outer shell by a covalent bond, preferably an amide bond between the amino group of the peptide N-terminal amino acid and the carboxyl group of the outer shell polymer, preferably PVA.
- the microcapsules of the invention may be prepared by a single emulsion technique as known in the art.
- the core polymer such as PLGA
- the SIRT3 activating compound in a suitable solvent, such as acetone
- the resulting mixture is emulsified, for example by using a sonicator, with a mixture of the outer shell polymer, such as PVA, in a suitable solvent, such as water.
- the microcapsules may be isolated by conventional means, such as evaporation of the solvent and ultracentrifugation.
- the microcapsules may be lyophilized.
- the microcapsules of the invention have a size
- SEM Scanning Electron Microscopy
- microcapsules of the invention have the advantage that they reach deep into the hair follicles, where the barrier possess only a few layers of differentiated corneocytes and can be considered highly permeable.
- the hair follicles can act as long-term reservoir, beneficial condition when transdermal delivery is intended. Follicular penetration of particles appear to be a promising mechanism for drug delivery.
- the hair follicle delivery has several pharmacokinetic advantages as a reduction or bypass of the tortuous pathway of the transepidermal absorption, decrease of the drug systemic toxicity when the follicle acts as long term delivery reservoir and increasing additionally the therapeutic index of some drugs as well as reducing the applied dose or frequency of administration.
- compositions comprising an effective amount of the combination comprising the SIRT3 activating compound and the peptide of formula (I) as defined above, together with one or more pharmaceutically or cosmetically acceptable excipients or carriers also form part of the invention.
- the invention relates to a cosmetic composition.
- the term "effective amount” means an amount that is sufficient to obtain the expected effect.
- the effective amount is the "therapeutically effective amount” and refers to the amount of a compound that, when administered, is sufficient to prevent development of, alleviate to some extent, one or more of the symptoms of the disorder, disease, or condition being treated.
- the particular dose of compound administered according to this invention will of course be determined by the particular circumstances surrounding the case, including the compound administered, the route of administration, the particular condition being treated, and the similar considerations.
- pharmaceutically acceptable excipients or carriers refers to pharmaceutically acceptable materials, compositions or vehicles for use in the pharmaceutical technology for preparing compositions with medical use.
- the pharmaceutical or cosmetic composition is a topical composition.
- the topical pharmaceutical or cosmetic composition of the present invention comprises an effective amount of the combination
- the invention relates to a topical cosmetic composition.
- suitable excipients or carriers for topical administration include, without limitation, repairing cutaneous barrier function agents, hydrating agents, sunscreens, emollients, emulsifiers, thickeners,
- humectants pH-regulating agents, antioxidants, preservative agents, vehicles, or their mixtures.
- the excipients or carriers used have affinity for the skin, are well tolerated, stable, and are used in an amount adequate to provide the desired consistency, and ease application.
- compositions of the present invention may contain other ingredients, such as fragrances, colorants, and other components known in the state of the art for use in topical formulations.
- Caprylic/Capric Triglyceride Caprylyl Glycol, Cetearyl Alcohol, Ceteth-20, Cetyl Alcohol, Cyclopentasiloxane, Decapeptide-22, Diethylhexyl Butamido Triazone, Dimer Tripeptide-43, Dimethicone, Dimethicone Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethiconol, Disodium EDTA, Ethylhexyl Triazone, Ethylhexylglycerin, Glycerin, Glycerylstearate,
- the cosmetic compositions of the invention may be in a solid, semi-fluid or fluid form, in particular in the form of emulsion, cream, milk, lotion, ointment, solid stick, foam, spray, oil, pomade and fluid, among others. They can be in anhydrous form, in an aqueous solution, in suspension form, or in the water- in-oil or oil-in water emulsion form.
- the topical composition used is formulated preferably as an emulsion.
- An emulsion is a dispersed system comprising at least two immiscible phases, one phase dispersed in the other as droplets.
- the emulsion When water is the dispersed phase and oil is the dispersion medium, the emulsion is termed a water-in-oil emulsion (w/o). When oil is dispersed as droplets throughout the aqueous phase, the emulsion is termed an oil-in-water emulsion (o/w).
- the emulsions used are preferably oil-in-water emulsions.
- the emulsions for use in the sense of the present invention are compatible with creams and lotions. In general any composition of the invention may be applied to the skin, in any parts of the skin, in any part of the body.
- Topical compositions of the present invention can be prepared according to methods well known in the state of the art.
- the appropriate excipients and/or carriers, and their amounts, can readily be determined by those skilled in the art according to the type of formulation being prepared.
- the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above is useful in the prevention and/or treatment of the cutaneous signs of aging.
- the combination of actives forms part of a cosmetic composition.
- aging is chronological aging.
- aging is photoaging.
- photoaging refers to the premature skin aging caused by solar radiation. This damage does not result from ultraviolet (UV) radiation alone, but also from longer wavelengths, in particular near-infrared radiation (IRA radiation, 760-1440 nm).
- photoaging relates to the effects of ultraviolet UV light exposure on skin and/or IR light exposure on skin associated with the formation of coarse wrinkles, uneven skin pigmentation, loss of skin elasticity, a disturbance of skin barrier functions, or a combination thereof. Cutaneous signs of photoaging include changes in pigmentation (mottled pigmentation), sallowness, deep wrinkling, dryness, telangiectasia, premalignant lesions, laxity, atrophy, leathery appearance, elastosis (a coarse, yellow,
- prevention means reducing the risk of manifestation of a phenomenon.
- treatment means compensating for a physiological dysfunction and more generally reducing or even eliminating an undesirable disorder, the manifestation of which is especially a consequence of this dysfunction.
- reducing means lessening, ameliorating, or relieving the deleterious effects.
- the invention relates to the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above for use in reducing the cutaneous signs of aging, in particular chronological aging.
- the invention relates to the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above for use in the prevention of cutaneous signs of photoaging, in particular induced or produced by UVA, UVB and IR
- UVA, UVB and IRA radiations are particularly, induced or produced by UVA, UVB and IRA radiations.
- the prevention and/or treatment of cutaneous signs of aging comprises regenerating, revitalizing and/or increasing longevity, repair or protection of the skin cell layers.
- the combination comprising a SIRT3 activating compound and a peptide of formula (I) of the invention can also be used for cosmetic purposes for the care of the skin.
- the combination comprising a SIRT3 activating compound and a peptide of formula (I) as defined above are forming part of a cosmetic composition.
- the skin care comprises ameliorating at least one of the following symptoms: roughness, flakiness, dehydration, tightness,
- the cosmetic composition of the invention comprises the appropriate effective amount of the combination for this use, i.e.
- the skin care agent is selected from the group consisting of a skin moisturizing agent and a skin barrier recovery agent.
- moisturizing agent refers to a material which increases the water content of the skin and helps keep it soft and smooth.
- skin barrier recovery agent refers to material whose composition and/or structure are similar to the skin barrier allowing the reparation of its deficiencies.
- CCCP carbonyl cyamide 3-chlorophenylhydrazone
- CTC 2-chlorotrityl resin
- DIPCDI N,N-diisopropylcarbodiimide
- DIPEA N,N-diisopropylethylamine
- DMEM Dulbecco's Modified Eagle Medium
- FCS Fetal Bobine Serum
- PBS Phosphate Buffer Saline
- TIS triisopropylsilane
- Trt trityl
- Fmoc-Gln(Trt)-OH (1 eq) was directly incorporated on the CTC-resin (1 .0 mmol/g) with DIPEA (3 eq) in DCM (aprox. 1 .25 mL/1 g resin). After 10 min more DIPEA was added (7 eq) and the mixture allowed to stir for 40 min.
- the resin was solvated with DMF (5 x 30 s), and the coupling with Fmoc-Lys(Ac)-OH (3 eq) was carried out in the presence of HOAt (3 eq) and DIPCDI (3eq) in DMF. After 1 h the resin was washed with DMF (5 x 30 s) and DCM (5 x 30 s). Kaiser test was used to verify that the coupling was successful. The same procedure was successively repeated 3 times with the following amino acids Fmoc-Lys(Boc)- OH, Fmoc-His(Trt)-OH, and Fmoc-Arg(Pbf)-OH. Finally, the cleavage of the peptide from the resin was carried out by treating the resin with TFA:TIS: H 2 O (95:2.5:2.5) for 1 h, yielding the peptide of sequence SEQ ID NO.1 .
- SDS-PAGE and Immunoblots Protein samples for electrophoresis were prepared by lysis buffer extraction and precipitation. The precipitates were dissolved in SDS-PAGE sample buffer and electrophoresed in 4.5-15% polyacrylamide gradient gels. The proteins were electrotransferred to nitrocellulose filters, and the membranes were treated with blocking buffer for 1 h at room temperature. This was followed by incubation at 4 °C overnight with an antibody to HSP70 (Santa Cruz Biotechnology, INC.) diluted 1 :1000 in blot buffer, washing, and incubation for 2 h at room temperature with peroxidase-conjugated goat-anti-rabbit IgG (Sigma, Germany) in blot buffer. Immunoreactivity was revealed by chemiluminescence (ECL-kit, Amersham Biosciences, UK). Table 1 shows the percentage of HSP70 in the different cell lines.
- the comet assay or single cell gel electrophoresis assay (SCGE) is a common technique for measurement of DNA damage in individual cells.
- the peptide of sequence SEQ ID NO.1 was coupled to the above obtained microcapsule via amide bound.
- carboxyl groups on the surface of the capsules were activated by re-suspending the capsules in isotonic 0.1 M 2- (N-morpholino)ethanesulphonic acid (MES) saline buffer pH 5.5, and then reacting them with 1 -ethyl-3-(3-dimethyl aminopropyl) carbodiimide (EDAC) (10 equiv.) and N-hydroxysuccinimide (NHS) (10 equiv.) for 1 h.
- the capsules were then centrifuged (15.000 rpm, 45 min) to remove excess EDAC/NHS and the water-soluble isourea byproduct.
- Activated capsules (1 g) were re- suspended in phosphate-buffered saline (PBS, 40 mL) and reacted with the N-terminal amine group of the peptide of sequence SEQ ID NO.1 (0.150 g) at room temperature for 2 hours.
- the coated capsules were centrifuged (15000 rpm, 30 min) and washed with PBS (3 x 10 mL) buffer to remove any unbound peptide. The presence of surface-bound peptide was confirmed by Kaiser ninhydrin tests.
- Unreacted peptide was separated from the capsules after the corresponding reaction step by analysis of the centrifugation supernatant (step described above) using 2,4,6-trinitrobenzenesulphonic acid (TNBS) as a colorimetric assay: 700 microliters of supernatant were added to 700 microliters of 0.1 M sodium borate buffer (pH 9.2). 350 microliter of TNBS aqueous solution (1 .65 mg/mL) were added and the solution was rapidly mixed. After incubation at 40 °C for 45 min., the reaction was stopped by adding 350 microliter of 0.1 M NaH 2 PO 4 containing 1 .5 mM Na 2 SO 3 and absorption at 420 nm was determined on a UVA/IS spectrometer.
- TNBS 2,4,6-trinitrobenzenesulphonic acid
- the amounts of peptide on the surface of the nanoparticles were calculated by substracting the free amount from the total amount added into the reaction system, being in that case 0.125%.
- the ratio of encapsulated hydrolyzed soy protein to peptide of sequence SEQ ID NO.1 is 25% to 0.125%.
- the diameter of the capsules was determined by Scanning Electron
- Human Dermal Fibroblasts and human keratinocytes were used. The isolated cells were cultured in DMEM culture medium supplemented with 10% FCS and were incubated at 37 °C for maintenance treatment. Untreated cells were used as negative control. The positive control was 0.1 % SDS.
- microcapsules as obtained in Example 2 were tested in the DMEM culture medium at two concentrations: 0.0032% and 0.032%. These weight percentages refer to the weight of the microcapsule in relation to the total weight.
- Human Dermal Fibroblasts and human keratinocytes were used.
- the isolated cells were cultured in DMEM culture medium supplemented with 10% FCS and were incubated at 37 °C for maintenance treatment. Untreated cells were used as negative control.
- the microcapsules as obtained in Example 2 were tested in the DMEM culture medium at two concentrations: 0.0032% and 0.032%. These weight percentages refer to the weight of the microcapsule in relation to the total weight.
- Sample preparation Based on the protein content of the sample (determined by the Bradford assay), the volume necessary to add in the different lanes of the gel was calculated. In a 10-well mini gel, a volume (including sample buffer and mercaptoethanol beta) of not more than 50 ⁇ in each lane was added. 10-15 ⁇ of Laemmli buffer in a microtube was added, beta
- the transfer was carried out on nitrocellulose membranes of 0.2 microns for 2 hours to a fixed voltage of 100V.
- the determination of the protein SIRT3 was performed with commercial antibodies (Rabbit polyclonal anti sirtuin 3 of mouse monoclonal) from Abeam, UK.
- Table 4 shows the percentage of SIRT3 protein in the different cell lines after the different treatments.
- microcapsules of Example 2 increased SIRT3 levels in human dermal fibroblasts and keratinocytes.
- the amount of ATP synthesized by the cells can be quantified by
- bioluminescence This assay is based on measurement of light emitted by the
- ATP determination kit ref. A22066 Invitrogen Molecular probes was used. Human Dermal Fibroblasts coming from biopsies of healthy donors were cultured in DMEM culture medium supplemented with 10% FCS and incubated at 37 °C for maintenance and treatment. Untreated cells were used as negative control. The microcapsules as obtained in Example 2 were tested in the DMEM culture medium at two concentrations: 0.0032% and 0.032%. These weight percentages refer to the weight of the microcapsule in relation to the total weight. Cells were seeded at 100000 cells per well in a 96-well plate.
- Example 2 increased ATP production in human dermal fibroblasts.
- the mitochondrial membrane potential evaluates the integrity of the mitochondrial membranes. This parameter is of great interest in studies of oxidative stress because mitochondria are affected significantly in the presence of ROS.
- the fluorescent marker JC-1 is able to enter the
- ROS Reactive Oxygen Species
- CCCP 50 ⁇
- CCCP CCCP (50 ⁇ ) was used, which was incubated with untreated cells without irradiation at 37 °C for 5 minutes.
- 10 mL of the cationic marker JC-1 was added to the different samples at a concentration of 200 ⁇ (2 ⁇ final concentration) and the samples were incubated at 37 °C, 5% CO 2 for 15 minutes.
- Cells were washed with PBS and centrifuged and the pellet obtained was resuspended in 500 ⁇ _ of PBS. Samples were analyzed on a flow cytometer at an excitation wavelength of 488 nm.
- Table 6 shows the fluorescence intensity (as well as the standard deviation (SD)) in human dermal fibroblasts after the different treatments.
- Example 2 increased mitochondrial membrane potential under the tested conditions, demonstrating their ability to reduce cellular oxidative stress.
- Cell longevity assay is related to the reduction of the galactosidase activity in senescent cells.
- X-gal (5-bromo-4-chloro-3-indolyl- -D- galactopyranoside) is an insoluble compound formed by an indole covalently linked to a galactoside, which is hydrolyzed in the presence of galactosidase giving a measurable blue color.
- Cellular Senescence Assay kit ref CBA-230 Cell Biolabs, INC. was used. Human Dermal Fibroblasts coming from biopsies of healthy donors were cultured in DMEM culture medium supplemented with 10% FCS and incubated at 37 °C for maintenance and treatment. Untreated non-senescent cells were used as negative control. Untreated senescent (after 12 cell divisions) cells were used as positive control. The microcapsules as obtained in Example 2 were tested in the DMEM culture medium at two concentrations:
- weight percentages refer to the weight of the microcapsule in relation to the total weight.
- Table 7 shows the percentage of senescence in human dermal fibroblasts after the different treatments.
- Example 2 decreased the beta galactosidase activity under the tested conditions, demonstrating their ability to increase cellular longevity.
- Protein carbonylation assay Protein oxidation is defined as the modification of proteins induced either directly by the effect of radicals (ROS) or indirectly by the action of secondary products resulting from oxidative stress.
- ROS radicals
- the oxidative modifications of proteins can be induced in vitro by numerous pro-oxidant agents.
- the present assay consists on the derivatization of the carbonyl groups with
- DNPH dinitrophenylhydrazine
- DNPH dinitrophenylhydrazine
- DNPH dinitrophenylhydrazine
- Untreated cells were used as negative control.
- Cells irradiated with UV were used as positive control.
- the microcapsules as obtained in Example 2 were tested in the DMEM culture medium at two concentrations: 0.0032% and 0.032%. These weight percentages refer to the weight of the microcapsule in relation to the total weight.
- Cells were seeded at 100000 cells per well in a 96-well plate of 35 mm. 24 hours after seeding, cells were incubated under the conditions described above. For dilution of the sample, DMEM culture medium supplemented with 10% FCS was used. After 72 hours cells were irradiated with UVB light 100 mJ/cm 2 and the samples were allowed to incubate for 24 hours. Measuring the carbonization of the proteins was performed at 96 hours. Table 8 shows the percentage of carbonylation in human dermal fibroblasts after the different treatments.
- microcapsules of Example 2 decreased levels of protein carbonylation after stimulation with UV radiation.
- Fluorescein-labeled microcapsules were prepared following an analogous process as described in Example 2, by additionally adding the marker DQ- BSA to the acetone mixture containing PLGA and hydrolyzed soy protein.
- Reconstituted skin (SkinEthic, RHE Reconstructed Human Epidermis) was cultured in DMEM culture medium supplemented with 10% FCS and incubated at 37 °C for maintenance and treatment. Untreated RHE was used as negative control.
- Formulations containing the labelled microcapsules with DQ-BSA were tested medium at three concentrations: 0.032%, 0.16%, 0.32%. These weight percentages refer to the weight of the microcapsule in relation to the total weight.
- the reconstructed skin models of size 0.5 cm 2 , 17 day, were reconstituted in the appropriate means provided by the supplier immediately upon arrival at laboratory and kept in the incubator at 37 °C for complete recovery. After 24 hours, treatment with the marked microcapsules was performed under the conditions detailed in the previous section. Incubation with the different treatments was carried out for 48 hours. Then, the samples were frozen and analyzed by fluorescence microscopy.
- the fluorescence signal indicated that the capsules penetrated and were uniformly distributed along the whole epidermis.
- the fluorescence did not appear in the nucleus of skin cells, but only in the cytoplasm where the capsule was degraded, DQ-BSA complex was cleaved and the fluorescent molecule released.
- the nucleus of the skin cells were stained in a darker color.
- the microcapsules of Example 2 showed a suitable penetration and a uniformly distribution on the entire epidermis.
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Abstract
L'invention concerne une combinaison comprenant un composé capable d'activer la synthèse endogène de la protéine SIRT3 dans des cellules de la peau et un peptide comprenant la séquence d'acides aminés de formule (I) où AA est un acide aminé ou un dérivé de celui-ci, n est 0, 1, 2 ou 3 et au moins un des résidus lysine est acétylé. L'invention concerne également une microcapsule la contenant, une composition pharmaceutique ou cosmétique la contenant, son utilisation dans la prévention et/ou le traitement de signes cutanés du vieillissement, et son utilisation en tant qu'agent de soin de la peau.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13763016.6A EP2892503A2 (fr) | 2012-09-10 | 2013-09-09 | Composition antivieillissement de la peau |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12382346 | 2012-09-10 | ||
PCT/EP2013/068615 WO2014037561A2 (fr) | 2012-09-10 | 2013-09-09 | Composition antivieillissement de la peau |
EP13763016.6A EP2892503A2 (fr) | 2012-09-10 | 2013-09-09 | Composition antivieillissement de la peau |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2892503A2 true EP2892503A2 (fr) | 2015-07-15 |
Family
ID=47018940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP13763016.6A Withdrawn EP2892503A2 (fr) | 2012-09-10 | 2013-09-09 | Composition antivieillissement de la peau |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP2892503A2 (fr) |
WO (1) | WO2014037561A2 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016064943A1 (fr) * | 2014-10-21 | 2016-04-28 | Us Cosmeceutechs, Llc | Procédé de caractérisation de la capacité protectrice d'une substance de protection de la peau topique |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH700735B1 (de) * | 2010-03-15 | 2010-10-15 | Labo Cosprophar Ag | Kosmetische Komposition für die Verjüngung des Erscheinungsbildes der Haut. |
ES2386177B1 (es) * | 2010-09-21 | 2013-09-23 | Lipotec, S.A. | Nanocapsulas conteniendo microemulsiones |
-
2013
- 2013-09-09 EP EP13763016.6A patent/EP2892503A2/fr not_active Withdrawn
- 2013-09-09 WO PCT/EP2013/068615 patent/WO2014037561A2/fr active Application Filing
Non-Patent Citations (1)
Title |
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See references of WO2014037561A2 * |
Also Published As
Publication number | Publication date |
---|---|
WO2014037561A3 (fr) | 2014-07-03 |
WO2014037561A2 (fr) | 2014-03-13 |
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