CA2202339C - Skin care compositions containing melinamide and a retinoid - Google Patents

Abstract

Melinamide in combination with either retinol or retinyl ester resulted in a synergistic enhancement in keratinocyte proliferation. The effects of the retinol or retinyl esters in combination with fatty acid amides were analogous to treatment with retinoic acid.

Description

J6271 (C) SKIN CARE COMPOSITIONS CONTAINING
MELINAMIDE AND A RETINOID
FIELD OF THE INVENTION
The invention relates to skin care compositions containing melinamide and retinol or retinyl ester.
BACKGROUND OF THE INVENTION
Retinol (vitamin A) is an endogenous compound which occurs naturally in the human body and is essential for normal epithelial cell differentiation.
Natural and synthetic vitamin A derivatives have been used extensively in the treatment of a variety of skin disorders and have been used as skin repair or renewal agents.
Retinoic acid has been employed to treat a variety of skin conditions, e.g., acne, wrinkles, psoriasis, age spots and discoloration. See e.g., Vahlquist, A. et al., J. Invest. Dermatol., Vol. 94, Holland D.B. and Cunliffe, W.J. (1990), pp. 496-498;
Ellis, C. N. et al., "Pharmacology of Retinols in Skin", Vasel, Karger, Vol.
3, (1989), pp. 249-252; Lowe, N.J. et al., "Pharmacology of Retinols in Skin", Vol. 3, ( 1989), pp. 240-248; PCT Patent Application No. WO 93/19743. Retinol and retinyl esters, such as retinyl acetate and retinyl palmitate, are easier to formulate/stabilize than retinoic acid. Unfortunately, retinol and retinyl esters are less effective than retinoic acid at providing skin benefits. The present invention is based, in part, on the discovery that a combination of retinol or retinyl esters with melinamide results in a synergistic improvement in keratinocyte proliferation. The effects of J6271 (C) melinamide combined with retinol or a retinyl ester were analogous to the effects of retinoic acid. Thus, a mixture of melinamide with retinol or retinyl esters mimics retinoic acid yet is easier to use than retinoic acid.
Thornfeldt (U.S. Patent No. 5,057,501 October 15, 1991 ) discloses a method for treatment of papulosquamous and eczematous diseases with a composition containing a sesquiterpene compound and from about 0.025% to about 35% of a monocarboxylic fatty acid, ester, or amide. The compositions may also include a retinoid; Thornfeldt teaches that certain retinoids, namely isotretinoin, tretinoin, etretin (all of which are stereoforms of retinoic acid) and etretinate (an ester of trimethoxyphenyl retinoic acid) have proven efficacy against papulosquamous diseases. PCT Application WO/9325177 (Procter and Gamble) discloses compositions for topical application to skin which contain a specific type of acyclic carboxamide coolant and may include retinoids such as retinoic acid and its derivatives (e.g., cis and trans). PCT application WO/9403156 (Rhone Poulenc) discloses a topical composition containing linoleic acid or a derivative as an active ingredient for treatment and prophylaxis of impure skin (e.g.. skin affected by pimples, pustules, or comedones); the composition may also contain 0.025-0.1 wt. ~ of tretinoin. European Patent Application No. 0 275 (Pierre Fabre Cosmetique) discloses compositions for treating seborrhea containing alkyl carboxamide and a zinc salt which may be zinc retinoate.
Klaus et al., (U.S. Patent No. 5,216,148 June 1, 1993) disclose the use of specific complex carboxamides for treating and preventing neoplasms, dermatoses, and aging of skin. Van Scott et al., (U.S. Patent No. 4,380,549 April 19, 1983) and Yu et al., (U.S. Patent No. 4,3b3,815 December 14, 1982) disclose treatment of acne, dry, flaky, scaly skin with a hydroxyacid or the amide thereof. EP 0 582 458 February 9, 1994 discloses use of N,N-( 1,4C alkyl) lauramide.
EP 0 559 304 August 9, 1993 disclose the use of an amide containing a hydrocarbyl chain of at F~-~ ~r ~ fl I

J6271 (C) least 25 carbon atoms as a skin smoothening agent. Beauquey et al., (U.S.
Patent No. 5,308,551 May 3, 1994) disclose a skin washing and conditioning composition containing, among other ingredients, a 1-4C alkanolamide of a 8-16C fatty acid. Great Britain Patent Specification No. 1,126,289 September 5, 1968 (Hoffman-La Roche) discloses a stock vitamin preparation containing vitamin A alcohol or a vitamin A ester, an emulsifier and a solvent which is selected from an alcohol or a dialkyl amide of a monocarboxylic acid (e.g., N,N-diethyl-acetamide, N,N-dimethyl acetamide or N,N-dimethyl formamide). The vitamin preparation has a very high vitamin content, i.e., the minimum concentration is 250,000 I.U. vitamin A/ml. Further, the amides disclosed in the '289 application do not include or mention melinamide.
An earlier filed European Patent Application EP O 742 005 (Unilever; priority date May 8, 1995), published November 13, 1996 (after the priority date of the present application) , discloses combinations fatty acid amides with retinol or retinyl esters. EP '005 however does not teach either melinamide or the general structure of an amide which would cover melinamide, i.e.e a fatty acid amide also containing an aromatic ring.
The art cited above does not disclose skin conditioning compositions based on synergistic combinations of melinamide with retinol or a retinyl ester.
None of the art cited above addresses the need for an effective alternative to retinoic acid.
SUMMARY OF THE INVENTION
The above objects are attained by the present invention which includes, in part, a skin conditioning composition containing:

J6271 (C) (a) from about 0.001 % to about 10% of a retinoid selected from the group consisting of retinol, a retinyl ester, and mixtures thereof;
(b) from about 0.0001 % to about 50% of melinamide; and (c) a cosmetically acceptable vehicle.
The term "conditioning" as used herein means prevention and treatment of dry skin, photodamaged skin, appearance of wrinkles, age spots, aged skin, acne, skin lightening psoriasis, atopic dermatosis, increasing stratum corneum flexibility, and generally increasing the quality of skin. The composition may be used in a cosmetic method to improve skin desquamation and cellular proliferation.
The present invention also includes the use of melinamide in combination with retinol or a retinyl ester for the manufacture of a medicament for the tratment of wrinkled, dry, flaky, aged, photodamaged skin and treating skin disorders (e.g., acne or psoriasis).
The invention further provides a cosmetic method of enhancing keratinocyte proliferation in skin, the method comprising applying to the skin the inventive composition as described above.
The presence of melinamide in the inventive product substantially improves the performance of retinol or a retinyl ester, i.e., melinamide substantially increases the ability of retinol or a retinyl ester to affect cellular proliferation.
Melinamide has no or little effect on improving skin benefit when used alone; a substantial increase in skin benefit is only realized when melinamide is combined with retinol _q_ J6271 ~C) or a retinyl ester. In short, the present invention is based, at least in part, on the discovery of synergistic interaction between retinol or a retinyl ester and melinamide.
In a preferred embodiment of the invention, a retinoid is selected from the group consisting of retinol or a retinyl ester. According to the present invention, by virtue of including an effective amount of melinamide into compositions containing retinol or a retinyl ester, the performance of the compositions is substantially improved. Alternatively, lower levels of retinol or a retinyl ester may be included in the composition containing melinamide to equal the performance of a similar formulation without the amide.
DESCRIPTION OF THE PREFERRED EMBODIMENT
All percentages are by weight of the final composition, unless other wise indicated.
The inventive compositions contain, as a first essential ingredient, a compound selected from the group consisting of retinol and/or a retinyl ester.
The term "retinol" includes the following isomers of retinol: all-trans-retinol, 13-cis-retinol, 1 1-cis-retinol, 9-cis-retinol, 3,4-didehydro-retinol.
Preferred isomers are all-trans-retinol, 13-cis-retinol, 3,4-didehydro-retinol, 9-cis-retinol. Most preferred is all-trans-retinol, due to its wide commercial availability.
Retinyl ester is an ester of retinol. The term "retinol' has been defined above.
Retinyl esters suitable for use in the present invention are C ,-C 3o esters of retinol, J6271 (C) preferably C 2 C 2o esters, and most preferably C 2, C 3, and C ,6 esters because they are more commonly available. Examples of retinyl esters include but are not limited to: retinyl palmitate, retinyl formate, retinyl acetate, retinyl propionate, retinyl butyrate, retinyl valerate, retinyl isovalerate, retinyl hexanoate, retinyl heptanoate, retinyl octanoate, retinyl nonanoate, retinyl decanoate, retinyl undecandate, retinyl laurate, retinyl tridecaroate, retinyl myristate, retinyl pentadecanoate, retinyl heptadeconoate, retinyl stearate, retinyl isostearate, retinyl nonadecanoate, retinyl arachidonate, retinyl behenate, retinyl linoleate, retinyl oleate, retinyl lactate, retinyl glycolate, retinyl hydroxy caprylate, retinyl hydroxy laurate, retinyl tartarate.
The preferred ester for use in the present invention is selected from retinyl palmitate, retinyl acetate and retinyl propionate, because these are the most commercially available and therefore the cheapest. Retinyl linoleate is also preferred, due to its superior efficacy.
The retinoid is employed in the inventive composition in an amount of from about 0.001 % to about 10%, preferably in an amount of from about 0.01 % to about 1 %, most preferably in an amount of from about 0.01 % to about 0.5%.
The second essential ingredient of the inventive compositions is melinamide.
The structure of melinamide is as follows:

J6271 (C) Melinamide is included in the inventive compositions in an amount ranging from about 0.0001 % to about 50%, preferably from about 0.01 % to about 10%, most preferably from about 0.1 % to about 5%.
Cosmetically Acceptable Vehicle The composition according to the invention also comprises a cosmetically acceptable vehicle to act as a dilutant, dispersant or carrier for the TCC in the composition, so as to facilitate its distribution when the composition is applied to the skin.
Vehicles other than or in addition to water can include liquid or solid emollients, solvents, humectants, thickeners and powders. An especially preferred nonaqueous carrier is a polydimethyl siloxane and/or a polydimethyl phenyl siloxane. Silicones of this invention may be those with viscosities ranging anywhere from about 10 to 10,000,000mm2~s(centistokes) at 25°C. Especially desirable are mixtures of low and high viscosity silicones. These silicones are available from the General Electric Company under trademarks Vicasil, SE and SF and from the Dow Corning Company under the 200 and 550 Series. Amounts of silicone which can be utilized in the compositions of this invention range anywhere from 5% to 95%, preferably from 25% to 90% by weight of the composition.
The cosmetically acceptable vehicle will usually form from 5% to 99.9%, preferably from 25~ to 80% by weight of the composition, and can, in the absence of other cosmetic adjuncts, form the balance of the composition.
_g_ J6271 (C) Preferably, the vehicle is at least 80 wt.% water , by weight of the vehicle.
Preferably, water comprises at least 50 wt.% of the inventive composition, most preferably from 60 to 80 wt.%, by weight of the composition.
Optional Skin Benefit Materials and Cosmetic Adjuncts An oil or oily material may be present, together with an emulsifier to provide either a water-in-oil emulsion or an oil-in-water emulsion, depending largely on the average hydrophilic-lipophilic balance (HLB) of the emulsifier employed.
The inventive compositions preferably include sunscreens. Sunscreens include those materials commonly employed to block ultraviolet light.
Illustrative compounds are the derivatives of PABA, cinnamate and salicylate. For example, octyl methoxycinnamate and 2-hydroxy-4-methoxy benzophenone (also known as oxybenzone) can be used. Octyl methoxycinnamate and 2-hydroxy-4-methoxy benzophenone are commercially available under the trademarks, Parsol MCX and Benzophenone-3, respectively. The exact amount of sunscreen employed in the emulsions can vary depending upon the degree of protection desired from the sun's U V radiation.
Another preferred optional ingredient is selected from essential fatty acids (EFAs), i.e., those fatty acids which are essential for the plasma membrane formation of all cells, in keratinocytes EFA deficiency makes cells hyperproliferative. Supplementation of EFA corrects this. EFAs also enhance lipid biosynthesis of epidermis and provide lipids for the barrier formation of the epidermis. The essential fatty acids are preferably chosen from linoleic acid, _g_ ' CA 02202339 1997-04-10 J6271 (C) y-linolenic acid, homo-y-linolenic acid, columbinic acid, eicosa-(n-6,9,13)-trienoic acid, arachidonic acid, y-linolenic acid, timnodonic acid, hexaenoic acid and mixtures thereof.
Yet another preferred optional ingredient is selected from azoles, e.g., climbazole, bifonazole, clotrimazole, ketoconazole, miconazole, econazole, itraconazole, fluconazole, terconazole, butoconazole, sulconazole, lionazole and mixtures thereof. The addition of an azole to the inventive compositions provides further synergistic improvement in skin proliferation benefit. The azole may be included in the inventive compositions in an amount of from 0.001 to 50 wt. %, preferably from 0.001 to 10 wt.%, most preferably from 0.1 to 5%.
Emollients are often incorporated into cosmetic compositions of the present invention. Levels of such emollients may range from about 0.5% to about 50%, preferably between about 5% and 30% by weight of the total composition.
Emollients may be classified under such general chemical categories as esters, fatty acids and alcohols, polyols and hydrocarbons.
Esters may be mono- or di-esters. Acceptable examples of fatty di-esters include dibutyl adipate, diethyl sebacate, diisopropyl dimerate, and dioctyl succinate. Acceptable branched chain fatty esters include 2-ethyl-hexyl myristate, isopropyl stearate and isostearyl palmitate. Acceptable tribasic acid esters include triisopropyl trilinoleate and trilauryl citrate. Acceptable straight chain fatty esters include lauryl palmitate, myristyl lactate, oleyl eurcate and stearyl oleate. Preferred esters include coco-caprylate/caprate (a blend of coco-caprylate and coco-caprate), propylene glycol myristyl ether acetate, diisopropyl adipate and cetyl octanoate.
-lo-J6271 (C) Suitable fatty alcohols and acids include those compounds having from to 20 carbon atoms. Especially preferred are such compounds such as cetyl, myristyl, palmitic and stearyl alcohols and acids.
Among the polyols which may serve as emollients are linear and branched chain alkyl polyhydroxyl compounds. For example, propylene glycol, sorbitol and glycerin are preferred. Also useful may be polymeric polyols such as poly-propylene glycol and polyethylene glycol. Butylene and propylene glycol are also especially preferred as penetration enhancers.
Exemplary hydrocarbons which may serve as emollients are those having hydrocarbon chains anywhere from 12 to 30 carbon atoms. Specific examples include mineral oil, petroleum jelly, squalene and isoparaffins.
Another category of functional ingredients within the cosmetic compositions of the present invention are thickeners. A thickener will usually be present in amounts anywhere from 0.1 to 20% by weight, preferably from about 0.5% to 10%
by weight of the composition. Exemplary thickeners are cross-linked polyacrylate materials available under the trademark Carbopol from the B.F. Goodrich Company. Gums may be employed such as xanthan, carrageenan, gelatin, karaya, pectin and locust beans gum. Under certain circumstances the thickening function may be accomplished by a material also serving as a silicone or emollient. For instance, silicone gums in excess of 10 centistokes and esters such as glycerol stearate have dual functionality.
Powders may be incorporated into the cosmetic composition of the invention. These powders include chalk, talc, Fullers earth, kaolin, starch, smectite clays, chemically modified magnesium aluminum silicate, organically modified J6271 (C) montmorillonite clay, hydrated aluminum silicate, fumed silica, aluminum starch octenyl succinate and mixtures thereof.
Other adjunct minor components may also be incorporated into the cosmetic compositions. These ingredients may include coloring agents, opacifiers and pertumes. Amounts of these other adjunct minor components may range anywhere from 0.001 % up to 20% by weight of the composition.
Use of the Composition The composition according to the invention is intended primarily as a product for topical application to human skin, especially as an agent for conditioning and smoothening the skin, and preventing or reducing the appearance of wrinkled or aged skin.
In use, a small quantity of the composition, for example from 1 to 100m1, is applied to exposed areas of the skin, from a suitable container or applicator and, if necessary, it is then spread over and/or rubbed into the skin using the hand or fingers or a suitable device.
Product Form and Packaging The topical skin treatment composition of the invention can be formulated as a lotion, a cream or a gel. The composition can be packaged in a suitable container to suit its viscosity and intended use by the consumer. For example, a lotion or cream can be packaged in a bottle or a roll-ball applicator, or a J6271 (C) propellant-driven aerosol device or a container fitted with a pump suitable for finger operation. When the composition is a cream, it can simply be stored in a non-deformable bottle or squeeze container, such as a tube or a lidded jar. ll-~e composition may also be included in capsules such as those described in U.S.
Patent 5,063,507 The invention accordingly also provides a closed container containing a cosmetically acceptable compositian as herein defined.
The following specific examples further illustrate the invention, but the invention is not limited thereto.
MATERIALS AND METHODS
Cell Culture:
Human keratinocytes, isolated from neonatal foreskin by trypsin treatment were grown in Dulbecco Modification Eagle (DME) Hams F12 (1:l) medium/10%
fietal calf serum in the presence of irradiated 3T3 mouse fibroblasts for establishing ~~ividing keratinocyte colonies. Cells were grown under the above condition until vrheir second passage and kept frozen for future use. Frozen second passage I;eratinocytes were thawed and plated into the above medium and grown for rive days before they were switched to a serum-free MCDB 153-based medium I;eratinocyte growth medium (KGM) from Clonetics Corporation, San Diego, CA, containing 0.15 mM Ca, or keratinocyte serum-free media (KSFM) from GIBCO
containing 0.09 mM Ca). On day 7; when the cells were 80-90% confluent, they were trypsinized and plated in the serum-free medium for the various experiments.

J6271 (C) Th~rmidine Assay 3H-Thymidine Incorporation and Keratinocyte Proliferation The incorporation of 3 H-thymidine by cultured keratinocytes was used as an assay of keratinocyte proliferation. Thymidine is one of four deoxynucleosides which are the monomeric units of DNA, the universal library of genetic information in the animal kingdom. Prior to cell division of a somatic cell such as a keratinocyte, the complete genome of the cell undergoing cell division is replicated. This involves large scale DNA synthesis by the cell and enables both daughter cells to receive identical copies of the genetic material. When 3 H-thymidine is included in the culture media of keratinocytes which are synthesizing DNA in preparation for cell division then the labelled nucleoside is incorporated into the newly synthesized DNA. The extent of incorporation of 3 H-thymidine into a population of cells is proportional to the rate of DNA
synthesis by this population of cells and therefore an indication of their cellular proliferation.
Keratinocytes (that were cultured as described above) were plated in 24 well plates at a density of 40,000 cells per well in 1 ml media. After incubation for four days or until the cells were 60-70% confluent, the media was changed.
Test compounds were added (in triplicate) to the wells 24 hours after the media change, and four hours later 1 NCi 3H-Thymidine in 50 NI media was added per well. Cells were incubated for a further 24 hours. Media was removed from the cells, 10% ice cold trichloroacetic acid (TCA) added and plates were incubated on ice for 30 minutes. Cells were washed five times with 5% TCA and allowed to dissolve in 500 ~I 0.1 M NaOH for at least one hour (usually overnight). The preparations were neutralized with 0.1 M HCI; 50 NI of the cell preparation was J6271 (C) used to determine total protein content. Disintegrations per minute (DPM) from 3 H labelling of DNA was determined by liquid scintillation counting of 900N1 of the cell preparation. Thymidine incorporation results were expressed as DPM/Ng protein.

Retinoic acid is more effective than retinol at increasingi keratinocyte proliferation A. The effect on incorporation of 3 H-thymidine Ng soluble protein 24 hours after the addition of retinoic acid or retinol at various concentrations was examined. The results that were obtained are summarized in Table 1.

J6271 (C) Effect of Retinoic Acid (RAJI and Retinol (ROH) on Keratinocyte Thymidine Incorporation Treatment mean Thymi~linep value Ys inac~rp.I~tg ~6ntrol 2.5x1E~ 2 5x'i0 2 5x0 M
M M

protein f RAH RtIH ROH
s d (% ~antrai) Control 2094140 (100%)- 0.202 0.501 0.203 2.5x10-'M 2475 116 0.005 0.032 0.004 0.002 RA (118%) 2.5x10-'M 2218 73 ( 0.202 - 0.021 0.005 ROH 106%) 2.5x10$M 2686 72 (128%)0.001 0.001 0.001 0.001 RA

2.5x10$M 2034 46 (97%)0.501 0.021 - 0.121 ROH

2.5x10-9M 2556 80 (122%)0.001 0.006 0.001 0.001 RA

2.5x10-9M 1977 19 (94%)0.203 0.005 0.121 -ROH

n=3 All concentrations of retinoic acid tested, i.e., 2.5 x 10 -' M, 2.5 x 10-$
and 2.5 x 10 -9M, significantly increased keratinocyte proliferation over both the ethanol control and each of the 2.5 x 10 -' M, 2.5 x 10 ~M and 2.5 x 10 -9M retinol treatments and they did so in a dose dependant manner. This is consistent with retinoic acid having a greater stimulatory effect on epithelial proliferation than retinol.

Melinamide and retinol act syrnergistically to enhance keratinoc~~te proliferation The effect on incorporation of 3 H-thymidine/Ng soluble protein 24 hours after Js271 (C) addition of the test compounds was examined and the combined results of three independent experiments were normalized to their respective ethanol controls.
The results that were obtained are summarized in Table 2.

Effect of Retinol and Melinamide on Keratinoc~~te Thymidine Incorlooration mean Thymidine Treatment incorp/Ng proteinvalue value valuevs vs vs vs lU'Mel S-d Cont- 2.sx 2.sx (% COntr01) f01 10' 1Q
RON RA

Control 5176 223 (100%)- - - -2.5x10-BM RA 671 1 402 0.004 o.o2s (130%) 2.5x10$M Retinol 3956 1303 o.~as - o.o2s (76%) 10''M Melinamide 4695 324 (91 o.t - - -%) ~s 2.5x10-8M ROH + 10-'M Melinamide5776 265 (1 o.oao o.m~ o.o2eo.o>
12%) >

n=3 2.5 x 10 -8M retinoic acid significantly increased keratinocyte thymidine incorporation over both the ethanol control and the 2.5 x 10-8M retinol treatment.
10-'M melinamide had no effect on keratinocyte proliferation on its own.
However, the combination of 2.5 x 10-$M retinol + 10-'M melinamide significantly increased keratinocyte proliferation over both the ethanol and the 2.5 x 10 -retinol treatments by 12% and 36~ respectively. Melinamide and retinol therefore, act synergistically to increase keratinocyte proliferation mimicking the stimulatory effect of retinoic acid.

J6271 (C) Melinamide and Retinyl Palmitate S~mergistically Enhanced Keratinocyte Proliferation The effect of melinamide and the retinyl ester (retinyl palmitate) on incorporation of 3H-thymidine was examined. The results that were obtained are summarized in Table 3.

Effect of Retinyl Palmitate I(RP) and Melinamide on Keratinocyte Thymidine Incorporation mean Thymidine Treatment incofp/Ng proteinvalue valuevs value vs vs 2.5x vs Cant- 2.5x l U' 1 Q' RA

(% COntf01) rol 10' Mel RP

Control 5498 484 (100%)- - - -2.5x10-'M RA 7795 370 (142%)o.ooa o.oot- -2.5x10-'M Retinyl palmitate5746 1 13 0.436 - o.oot -(104%) 10-'M Melinamide 4635 608 (84%)o.tv - - -2.5x10-'M ROH + 10-'M Melinamide6395 286 (1 o.oso 0.0220.00 o.oto 16%) n=3 2.5 x 10 -'M retinoic acid significantly increased keratinocyte thymidine incorporation over both the ethanol control and the 2.5 x 10-'M retinyl palmitate J6271 (C) treatment. 10 -'M melinamide had no effect on keratinocyte proliferation on its own. However, the combination of 2.5 x 10 -'M retinyl palmitate + 10 -'M
melinamide significantly increased keratinocyte proliferation over both the ethanol (by 16%j and the 2.5 x 10 -'M retinyl palmitate control treatments (by 12%).
Melinamide and retinyl palmitate therefore, act synergistically to increase keratinocyte proliferation mimicking the stimulatory effect of retinoic acid.
Examples 1-3 demonstrate that retinoic acid, in a dose dependent manner, increased thymidine incorporation in skin keratinocytes. In other words retinoic acid increased keratinocyte proliferation. In Examples 1-3, retinoic acid was used as positive control and reference compound against which the other compounds under analysis were compared. Retinol was completely ineffective at increasing keratinocyte proliferation.
The unexpected results of Examples 1-3, however, were that the effect of retinol on cultured keratinocytes can be enhanced to levels approaching those of retinoic acid by combining retinol or retinyl ester with melinamide - a compound which exerts little or no benefit on its own. The results documented above demonstrate that melinamide acts synergistically with retinol or retinyl ester, to increase keratinocyte proliferation, mimicking the effect of retinoic acid.
Examples 4-9 illustrate topical compositions according to the present invention. The compositions can be processed in conventional manner. They are suitable for cosmetic use. In particular the compositions are suitable for application to wrinkled, rough, dry, flaky, aged and/or UV-damaged skin to improve the appearance and the feel thereof as well as for application to healthy skin to prevent or retard deterioration thereof.

J6271 (C) This example illustrates a high internal phase water-in-oil emulsion incorporating the inventive composition.
wlw Retinol 0.5 Fully hydrogenated coconut 3.9 oil Melinamide 5 Brij 92* 5 Bentone 38 0.5 MgS047H20 0.3 Butylated hydroxy toluene 0.01 Perfume qs Water to 100 * Brij 92 is polyoxyethylene (2) oleyl ether J6271 (C) This example illustrates an oil-in-water cream incorporating the inventive composition.
wiw Retinyl linoleate 0.15 Mineral oil 4 Melinamide 1 Brij 56* 4 Alfol 16RD* 4 Triethanolamine 0.75 Butane-1,3-diol 3 Xanthan gum 0.3 Perfume qs Butylated hydroxy toluene 0.01 Water to 100 * Brij 56 is cetyl alcohol POE (10) Alfol 16RD is cetyl alcohol J6271(C) This example illustrates an alcoholic lotion incorporating the composition according to the invention.
Q~a llii~illl Retinyl palmitate 0.15 Melinamide 0.1 Ethanol 40 Pertume qs Butylated hydroxy toluene 0.01 Water to 100 J6271 (C) This example illustrates another alcoholic lotion containing the inventive composition.
t wlw Retinol 0.15 Melinamide 0.1 Ethanol 40 Antioxidant 0.1 Perfume qs Water to 100 J6271 (C) This example illustrates a suncare cream incorporating the composition of the invention:
fo WIW '' l Retinol 0.01 Melinamide 0.1 Silicone oil 200 cts 7.5 Glycerylmonostearate 3 Cetosteryl alcohol 1.b Polyoxyethylene-(20)-cetyl alcohol 1.4 Xanthan gum 0.5 ;, Parsol 1789TM ~ , 1.5 Octyl methoxycinnate (I'ARSUL. Mt'X~e"1.),a Perfume qs Color qs Water to 100 J6271 (C) This example illustrates a non-aqueous skin care composition incorporating the inventive combination.
1a uulw Retinyl acetate 0.15 Melinamide 1 Silicone gum SE-30' 10 Silicone fluid 3452 20 Silicone fluid 3443 55.79 Squalene 10 Linoleic acid 0.01 Cholesterol 0.03 2-hydroxy-n-octanoic acid 0.7 Vitamin E linoleate 0.5 Herbal oil 0.5 Ethanol 2 ' A dimethyl silicone polymer having a molecular weight of at least 50,000 and a viscosity of at least 10,000 ceritistokes at 25°C, available from GEC
Dimethyl siloxane cyclic pentamer, available from Dow Corning Corp.
3 Dimethyl siloxane tetramer, available from Dow Corning Corp.

Claims (7)

1. A skin conditioning composition comprising (a) from 0.001 % to about 10% of a compound selected from the group consisting of retinol, a retinyl ester, and mixtures thereof;
(b) from 0.0001 % to about 50 % of melinamide; and (c) a cosmetically acceptable vehicle.

2. The composition of claim 1 wherein the retinyl ester is selected from the group consisting of retinyl linoleate, retinyl palmitate, retinyl acetate, retinyl propionate, and mixtures thereof.

3. The composition of claim 1 wherein ingredient (a) is retinol.

4. The composition of claim 1 wherein ingredient (a) is a retinyl ester.

5. A cosmetic non-therapeutic method of conditioning skin, the method comprising applying topically to skin the composition according to any one of claims 1-4.

6. Use of a composition according to any one of claims 1-4 in the manufacture of a medicament for treating the appearance of wrinkled, dry, rough, flaky, aged, or photodamaged skin and for treating skin disorders.

7. Use of a composition according to any one of claims 1-4 in the manufacture of a medicament for mimicking the effect on skin of retinoic acid.