Diacerein or rhein topical formulations and uses thereof

Abstract

To provide a topical pharmaceutical composition containing diacerein and / or its analogs, and also to provide a method for treating various diseases using the composition.SOLUTION: Provided is a topical pharmaceutical composition containing a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein, and salts or esters or prodrugs thereof, and one or more pharmaceutically acceptable excipients, the composition being in the form of ointment, cream, or gel, and at least about 90 vol.% of the compound having a particle size of about 0.5 to about 35 μm.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. Provisional Patent Application No. 62 / 187,743, filed July 1, 2015, which is incorporated herein by reference in its entirety.

[0002] The present invention relates to a topical pharmaceutical composition containing diacerein and / or its analogues, and also to the use of this topical pharmaceutical composition in the treatment of various diseases or conditions. [Background technology]

[0003] Chemically, rhein is 9,10-dihydro-4,5-dihydroxy-9,10-dioxo-2-anthracene carboxylic acid having the structure of formula (I), and one of its prodrugs, diacerein, is 4,5-bis(acetyloxy)9,10-dihydro-4,5-dihydroxy-9,10-dioxo-2-anthracene carboxylic acid having the structure of formula (II). Diacerein is completely converted to rhein before reaching the systemic circulation, and in the body, it exerts its physiological functions in the form of rhein.

[0004] Formula (I)

[0005] [ka]

[0006] Formula (II)

[0007] [ka]

[0008] Diacerein is an anti-inflammatory drug that is widely used in the treatment of osteoarthritis and has been shown to inhibit interleukin 1 (IL-1) signal transduction. Currently, diacerein capsules are available in 50 mg strength and are marketed in various countries under various trade names, including Art 50®, Artrodar®, etc. As disclosed in U.S. Patent Nos. 8,536,152 and 8,865,689, diacerein can be used as an adjunct therapy for type II diabetes, and has also been found to be effective in lowering blood uric acid levels, and therefore can be used to treat hyperuricemia or metabolic disorders associated with hyperuricemia. In addition, diacerein has been reported to have potential effects in the treatment of epidermolysis bullosa (Wally et al., Orphanet Journal of Rare Diseases, 2013, vol. 8, issue 69).

[0009] Although diacerein can be administered by the oral route, it cannot be completely absorbed by the digestive tract, and the oral bioavailability of diacerein is estimated to be about 40% to 60%. Incomplete absorption of diacerein can result in undesirable side effects such as diarrhea or loose stools. In vitro and in vivo studies have shown that unabsorbed diacerein is metabolized to rhein in the colon, which then induces a laxative effect.

[0010] Because such side effects can result from oral administration, parenteral diacerein compositions have been proposed to overcome these problems.

[0011] PCT International Application No. WO2009 / 133430 discloses topical compositions containing diacerein or rhein, which may be in various forms, such as lotions, creams, ointments, pastes, gels, etc. However, these compositions are not intended for any particular disease, and therefore, from the context of this paper, it is not possible to know which form is most suitable for the particular type of disease being treated.

[0012] Wally et al. disclosed a cream diacerein formulation for epidermolysis bullosa (Wally et al., Orphanet Journal of Rare Diseases, 2013, vol. 8, issue 69). However, it is not clear from this paper whether or how the properties of the formulation have a therapeutic effect on epidermolysis bullosa.

[0013] The exact properties of the diacerein preparation appear to be of great importance for the therapeutic efficacy of this preparation against various diseases. [Prior art documents] [Patent documents]

[0014] [Patent Document 1] U.S. Pat. No. 8,536,152 [Patent Document 2] U.S. Pat. No. 8,865,689 [Patent Document 3] International Application No. 2009 / 133430 [Non-patent literature]

[0015] [Non-Patent Document 1] Wally et al.,Orphanet Journal of Rare Diseases,2013,vol.8,issue 69 Summary of the Invention [Problem to be solved by the invention]

[0016] Considering that the literature provides little information on the physicochemical properties of diacerein / rhein topical formulations and their relationship to their therapeutic effect, the present invention provides topical formulations that are appropriately adapted to various diseases. [Means for solving the problem]

[0017] The present invention provides a topical composition comprising a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, wherein the composition is in the form of an ointment, cream or gel, and at least about 90% by volume of the compound has a particle size of about 0.5 to 35 μm.

[0018] The present invention also provides a topical composition comprising a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, wherein the composition is in the form of a gel, and at least about 90% by volume of the compound has a particle size of less than about 1 μm.

[0019] The present invention also provides methods for treating inflammatory and / or hyperproliferative and pruritic skin diseases, as well as diseases associated with epidermal barrier dysfunction, including aging skin and epidermolysis bullosa, comprising administering to a subject in need of treatment an effective amount of a composition of the present invention.

[0020] The present invention also provides a method for treating hyperuricemia, metabolic disorders associated with hyperuricemia, osteoarthritis, or type 2 diabetes, comprising administering to a subject in need of treatment an effective amount of a composition of the present invention.

[0021] In some embodiments, the methods of treatment of the present invention specifically exclude the administration of any other active agents to treat a disease treatable by the compositions of the present invention, however, in some embodiments, the methods of the present invention contemplate the administration of other active agents.

[0022] Preferably, the treatment methods of the invention result in effective treatment of the relevant disease in at least one treated subject, preferably in a substantial number of treated subjects, and more preferably in a majority of treated subjects.

[0023] Detailed techniques and preferred embodiments implemented for the present invention are described in the following paragraphs accompanied with accompanying drawings for those skilled in the art to fully understand the features of the claimed invention. [Brief description of the drawings]

[0024] [Figure 1] FIG. 1 is a statistical bar graph showing rhein concentrations in the dermis and epidermis 8 hours after treatment with three test diacerein formulations (G1, C1 and O1, n=4). [Figure 2A] 1 is a plot of cumulative rhein penetration (ng / cm2) from skin tissue into the receiver solution versus time for three tested diacerein formulations (G1, C1 and O1, n=4). [Figure 2B] 1 is a plot of cumulative rhein penetration (ng / cm2) from skin tissue into the receiver solution versus time for three tested diacerein formulations (G1, C1 and O1, n=4). [Diagram 3] 1 is a statistical bar graph showing rhein concentrations in the dermis and epidermis 8 hours after treatment with two test diacerein ointment formulations (O2 and O3, n=3). [Figure 4] 1 is a plot of cumulative rhein penetration (ng / cm2) from skin tissue into the receiver solution versus time for two test diacerein ointment formulations (O2 and O3, n=3). [Diagram 5] 1 is a statistical bar graph showing rhein concentrations in the dermis and epidermis 8 hours after treatment with the test diacerein ointment formulation (O3, n=3) or the comparative formulation (n=3). [Figure 6] 1 is a plot of cumulative rhein penetration (ng / cm2) from skin tissue into receiver solution versus time for a test diacerein ointment formulation (O3, n=3) and a comparative formulation (n=3). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0025] As used herein, the term "therapeutically effective amount" refers to an amount that relieves or reduces one or more symptoms of a disease.

[0026] As used herein, the term "diacerein or an analog thereof" refers to diacerein, rhein, monoacetylrhein, or a pharma- ceutically acceptable salt or ester or prodrug thereof.

[0027] Unless otherwise stated herein, the terms "a," "an," "the," and the like as used herein (particularly in the claims below) are understood to encompass both the singular and the plural.

[0028] As mentioned above, topical administration of diacerein avoids the gastrointestinal route with limited tolerance and reduces the amount of diacerein that enters systemic circulation compared with oral administration, so that it can prevent the undesirable side effects of oral administration.In addition, when diacerein is used to treat skin diseases, it is advantageous that diacerein can easily penetrate the stratum corneum to reach the target site (e.g., the dermis or epidermis, where skin disorders may occur).At the same time, it is also desirable that diacerein is retained in the skin as long as possible to fully perform its function.For this reason, a delicate balance needs to be achieved so that, on the one hand, diacerein or rhein can penetrate into the target site quickly, but on the other hand, it can be retained in the target site for sustained exposure.

[0029] The inventors of the present invention have discovered that the form of a topical diacerein / rhein composition and / or the particle size of the active ingredient contained in the composition play an important role in the permeability (or diffusion rate) and retention rate in the skin.

[0030] The present invention therefore provides a topical diacerein / rhein pharmaceutical composition suitable for skin diseases and meeting the above requirements. The topical pharmaceutical composition comprises a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and its salts or esters or prodrugs, and one or more pharma- ceutically acceptable excipients, wherein the composition is in the form of an ointment, cream or gel, and at least about 90% by volume of the compound has a particle size of about 0.5 to 35 μm.

[0031] In the context of this application, particle size distribution is based on volumetric D values ​​(i.e. Dv values ​​such as Dv10, Dv50 and Dv90), which are commonly used to describe the range of particle sizes of a given sample.

[0032] Preferably, the composition is provided as an ointment or cream, more preferably as an ointment. Surprisingly, it has been found that an ointment or cream formulation provides a higher retention rate and a longer retention time on the skin compared to a gel formulation.

[0033] In one embodiment, at least about 90% by volume of the compound in the composition has a particle size of about 1 to about 15 μm, preferably about 2 to about 5 μm. Preferably, the composition containing the compound with this particle size is in the form of an ointment or cream, and when administered to the skin of a subject, more than 90% of the number of compounds, preferably substantially all of the compounds, are retained on the skin for at least about 2 hours, more preferably about 4 hours, even more preferably about 6 hours, and most preferably about 8 hours after administration. The retention rate and retention time of the compound in the skin can be measured, for example, via a diffusion cell test. In this test, a diffusion cell apparatus is set up that essentially consists of a piece of skin fixed between two clamps, a formulation containing the compound is applied to one side (top) of the skin, and the compound concentration is measured at regular time intervals in the receiver part (bottom) of the apparatus (which can be a buffer-filled container in contact with the skin).

[0034] Further, when administered to the skin of a subject, the concentration of the compound can be, for example, from about 8 to about 20 μg per gram of epidermal tissue and / or from about 1 to about 3 μg per gram of dermal tissue 8 hours after administration.

[0035] In another embodiment, at least about 90% by volume of the compounds in the composition have a particle size of about 10 to about 30 μm, preferably about 12 to about 25 μm. Preferably, the composition containing the compounds having this particle size is in the form of an ointment or cream, more preferably an ointment, and when administered to the skin of a subject, greater than 90% by number of the compounds, preferably substantially all of the compounds, are retained on the skin, preferably for at least about 4 hours, more preferably for about 6 hours, and most preferably for about 8 hours, after administration.

[0036] Additionally, when administered to the skin of a subject, the concentration of the compound can be, for example, from about 3 to about 6 μg per gram of epidermal tissue and / or from about 0.2 to about 2 μg per gram of dermal tissue 8 hours after administration.

[0037] Topical pharmaceutical compositions having the above properties provide a good balance between penetration and retention and are therefore useful in the treatment of skin diseases, such as inflammatory and / or hyperproliferative and pruritic skin diseases selected from atopic dermatitis, psoriasis, cystic psoriasis, rosacea, keloids, hypertrophic scars, acne, Netherton syndrome, or other pruritic dermatoses including prurigo nodularis, non-specific itch in the elderly, and diseases involving epidermal barrier dysfunction including aging skin and epidermolysis bullosa.Preferably, said compositions are useful in the treatment of epidermolysis bullosa.

[0038] The present invention also relates to methods of treating inflammatory and / or hyperproliferative and pruritic skin diseases, as well as diseases associated with epidermal barrier dysfunction, including aging skin and epidermolysis bullosa, comprising administering to a subject in need of treatment an effective amount of a composition of the present invention.

[0039] The present invention further provides a topical diacerein / rhein pharmaceutical composition useful in the treatment of hyperuricemia, disorders related to hyperuricemia (such as acute gout, chronic gout, gouty flare, uric acid nephrolithiasis, gouty nephropathy, etc.), osteoarthritis and type 2 diabetes.Unlike compositions used to treat skin diseases, the compositions of the present invention allow active compounds to easily penetrate the skin and enter the body relatively quickly to reach the systemic circulation and perform their functions in the body.The topical composition contains a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and its salts or esters or prodrugs, and one or more pharma- ceutically acceptable excipients, wherein the composition is in the form of a gel, and at least about 90% by volume of the compound has a particle size of less than about 1 μm, and preferably greater than about 0.1 μm.

[0040] Preferably, when the composition is administered to the skin of a subject, the compound is released from the skin into the body within about 6 hours, more preferably within about 4 hours, and most preferably within about 2 hours after administration.

[0041] The present invention also provides methods for treating hyperuricemia, disorders associated with hyperuricemia (e.g., acute gout, chronic gout, gouty flares, uric acid nephrolithiasis, gouty nephropathy, etc.), osteoarthritis, and type 2 diabetes, comprising administering to a subject in need of treatment an effective amount of a composition of the present invention.

[0042] In some embodiments, the treatment methods of the present invention specifically exclude the administration of any other active agents to treat a disease treatable by the compositions of the present invention. In some embodiments, however, the methods of the present invention contemplate the administration of other active agents.

[0043] Preferably, the treatment methods of the invention result in effective treatment of the relevant disease in at least one treated subject, preferably in a substantial number of treated subjects, and more preferably in a majority of treated subjects.

[0044] The topical pharmaceutical compositions of the present invention may contain preferably from about 0.1% to about 10% by weight, more preferably from about 0.1% to 5% by weight, and most preferably from about 0.5% to about 2% by weight of the compound, based on the total weight of the composition.

[0045] Pharmaceutically acceptable excipients in the composition may include antioxidants, gelling agents / hydrogel bases, pH adjusters / buffers, penetration enhancers, preservatives, chelating agents, humectants, surfactants, emulsifiers, thickeners, solvents, stabilizers, etc. As used herein, an excipient / ingredient in the present invention may have multiple functions, e.g., one excipient may be used as a surfactant and / or stabilizer and / or emulsifier, etc.

[0046] Examples of antioxidants include, but are not limited to, one or more of vitamin C, vitamin A, and alpha-lipoic acid, ascorbyl palmitate, sodium metabisulfite, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), and the like.

[0047] Suitable gelling agents / hydrogel bases may include, but are not limited to, one or more of guar gum, xanthan gum and carrageenan gum, anionic, nonionic, cationic and lipophilically modified guar gum, polyacrylic acid (e.g., carbomer), polymethacrylic acid, cellulosics, polyethylene glycols, hydroxyalkylcelluloses, carboxyalkylcelluloses, polyalkyleneamines, and the like.

[0048] Examples of pH adjusters / buffers include, but are not limited to, one or more of sodium bicarbonate, potassium bicarbonate, magnesium hydroxide, magnesium lactate, magnesium gluconate, aluminum hydroxide, aluminum hydroxide / sodium bicarbonate coprecipitate, amino acids, aluminum glycinate, sodium citrate, sodium tartrate, sodium acetate, sodium carbonate, sodium polyphosphate, potassium polyphosphate, sodium pyrophosphate, potassium pyrophosphate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, trisodium phosphate, tripotassium phosphate, sodium phosphate, sodium acetate, potassium metaphosphate, magnesium oxide, magnesium hydroxide, magnesium carbonate, magnesium silicate, calcium acetate, calcium glycerophosphate, calcium chloride, calcium hydroxide, calcium lactate, calcium carbonate, calcium bicarbonate, citric acid, and the like.

[0049] Examples of penetration enhancers include diethylene glycol monoethyl ether, dimethyl sulfoxide, propylene glycol, isopropyl myristate (IPM), calcipotriene, detergents, emollients, ethoxydiglycol, triacetin, propylene glycol, benzyl alcohol, sodium laureth sulfate, dimethyl isosorbide, isopropyl myristate, medium chain triglyceride oil (MCT oil), menthol, isopropyl palmitate, isopropyl isostearate, propylene glycol monostearate, lecithin, and the like. The preferred oleic acid, ethyl oleate, urea, glyceryl oleate, caprylic / capric triglyceride, propylene glycol dicaprylate / dicaprate, laureth 4, oleth-2, oleth-20, propylene carbonate, nonoxynol-9,2-n-nonyl-1,3-dioxolane, C7-C14-hydrocarbyl substituted 1,3-dioxolanes, 1,3-dioxanes or acetals, and nonoxynol-15.

[0050] The preservative may be, for example, one or more of sodium benzoate, butylated hydroxytoluene, butylated hydroxyanisole, ethylenediaminetetraacetic acid (EDTA), paraoxybenzoic acid esters, chlorobutanol, benzyl alcohol, phenylethyl alcohol, dehydroacetic acid, sorbic acid, benzalkonium chloride, benzethonium chloride, phenol, phenylmercuric nitrate (II), thimerosal, methylparaben, ethylparaben, and / or propylparaben.

[0051] Examples of suitable solvents include, but are not limited to, one or more of alcohol, castor oil, diisopropyl adipate, ethoxylated alcohol, ethyl alcohol, fatty alcohol citrate, glycerin, 1,2,6-hexanetriol, hexylene glycol, isopropyl alcohol, isopropyl myristate, isopropyl palmitate, mineral oil, phosphoric acid, polyethylene glycol 300, polyethylene glycol 400, polyethylene glycol 1450, polyethylene glycol 8000, polyethylene glycol 1000 monocetyl ether, polyethylene glycol monostearate, polyethylene glycol 400 monostearate, polyethylene glycol, polyoxyl 20 cetostearyl ether, polyoxypropylene 15-stearyl ether, polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 80, polysorbate, propylene carbonate, propylene glycol, pure water, SD alcohol 40, triglycerides of saturated fatty acids, and the like.

[0052] Suitable stabilizers or surfactants may be, for example, one or more of ionic polysorbate surfactants, Tween 20, Tween 40, Tween 60, Tween 80, nonylphenol polyethylene glycol ether, (alkylphenol-hydroxypolyoxyethylene), poly(oxy-1,2-ethanediyl), α-(4-nonylphenol)-ω-hydroxy-, branched (i.e., Tergitol® NP-40 surfactant), nonylphenol polyethylene glycol ether mixture (i.e., Tergitol® NP-70 (70% aqueous solution) surfactant), phenoxypolyethoxyethanol and polymers thereof, such as Triton®, Poloxamer®, Spans®, Tyloxapol®, various grades of Brij, sodium dodecyl sulfate, cetyl alcohol, stearic acid, polyoxyl stearates, and the like.

[0053] Examples of chelating agents include, but are not limited to, antioxidants, citric acid, edetate disodium (EDTA), edetate calcium disodium, edetate, malic acid, maltol, pentetic acid, edetate sodium, edetate trisodium, and the like.

[0054] Examples of humectants include, but are not limited to, glycerin, propylene glycol, sorbitol, polyethylene glycol, polysaccharides (e.g., fructose, glucose, maltose, etc.), corn syrup, polyols, urea and derivatives, and natural honey. Preferred humectants are propylene glycol and glycerin.

[0055] Examples of thickening agents include, but are not limited to, stearic acid, cellulose polymers, carbomer polymers, carbomer derivatives, cellulose derivatives, polyvinyl alcohol, poloxamers, polysaccharides, and the like.

[0056] Examples of oily bases for creams include, but are not limited to, vegetable oils (eg, castor oil), white petrolatum, mineral oil, and the like.

[0057] Examples of ointment bases include, but are not limited to, petrolatum, fatty oils, lanolin, petrolatum, glycerin, paraffin, poloxamer, polyethylene glycol, stearic acid, beeswax, etc. Examples of ointment base modifiers include, but are not limited to, mineral oil, liquid paraffin, etc.

[0058] In one embodiment, the topical pharmaceutical composition of the present invention is in the form of a gel and contains about 0.1% to about 10% by weight of diacerein or an analog thereof, about 0.1% to about 5% by weight of a hydrogel base, about 2% to about 50% by weight of a humectant, and about 0.1% to about 2.5% by weight of a stabilizer / surfactant.

[0059] In one embodiment, the topical pharmaceutical composition of the present invention is in the form of a cream and contains about 0.1% to about 10% by weight of diacerein or an analog thereof, about 0.5% to about 25% by weight of a surfactant, about 0.5% to about 25% by weight of an oil base, about 2% to about 50% by weight of a humectant, and water.

[0060] In one embodiment, the topical pharmaceutical composition of the present invention is in the form of a cream and contains Part A and Part B, where Part A contains about 0.1% to about 10% by weight of diacerein or its analogue, about 1.5% to about 40% by weight of a thickening agent, about 1% to about 40% by weight of an oil base and about 0.4% to about 10% by weight of a surfactant, and Part B contains about 0.2% to about 5% by weight of a stabilizer, about 0.6% to about 15% by weight of a humectant, and water.

[0061] In one embodiment, the topical pharmaceutical composition of the present invention is in the form of an ointment and contains 0.1% to about 10% by weight of diacerein or an analog thereof, about 15% to about 99% by weight of an ointment base, about 0% to about 60% by weight of a base improver, and about 0% to about 10% by weight of a surfactant.

[0062] Preferably, the topical pharmaceutical compositions of the present invention are once-daily or twice-daily compositions, i.e., suitable for administration once or twice daily to achieve the desired therapeutic effect.

[0063] The topical pharmaceutical compositions of the present invention have the following advantages. First, they can be administered directly to the affected area of ​​dermatological subcutaneous lesions, avoiding the gastrointestinal route and greatly reducing systemic exposure. Second, they are easy to apply, and therefore more convenient for patients. Third, these topical formulations are also preferable to oral formulations for patients who suffer from dysphagia or dislike the taste of medicine. Fourth, they are easier to achieve sustained exposure to target areas.

[0064] The present invention also relates to a method for treating inflammatory and / or hyperproliferative and pruritic skin diseases, as well as diseases associated with epidermal barrier dysfunction, including aging skin and epidermolysis bullosa, comprising administering to a subject in need of treatment an effective amount of a topical pharmaceutical composition, wherein the composition contains a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, and wherein when the composition is administered to the skin of a subject, more than 90% of the compound (by number) is retained on the skin for at least about 2 hours, preferably at least about 4 hours, even more preferably about 6 hours, and most preferably about 8 hours after administration.

[0065] The present invention also relates to a method for treating inflammatory and / or hyperproliferative and pruritic skin diseases, as well as diseases associated with epidermal barrier dysfunction, including aging skin and epidermolysis bullosa, comprising administering to a subject in need of treatment an effective amount of a topical pharmaceutical composition, wherein the composition contains a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, and wherein when the composition is administered to the skin of a subject, the concentration of the compound may be, for example, about 8 to about 20 μg per gram of epidermal tissue and / or about 1 to about 3 μg per gram of dermal tissue 8 hours after administration.

[0066] The present invention also relates to a method for treating inflammatory and / or hyperproliferative and pruritic skin diseases, as well as diseases associated with epidermal barrier dysfunction, including aging skin and epidermolysis bullosa, comprising administering to a subject in need of treatment an effective amount of a topical pharmaceutical composition, wherein the composition contains a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, and wherein when the composition is administered to the skin of a subject, the concentration of the compound may be, for example, about 3 to about 6 μg per gram of epidermal tissue and / or about 0.2 to about 2 μg per gram of dermal tissue 8 hours after administration.

[0067] The present invention further relates to a method for treating hyperuricemia, disorders associated with hyperuricemia, osteoarthritis and type 2 diabetes, comprising administering to a subject in need of treatment an effective amount of a topical pharmaceutical composition, wherein the composition contains a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and salts or esters or prodrugs thereof, and one or more pharma- ceutically acceptable excipients, and wherein when the composition is administered to the skin of a subject, the compound is released from the skin into the body within about 6 hours, more preferably within about 4 hours, and most preferably within about 2 hours after administration.

[0068] Hereinafter, the present invention will be further described with reference to the following examples, which are provided for illustrative purposes only and are not intended to limit the scope of the present invention. EXAMPLES

[0069] [Preparation Example] Preparation of Diacerein Topical Composition Seven diacerein topical compositions (G1, C1, C2 and O1 to O4) with three different forms (gel, cream and ointment) were prepared according to Tables 1 to 4. The particle size (Dv90) of the compound in each composition was measured by Mastersizer 2000 version 5.60. The excipients / ingredients listed in the following tables may have multiple functions, for example, one excipient is used as a surfactant and / or stabilizer and / or emulsifier, etc.

[0070] [Table 1]

[0071] [Table 2]

[0072] [Table 3]

[0073] [Table 4]

[0074] [Example 1] Diffusion Cell Testing of Topical Diacerein Compositions Procedure: Mice were sacrificed by cervical dislocation. Full thickness flank skin was removed and placed on a diffusion cell in contact with the receptor phase, which was PBS (pH 5.4) containing 30% PEG 300 (37°C). The buffer was pumped into the receiver compartment at a flow rate of 3 to 4 mL / h. A dose of 20 μl of 1% diacerein gel (formulation G1), 1% diacerein cream (formulations C1 and C2) or 1% diacerein ointment (formulations O1, O2 and O3) was added to the skin surface in the donor compartment. The receiver solution was collected at 0, 1, 2, 4, 6 and 8 hours. After 8 hours of treatment with the formulations, the skin was removed from the diffusion cell and the skin surface was carefully cleaned with three alcohol swabs (no tape stripping). The epidermis was separated from the dermis using a scalpel blade. Both the separated epidermis and dermis were weighed, minced and extracted twice with 0.5 ml of acetonitrile:acetic acid:water (60:0.1:40) by vigorous shaking for 1 h. The skin extract was then centrifuged at 14,500 rpm for 20 min. All procedures were carried out under reduced light. Both the skin extract and the receiver solution were stored at -20°C until subjected to analysis of diacerein and rhein concentrations by HPLC (diacerein is easily converted to rhein during the experiment). The skin flux was calculated from the slope of the linear portion of the curve of cumulative permeation of rhein concentration versus time. The results are summarized as follows:

[0075] [Effect of morphology on permeability and retention] transparency As shown in Figure 1, the gel diacerein formulation (G1) penetrates the stratum corneum better than the cream and ointment formulations (C1 and O1). Eight hours after administration, the rhein concentration per gram of epidermis is 204.0 μg for G1, 16.1 μg for C1, and 31.2 μg for O1, and the rhein concentration per gram of dermis is 11.9 μg for G1, 2.53 μg for C1, and 3.14 μg for O1.

[0076] retention As shown in Figures 2A and 2B, rhein penetrated into the skin tissue and was released into the receiver solution after 1 hour for the gel formulation (G1) and after 2 hours for the cream formulation (C1), whereas for the ointment formulation (O1), rhein did not penetrate into the skin tissue and did not enter the receiver solution until 4 hours later, indicating that the ointment formulation had a higher retention rate and a longer retention time than the gel and cream formulations.

[0077] The results show that diacerein / rhein has higher penetration into the stratum corneum in the gel formulation compared to the cream or ointment formulations, and has a longer retention time at the skin target site in the ointment formulation compared to the cream or gel formulations. The gel formulation has the shortest retention time at the skin target site among the three formulations.

[0078] Effect of particle size on permeability and retention Figure 3 shows that the ointment formulation with smaller particle size (O2) penetrated faster than the formulation with larger particle size (O3). Eight hours after administration, the rhein concentration per gram of epidermis was 10.7 μg for O2 and 4.8 μg for O3, and the rhein concentration per gram of dermis was 1.6 μg for O2 and 0.7 μg for O3.

[0079] Figure 4 shows that ointment formulation O2 released rhein after 4 hours, while ointment formulation O3 did not release rhein until 8 hours or even longer. Ointment formulation O3 showed similar compound concentrations in the skin layer, but had a longer retention time compared to O2.

[0080] [Example 2] Comparative Example Wally et al. discloses a cream formulation containing 1% diacerein in the commonly used care cream Ultraphil® (Wally et al., Orphanet Journal of Rare Diseases, 2013, vol. 8, issue 69). A comparison test was carried out between this cream formulation (comparative formulation) and the ointment formulation O3 of the present invention. The results are shown in Figures 5 and 6.

[0081] As shown in Figure 5, the ointment formulation O3 penetrated the stratum corneum more than the comparative formulation, revealing higher retention in the skin layers. Furthermore, as shown in Figure 6, rhein in the comparative formulation penetrated the skin tissue and was detectable in the receiver solution after 4 hours, whereas rhein in the O3 formulation did not penetrate the skin tissue into the receiver solution until 6 hours later.

[0082] The results revealed that the O3 formulation had higher penetration into the stratum corneum, higher retention rate and longer retention time than the comparative formulations, indicating that the O3 formulation maintained a higher drug concentration in the skin layer.

[0083] The above disclosure relates to the detailed technical contents and inventive features of the present invention. Those skilled in the art may make various modifications and replacements based on the above disclosure and suggestions of the present invention without departing from its features. Nevertheless, although such modifications and replacements are not fully disclosed in the above description, they are substantially encompassed in the following claims.

Claims

1. A topical pharmaceutical composition for use in the treatment of epidermolysis bullosa comprising a therapeutically effective amount of a compound selected from the group consisting of diacerein, rhein, monoacetylrhein and their salts or esters, and one or more pharma- ceutically acceptable excipients, said composition being in the form of an ointment, at least about 90% by volume of said compound having a particle size of about 10 to about 30 μm, and said composition comprising, based on the weight of the total composition, about 0.1% to about 10% by weight of said compound, about 15% to about 99% by weight of white petrolatum, about 0% to about 60% by weight of mineral oil, and about 0% to about 10% by weight of cetyl alcohol.

2. The composition described in claim 1, wherein at least about 90% by volume of the compound has a particle size of about 12 to about 25 μm.

3. The composition described in claim 1, wherein the compound is present in an amount of about 0.1% to 5.0% by weight of the total composition.

4. The composition described in claim 1, wherein the compound is present in an amount of about 0.5% to about 2.0% by weight of the total composition.

5. The composition of claim 1, administered once daily or twice daily.

6. Use of the composition described in claim 1 in the manufacture of a medicament for the treatment of epidermolysis bullosa, wherein an effective amount of the composition is administered to a subject in need of treatment.

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