NZ200179A - Non-yellowing topical pharmaceutical compositions containing tetracyclines - Google Patents

Description

New Zealand Paient Spedficaiion for Paient Number £00179 2001 7 Priority Date(s): -f?2.

Complete Specification Filed: tvt.......

C,as, Publication Date: ... B55EPJ9M..

, " J2.75" P.O. Journal, No: NEW ZEALAND PATENTS ACT, 1953 [rife1.

:°HARl982r No.: Date: COMPLETE SPECIFICATION "NON-YELLOWING TOPICAL PHARMACEUTICAL COMPOSITION" X/We, THE PROCTER AND GAMBLE COMPANY, a corporation organised under the laws of the State of Ohio, U.S.A., of 301 East Sixth Street, Cincinnati, Ohio 45202, United States of America, hereby declare the invention for which ± / we pray that a patent may be granted to ncae^us, and the method by which it is to be performed, to be particularly described in and by the following statement: - (followed by page la) 2001 7 - ]a- NON-YELLOWING TOPICAL PHARMACEUTICAL COMPOSITION Burt P. Koonsvitsky and Gary L. Manring BACKGROUND OF THE INVENTION The invention described and claimed herein relates to pharmaceutical compositions formulated for topical application, containing tetracycline, tetracycline salts 5 or tetracycline derivatives, used in the treatment of a variety of skin disorders.

The use of antibiotics, especially tetracycline, is a widely accepted mode of therapy for a variety of conditions, including skin disorders, such as acne. 10 Especially in the case of skin disorders, the convenience and the fact that application of the active ingredient is made directly to the afflicted situs with only a minimal systemic exposure to the active component, makes topical application a preferred mode of administration. However, 15 the topical use of tetracycline or tetracycline-derived compounds, can lead to a yellowing of the skin at the site of application, particularly in people with fair complexions and pink skin tones. Although this skin yellowing is temporary and can be washed away by normal soap 20 and water washing, it can be viewed by users of the topical tetracycline composition as a cosmetically undesirable characteristic and can even be perceived in efficacy terms since, as a result of the skin yellowing, the patient may decrease usage of the tetracycline com-25 position, causing an exacerbation of the condition being treated. Thus, it would be very desirable from both cosmetic and treatment viewpoints, to be able to formulate / 2001 7 9 a tetracycline-containing topical composition which does not exhibit this skin yellowing characteristic.

The use of topical pharmaceutical compositions, some of which contain tetracycline, in the treatment of a wide variety of conditions, such as acne, is known in the art. See, for example, U.S. Patent 3,896,238, Smith, issued July 22, 1975, and U.S. Patent 3,527,864, MacMillan and Lyness, issued September 8, 1970, both of which are incorporated herein by reference. Citric acid is known for use as a component in a variety of therapeutic treatments, such as in the preparation of effervescent granules, the enhancement of antioxidant effectiveness, as a disinfectant, and in a lotion for the neutralization of alkali materials in the eyes. See, Martindale, The Extra Pharmacopoeia, 26th Edition, The Pharmaceutical Press, 1972, pages 880-^ 881, incorporated herein by reference. In addition, citric acid has been used at low levels (i.e., less than about 0.1%) as a stabilizer in various pharmaceutical products.

It has now been found that by carefully controlling 20 the size and configuration of tetracycline crystals as they recrystallize at the skin surface after application, it is possible to formulate topical tetracycline-con-taining compositions which do not yellow the skin upon use. A preferred way of accomplishing this is to buffer the compositions at a pH between about 2.0 and about 4, preferably using citric acid as the buffering acid.

It is, therefore, an object of the present invention to provide topical pharmaceutical compositions, containing tetracycline or tetracycline-derived compounds, which do "O n not yellow the skin upon use.

It is a further object of the present invention to provide a method for topically treating skin disorders with tetracycline or tetracycline derivatives in a manner which does not cause yellowing of the skin area being ^ treated. a 2.0 01 7 3 SUMMARY OF THE INVENTION The present invention encompasses topical pharmaceutical compositions for use in the treatment of skin disorders, containing from about 0.005% to about 5% of a tetracycline compound selected from the group consisting of tetracycline, a tetracycline salt, or a tetracycline derivative in solution, said compositions formulated such that following application the tetracycline recrystallizes at the skin forming irregularly shaped crystals having an 10 average size of no greater than about 30 microns. (1) from about 0.005% to about 5% of a tetracycline coiu pound selected from the group consisting of tetracycline, a tetracycline salt or a tetracycline derivative, in 15 solution; (2) from about 0.5% to about 10% of a pharma-ceutically-acceptable acid which buffers the composition at a pH of from about 2.0 to about 4; and (3) a phar-maceutically-acceptable topical carrier. The preferred buffering acid for use in these compositions is citric 20 acid. The method of treating skin disorders with these compositions is also disclosed and claimed. compositions, containing tetracycline, which may be used topically (as in the treatment of skin disorders, such as acne) without yellowing the skin of the user. The formulation of these compositions revolves around the discovery that by controlling the size and shape characteristics of 30 the tetracycline compound as it recrystallizes on the skin after application, the tendency to yellow the skin can be eliminated. Generally, when applied to the skin from a solution, tetracycline recrystallizes at the skin surface in relatively large, yellow rhombohedron-shaped crystals, 35 having an average size of at least about 35-4 0 microns.

Preferred compositions are those which comprise DETAILED DESCRIPTION OF THE INVENTION The present invention encompasses pharmaceutical 2001 The flat surfaces of these crystals reflect light, imparting a yellow coloration to the skin. By formulating the compositions such that the tetracycline compound recrystallizes at the skin surface in small crystals, i.e., 5 having an average size of about 30 microns or less, preferably less than about 25 microns, of irregular shape, the perception of skin yellowing is eliminated.

One way to achieve this result is to lower the pH of the skin prior to application of the tetracycline cora-10 position. This may be accomplished by washing the area to be treated with an acidic soap just prior to application of the tetracycline-containing composition. A far superior way to achieve this result, both in terms of convenience and elimination of yellow coloration, is by controlling the 15 pH of the composition itself. Thus, preferred compositions r} of the present invention are those containing from about 0.5% to about 10%, preferably from about 0.75% to about 6%, most preferably from about 1% to about 3%, of an acid which buffers the compositions at a pK of from about 2.0 to about '20 4, preferably from about 2.5 to about 3.5. Examples of such acids include hut are not limited to, citric acid, lactic acid, ascorbic acid, glutaric acid, oxalic acid, hydrochloric acid, and mixtures thereof, with citric acid being preferred. In addition to the crystal modification 25 effect, the lowering of the pH of the composition may act to shift its light absorption characteristics, thereby eliminating skin yellowing.

Excellent therapeutic and skin yellowing results are also obtained where acid is added to the composition, 30 bringing the pH. down to from about 2.0 to about 2.5, and then an alkaline compound, such as sodium hydroxide, is added to bring the composition pH to from about 3.0 to about 3.5. Similar results are obtained where the composition is formulated to include a weak acid Ce.g., 200179 citric acid) and its basic salts (e.g., sodium citrate), such that the final composition has a pH between about 3.0 and about 3.5 and^'contains from about '0.75% to about 6%, preferably from about 1% to about 3%, of the acid/salt 7.* mixture.

The compositions of the present invention contain ri' from about 0 .005% to about 5%, preferably from about 0.05% t to about 2%, and most preferably about 0.5%, of tetracycline, a tetracycline salt or a tetracycline derivative. 10 Mixtures of such tetracycline compounds may be used. The tetracycline compound contained in the composition must be present in solution; the skin yellowing effect is not present when the tetracycline compound is in a suspension, as in an ointment formulation. Tetracycline 15 compounds useful in the present invention include tetracycline itself, as well as the salts thereof, for example, tetracycline hydrochloride and the tetracycline phosphate complex marketed under the trademarks "Tetrex" and "Panmycin Phosphate", and the like. Tetracycline analogues, 20 for example, the oxytetracyclines or terramycins, such as terramycin hydrochloride, terramycin disodium salt di-hydrate, and the like are also suitable herein. Preferred tetracycline compounds for use herein include tetracycline, tetracycline hydrochloride, and equilibrium mixtures of• 25 epi-tetracycline hydrochloride and tetracycline hydrochloride (formed on dissolution of tetracycline hydrochloride in waterl. Especially preferred tetracycline compounds include tetracycline hydrochloride and the equilibrium mixture of tetracycline hydrochloride and epi-30 tetracycline hydrochloride which forms spontaneously after aqueous solutions of tetracycline hydrochloride have been allowed to age at about 90°P for about 7 days. In general, this equilibrium mixture comprises about 40-45% by weight tetracycline hydrochloride and 55-60% by weight 35 epi-tetracycline hydrochloride. 200179 Other additives conventionally used in topical pharmaceutical compositions, such as perfumes, colorants, thickeners, preservatives, and penetration enhancers, may be included in the compositions of the present invention.

Examples of such penetration enhancers include sugar esters, sulfoxides or phosphine oxides, and the combinations of these components described in U.S. Patent 3,896,238, Smith, issued July 22, 1975, and U.S. Patent 3,952,099, Smith, issued April 20, 1976, both incorporated 10 herein by reference. Compositions of the present invention may contain up to about 10%, preferably about 0.1% to about 1% by weight of a sugar ester of the type hereinafter disclosed. The sugar esters suitable for use in this invention can be classified as hydrocarbyl and alkyl 15 polyoxyalkylene esters of cyclic polyhydroxy saccharides wherein one or more of the hydroxyl groups on the saccharide moiety is substituted with an acyl or polyoxyalkylene group.

Preferred sugar esters herein are those prepared by 20 the esterification of sugars in a mole ratio of esteri-fication agent:sugar of 1:1 and 2:1, i.e., the mono-acyl and di-acyl sugar esters. Especially preferred are the mono-acyl and di-acyl sugar esters wherein the acyl substituents contain from about 8 to about 20 carbon 25 atoms. Of the mono-acyl and di-acyl sugar esters, the respective esters of di-saccharide sugars, especially sucrose, wherein the acyl groups contain from about 8 to about 20 carbon atoms are especially preferred. Sucrose monooleate has been found to be particularly efficacious. 30 The following is a list of typical sugar esters suitable for use in the instant invention but is not intended to be limiting of such, esters and is only mentioned by way of example: glucose monooctanoate, glucose mono-caprate, glucose monolaurate, glucose monomyristate, 35 galactose monopalmitate, galactose monostearate, galactose monooleate, mannose dipalmitate, xylose diooleate, xylose 2001 7 di-eicosanate, sucrose monooctanoate, sucrose monocaprate, sucrose monolaurate, sucrose monomyristate, sucrose mono-palmitate, sucrose monostearate, sucrose monooleate, sucrose di-octanoate, sucrose dilaurate, sucrose dimy-5 ristate, sucrose dioleate, sucrose trilaurate, sucrose tripalmitate, sucrose trioleate, maltose monooleate, maltose dilaurate, galactose monolaurate, galactose dilaurate, cellibiose trilaurate, raffinose monomyristate, gentianose dioctanoate, and gentianose trioleate. Preferred 10 sugar esters include sucrose monooctanoate, sucrose monodecanoate, sucrose monolaurate, sucrose monomyristate, sucrose monopalmitate, sucrose monostearate, sucrose monooleate, and sucrose dioleate.

Preferred compositions herein, having improved skin 15 penetration properties, contain a compound selected from sulfoxides of the formula R^SCO)!^, wherein R-^ is a straight chain or branched chain alkyl, alkenyl, substituted alkyl, heteroalkyl or hydroxy-substituted alkyl substi-tuent containing from 4 to 12 carbon atoms, and R£ is a 20 low molecular weight (C-^-Cg) alkyl or low molecular weight (Ci-C8) hydroxy-substituted alkyl substituent; and pho's-phine oxides of the formula R-jR^R^P CO) , wherein is an alkyl, aralkyl, substituted alkyl, heteroalkyl, or hydroxy-substituted alkyl substitutent containing from 1 25 to 12 carbon atoms, or aryl Ce.g., phenyl or tolyl) containing from 6 to 9 carbon atoms; and R^ and R^ are each low molecular weight alkyl CC^-C^) or low molecular weight hydroxy-substituted alkyl CC^-C^] substituents. Preferred herein are the alkyl sulfoxides wherein R-j^ is an alkyl or 30 hydroxyalkyl substitutent containing about 8 to 12 carbon atoms and Rj is a low molecular weight alkyl or low molecular weight hydroxyalkyl group containing about 1- to 8 carbon atoms. Alkyl tertiary phosphine oxides wherein R^ is an alkyl or hydroxyalkyl substituent containing 8 to 35 12 carbon atoms and R^ and R^ are each lower alkyl or 01 7 % lower hydroxyalkyl substitutents are the preferred phosphine oxides herein.

The concentration of sulfoxide or phosphine component oxide employed in the preferred compositions of the 5 present invention is at least about 0.1% by weight of the composition and can range from about 0.1% to about 10%. by weight. If concentrations less than about 0.1% are used, the degree of penetration enhancement attained, especially with the lower chain lengths is not appreciable. If con-10 centrations greater than about 10% are employed, solubility problems may be encountered with the higher chain length materials. Preferably, the concentration of sulfoxide or phosphine oxide will range from about 0.1% to about 1% by weight of the total composition.

The balance of the compositions of the present in vention, generally from about 50% to about 99.5%jp>ftne compositions, comprises a conventional pharmaceutical carrier material, generally in liquid or semi-liquid state, especially adapated for topical application, it is 20 desirable that the carrier selected be capable of co- dissolving the materials used in the composition. Carrier materials suitable for use in the instant compositions include those well-known for use in the cosmetic and medical arts as bases for ointments, lotions, salves, 25 aerosols, suppositories and the like. Suitable carriers include, for example, water, liquid alcohols, liquid glycols, liquid polyalkylene glycols, liquid esters-, liquid amides, liquid protein hydrosylates, liquid alkylated protein hydrosylates, liquid lanolin and lanolin 30 derivatives, and like materials commonly employed in cosmetic and medicinal compositions. Exemplary carriers include alcohols, including both monohydric and polyhydric alcohols, for example, ethanol, isopropanol, glycerol, sorbitol, 2-methoxyethanol, diethylene glycol, ethylene. 35 glycol, hexylene glycol, mannitol, and propylene glycol; ethers, such as diethyl or dipropyl ether; polyethylene 2 001 7 glycols and methoxypolyoxyethylenes (such as carbowaxes having molecular weights ranging from 200 to 20,000); polyoxyethylene glycerols, polyoxyethylene sorbitols, and stearoyl diacetin. Oil-in-water emulsions such as cold 5 cream bases, can also be used.

Preferably the carrier herein is a pharmaceutically-acceptable liquid alcohol containing from about 2 to about 6 carbon atoms. Mixtures comprising from about 0 to 80% by weight of water and about 20 to 100% by weight of said 10 C2~C6 alc°h°ls are also suitable. Alcohols useful herein include ethanol, isopropanol, hexanol, and the like. Especially preferred carriers are water-ethanol mixtures at a weight ratio of about 1:20 to 5:1. Ethanol containing from about 5 to about 50% by weight of water, 15 especially 40:60 by volume ethanol-water, is preferred as the carrier.

Because of storage stability considerations relating to tetracycline hydrochloride and epi-tetracycline hydrochloride when formulated in solution, for particular 20 formulations it may be preferable to package the compositions of the present invention in kit form. In such executions the tetracycline compound is packaged separately from any water-based carrier material, such as a mixture of ethyl alcohol, water, sucrose monooleate and 25 decyl methyl sulfoxide, used in the composition. Accordingly, a preferred embodiment of the present invention encompasses a separately packaged portion of the tetracycline component, such as an equilibrium mixture of tetracycline hydrochloride and epi-tetracycline hydro-30 chloride and a separately packaged portion of a penetration enhancing carrier. Such separately packaged portions are stable on prolonged storage and can be admixed by the user immediately before the course of treatment. It is convenient to package the two portions to provide a 35 sufficient quantity of the composition to last for about 4 to 8 weeks of treatment. This, of course, is not critical to the present invention inasmuch as the clinical efficacy 2001 of the compositions herein is satisfactory even after storage. However, the use of separate packages for the tetracycline active and for the fluid ointment base insures that fresh material will be provided to the user.

The buffering acid component of the present invention, preferably citric acid, may be included either with the tetracycline portion or the liquid carrier portion of such a kit.

The size of the kits herein are of no consequence 10 to the practice of the invention. For example, such kits can be provided which contain only a few grams of material and which are suitable for but a single application. Alternatively, kits can be provided which comprise a relatively large volume of the composition. The user can 15 then measure aliquots of the carrier material and add thereto a premeasured packet of the tetracycline component. A preferred example of a composition of the present invention, used to provide an anti-acne benefit, contains a separately packaged, fluid ointment base com-20 prising from about 0.1 to about 1% by weight of sucrose monooleate, from about 0.1 to about 8% by weight of decyl methyl sulfoxide, from about 30 to about 70% by weight of water, from about 30 to about 7 0% by weight of ethyl alcohol, and from about 1 to about 6% by weight of citric 25 acid. The second component of the kit comprises a separately packaged, dry portion of an anti-acne agent comprising an equilibrium mixture of tetracycline hydrochloride and epi-tetracycline hydrochloride in an amount sufficient to provide a 0. .1% to 1% by weight concentration 30 of said equilibrium mixture when dissolved in the fluid ointment base composition. The equilibrium mixture of tetracycline hydrochloride and epi-tetracycline hydrochloride may also contain from about 0.05 to about 0.15% by weight (based on the total weight of all components), of 35 a color stabilizer, especially sodium bisulfite. Alternatively, the second component can be an equivalent amount 200179 - n - of either tetracycline hydrochloride or epi-tetracycline hydrochloride, since these materials are stable in the dry state, and may contain the citric acid component rather than having it in the liquid portion of the kit.

Topical treatment regimens according to the practice of this invention comprise applying the compositions herein directly to the skin, e.g., at the situs of a dermatosis, such as acne. The rate of application and duration of treatment will, of course, depend on the 10 severity of the condition, the response of the particular patient, and related factors within the sound medical judgment of an attending physician. In general, for the compositions of the present invention, application rates of 2 2 from about 0.01 ml/cm to about 25 ml/cm per day are used.

Application can be made once, or preferably several times, daily for periods of a week or more, and do not result in a yellow coloration of the skin at the site of application.

The following examples illustrate topical compositions prepared and used in the manner of this in-2 0 vention, but are not intended to be limiting thereof.

EXAMPLE I The skin yellowing effect of the compositions of the present invention, as compared with control compositions, was tested as follows using a control com-25 position having the following formulation.

CONTROL Tetracycline hydrochloride 154 mg. 4-Epitetracycline hydrochloride 196 mg. n-Decyl methyl sulfoxide 87.5 mg.

Sucrose monooleate 87.5 mg.

Sodium bisulfite 7Q mg.

Vehicle = 70 ml. of a 4 0% Cby volume] ethanol/water mixture. 2 001 12 Compositions of the present invention were formulated by adding citric acid to the control composition in an amount such that the final composition contained 1%, by weight, of the citric acid (Composition A) and another composition was formed such that the final composition contained 2% citric acid (Composition B). Compositions A and B both have pH's between about 2.5 and about 3.5. These 2 compositions were applied to skin once at 4 ml/cm . The skin yellowing effect of these compositions was then graded 10 on a 0 to 5 grading scale, with 0 indicating the yellow staining effect of the control compositions and 5 indicating no yellow skin coloration at all. The tests were repeated on 8 subjects and the skin staining was evaluated by two graders for each subject. The results were averaged 15 and are summarized in the table below.

Test Control Composition A Composition B 1 0 4.25 4.75 2 0 -- 4.40 yellowing is dramatically demonstrated by the data contained in the above table. Substantially similar results are obtained where the citric acid component is replaced, in whole or in part, by lactic acid, ascorbic acid, hydrochloric acid, glutaric acid, oxalic acid, or mixtures 25 of these components. Substantially similar results are also obtained where a composition similar to Composition A is formulated but with, the ' " " • ■ - ' ' .g composition. Similar results are also obtained where the 30 tetracycline components in the above compositions are replaced, in whole or in part, by tetracycline, tetracycline phosphate complexes, terramycin hydrochloride, terramycin disodium salt dihydrate, or mixtures of these components.

The benefit in terms of minimization of skin 0.5%, 0.75%, 1.5%, 3%, 4%, 1 7 9 s « A study of crystals formed on the skin surface in the above test indicates that the control composition resulted in the formation of crystals having a rhornbo-hedral shape and an average size of greater than 30 microns, 5 while the crystals formed from Composition B on the skin surface had an average crystal size of less than 28 microns and were irregular in shape.

EXAMPLE II The control composition, described in Example I, and compositions of the present invention, formulated by adding amounts of citric acid ranging from 0.5% to 10%, by weight, of the final composition to the control were applied to white press-apply labels; the amount applied was approxi-2 mately 3 ml/cm . The color differences obtained from these 15 compositions, as judged under white light, were found to be as follows: (1) Composition obtained by adding 0.5% citric acid to the control resulted in noticeably less yellow color than did the control composition. 20 (2) Compositions formulated by adding 2 to 4% citric acid to the control composition resulted in noticeably less yellow coloration than that obtained using the control plus 0.5% citric acid and, when compared to the control, showed al-25 most no yellow coloration. (3) Levels of citric acid above the range of 2-4% did not give any significant improvement over the 2-4% citric acid level, but were significantly better than the control composition. 30 Substantially similar results are obtained where the citric acid is replaced, in whole or in part, by lactic acid, ascorhic acid, hydrochloric acid, glutaric acid, oxalic acid, and mixtures thereof.

V a 4 - 0 01 EXAMPLE III A composition of the present invention, having the formulation given below, is formulated in a conventional manner.

COMPONENT Weight % Tetracycline hydrochloride 0.22 4-Epitetracycline hydrochloride 0.28 Citric acid 2.0 Sodium bisulfite 0.1 1° Propylene glycol monoisostearate 1.5 40/60(approximately) ethanol/water Balance to 100 This composition when applied to the skin at an 2 application rate of about 10 mg/cm per day, provides effective therapy in the treatment of acne without 15 causing the treated skin area to become yellow.

EXAMPLE IV A composition of the present invention, having the formulation given below, is formulated in a conventional manner.

COMPONENT Weight % Tetracycline hydrochloride 0.22 4-Epitetracycline hydrochloride 0.22 Citric acid 2.0 Sodium bisulfite 0.1 Myristyl alcohol 1-5 40/60(approximately) ethanol/water Balance to 100 This composition, when applied m a daily dosage 2 of about 5 ml/cm , provides an effective topical treatment for a variety of skin disorders, including acne, 30 without causing the treated skin area to become yellow stained. 2001 EXAMPLE V A composition of the present invention, having the formulation given below, is formulated in a conventional manner. 2.2 mg/ml 3.25 mg/ml 1.25 mg/ml 18.95 mg/ml 1 mg/ml COMPONENT Tetracycline hydrochloride 4-Epitetracycline hydrochloride Decyl methyl sulfoxide Citric acid 10 Sodium bisulfite Appropriate amounts of the above components are dissolved in 40/60 ethanol/water vehicle to form about 70 ml. of the desired composition. The composition has a pH between about 2.5 and 3.0. This composition, when 2 applied in a daily dosage of about 5 ml/cm , provides an effective topical treatment for a variety of skin disorders, including acne, without causing the treated area to become yellow stained. Excellent results are also obtained where sodium hydroxide is added to the 20 above composition in an amount to raise the pH of the composition to 3.5. 2 001 EXAMPLE VI A composition, effective in the topical treatment of acne, sold in kit form, and having the 'formulation given below is made in a conventional manner.

COMPONENT Weight % Component 1 Tetracycline hydrochloride/epi- tetracycline hydrochloride 0.06 oz. mixture Sodium bisulfite 0.02 oz.

Citric acid 0.25 oz.

Component 2 Ethanol 4.0 oz.

Sucrose monooleate 0.06 oz.

Decyl methyl sulfoxide 0.06 oz.

Water 2.5 oz.

In the above composition, Component 1 is packaged in a dry, water-proof foil packet; Component 2 is packaged in a bottle having sufficient head space to allow mixing. 20 Immediately prior to use, Component 1 is added to Component 2 and the mixture is shaken to mix. The user applies an effective amount of the composition to the acne lesions, ad lib, and alleviation of the acne is secured; such use does not cause the treated situs to take on a 25 yellow coloration.

In the above composition, the citric acid component may be included in Component 2 rather than in Component 1, while retaining its yellow stain reduction benefit.

Further, in the above example, the' mixture of tetracycline 30 hydrochloride and epi-tetracycline hydrochloride may be replaced by tetracycline hydrochloride and epi-tetracycline hydrochloride, respectively, and equivalent results are secured. Similar results are also obtained where the above composition is formulated without the sucrose monooleate 35 and/or the sodium bisulfite components. 200179

Claims (10)

WHAT WE CLAIM IS:

1. A topical pharmaceutical composition comprising by weight: (1) from 0.005% to 5% of a tetracycline compound selected from the group consisting of tetracycline, a tetracycline salt or a tetracycline derivative in a water containing solution; (2) from 0.5% to 10% of a pharmaceutically-acceptable acid which buffers the composition at a pH of from 2.0 to 4 selected from the group consisting of citric acid, lactic acid, ascorbic acid, hydrochloric acid, glutaric acid and mixtures thereof; and (3) a pharmaceutically-acceptable topical carrier.

2. A composition according to claim 1 which contains from 0.05% to 2% of the tetracycline compound.

3. A composition according to claim 2 which contains from 0.75% to 6% of the pharmaceutically-acceptable acid.

4; A composition according to claim 3 wherein the pharmaceutically-acceptable acid is citric acid.

5. A composition according to claim 4 which contains from 1% to 3% of said pharmaceutically-acceptable acid.

6. A composition according to claim 5 which contains 0.5% of the tetracycline compound.

7. A composition according to claim 3 which contains from 0.1% to 10% of a sugar ester selected from the group consisting of hydrocarbyl polyoxyalkylene esters of cyclic polyhydroxysaccharides wherein one or more of the hydroxyl groups on the saccharide moiety is substituted with an acyl or polyoxyalkylene group, and from 0.1% to 10% of a sulfoxide having the formula R1S(0)R2 wherein Rj is a Cg - C12 alkyl or hydroxyalkyl substituent and R2 is a substituent selected from the group consisting of C.-C. alkyl and hydroxy-substituted alkyl substituents. ^ - 18 - 2.00179

8. A topical pharmaceutical composition comprising by weight: (1) from 0.005% to 5% tetracycline compound selected from the group consisting of tetracycline, a tetracycline salt or a tetracycline derivative in a water containing solution; (2) from 0.5% to 10% of a pharmaceutically-acceptable acid which buffers the composition at a pH of from 2.0 to 2.5, and (3) a pharmaceutically-acceptable topical carrier.

9. A composition according to claim 8 wherein the pharmaceutically-acceptable acid is citric acid.

10. A topical pharmaceutical composition as claimed in claim 1 substantially as hereinbefore described with reference to the Examples. dated this jCW of "3^ 1985" \ PARK & SON