GB2084465A - Topically administrable pharmaceutical compositions containing anti-inflammatory steroids - Google Patents
Topically administrable pharmaceutical compositions containing anti-inflammatory steroids Download PDFInfo
- Publication number
- GB2084465A GB2084465A GB8129992A GB8129992A GB2084465A GB 2084465 A GB2084465 A GB 2084465A GB 8129992 A GB8129992 A GB 8129992A GB 8129992 A GB8129992 A GB 8129992A GB 2084465 A GB2084465 A GB 2084465A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pharmaceutical composition
- composition according
- steroid
- oily phase
- liquid oily
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Pharmaceutical compositions such as ointments and creams are provided by admixture of anti- inflammatory steroids active on topical application with a liquid oily phase containing at least one oil possessing a viscosity less than 10 centistokes and in which the steroid has a solubility of at least 0.5% by weight at 25 DEG C, the degree of unsaturation of the steroid in the liquid oily phase of the composition at 25 DEG C being at least 3. Examples of steroids which may be used are betamethasone, beclomethasone and clobetasol derivatives. Suitable oils include esters of mono- and dibasic aliphatic acids. The compositions may include further oils such as liquid paraffin and conventional additives used in the preparation of ointments and creams. The local anti- inflammatory effect of the steroids is maintained in such formulations but systemic side effects are decreased. <IMAGE>
Description
SPECIFICATION
Topically administrable pharmaceutical compositions containing anti-inflammatory steroids
The present invention relates to novel pharmaceutical compositions containing anti-inflammatory steroids.
Anti-inflammatory steroids such as clobetasol 17-propionate are commonly formulated for topical application in solution in relatively polar solvents such as propylene glycol which, in the case of ointments, may be dispersed in white soft paraffin. Such formulations permit some penetration of the active steroid into the skin to exert a topical anti-inflammatory effect. It is thought to be particularly important that the steroid should not, however, be so completely absorbed that it can exert a systemic effect which would be likely to lead to the various unwanted side effects observed with antiinflammatory steroids such as cortisol suppression.
The use of isopropyl and butyl adipates as well as of ethyl lactate and ethanol as vehicles for the topical formulation of triamcinolone acetonide and its dicoumaryl ester is described in a paper by
Altmeyer and Zaun in Arch. Derm. Forsch 1 974, 248, 387-390. The effects of these vehicles on the vasoconstrictor properties of the compounds is discussed, and it is concluded that the base in which a corticosteroid is administered determines to a great extent its penetration rate, strength and duration of topical anti-inflammatory activity. There is no discussion, however, of the possible dangers of enhanced penetration in increasing systemic absorption. As far as can be determined, the solutions of triamcinolone acetonide concerned were saturated or even supersaturated which we believe would have tended to maximise release of the steroid into the aqueous fluids.
We have now found that the systemic side effects produced by anti-inflammatory steroids on topical administration can be significantly decreased if they are applied in solution in certain oils, provided that the degree of unsaturation of the steroid in the oil is relatively high, and that the local anti-inflammatory effect and clinical efficacy of the steroids are not correspondingly reduced.
Consequently, it is possible to apply about the same amount of the steroid to achieve the same local anti-inflammatory effect but to correspondingly reduce unwanted systemic effects.
The formulations according to the invention comprise an anti-inflammatory steroid dissolved in a liquid oily phase as defined hereinafter. The quantity of the liquid oil phase in relation to the quantity of steroid and the solubility of the steroid in the liquid oily phase have been found to be particularly important: the solution of the steroid in the liquid oily phase of the composition should be not more than one third saturated at 250C, i.e. have a degree of unsaturation at 250C of at least 3. This means that the quantity of the liquid oil phase present should be sufficient to dissolve, at 250C, at least three times the amount of steroid which is actually present.
Thus, according to the present invention we provide pharmaceutical compositions comprising an anti-inflammatory steroid active on topical application dissolved in a liquid oily phase containing at least one oil possessing a viscosity less than 10 centistokes and in which the steroid has a solubility of at least 0.5% by weight at 250C, the degree of unsaturation of the steroid in the liquid oily phase of the composition at 250C being at least 3.
Examples of steroids which can benefit by this type of formulation are Beclomethasone 1 7,21 - dipropionate, Betamethasone, 1 7-valerate, Betamethasone 1 7,21 -dipropionate, Clobetasol 17propionate, Clobetasone 17-butyrate and chloromethyl 1 7m-acetoxy-9a-fluoro-1 1 P-hydroxy-l 6P- methyl-3-oxoandrosta- 1,4-diene-17/3-carboxylate.
Formulations containing betamethasone 17-valerate, beclomethasone 1 7,21 -dipropionate and clobetasol 1 7-propionate are preferred. Formulations containing clobetasol 17-propionate are particularly preferred since incidence of dermal atrophy has been shown to be significantly reduced in healthy volunteers when this formulation is used.
Suitable oils for inclusion as solvents for the steroids include esters of mono- and dibasic aliphatic acids, such esters having, for example, 6 to 1 8 carbon atoms, such as the butyl and isopropyl esters of adipic, lauric, palmitic and myristic acids. Dibutyl adipate is particularly useful. Mixtures of the above esters can also be employed.
The compositions according to the invention may contain a mixture of the solvent oil with one or more further oils in which the steroid is soluble and/or one or more oils in which the steroid is substantially insoluble, such as hydrocarbon oils, e.g. liquid paraffin. The liquid paraffin can either be the standard, relatively viscous kind (viscosity about 100 centistokes) or may more advantageously be a light paraffin having a much lower viscosity, for example about 7 centistokes. Use of such light liquid paraffin improves the penetration of the liquid oily phase into the skin.
It will be appreciated that when the principal solvent oil, such as dibutyl adipate, is present in admixture with a non-solvent oil such as hydrocarbon, the solubility of the steroid in the liquid oily phase will not be a linear function of the concentration of the solvent oil in the mixture. The solubility of the chosen active steroid in any mixture of solvent and non-solvent oils can readily be determined by experiment.
The following Tables illustrate typical solubility values, at 250 C, of various steroids in various mixtures of solvents.
TABLE I
Mixture: dibutyl adipate + liquid paraffin % dibutyl adipate % solubility of Clobetasol
in mixture 17-propionate in mixture
25 0.025
28 0.07
36 0.22
50 0.45
65 0.65
75 1.2
85 1.5
100 1.9
TABLE II
Mixture A: dibutyl adipate + isopropyl myristate
Mixture B: dibutyl adipate + liquid paraffin
% dibutyl adipate % solubility of Ciobetasone in mixture (A or B) 17-butyrate in mixture
A B
0 0.65 0.02
10 0.70
20 1.02 0.08
30 1.6 0.15
40 2.1 0.45
50 2.55 0.8
60 2.95 2.0
70 3.5 2.75
TABLE Ill
Mixture: diisopropyl adipate + liquid paraffin
% solubility in mixture of:
% diisopropyl adipate Clobetasone Clobetasol
in mixture 17-butyrate 17-propionate
25 0.15 0.095
50 2.45 0.75
65 2.85 1.25
75 2.95 1.45
85 4.4 2.1
100 7.0 3.0
Table IV shows the solubility of betamethasone 1 7-valerate at 250C in two solvent oils:- TABLE IV
% solubility
Solvent Oil Betamethasone 17-valerate Dibutyi adipate 0.9
Diisopropyl adipate 1.4
The degree of unsaturation appears to be particularly important in relation to the absence of systemic side effects, and while it should be above 3 it is not necessary for the degree of unsaturation to exceed about 5.0, although higher values may not be disadvantageous.
The concentrations of the active steroids in the formulations according to the invention are conveniently in the range 0.02% to 0.5%, e.g. 0.05% to 0.25% by weight, although higher percentages e.g. up to 1.5% may be employed. Preferably the compositions contain 0.05% to 0.50% by weight of active steroid.
The compositions of the invention may, for example, take the form of ointments or creams. In ointments, solid wax will commonly be present. Such an ointment may, for example, contain 55 to 90% by weight of liquid phase and 1 0-45% of solid wax, more usually 6580% by weight liquid phase and 2035% by weight of solid wax. Cream formulations will normally be emulsions, commonly oil-inwater or water-in-oil emulsions, containing 1080%, more usually 2060%, by weight of oil phase.
Such creams can also contain emulsifying agents, which may be surfactants or emulsifying waxes, for
example, cetostearyl alcohol, Cetomacrogol 1000 or self-emulsifying monostearin, as well as
preservatives, buffers, stabilisers etc.
The foregoing formulations for topical application to the skin may be used for the treatment of
inflammatory dermatoses of humans and animals, for example eczema, which are normally responsive
to corticosteroid therapy, and also of less responsive conditions such as psoriasis in humans. The
preparation may be administered by one or more applications per day to the affected area; over skin
areas occlusive dressings may often be used with advantage.
The following examples are given by way of iliustration only: EXAMPLE 1
Ointment % w/w Clobetasol 17-propionate 0.05
Dibutyl adipate 25.00
Microcrystalline Wax 140/145 30.00
Liquid paraffin BP to 100.00
The ointment formulation in Example 1 contains 0.07% of clobetasol 17-propionate in its liquid oily phase (dibutyl adipate + liquid paraffin). As can be seen from the solubility values in Table 1 above. to dissolve that level of clobetasol 17-propionate requires 28% of dibutyl adipate in the liquid oily phase.
The liquid oily phase in fact contains about 36% of dibutyl adipate which as indicated in Table 1 is sufficient to dissolve 0.22% of clobetasol 17-propionate, i.e. more than 3 times the amount of steroid which is actually present in the formulation. Similarly the formulations of Examples 2-10 may be arrived at from the solubility values given in the tables or else the values may be determined by experiment.
EXAMPLE 2
Ointment % w/w
Clobetasol 17-propionate 0.05
Dibutyl adipate 40
Beeswax 15
Isopropyl myristate to 100
EXAMPLE 3
Ointment % w/w
Clobetasone 17-butyrate 0.1
Microcrystalline wax 140/145 40.0
Dibutyl adipate 25.0
Ultra light liquid paraffin to 100.0
EXAMPLE 4
Cream % w/w Clobetasol 17-propionate 0.05
Dibutyl adipate 30.0
Microcrystalline wax 140/145 7.5
Cetostearyl alcohol 7.5
Cetomacrogol 1000 1.0
Sodium citrate 0.05
Citric acid 0.05
Chlorocresol 0.1
Water to 100.0
EXAMPLE 5
Cream % w/w Clobetasol 17-propionate 0.05
Dibutyl adipate 50.0
Beeswax 7.0
Cetostearyl alcohol 7.0
Self-emulsifying monstearin 2.0
Sodium citrate 0.05
Citric acid 0.05
Chlorocresol 0.1
Water to 100.0
EXAMPLE 6
Ointment % w/w Betamethasone 1 7-valerate 0.12
Dibutyl adipate 60
Microcrystalline wax 140/145 20
Beeswax 10
Liquid paraffin to 100
EXAMPLE 7
Ointment % w/w
Beclomethasone 1 7,21 -dipropionate 0.025
Dibutyl adipate 37.5
Microcrystalline wax 140/145 30
Liquid paraffin to 100
EXAMPLE 8
Cream-like ointment % w/w
Clobetasol 17-propionate 0.05
Dibutyl adipate 22.0
Microcrystalline wax 140/145 30.0
Beeswax 3.0
Cetomacrogol 1000 3.0
Titanium dioxide 2.0
Ultra-light liquid paraffin to 1 00.0 EXAMPLE 9
Ointment % w/w Chloromethyl 1 7a-acetoxy- 9cr-fluoro-11,B-hydroxy-16j3- methyl-3-oxoandrosta- 1,4 diene-17P-carboxylate 0.1
Dibutyl adipate 84.9
Beeswax 15.0
EXAMPLE 10
Ointment % w/w Betamethasone 17,21 -dipropionate 0.05
Beeswax 10.00
Microcrystalline wax 140/145 20.00
Dibutyl adipate to 100.00
The method used for making up the formulations is as follows: the steroid is dissolved in a portion of or all of the dibutyl adipate. The other ingredients are mixed together at 60-700C and the steroid solution added to the mixture which is then stirred and cooled until semi-solid.
Claims (14)
1. A pharmaceutical composition comprising an anti-inflammatory steroid active on topical application dissolved in a liquid oily phase containing at least one oil possessing a viscosity less than 10 centistokes and in which the steroid has a solubility of at least 0.5% by weight at 250C, the degree of unsaturation of the steroid in the liquid oily phase of the composition at 250C being at least 3.
2. A pharmaceutical composition according to claim 1 wherein the anti-inflammatory steroid is selected from beclomethasone 17,21 -dipropionate, betamethasone 17-valerate, betamethasone 17,21 dipropionate, clobetasol 17-propionate, clobetasone 17-butyrate and chloromethyl 1 7ar-acetoxy-9a- fluoro- 11 -hydrnxy- 1 6-methyI-3-oxoandrnsta- 1 ,4-diene- 1 7/3-carboxylate.
3. A pharmaceutical composition according to claim 1 or claim 2 wherein the liquid oily phase contains at least one oil selected from the esters of mono- and dibasic aliphatic acids the said ester having from 1 6 to 1 8 carbon atoms.
4. A pharmaceutical composition according to claim 3 wherein the liquid oily phase contains at least one oil selected from the butyl and isopropyl esters of adipic, lauric, palmitic and myristic acids.
5. A pharmaceutical composition according to claim 4 wherein the liquid oily phase contains dibutyl adipate.
6. A pharmaceutical composition according to claim 5 which contains clobetasol 17-propionate.
7. A pharmaceutical composition according to claim 5 which contains betamethasone 17valerate.
8. A pharmaceutical composition according to claim 5 which contains beclomethasone 1 7,21 - dipropionate.
9. A pharmaceutical composition according to any preceding claim wherein the liquid oily phase contains further oil(s).
1 0. A pharmaceutical composition according to claim 9 wherein the liquid oily phase contains liquid paraffin having a viscosity of about 7 centistokes.
11. A pharmaceutical composition according to any preceding claim in which the degree of unsaturation of the steroid is in the range 3.0 to 5.0.
12. A pharmaceutical composition according to any preceding claim wherein the concentration of the steroid is from 0.02 to 1.5% by weight of the composition.
1 3. A pharmaceutical composition according to any preceding claim in the form of an ointment or cream.
14. A pharmaceutical composition according to claim 1 3 containing, as additional ingredients, substances selected from solid wax, emulsifying agents, preservatives, buffers, stabilisers and other conventional additives.
1 5. A pharmaceutical composition substantially as described herein with reference to Examples 1-10.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8129992A GB2084465B (en) | 1980-10-06 | 1981-10-05 | Topically administrable pharmaceutical compositions containing anti-inflammatory steroids |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8032111 | 1980-10-06 | ||
GB8129992A GB2084465B (en) | 1980-10-06 | 1981-10-05 | Topically administrable pharmaceutical compositions containing anti-inflammatory steroids |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2084465A true GB2084465A (en) | 1982-04-15 |
GB2084465B GB2084465B (en) | 1984-09-12 |
Family
ID=26277114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8129992A Expired GB2084465B (en) | 1980-10-06 | 1981-10-05 | Topically administrable pharmaceutical compositions containing anti-inflammatory steroids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2084465B (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2123292A (en) * | 1982-07-07 | 1984-02-01 | Schering Ag | Topical corticoid-containing preparations |
EP0147535A2 (en) * | 1983-10-06 | 1985-07-10 | American Cyanamid Company | Pharmaceutical composition comprising an E-type prostaglandin compound and useful as a topical medicament |
EP0196121A1 (en) * | 1985-02-22 | 1986-10-01 | Pera Dr. Visnjic | Process for obtaining the preparation for the treatment of the disease psoriasis; drug for the treatment of psoriasis and its application |
AU602871B2 (en) * | 1986-02-14 | 1990-11-01 | Pero Visnjic | Procedure for obtaining the preparation for the treatment of the disease psoriasis; drug for the treatment of psoriasis and its application |
GB2390540A (en) * | 2002-07-09 | 2004-01-14 | Denis Tenant-Flowers | Composition for the prevention of hair colour loss |
WO2009047788A2 (en) * | 2007-08-06 | 2009-04-16 | Glenmark Pharmaceuticals Limited | Topical composition containing the combination of mupirocin and beclomethasone |
-
1981
- 1981-10-05 GB GB8129992A patent/GB2084465B/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2123292A (en) * | 1982-07-07 | 1984-02-01 | Schering Ag | Topical corticoid-containing preparations |
EP0147535A2 (en) * | 1983-10-06 | 1985-07-10 | American Cyanamid Company | Pharmaceutical composition comprising an E-type prostaglandin compound and useful as a topical medicament |
EP0147535A3 (en) * | 1983-10-06 | 1986-01-08 | American Cyanamid Company | Pharmaceutical composition comprising an e-type prostaglandin compound and useful as a topical medicament |
EP0196121A1 (en) * | 1985-02-22 | 1986-10-01 | Pera Dr. Visnjic | Process for obtaining the preparation for the treatment of the disease psoriasis; drug for the treatment of psoriasis and its application |
AU602871B2 (en) * | 1986-02-14 | 1990-11-01 | Pero Visnjic | Procedure for obtaining the preparation for the treatment of the disease psoriasis; drug for the treatment of psoriasis and its application |
US5004736A (en) * | 1986-02-14 | 1991-04-02 | Pero Visnjic | Procedure for obtaining the preparation for the treatment of the disease psoriasis: drug for the treatment of psoriasis and its application |
GB2390540A (en) * | 2002-07-09 | 2004-01-14 | Denis Tenant-Flowers | Composition for the prevention of hair colour loss |
GB2390540B (en) * | 2002-07-09 | 2005-11-30 | Denis Tenant-Flowers | Composition when used for the prevention of hair colour loss |
WO2009047788A2 (en) * | 2007-08-06 | 2009-04-16 | Glenmark Pharmaceuticals Limited | Topical composition containing the combination of mupirocin and beclomethasone |
WO2009047788A3 (en) * | 2007-08-06 | 2009-07-02 | Glenmark Pharmaceuticals Ltd | Topical composition containing the combination of mupirocin and beclomethasone |
Also Published As
Publication number | Publication date |
---|---|
GB2084465B (en) | 1984-09-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4370322A (en) | Topically administrable pharmaceutical compositions containing anti-inflammatory steroids | |
JP5721927B2 (en) | Topical composition containing at least one vitamin D or one vitamin D analog and at least one corticosteroid | |
US4083974A (en) | Topical steroidal anti-inflammatory preparations containing polyoxypropylene 15 stearyl ether | |
RU2238734C2 (en) | Pharmaceutical composition | |
US4794106A (en) | Cream | |
US4233295A (en) | Corticosteroid formulations containing sebacate carrier | |
US4048310A (en) | Topical steroid formulation in form of lotion or cream | |
US5612327A (en) | 1α,24-(OH)2 -cholecalciferol emulsion composition and method for treating psoriasis | |
CA2670425A1 (en) | Pharmaceutical compositions including vitamin d and corticosteroid | |
US5094851A (en) | Water-containing external preparations | |
GB2084465A (en) | Topically administrable pharmaceutical compositions containing anti-inflammatory steroids | |
JPS58225009A (en) | Pharmaceutical preparation of corticosteroid for external use | |
WO2002013868A1 (en) | Dermatological formulation | |
JP3150021B2 (en) | External cream for skin | |
JPH0676327B2 (en) | Steroid ointment formulation | |
IE58042B1 (en) | Improved betamethasone dipropionate cream | |
CA1045974A (en) | Oil-free pharmaceutical cream | |
US4279901A (en) | Topical ointment | |
EP0325949B1 (en) | Concentrated solutions of corticosteroids and method of making them | |
US20030216364A1 (en) | Dermatological Formulation | |
LU84059A1 (en) | NOVEL PHARMACEUTICAL COMPOSITIONS COMPRISING ANTI-INFLAMMATORY STEROIDS | |
JPH0219090B2 (en) | ||
KR830010126A (en) | Method for preparing pharmaceutical composition for micro administration containing steroid anti-inflammatory |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |