EP2155186A2 - Pharmazeutische oder kosmetische präparate zur topischen und/oder parenteralen anwendung, verfahren zu ihrer herstellung und ihre anwendung - Google Patents
Pharmazeutische oder kosmetische präparate zur topischen und/oder parenteralen anwendung, verfahren zu ihrer herstellung und ihre anwendungInfo
- Publication number
- EP2155186A2 EP2155186A2 EP08788214A EP08788214A EP2155186A2 EP 2155186 A2 EP2155186 A2 EP 2155186A2 EP 08788214 A EP08788214 A EP 08788214A EP 08788214 A EP08788214 A EP 08788214A EP 2155186 A2 EP2155186 A2 EP 2155186A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- hyaluronic acid
- derivatives
- acid
- inhibitor
- degradation
- 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- Withdrawn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
- 239000002537 cosmetic Substances 0.000 title claims abstract description 14
- 230000000699 topical effect Effects 0.000 title claims abstract description 8
- 238000002360 preparation method Methods 0.000 title description 4
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims abstract description 80
- 229920002674 hyaluronan Polymers 0.000 claims abstract description 80
- 229960003160 hyaluronic acid Drugs 0.000 claims abstract description 79
- 239000000203 mixture Substances 0.000 claims abstract description 71
- 230000015556 catabolic process Effects 0.000 claims abstract description 28
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- 238000006731 degradation reaction Methods 0.000 claims abstract description 25
- 239000003112 inhibitor Substances 0.000 claims abstract description 24
- 150000004492 retinoid derivatives Chemical class 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 17
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 claims description 16
- 239000004378 Glycyrrhizin Substances 0.000 claims description 15
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 claims description 15
- 229960004949 glycyrrhizic acid Drugs 0.000 claims description 15
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 claims description 15
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- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 claims description 15
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 14
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- 239000004480 active ingredient Substances 0.000 claims description 5
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- WXUQMTRHPNOXBV-UHFFFAOYSA-N Urolithin B Chemical compound C1=CC=C2C3=CC=C(O)C=C3OC(=O)C2=C1 WXUQMTRHPNOXBV-UHFFFAOYSA-N 0.000 claims description 4
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 230000002265 prevention Effects 0.000 claims description 4
- 238000002278 reconstructive surgery Methods 0.000 claims description 4
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- 239000000725 suspension Substances 0.000 claims description 4
- 239000002211 L-ascorbic acid Substances 0.000 claims description 3
- 235000000069 L-ascorbic acid Nutrition 0.000 claims description 3
- MQUQNUAYKLCRME-INIZCTEOSA-N N-tosyl-L-phenylalanyl chloromethyl ketone Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N[C@H](C(=O)CCl)CC1=CC=CC=C1 MQUQNUAYKLCRME-INIZCTEOSA-N 0.000 claims description 3
- VEAUNWQYYMXIRB-UHFFFAOYSA-N Nyasol Natural products C1=CC(O)=CC=C1C=CC(C=C)C1=CC=C(O)C=C1 VEAUNWQYYMXIRB-UHFFFAOYSA-N 0.000 claims description 3
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 claims description 3
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- 229920001467 poly(styrenesulfonates) Polymers 0.000 claims description 3
- 229960001727 tretinoin Drugs 0.000 claims description 3
- 239000001100 (2S)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one Substances 0.000 claims description 2
- RDJGLLICXDHJDY-NSHDSACASA-N (2s)-2-(3-phenoxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](C)C1=CC=CC(OC=2C=CC=CC=2)=C1 RDJGLLICXDHJDY-NSHDSACASA-N 0.000 claims description 2
- AXNVHPCVMSNXNP-IVKVKCDBSA-N (2s,3s,4s,5r,6r)-6-[[(3s,4s,4ar,6ar,6bs,8r,8ar,9r,10r,12as,14ar,14br)-9-acetyloxy-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-[(e)-2-methylbut-2-enoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-3, Chemical compound O([C@@H]1[C@H](O[C@H]([C@@H]([C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@]([C@@]3(CC[C@H]2[C@]1(CO)C)C)(C)C[C@@H](O)[C@@]1(CO)[C@@H](OC(C)=O)[C@@H](C(C[C@H]14)(C)C)OC(=O)C(/C)=C/C)C(O)=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O AXNVHPCVMSNXNP-IVKVKCDBSA-N 0.000 claims description 2
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical compound C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 claims description 2
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- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
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- NCYCYZXNIZJOKI-OVSJKPMPSA-N retinal group Chemical group C\C(=C/C=O)\C=C\C=C(\C=C\C1=C(CCCC1(C)C)C)/C NCYCYZXNIZJOKI-OVSJKPMPSA-N 0.000 description 1
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- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical class CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
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Classifications
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Definitions
- compositions for topical and / or parenteral application comprising, in a physiologically acceptable medium, a retinoid and / or its salts and / or derivatives, and an inhibitor of the degradation of hyaluronic acid.
- Said compositions are intended for the treatment of dermatological conditions, in particular, the filling treatment of wrinkles, fine lines, fibroblastic depletions and any scarring.
- the aging of the skin is one of the most visible changes in the senescence process.
- the skin is exposed to many factors that can accelerate this physiological process.
- intrinsic aging which is easier to evaluate in areas that are normally not exposed to the sun and, on the other hand, extrinsic aging, caused by the interaction of environmental factors, in particular UV rays. These environmental factors have a much greater effect on sun-exposed body parts, especially in light-skinned people.
- actinic aging Other factors such as eating habits, smoking, excessive alcohol consumption, Chronic diseases and dysfunctions of the endocrine glands also contribute to this aging.
- the stratum corneum is little modified.
- the epidermis is atrophic and the dermal-epidermal junction is flattened, so that adhesion to the dermis is less good, facilitating the formation of bubbles.
- the thickness of the dermis is significantly reduced; there are fewer blood vessels. There are also fewer fibroblasts and their biosynthesis and proliferation abilities are diminished.
- the elastic fibers undergo modifications first, and then disappear.
- Wrinkles are the most visible signs of aging. We can distinguish it from several natures, in particular superficial and deep wrinkles. Deep wrinkles may be due to dermo-hypodermic changes, while superficial wrinkles could be explained by dermal and possibly epidermal changes. Wrinkles are mainly due to the loss of elasticity of the skin. The reaching of the network elastic subepidermal gives rise to a superficial laxity of the aged skin and a fold of its surface. The destruction of elastic fibers in the reticular dermis is responsible for the loss of elasticity and the ability of the skin to regain its shape after stretching. Depending on the type, intensity and topography, a suitable treatment will be possible.
- dermal implants that is to say as substances injected directly into the skin, in order to remedy the skin changes resulting from aging. , trauma or disease.
- Botulinum toxin inactivated Botox ®
- laser techniques These different types of treatment are not exclusive and their combination has even been recommended.
- collagen and hyaluronic acid are the ones that are at the origin of the majority of the products available on the market.
- Hyaluronic acid is a ubiquitous natural polysaccharide that exists in the same form from the simplest bacterium to humans. It is a polysaccharide composed alternately of D-glucuronic acid and N- acetylglucosamine, linked together by alternating glycosidic bonds beta-1,4 and beta-1,3. According to Saari H et al. Differential effects of reactive oxygen species on a native synovial fluid and purified human umbilical cord hyaluronate. Inflammation 17 (1993): 403-415, the polymers of this repeating unit can have a size between 10 2 and 10 4 kDa in vivo, the hyaluronic acid taken from the umbilical cord having a weight of 2500 kDa.
- Hyaluronic acid is a natural component of the dermis where it plays an important role in the hydration and elasticity of the skin. However, it decreases in quantity and quality with age, resulting in drying of the skin that wrinkles. It is highly water soluble and forms high viscosity solutions in water. Because of these particular properties, hyaluronic acid is one of the most widely used pharmaceutical products.
- hyaluronic acid is very quickly eliminated from the plasma by degradation. Its plasma half-life after intravenous injection is very short, between 2.5 and 5.5 minutes, while in the skin, its half-life is 0.5 to 2 days depending on its concentration. Urinary excretion is low, less than 1% of total clearance. In rabbits, the rate of elimination in the skin was measured (Reed RK, Laurent UB, JR Fraser, Laurent TC., Removal rate of [3H] hyaluronan injected subcutaneously in rabbits.) Am J Physiol 1990 Aug; 259 (2Pt 2): H532-5). It is non-exponential with a half-life of 0.5 to 1 day when its concentration is 5 mg / ml. The tolerance of hyaluronic acid is very good and no immunogenicity has been associated with this substance. This has a very low incidence of side effects.
- hyaluronic acid alone or in combination
- injectable compositions such as, for example, hyaluronic acid alone, collagen alone or the combination "hyaluronic acid and collagen" have already been used in reconstructive surgery, in the context of treatment by filling wrinkles, fine lines, fibroblastic depletions and all scars.
- hyaluronic acid because of its low bioavailability after injection and its too high injection frequency, can not be used as such.
- compositions based on hyaluronic acid having a very good bioavailability and likely to better withstand the action of degradation enzymes. This allows, in particular, to space interventions and reduce their number.
- compositions used as a dermal implant are all composed of stabilized hyaluronic acid and many of them comprise hyaluronic acid chemically modified for this purpose.
- hyaluronic acid included in these products is predominantly of non-human origin such as for example of avian or bacterial origin.
- compositions there are thus in these compositions numerous hyaluronic acid derivatives chemically modified in the form, in particular of esters, of amides, as well as derivatives having "intra and / or interchain bridges"
- a problem to be solved by the invention is to provide compositions which make it possible to ensure that hyaluronic acid has a better bioavailability while retaining its physico-chemical characteristics and its biological properties, as well as a method of manufacturing such compositions.
- the solution of the invention to this problem has as its first object a pharmaceutical or cosmetic composition, especially for topical and / or parenteral application comprising, as sole active ingredients, in a physiologically acceptable medium:
- At least one compound chosen from retinoids, their salts and derivatives, and at least one inhibitor of the degradation of hyaluronic acid at least one compound chosen from retinoids, their salts and derivatives, and at least one inhibitor of the degradation of hyaluronic acid.
- the composition does not comprise an oligosaccharide.
- composition according to the invention indeed contains as active ingredients only the retinoid (s) and the (s) inhibitor (s) of the degradation of hyaluronic acid; any other active ingredient is excluded.
- Its second object is a process for the manufacture of such a pharmaceutical or cosmetic composition, comprising a step of mixing at least one compound chosen from retinoids, their salts and derivatives, and at least one degradation inhibitor. hyaluronic acid with a physiologically acceptable medium.
- the method according to the invention also comprises a step of preparing a physiologically acceptable medium, in which the active ingredients are mixed.
- its third object is the use of at least one compound chosen from retinoids, their salts and derivatives, and at least one inhibitor of the degradation of hyaluronic acid, or a composition according to the invention, for the manufacture of a medicament for the treatment and / or prevention of dermatological conditions.
- a pharmaceutical or cosmetic composition according to the invention significantly increases the bioavailability of a hyaluronic acid, which is further included in said composition, or which is administered separately.
- the composition according to the invention makes it possible to space the applications of hyaluronic acid and to reduce the number thereof and it has a significant effectiveness in the filling of wrinkles, fine lines, fibroblastic depletions and all scars.
- the Applicant has demonstrated a decrease in the catabolism of hyaluronic acid in human keratinocytes in vivo on which hyaluronic acid, an inhibitor of hyaluronic acid degradation and a retinoid, are applied in the absence of oligosaccharide.
- the absence of oligosaccharide in a composition comprising a hyaluronic acid degradation inhibitor and a retinoid confers on hyaluronic acid also applied a better stability and a better bioavailability.
- compositions of the prior art are more effective than the compositions of the prior art, and in particular compositions comprising oligosaccharides, in the filling of wrinkles, fine lines, fibroblastic depletions and all scars, as well as in the hydration of the skin.
- composition according to the invention comprises, in a physiologically acceptable medium, at least one retinoid and / or its salts and / or derivatives and an inhibitor of the degradation of hyaluronic acid.
- a physiologically acceptable medium at least one retinoid and / or its salts and / or derivatives and an inhibitor of the degradation of hyaluronic acid.
- it does not include an oligosaccharide.
- composition according to the invention may further comprise hyaluronic acid.
- the composition according to the invention may be administered to a subject to whom hyaluronic acid is independently administered.
- the hyaluronic acid may be included in a separate composition, which may be administered simultaneously or in a different time from that of the administration of the composition according to the invention.
- the distinct composition comprising hyaluronic acid can be administered topically, orally or parenterally, for example by injection.
- Physiologically acceptable medium means a medium compatible with the skin and optionally with its integuments (eyelashes, nails, hair) and / or mucous membranes.
- the retinoid and / or its salts and / or its derivatives, and the inhibitor of the degradation of hyaluronic acid and, where appropriate, hyaluronic acid are present in proportions that can go from 0.0000001% to 10%, preferably from 0.00001% to 1% by weight, relative to the total weight of the composition.
- intervals of concentrations are given, they include the upper and lower bounds of that range.
- compositions according to the invention may comprise hyaluronic acid.
- hyaluronic acid is meant a ubiquitous natural polysaccharide existing in the same form from the simplest bacterium to humans. It is a polysaccharide composed alternately of D-glucuronic acid and N-acetylglucosamine, linked together by alternating glycoside bonds beta-1,4 and beta-1,3.
- the polymers of this repeating unit can have a size between 10 2 and 10 4 kDa in vivo, the hyaluronic acid taken from the umbilical cord having a weight of 2500 kDa.
- hyaluronic acid is natural.
- natural hyaluronic acid is meant an unstabilized hyaluronic acid, not chemically modified in the form, in particular of esters, amides, or in the form of derivatives having "intra and / or interchain bridges"
- compositions according to the invention comprise a retinoid and / or its salts and / or its derivatives, taken alone or as a mixture.
- retinoids that may be used in the compositions according to the invention, retinol, retinal, retinoic acid (or tretinoin), adapalene or their salts and derivatives, taken alone or as a mixture, more preferably, will be chosen more preferentially. retinol.
- retinoid salt is meant in particular an alkali metal salt, or an alkaline earth salt, or an organic amine salt.
- retinoid derivative is meant in particular the esters, such as retinyl palmitate, retinyl acetate, retinyl stearate, retinyl oleate, retinyl propionate or retinyl linoleate.
- the retinoids used in the compositions according to the invention are retinoids naturally occurring in the human body.
- compositions according to the invention do not comprise in particular any oligosaccharide.
- oligosaccharide polymers formed of a number n (with n less than or equal to 100) of monosaccharides by glycosidic bonding, in particular any oligosaccharide limiting the penetration of hyaluronic acid into skin cells, in particular keratinocytes and fibroblasts.
- oligosaccharides mention may be made of the oligomers of hyaluronic acid, such as di- to dodecamers of the acid hyaluronic acid, said dimer comprising a disaccharide unit component of hyaluronic acid, and the dodecamer comprising six of these disaccharide units, in particular the tetra-to-hexamers of hyaluronic acid, in particular the pentamer of hyaluronic acid.
- the molecular weight of a disaccharide unit of hyaluronic acid is about 400 Da.
- An oligomer of one to six disaccharide units of hyaluronic acid therefore has a molecular weight of between 400 and 2400 Da.
- Oligomer means, according to IUPAC in Pure Appl. Chem., Vol. 68, No.12, pp. 2287-2311, 1996, a molecule of intermediate molecular weight, the structure of which comprises a small amount of molecules having a lower molecular weight.
- a molecule having an intermediate molecular mass we will speak of a molecule having an intermediate molecular mass, when the removal of one or a few constituent units will significantly modify the properties of the molecule.
- compositions according to the invention further comprise an inhibitor of the degradation of hyaluronic acid.
- inhibitor of the degradation of hyaluronic acid is meant a compound capable of reducing, or even blocking, the catabolism either extracellular or intracellular of hyaluronic acid, preferably a compound capable of reducing or even blocking the extracellular catabolism of hyaluronic acid, more preferably a compound capable of inhibiting the extracellular hyaluronidase present in the skin.
- 1,2,3,4,6-penta-O-galloylglucose will be chosen in particular.
- TDSS a C14: 1 to C24: 1 unsaturated fatty acid with a double bond
- urinary trypsin inhibitor a C14: 1 to C24: 1 unsaturated fatty acid with a double bond
- the inhibitors of the degradation of hyaluronic acid used in the compositions according to the invention are natural.
- the inhibitor is used at concentrations of between 10 -9 M and 10 -2 M, preferentially between 10 -6 M and 10 -3 M.
- derivatives of glycyrrhizin or of glycyrrhetinic acid is meant in particular the salts, substituted derivatives, enantiomers and racemates of said compounds.
- salts of said compounds mention may be made of the salts obtained by addition of said compounds with an inorganic base, chosen in particular from the hydroxides of sodium, lithium, calcium, potassium, magnesium, ammonium or zinc, the carbonates of alkali or alkaline earth metals such as carbonates and bicarbonates of sodium, lithium, calcium, potassium, magnesium, ammonium or zinc, or with an organic base, chosen in particular from methylamine, propylamine, trimethylamine, diethylamine, triethylamine, N, N-dimethylethanolamine, tris (hydroxymethyl) aminomethane, ethanolamine, pyridine, picoline, dicyclohexylamine, morpholine, procein, lysine, arginine, histidine, N-methylglucamine or even phosphonium salts such as alkylphosphonium salts, arylphosphonium salts, alkylarylphosphonium salts, alkenylarylphosphonium salts or quaternary ammonium
- Such salts are in particular the potassium salt of glycyrrhetinic acid, the sodium salt of glycyrrhetinic acid, or the salt monoammonium of glycyrrhetinic acid (ammonium glycyrrhetinate).
- Analogous is understood to mean, in particular, the enzymatic or biomimetic analogs of said compounds, capable of binding to the catalytic or non-catalytic site of hyaluronidases and of thus inhibiting their activation. Such analogs can be selected in vitro by hyaluronidase binding or inhibition tests according to conventionally used techniques.
- the derivatives and / or analogues must be of natural origin.
- the compounds and their derivatives and / or analogues of natural origin are compounds in the pure state or in solution at different concentrations, obtained by various methods of extraction or hydrolysis of biological material of natural origin.
- compositions according to the invention may also contain the usual adjuvants well known to those skilled in the art.
- compositions according to the invention may be formulated for topical and / or parenteral application.
- compositions may be in any dosage form normally used for topical administration.
- topical compositions mention may be made of compositions in liquid form, pasty, or solid and, more particularly, in the form of ointments, aqueous, hydroalcoholic or oily solutions, dispersions of the lotion type which may be biphasic, serum, aqueous, anhydrous or lipophilic gels, powders, soaked swabs, syndets, wipes, sprays, foams, sticks, shampoos, compresses, washing bases, emulsions of liquid or semi-liquid consistency of the milk type, obtained by dispersion of a fatty phase in an aqueous phase (O / W) or conversely (W / O), a microemulsion, suspensions or emulsions of soft, semi-liquid or solid consistency of the white or colored cream, gel or ointment type, suspensions of microspheres or nanospheres or lipid or polymeric vesicles,
- compositions according to the invention can be applied subcutaneously or intradermally.
- parenteral compositions mention may be made of compositions in the form of solutions or suspensions for infusion or for injection.
- hyaluronic acid may be administered in the form of an injectable aqueous solution, a composition according to the invention.
- invention comprising retinol, and glycyrrhizin being administered as a cream.
- the administration frequencies may be identical or different.
- the frequency of administration of hyaluronic acid injected in the form of an aqueous solution for injection may vary from 4 to 24 months, preferably from 4 to 16 months, while those of composition according to the invention, administered topically, for example in cream form, may vary from 1 to 7 days, preferably from 1 to 3 days.
- the method of manufacturing a composition comprises the steps of preparing a physiologically acceptable medium and mixing an effective amount of retinol, and glycyrrhizin and / or its derivatives and / or like.
- the invention also relates to the use of at least one compound chosen from retinoids, their salts and derivatives, and at least one inhibitor of the degradation of hyaluronic acid, or a composition such as previously described for the manufacture of a cosmetic or pharmaceutical composition for the treatment, improvement and / or prevention of dermatological conditions.
- the invention relates to the use of at least one compound chosen from retinoids, their salts and their derivatives, and at least one inhibitor of the degradation of hyaluronic acid, or of a composition as described above for the manufacture of a cosmetic or pharmaceutical composition for the treatment, improvement and / or prevention of skin aging.
- Skin aging is understood to mean wrinkles, fine lines, fibroblastic depletions and scars.
- Such a medicine is adapted to the treatment of wrinkled and / or aged skin, and aims in particular to prevent and / or reduce the effects.
- the treatment of wrinkles, fine lines, fibroblastic depletions and all scars is done by filling.
- composition according to the invention can be applied to the areas of the face or forehead marked by expression lines.
- the invention also relates to the use of at least one compound chosen from retinoids, their salts and derivatives, and at least one inhibitor of the degradation of hyaluronic acid, or a composition such as previously described for the manufacture of a cosmetic or pharmaceutical composition for use in reconstructive surgery.
- IC50 of GLZ Determination of IC50 of GLZ, with or without pre-incubation at 37 ° C: The GLZ, at different concentrations, is preincubated or not 20 minutes at 37 ° C in the presence of the enzyme. The enzymatic reaction is triggered by adding the hyaluronic acid solution (TO time). After 20 minutes of incubation, the unhydrolysed hyaluronic acid is precipitated by adding the acid solution of bovine albumin.
- the turbidimetry of the solutions is determined spectrophotometrically at a wavelength of 600 nm.
- the optical density (OD) of these solutions is deduced from the OD of a control solution of hyaluronic acid (of the same concentration) not hydrolyzed by the enzyme. This difference in OD, which is inversely proportional to the concentration of hyaluronic acid, is used to measure the activity of hyaluronidase.
- the inhibitory effect of GLZ on bovine hyaluronidase is illustrated in Figure 1 (semi-logarithmic representation).
- the IC50 is 350 ⁇ M.
- composition is prepared in a conventional manner for the person skilled in the art:
- Example 3 Composition No. 2
- Stearic acid 3.00% mixture of glyceryl monostearate and PEG stearate (100 EO) 2.5%
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Molecular Biology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0755026 | 2007-05-11 | ||
| PCT/FR2008/050726 WO2008139124A2 (fr) | 2007-05-11 | 2008-04-22 | Preparations pharmaceutiques ou cosmetiques pour application topique et/ou parenterale, leurs procedes de preparation, et leurs utilisations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2155186A2 true EP2155186A2 (de) | 2010-02-24 |
Family
ID=38786904
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP08788214A Withdrawn EP2155186A2 (de) | 2007-05-11 | 2008-04-22 | Pharmazeutische oder kosmetische präparate zur topischen und/oder parenteralen anwendung, verfahren zu ihrer herstellung und ihre anwendung |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20100298249A1 (de) |
| EP (1) | EP2155186A2 (de) |
| CA (1) | CA2686511A1 (de) |
| WO (1) | WO2008139124A2 (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3278800B1 (de) * | 2010-12-23 | 2019-04-10 | Amazentis SA | Zusammensetzungen und verfahren zur verbesserung der mitochondrienfunktion und behandlung von pathologischen muskulären erkrankungen |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US523139A (en) * | 1894-07-17 | Thread-package | ||
| US4439614A (en) * | 1982-09-22 | 1984-03-27 | Sri International | 5,6-Methano-5,6-dihydroretinoids |
| US4879114A (en) * | 1985-12-20 | 1989-11-07 | Angio-Medical Corporation | Lipids from omentum and methods for cosmetic use |
| WO1994001074A1 (en) * | 1992-07-13 | 1994-01-20 | Shiseido Company, Ltd. | Composition for dermatologic preparation |
| US5723139A (en) * | 1996-09-27 | 1998-03-03 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Skin care compositions containing a polycyclic triterpene carboxylic acid and a retinoid |
| US6008254A (en) * | 1997-05-09 | 1999-12-28 | Kligman; Douglas E. | Method of treating skin disorders with high-strength tretinoin |
| DE19806946A1 (de) * | 1998-02-19 | 1999-09-09 | Beiersdorf Ag | Kosmetische oder dermatologische Wirkstoffkombinationen aus mindestens einer Substanz gewählt aus der Gruppe, bestehend aus Carnitin und den Acylcarnitinen, und mindestens einem Retinoid sowie Zubereitungen mit einem Gehalt an solchen Wirkstoffkombinationen |
| US8093293B2 (en) * | 1998-07-06 | 2012-01-10 | Johnson & Johnson Consumer Companies, Inc. | Methods for treating skin conditions |
| WO2000038647A1 (de) * | 1998-12-23 | 2000-07-06 | Esparma Gmbh | Mittel zum schutz der haut, enthaltend ein aus hyaluronsäure durch hydrolyse hergestelltes fragmentgemisch |
| JP2000212082A (ja) * | 1999-01-26 | 2000-08-02 | Showa Denko Kk | 皮膚用剤 |
| KR100332031B1 (ko) * | 1999-06-03 | 2002-04-10 | 서경배 | 피부 주름의 개선 및 생성 억제 효과를 갖는 외용제 조성물 |
| EP1280508B1 (de) * | 2000-05-05 | 2009-08-12 | Johnson & Johnson Consumer Companies, Inc. | Hautpflegezusammensetzung |
| KR100866671B1 (ko) * | 2000-06-30 | 2008-11-04 | 유니레버 엔.브이. | 피부에 대한 레틴산의 효과를 모방하는 화합물을 함유하는피부 컨디셔닝 조성물 |
| ITMI20020756A1 (it) * | 2002-04-09 | 2003-10-09 | Sinclair Pharma S R L | Composizioni farmaceutiche topiche per il trattamento delle dermatiti |
| JP2005535614A (ja) * | 2002-06-25 | 2005-11-24 | コズメシューティック ソリューションズ プロプライエタリー リミテッド | 局所用美容組成物 |
| FR2894827B1 (fr) * | 2005-12-21 | 2010-10-29 | Galderma Res & Dev | Preparations pharmaceutiques ou cosmetiques pour application topique et/ou parenterale, leurs procedes de preparation,et leurs utilisations |
-
2008
- 2008-04-22 WO PCT/FR2008/050726 patent/WO2008139124A2/fr active Application Filing
- 2008-04-22 EP EP08788214A patent/EP2155186A2/de not_active Withdrawn
- 2008-04-22 US US12/599,645 patent/US20100298249A1/en not_active Abandoned
- 2008-04-22 CA CA002686511A patent/CA2686511A1/fr not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2008139124A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20100298249A1 (en) | 2010-11-25 |
| CA2686511A1 (fr) | 2008-11-20 |
| WO2008139124A2 (fr) | 2008-11-20 |
| WO2008139124A3 (fr) | 2009-02-05 |
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