NZ210943A - Dehydroepiandrosterone compositons for skin treatment - Google Patents

Description

2109 ' M iiii Priority Date{s): c— , Pi. r- Prcri.'ication Filed: Class: (£AUJ.

Publication Date: . ^ " MR J992 P.O. Journal,-No: JAN 1985 received No. Dale.

NEW ZfcALAN!) PATtNTS AIT. 195.1 COMFU TF SPECIFICATION TOPICAL COMPOSITIONS FOR PREVENTING OR TREATING DRY SKIN i/We, NORMAN OREnTREICH, AN American citizen of 140 E. 72nd Street. New York, New York 10021, U.S.A. hereby declare the invention for which I / we pray that a patent may be granted to me/us, and the method by which it is to be performed, to be particularly described in and by the following statement:- - 1 - (followed by page -la-} n 1 ■ L s •< TOPICAL ffiftPC&I5UX)H£LJXiE-.PREKEmNfiLI>R- TitfATIlUL£IUr_SlIU PieljL i?i_ Jny^r-.tijQii The present invention relates to compositions for preventing and/or treating dry skin and loss of natural oiliness by the external application of effective dosages of the free alcohol of dehydroepiandrosterone (DHEA) or its derivatives, for example* acetate, in suitable vehicles. DHEA compositions which are particularly useful for dry skin patients who are susceptible to acne-like lesions when the production of sebum in the skin is increased also contain a keratolytic agent.

Ej.cJkgjc.aj;p,d-_&f ir-y-ent i on Almost all menopausal and post-menopausal women, many women over thirty-five, and most women over forty years of age, and some older men frequently complain that the natural oiliness of their skir. is markedly diminished.

A paper entitled "The Effect of Aging on the Activity of the Sebaceous Gland in Man" by Pochi. P.E. and Strauss, J.S. that was published in Advances in Biology of Skin, Vol VI: Aging, edited by Kontagna, W., Pergamon Press, N.Y. (1965), described the reduction in mean sebum (oil) secretion in males and females in relation to advancing age. Figure 1 herein illustrates this reduction in mean sebum production with aging.

- Iq - • . 3 Testosterone therapy increases skin oil production in menopausal and post-menopausal women. However, it produces unwanted superfluous facial and body hair and other systemic masculinizing side effects and is therefore rarely used.

Dehydroepiandrosterone (DHEA) is a steroid. It and its sulfate are secreted by the adrenal glands, circulate in the bloodstream, and are excreted in urine as derivatives of DHEA.

As shown in Figure 2, dehydroepiandrosterone sulfate levels in the blood have been shown to reach a peak in early adult life and then gradually decline with advancing age (Orentreich Foundation for the Advancement of Science, Inc., Annual Report, 1979).

The structure for DHEA is as follows: In as study entitled "Biological Activity of Dehydroepiandrosterone Sulfate in Man" by Drucker, W.D., Blumberg, A.M., Gandy, B.M., David, R.R., and Verde, A.L., that was published in the Journal of Clinical Endocrinology and Metabolism. 35: 4 8-54 (1972), sebum production was used as a measure of androgenic activity associated with the oral administration of dehydroepiandrosterone sulfate. Drucker et al., however, did not address 2 the probleir of dry skin in normal older women and some cider men. Indeed, the experiments of Drucker et al. were conducted with five abnormal, androger.-def icient, hypogonadal males, ages 15, 20, 30, 34, and 35, and a three-month-old female with 21-trisomy syndrome.

In U.S. Patent 4,005,200, a new use of dehydroepiandrosterone sulfate as a parturient canal conditioning agent was disclosed. Patent 4,005,200 describes systemic administration of dehydroepiandrosterone sulfate to a pregnant female during the 37th to 39th week of pregnancy to improve the maturity of the parturient canal and the sensibility of the uterine musculature to oxytocin. Patent 4,005,200 mentions that it had been proposed to use dehyroepiandrosterone sulfate clinically in combination with estrogens in the treatment of various syndromes assoicated with climacterium, but the problem of skin dryness was not addressed in this patent.

In recent articles (January 17, 1982 edition of Science JSfiKJS, "Antiobesity Drug Kay Counter Cancer, Acing"; January 22, 1981 edition of the £lii£.as£> JxiiPJiJie, "Amazing New Drug That May Lead to Longer Life", Kotulak, P.), uses of DHEA and analogs thereof were described to counter obesity and prevent cancer. These articles did not, however, address the problem of skin dryness.

I previously discovered a method for treating dry skin in humans by internally administering an effective dosage of the alcohol and/or one or more salts of DHEA. This treatment is particularly useful in treating dry skin in menopausal women. 3 m 2109^3 This treatrent car. alsrc be employed tc treat prerrenopausal females vith a low endogenous DHEA production. Furthermore, males who suffer from dry skin due to low plasma levels of testosterone and/or DHEA and its sulfate can be treated in accordance with my previous invention.

Menopausal and post-menopausal and other older women usually have a distinct reduction in dehydroepiandrosterone sulfate levels in the blood which is generally accompanied by a reduction in the oil production of the skin and results in dryness of the skin. Such dry skin problems generally affect the entire body. The face and head, however, have the highest population of sebaceous glands and therefore those areas are the most vulnerable to these problems. I previously found that the internal adminstration of the alcohol or one or more salts of DHEA increases the blood level of DHEA and its sulfate and reduces skin dryness. The reduction of activity of sebaceous glands with aging and at the onset of menopause is reversed by the internal administration of dehydroepiandrosterone alcohol or dehydroepiandrosterone sulfate.

Xeroderma, i.e., dry skin, can be caused by a multiplicity of factors and can be aided by the use of exogenous and water retentive products. I previously found that internal adminstration of dehydroepiandrosterone alcohol or dehydroepiandrosterone sulfate increases the endogenous production and secretion of natural sebum and enhances the water protective barrier of the skin, thus acting as a natural moisturizer.

Oral ingestion or other systemic administration of DHEA or its derivatives results in an increase in oil production by 4 all sebaceous elands ever the entire tody, an effect that is frequently undesirable or unnecessary. The present invention permits obtaining the above-described desirable effects on a localized basis, only at the places vhere such effects are desired or necessary.

Surjr.aiA'_ _c£. I nYeniiCLn There have now been discovered compositions for treating dry skin in a patient which involves topically administering to the area of dry skin on the patient a topical vehicle containing an effective amount of DHEA and/or a pharmaceutical^' acceptable, therapeutically effective derivative thereof. One such derivative of DHEA is the acetate derivative. Other non-liir iting derivatives which may be utilized in this invention include valerate, enanthate, and fatty acid ester derivatives.

For patients who have a genetic tendency for acne, the topical compositions of the invention comprise DHEA and/or a pharmaceutical!}* acceptable, therapeutically effective derivative or analog thereof; a keratolytic agent; and a non-toxic, deriratolocical ly pcc^ptahle "ehicle. The DHEA end'or derivative thereof is present in an amount which is effective to increase sebum production, while the keratolytic agent is present in an amount sufficient to counteract the formation of acne-like skin lesions without diminishing the effectiveness of DHEA or its derivative.

The preferred keratolytic agents are selected from hydroxybenzoic acids, alpha-hydroxycarboxylic acids and urea. Ortho-hydroxybenzoic acid (salicylic acid) is particularly preferred. The vehicle rcsv be cnv of a wide varietv of o < ^ ^ '-0943 l^referably non-drying preparations such as tinctures, creams, ointments, gels and lotions.

Accordingly in one aspect of the invention a topical composition for treating dry skin in a patient comprising: (a) dehydroepiandrosterone and/or pharmaceutically acceptable, therapeutically effective derivative thereof in an amount effective to increase sebum production. (b) a keratolytic agent in an amount sufficient to counteract the formation of acne-like skin lesions without diminishing the effectiveness of dehydroepiandrosterone or its derivative, and (c) a non-toxic, dermatologica1ly acceptable vehicle..

In a further aspect the present invention consists in a topical composition for treating dry skin in a patient comprising: (a.) dehydroepiandrosterone and/or pharmaceutically acceptable, l I £ ^ therapeutically effective derivative thereof in an amount effective So incr/a; / ' . sebum production; and ^ JA ' (b) a non-toxic, dermatologically acceptable vehicle, said ^ '•'992 dehydroepiandrosterone and/or derivative thereof being present in which is sufficient to increase sebum production to an exteW.^yfJicient to reduce or retard dryness of the skin, but said amount being sucTT^n^-^****^-.- - "X w substantially no undesirable effects are caused locally or systemically, said amount being in the range of 0.01 to 1.0 weight percent of the composition.

In still a further aspect the invention consists in the use of dehydroepiandrosterone and/or a pharmaceutically acceptable, therapeutically effective derivative thereof in the preparation of a topical composition for treating dry skin in a patient, said composition comprising: (i) dehydroepiandrosterone and/or a pharmaceutically acceptable, therapeutically effective derivative thereof in an amount effective to increase sebum production; and (ii) a non-toxic, dermatologically acceptable vehicle.

In yet another aspect of the present invention consists in a method of treating skin on a non-human mammal to enhance sebum production available to the skin * , no- comprising topically administering to the skin a composition of the present invent, ion. ii£ii_af_±b£. Pre fleas For the purpose cf illustrating the invention, there are provided in the cravings forms which are presently preferred; it teir.g understood, however, that this invention is net limited to the precise arrangements anc instrumentalities shewn.

Figure 1 is a graph demonstrating the reduction ir. mean sebum (oil) secretion in males anc females in relation to advancing ace.

Figure 2 is a graph of dehydroepiencrcsterone sulfate levels in the blccc as a function of age.

Figure 3 is a pair of bar plots depicting the change in the sice of the setaceous clancs of an animal after treatment according tc this invention and with various androgens.

Figure 4 is a bar graph comparing DHEA at two different dosages causing equivalent responses as certain doses of testosterone ap.c cihvdrotestosterone, respectively.

Figure 5 is a plot of the mean size of the sebaceous gland of the animal ears treated with DHEA in a gel, untreated ears and control animals treated with the gel without DHEA all varying as a function of time. t ailgj3_i?^.s^xlpli^xi_x>f_i:ii e_lpygr..t j g n The sebum excretion rate in animal skin, particularly human skin, may be increased by the topical application of DHEA, either in the form cf the free alcohol or in the fcrm cf one or more of the analogs or derivatives of DHEA, e.g., the acetate, if o 6 a A; 23 A UGI988Z 2109 43 valerate, enanthate, and fatty acid ester derivatives. As used hereafter in this application unless indicated otherwise, any reference to DHEA will be understood to refer to DHEA ana/or derivatives or analogs thereof. The free alcohol form of DHEA is preferred.

Typical formulations contain about 1 weight percent DHEA based on the total weight of the formulation, as that amount was found to be effective when topically applied to the area of dry skin to increase the sebum production rate and thereby reduce or retard dryness of the skin. Such topical applications were found to be essentially local in effect with substantially no systemic effect or undesirable side effects.

It has been found, however, that there are concentrations at which DHEA is used in treating dry skin such that the increase in sebum has been accompanied by or associated with the formation of acne-like skin lesions in people who have the genetic tendency for acne. Conventional over-the-counter preparations for treating acne generally act as drying agents and exfoliatois, which ate generally irritating to the skin and counterproductive to the general treatment of dry skin. According, it would be advantageous to have a composition which could counteract the formation of acne-like skin lesions without diminishing the effectiveness of DHEA in improving the sebaceous gland activity of the skin.

For patients who have a cenetic tendency for acne, effective formulations may contain about 0.01 to 1.0 weight percent DHEA, typically about 1 weight percent. It has been 7 210943 found that DHEA concentrations on the order of about 0.1 weight percent of the formulations are as effective as the abcve DHEA formulations in sebum production while preventing the side effect of acne-like skin lesions in certain patients. Concentrations above about 1.0 weight percent DHEA could be used but produce no significant increased effect and are therefore wasteful.

DHEA has been found to be so potent in increasirg sebum production that acne is caused in patients who have the genetic tendency to such conditions. That is, the increased sebum was found to form the hardened plugs which clog the pores and cause the formation of cysts which are characteristic of acne and acnelike conditions. The incorporation of a keratolytic agent in the compositions of the present invention was found to substantially prevent the occurence of such conditions.

The keratolytic agents used in the formulations and methods of the present invention may include hydroxybenzoic acids, including ortho, meta or para hydroxybenzoic acids; alpha-hydroxycarboxylic acids, such as glycolic, tartaric, lactic or mandelic acids; or urea. Particularly preferred according to the invention is ortho-hydrcxybenzoic acid (salicylic acid), which is a known exfoliator in topical over-the-counter acne treatment preparations, as well as being used in topical preparations for the treatment of warts, corns, calluses, seborrheic disorders, etc.

It has been reported that alpha-hydroxycarboxyclic acids such as glycolic, tartaric, lactic and mandelic acid have been reported in the literature to be effect keratolytic agents. See e.g., E.J. Van Scott and R.J. Yu, "Substances that Modify the 8 2 1094 Stratum Corneum by Modulating its Formation", Chapter 10 of edited by Philip Frost and Stephen N. Horwitz. Moreover, salicylic acid (ortho-hydroxybenzcic acid) is a known keratolyic agent present in an amount of about 2 percent by weight in over-the-counter preparations such as "PERKOX", "FOSTEX" and "FOSTKIL", used in the treatment of acne. However, these known exfoliators have not to applicant's knowledge been used in preparations to prevent acne formation.

When salicylic acid is used as the keratolytic agent in the formulations of the invention, it is preferably present in the amount of about 0.1 to 2 percent by weight. Other keratolytic agents, which are not as strong as salicyclic acid, maybe used in the formulations of the invention in concentrations of about 0.1 to 10 percent by weight of the formulation. The exact concentration of keratolytic agent to be used in the invention will vary somewhat depending upon the particular form of dosage chosen, e.g., ointment, cream, loticn, etc., but may be determined by one of orciinarv skill in the art with a niinimiun; of experimentation.

As demonstrated in the specific examples below the compositions of the present invention may contain conventional vehicle ingredients to form lotions, tinctures, creams, gels or ointments which are non-toxic and dermatologically acceptable. In addition to these and other vehicles which will be obvious to those of ordinary skill in the art, it will be understood that the compositions of the present invention may include other 9 ^ " a 9 4 3 ingredient? such as hydrocortisone rcisturizers, benzoyl peroxide, antibiotics, etc.

Tc perr.it quantitative evaluation of the effectiveness and degree of localization of the topical application of various amounts of the free alcohol form cf DHEA and its derivatives, e.g., acetate, an animal model (harr.sters) was chcsen that would permit direct examination and quantitation of the size of sebaceous glands as a function of the treatment according to this invention. The use of a hamster ear for sebaceous gland testing was described by Flewig, G. and Luderschmidt, "Hamster Ear Model for Sebaceous Glands", JDuiD3l_rf_lEy££iisa£i¥£_I£xir.5Lfc.P.l.e.ai, 68: 171-176 (1977).

Hamster sebaceous glands have been used by numerous medical researchers as an effective and medically accepted animal model for the evaluation of pharmacological products and are directly translatable to their use on human subjects. This model has the advantage of reacting to androgens, estrogens, and other hormones and steroid formulations in a manner closely related to those experienced in the treatment of human beings.

Sebaceous gland cells grow in size as they fill with sebum until they reach full maturity at which point they break open and release their sebum to the surface of the skin. Measurement of sebaceous gland size is thus an effective indicator of the amount of sebum (oil) that is delivered to the surface of the skin. Large glands produce large amounts of sebum, while small glands produce small amounts, thus large glands are associated with oily skin; small glands with dry skin. Hamster ears have sebaceous glands which are readily treatable 21094 and easily measured. Accordingly, tests were conducted in which one ear of the hamster was treated with DHEA and/or a pharmaceutically acceptable, therapeutically effective derivative thereof in a suitable base vehicle while the contralateral ear (the control) was treated with the same base vehicle without the DHEA, and the resultant changes in the gland size of the e£.r treated with DHEA and the control animal ear vere compared.

When the effect of treatment is systemic, both ears will be affected and significant gland size changes will occur on both ears. It is preferred during testing to have a response at the site of application only, e.g., no systemic effect from local application.

The treatment according to this invention was also compared to other known treatments (use of androgens such as testosterone) to produce sebaceous gland enlargement. These other treatments are generally not usable because of their undesirable side effects and systemic action. In the tests used for evaluation, hamsters were treated on one ear with 1% by weight of the free alcohol form of DHEA in 50 microliters of a suitable vehicle and on the other ear with 50 microliters of the vehicle alone. Similar applications of 1% by weight of various androgens in the same vehicle on other hamsters were used for comparison. A total of 149 hamsters were used to insure statistical validity. Both gel and tincture vehicles were used.

Figure 3 shows a bar plot of the increase in the size of the sebaceous glands of between about 6 and 10 hamsters per group after treatment with the free alcohol form cf DHEA and with 11 7 109 4 various ether androgens. The outer tar in each instance is the ratio of the mean size of sebaceous elands of the treated hamster ear to the mean size of the sebaceous glands of the ears of control hamsters. The inner bar is the ratio of the mean size of sebaceous elands of the untreated contralateral ear of treated hamsters to the mean size of the sebaceous elands of the ears of control hamsters. The scale is on the left of the plot.

It can be seen from Figure 3, that all the androgens tested produced statistically significant systemic effects as measured by the increase of the gland sizes of the contralateral ear (inner bar), while DHEA had no statistically significant systemic effects. In these tests the hamsters were treated once per day for five days a week for two weeks with 50 microliters of a 1% solution (weight/volume) in a tincture vehicle.

Figure 3 shows the statistically insignificant systemic effect of DHEA compared to the other androgens tested. The curve interconnecting the points in the center of each bar is a plot of the systemic effect as a percent of contralateral untreated ear sebaceous gland size versus the sebaceous gland size of the treated ear. The percentage scale is on the right side of the plot; no systemic effect is at the bottom of the araph corres- ■"*» J ponding to no increase on the contralateral side and 100% systemic effect is at the top. As is shown, the systemic effect of DHEA was about 15% (statistically insignificant) whereas all the other androgens tested had systemic effects in excess of 50%.

Figure 4 shows a bar graph comparing DHEA at 1% weight/volume in a tincture vehicle to a dose of testosterone ("testo") (0.1%) causing an equivalent response and dehydroepi- 12 m / androsterone at 5% weight/volume to a dose of dihydrotestosterone ("DHT") (0.1%) causing an approximately equivalent response. Treatment was once per day for five days a week for two weeks. All values represent the ratio of the mean size of sebaceous glands of treated hamsters to the mean size of sebaceous glands of control hamsters. The outer and inner bars are defined as set forth above for Figure 3. The scale is on the left of the plot. Only DHEA showed unilateral performance. The curve (as in Figure 3 and with its scale on the right) shows the systemic effect of DHEA as less than 10% (statistically insignificant), whereas testosterone and dihydrotestosterone have systemic effects of over 80%.

Figure 5 shows a plot of the mean size of sebaceous glands of ears treated once per day for five days a week with DHEA (1% weight/volume) in a gel vehicle, untreated contralateral ears of the same hamsters (designated as contralateral), and control hamsters treated with the gel vehicle without any DHEA (designated as gel), as a function of the time of treatment. The plot shows that two weeks of treatment produced equilibrium and that the effect on the contralateral ears' sebaceous glands was 1 negligible.

The invention will now be described in further detail by reference to the following specific, non-limiting examples.

Examples 1-4 These examples concern the preparation of a tincture, topical cream, topical ointment and topical gel, respectively, using vehicles previously used in other preparations and 13 2 109 reforirulcted to optiir.ize the efficacy of the DHEA. The formulations for these preparations are given in the Table I hereinbelcw. ■a 14 210943 TABULJ. J3.e^'^.rcj_ijji_aj:jo.£.tej:cAe. _ FDiUj;l£ti.Ciis Example Example Example Example MA._1 ilD-*. 2 Jia._3 Ingredients Topical Topical Topical Topical Tincture Cream/Lotion Ointment Gel ib'/M. S v/v 1 v/x %V/K_ alcohol 1. DHEA acetate 1.0 1.0 1.0 1.0 valerate, etc any fatty acid ester 2. Methyl Faraben NF .01 3. Propyl Paraben NF .01 4. Hydroxy Propyl Cellulose (1) 1.0 . PPG-12-Buteth-16 (2) 2.0 6. Squalane (3) 2.0 7. Glyceryl Konostearate NF 2.0 8. Stearyl Alcohol NF 2.8 9. Cetyl Alcohol NF 4.2 . Polyethylene Glycol Cetyl Ether (4) 5.0 11. Mineral Oil NF 5.0 12. Butylene Glycol 4.0 12.0 4.0 13. Petrolatum USP 5.4 85.0 14. Alcohol (5) 89.0 47.0 . Water 6.0 45.0 100.0 100.0 100.0 100.0 Notes: (1) available under the trademark KLUCEL from Hercules (2) available under the trademark UCON fluid 50HB from Union Carbide (3) available under the trademark ROBANE from Robeco (4) available under the trademark BRIG 58 from ICI (5) contains 95% ethanol and 5% water i\2LaRFJ-«-- Butylene clycol and water were mixed and dissolved into alcohol. The resultant vehicle mixture anc DHEA were irixed and dissolved. The resultant formulation was a tincture.

In this example a topical cream was prepared by first mixing and melting squalane, stearyl alcohol NF, cetyl alcohol, polyethylene glycol cetyl ether, mineral oil NF and petrolatum USP, at 70 degrees C. A second mixture was formed by mixing and dissolving methyl paraben NF and propyl paraben NF in water, at 70 degrees C. The second mixture was slowly added to and mixed with the first mixture to form an emulsion. DHEA was dispersed in the resultant emulsion at 50 degrees C. The resultant composition was slowly cooled with mixing until the composition reached room temperature.

Example No. 3 In this example a topical ointment was prepared. As a first step, glyceryl monostearate was mixed and melted in petrolatum USP at 70 degrees C. As a second step, DHEA was mixed and dissolved in butylene glycol at 70 degrees C. The resultant composition of step 2 was slowly added to the resultant composition of step 1, with mixing. This mixture was then cooled to its congealing point with mixing and then cooled to room temperature without mixing. 16 2 1094 EjCiUOPijL 4_ In this example a topical gel was prepared. As a first step, hydroxy propyl cellulose was hydrated and dissolved into water. As a second step, DHEA, butylene glycol ana PPG-12-Buteth-16 was dissolved in alcohol. Slowly the resultant mixture of step 2 was added into the resultant mixture of step 1 with mixing until a gel formed.

The following specific, non-limiting examples concern the preparation of a topical lotion, topical cream, topical ointment and topical gel, respectively, using vehicles previously used in other preparations and reformulated to optimize the efficacy of the DHEA and keratolytic agent. The formulations for these preparations are given in Table II hereinbelow.

Propylene glycol and water were mixed and dissolved into alcohol. The resultant vehicle mixture, salicylic acid and DHEA were mixed and dissolved. The resultant formulation was a topical lotion or tincture.

£* HP. 6 In this example a topical cream was prepared by first mixing and melting propylparaben, stearic acid, cetyl alcohol, glyceryl monostearate, lanolin oil, mineral oil and sesame oil at 70 degrees C. A second mixture was formed by mixing and dissolving methylparaben, triethanolamine and propylene glycol in water at 70 degrees C. The second mixture was slowly added to and mixed with the first mixture to form an emulsion. DHEA, 17 u salicylic acid and Carbomer 940 were dispersed in the resultant emulsion at 50 degrees C. The resultant composition was slowly cooled with mixing until the composition reached room temperature .

J&KAFjpjjeL Jto. 7 In this example a topical ointment was prepared. As a first step, glyceryl monostearate was mixed and melted in petrolatum at 70 degrees C. As a second step, DHEA and salicylic acid were mixed and dissolved in propylene glycol at 70 degrees C. The resultant composition of step 2 was slowly added to the resultant composition of step 1, with mixing. This mixture was then cooled to room temperature without mixing.

Hj^jupl.e. .No.,- 8 In this example a topical gel was prepared. As a first step, hydroxy propyl cellulose was hydrated and dissolved into water. As a second step, DHEA, salicylc acid, butylene glycol and PPG-12-Buteth-16 were dissolved in alcohol. Slowly the resultant mixture of step 2 was added into the resultant mixture of step 1 with mixing until a gel formed. 18 2109 43 Pi)£A_ r. ^iirylic. Ac isL FoiEuJ..aii j?hs_ Example No. 5 Example No. 6 Example No. 7 Example No. 8 Topical Lotion Topical Cream Topical Oint. Topical Gel 1-K/.K i-KZw ±y/x IvJv Actives DHEA (free alcohol) 1.0 1.0 1.0 1.0 Salicylic acid 1.0 1.0 1.0 1.0 IHiL£LtiiL£5 Methylparaben 0.1 Propylparaben 0.1 0.1 Hydroxy propyl cellulose (1) 1.0 PPG-12-Buteth-16 (2) 2.0 Lanolin oil 5.0 Mineral oil 4.0 Sesame oil 4.0 Cetyl alcohol 5.0 Glyceryl monostearate 2.0 3.0 Stearic acid 2.0 Tr lethanolair.ine 1.0 0.2 Propylene glycol 5.0 5.0 12.0 5.0 Alcohol (3) 87.0 45.0 Carbomer 940 (4) 0.1 0.2 Petrolatum 82.9 Water 6.0 _6iL2_ ! 100.0 100.0 100.0 100.0 Notes: (1) available under the trademark KLUCEL from Hercules (2) available under the trademark UCON fluid 50 HB from Union Carbide (3) contains 95% ethanol and 5% water (4) available under the trademark CARBOPOL 940 from B.F. Goodrich 19 21094-3 It will be recognized by those skilled in the art that changes may be made to the above-described embodiments of the invention without departing from the broad inventive concepts thereof. It is understood, therefore, that this invention is not limited to the particular embodiments disclosed, but it is intended to cover all modifications which are within the scope and spirit of the invention as defined by the appended claims. •210" :J

Claims (13)

WHAT WE CLAIM IS:

1. A topical composition for treating dry skin in a patient comprising: acceptable, therapeutically effective derivative thereof in an amount effective to increase sebum production; the formation of acne-like skin lesions without diminishing the effectiveness of dehydroepiandrosterone or its derivative, and

2. A composition according to Claim 1 wherein said keratolytic agent is selected from the group consisting of hydroxybenzoic acids, alpha-hydroxycarboxylic acids and urea.

3. A composition according to Claim 2 wherein said alpha-hydroxycarboxylic acid is selected from the group consisting of glycolic, tartaric, lactic and mandelic acids.

U. A composition according to Claim 3 wherein said keratolytic agent is present in an amount of 0.1 to 10 weight percent of the composition.

5. A composition according to Claim 2 wherein said keratolytic agent is salicylic acid.

6. A composition according to Claim 5 wherein said salicylic acid is present in an amount of 0.1 to 2 weight percent of the composition.

7. A composition according to Claim 1 wherein said dehydroepiandrosterone and/or derivative thereof is present in an amount of 0.01 to 1.0 weight percent of the composition.

8. A composition according to Claim 2 wherein dehydroepiandrosterone free alcohol is present in an amount of about 1.0 weight percent and said (a) dehydroepiandrosterone and/or a pharmaceutically (b) a keratolytic agent in an amount sufficient to counteract (c) a non-toxic, dermatologii.-ally acceptable vehicle. r 2 3 AUG 1988 -21- 094 3 " keratolytic ag»r>.: is salicylic acid present, in an amount of about 1.0 weight percent of the compos it ior..

9. A composition according to Claim 1 wherein said dehydroepiandrosterone is in the form cf the free alcohol or a derivative selected from the group consisting of acetate, enar.thate, valerate and fatty acid esters.

10. A composition fccordir.g to any one of the preceding claims wherein said vehicle is selected from the group consisting of tinctures, creams, ointments, gels and lotions.

11. A composition cf claim 10 when in the form of a gel.

12. A composition as claimed in any one of claims 1 to 11 substantially as hereinbefore desribed.

13. A topical composition for treating dry skin in a patient comprising: a. dehydroepiandrosterone and/or pharmaceutically acceptable, therapeutically effective derivative thereof in an amount effective to increase sebum production; and b. a r.on-toxic , dermatologically acceptable vehicle, said dehydroepiandrosteror.e anc/or derivative thereof being present in an amount which is sufficient to increase sebum production to an extent sufficient to reduce or retard dryness of the skin, but said amount being such that substantially no undesirable effects are caused locally or systemically, said amount being in the range of 0.01 to 1.0 weight percent of the composition. I*- A method of treating skin on a non-human mammal to enhance sebum production available to the skin comprising topically administering to the skin a composition as claimed in any one of claim 1 to 13.;^ D . " - ^ ^ I2nj f i.V,' ~;..v. C'.' C: 30'i;P L • 1 sf/ty;Ai jI .5 F,;r THE APPLICANTS*