GB2124485A - Penetrating topical medicament - Google Patents
Penetrating topical medicament Download PDFInfo
- Publication number
- GB2124485A GB2124485A GB08222494A GB8222494A GB2124485A GB 2124485 A GB2124485 A GB 2124485A GB 08222494 A GB08222494 A GB 08222494A GB 8222494 A GB8222494 A GB 8222494A GB 2124485 A GB2124485 A GB 2124485A
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- GB
- United Kingdom
- Prior art keywords
- medicament
- set forth
- volume
- level
- group
- 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.)
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Classifications
-
- 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
-
- 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
- A61K31/095—Sulfur, selenium, or tellurium compounds, e.g. thiols
- A61K31/10—Sulfides; Sulfoxides; Sulfones
-
- 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
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/60—Salicylic acid; Derivatives thereof
-
- 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
- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
Abstract
An improved topical medicament useful in treating athletic injuries or other painful subdermal conditions comprises a penetrating solvent such as dimethylsulfoxide (DMSO) along with a corticosteroid (e.g., hydrocortisone acetate), a counter- irritant/analgesic such as methyl salicylate, and optionally one or more emulsifiers, a rubifacient and an alcoholic carrier.
Description
SPECIFICATION
Penetrating topical medicament
Background of the invention
1. Field of the invention
The present invention is concerned with greatly improved topical medicaments which can penetrate the skin and transport an anti-inflammatory corticosteroid and/or an analgesic to enhance the effectiveness of such components.
More particularly, it is concerned with such topical medicaments which include a penetrating solvent such as dimethylsulfoxide (DMSO) or an alcohol along with a corticosteroid and/or a counterirritant/analgesic, and, preferably, a rubefacient, one or more suspending agents (e.g., emulsifiers), and a carrier.
2. Description of the prior art
Corticosteroids such as the hydrocortisones and their various derivatives are known to be useful medicinal agents. For example, these substances can be applied topically for the purpose of treatment of dermatoses of various types. These materials are known to have antiinflammatory, antipruritic and vascconstrictive actions. The clinical efficacy of topical corticosteroids is dependent upon the extent of percutaneous absorption or penetration of the active drug through the skin. Factors influencing absorption include the agent used, the concentration of the drug, the vehicle used, and the anatomical site of application.Topically applied corticosteroid preparations are available in nonprescription form forth temporary relief of minor skin irritations, itching and rashes due to eczema, dermatitis, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, jewelry and itchy genital and anal areas.
In addition, corticosteroids have been prepared in injectable form for treatment of inflamed body parts such as kness or other joints. To give but one example, these preparations can be injected for the treatment of painful athletic injuries such as knee sprains and the like.
Dimethylsulfoxide (DMSO) is an extra-ordinary chemical in the form of a highly polar, stable, hygroscopic organic liquid with exceptional solvent properties. Its industrial applications are numerous and diverse, being used as a solvent for resins, fungicides, dyes, pigments, etc., as a reactant for chemical synthesis, as an extractant, and as a reaction medium to accelerate rates of chemical combination.
DMSO has also been tested for use in certain types of topical preparations, e.g., see "Topical
Pharmacology and Toxicology of Dimethyl Sulfoxide-Part I", Journal of the American
MedicalAssociation, Vol. 193, No. 10, p. 796, and literature cited therein.
Counterirritants are sometimes employed in topical medicaments for the symptomatic relief of pain. Counterirritants are agents that are applied locally to produce an inflammatory reaction with the object of affecting another site usually adjacent to or underlying the surface irritated. The intensity of response of the skin depends on not only the nature of the irritant employed, but also its concentration, the solvent in which it is dissolved, and the period of contact. A counterirritant drug is typically applied to the skin where pain is experienced. Pain is only as intense as it is perceived, and the perception of other sensations from the application of the counterirritant, such as massage and warmth, tend to crowd out perception of the pain.In addition, such products may produce an increase in the flow of blood to the muscles which, with concomitant waste disposal and other chemical changes, enhances recovery. Various types of counterirritants have been employed in the past, e.g., methyl salicylate, camphor, menthol, eugenol, eucalyptol and thymol.
Additional background patents and literature references in connection with the instant invention include:
U.S. Pat. No. 2,801,202-Compositions Containing Cortisone or Hydro-Cortisone and
Phenylphrine
U.S. Pat. No. 2,81 5,315-Analgesic and Anti
rheumatic Preparation
U.S. Pat. No. 2,880,1 30-Anti-inflammatory Steroid Solutions
U.S. Pat. No. 2,880,1 38-Anti-inflammatory Steroid Solutions
U.S. Pat. No. 2,890,152-Topical Anti-inflam
matory Compositions
U.S. Pat. No. 3,019,1 62-Cinchophen-Hydro- cortisone Topical Compositions
U.S. Pat. No. 3,053,737-N-Acetyl-p-Amino- phenol Anti-inflammatory Steroid
Compositions
U.S.Pat. No. 3,474,168-Prevention of
Corticosteroid Side Effects
U.S. Pat. No. 4,012,508-Topical Composition
and Method
"Rubs and Liniments", Facts and Comparisons, pp.1653-1655(1981) "Emulsifying and Suspending Agents",
Pharmaceutical Necessities-Remingtons
Pharmaceutical Science, Chapter 64, pp.
1244-1253(1980) "Emulsions", Particle Phenomena and Coarse
Dispersions-Remingtons Pharmaceutical
Science
"Hormones", Remingtons Pharmaceutical
Science, 16th Ed., pp.901-912(1980) "Corticosteroids Topical", Fact S Comparisons, pp.1620-1628(1981) Summary of the invention
The present invention provides a greatiy improved topical medicament which includes a member selected from the group consisting of the corticosteroids, derivatives of the corticosteroids, and mixtures thereof, a substance selected from the group consisting of methyl salicylate, triethanolamine salicylate, salicyamide, oil of eucalytus, menthol and mixtures thereof, and an amount of a penetrating solvent such as DMSO or a lower alcohol (i.e., an alcohol having from 1-4 carbon atoms, inclusive). A medicament of this type is particularly useful for the topical treatment of sprains or other types of athletic injuries. In use, the penetrating solvent serves to transport at least the corticosteroid component to a subcutaneous site of inflammation in order to reduce and ameliorate the effects thereof. At the same time, the counterirritant substance serves to lessen the pain and discomfort commonly experienced with such athletic injuries, and serves to increase blood flow. In particularly preferred forms, the counterirritant substance is selected from the group consisting of methyl salicylate, triethanolamine salicylate, and salicyamide. These materials are converted to salicyclic acid in the bloodstream, and in this form serve as effective pain killers.
The topical medicament hereof can be in various forms such as lotions, creams, jellies or aerosols. Depending upon the desired form, the medicament may include one or more suspending agents such as sodium lauryl sulfate, stearyl alcohol, cetyl alcohol, glycerol monostearate, the polyethyien glycols, bentonite, tragacanth, and mixtures thereof. In the case of a lotion product for example, a plurality of emulsifiers may be employed.
Description of the preferred embodiments
As noted above, the medicaments of the present invention include a corticosteroid or derivative thereof, and most preferably a member selected from the group consisting of the hydrocortisones and derivatives thereof, with hydrocortisone acetate being a typical example. This component is preferably present at a level of up to about 10% by volume in the final medicament, and more preferably from about 0.5 to 5% by volume, and most preferably about 0.5% by volume.
The counterirritant/anaigesic substance is preferably present at a level of up to about 50% by volume, more preferably from about 10 to 35% bylvolume, and more preferably about 1 5% by volume. On the other hand, the solvent component is advantageously used at a level of from about 5 to 90% by volume, more preferably from about 5 to 50% by volume, and most preferably about 15% by volume.
Although the amounts of suspending agents may vary depending upon desired characteristics in the final medicament, as a general rule the total amount of suspending agent should be present at a level of up to about 15% by volume.
In certain compositions in accordance with the invention, the medicament may include a rubefacient such as camphor, normally at a level of up to about 5% by volume.
The following table sets forth preferred components useful in the preparation of a lotion type topical medicament in accordance with the invention. The ranges of use of the respective
components are set forth, along with the most
preferred amounts:
Table
Usual Most
ranges preferred
Component (Vol. /OJ (Vol%) DMSO 5-90 15 Hyd rocortisone acetate 0--10 0.5
Methyl salicylate 0-50 1 5 Camphor 0-5 Cetyl alcohol 0--4 0.5
Stearyl alcohol 0-4 0.5
Glycerol
monostearate 0-6 1 Menthol 0--5 Isopropyl
alcohol 0-50% 10
Distilled Water 0-80% 57.5
100.0
In preparative procedures using the most preferred components in the foregoing Table, an aqueous phase is formulated by adding the glycerol monostearate to 50% distilled water, followed by heating until the monostearate is dissolved and a homogeneous mixture results. The aqueous phase is then allowed to cool. An oleaginous phase is next prepared by adding the hydrocortisone to isopropyl alcohol, with gentle stirring to dissolve the hydrocortisone. The DMSO is next added to the methyl salicylate, again with gentle stirring. The hydrocortisone/alcohol and
DMSO/methy salicylate mixtures are then blended together, and the cetyl and stearyl alcohol are added thereto. The entire mixture is then heated until all components are fully dissolved.
The oleaginous phase is slowly added to the cooled aqueous stage, with vigorous stirring (e.g., using an electric stirrer or Hobart mixer), whereupon the remaining 7.5% distilled water is added with stirring until a uniform emulsidn has been obtained.
In the use of a lotion-type composition as described, the medicament is simply applied to the skin at the region of pain. For example, in the case of a knee sprain, the lotion is applied on the skin adjacent the affected knee. The DMSO or alcoholic solvent serves to transport the hydrocortisone component to a subcutaneous site for treatment of inflammation whereas the methyl salicylate and other components (if used) serve as counterirritants or rubifacients in order to lessen pain. The methyl salicylate is transported subcutaneously and is converted in the bloodstream to the analgesic salicylic acid. This also serves to
kill the pain associated with the injury.
Claims (17)
1. A penetrating topical medicament, comprising:
a member selected from the group consisting of the corticosteroids, derivatives of the corticosteroids, and mixtures thereof;
a substance selected from the group consisting of methyl salicylate, triethanolamine salicylate, salicyamide, oil of eucalyptus, menthol and mixtures thereof; and
an amount of a penetrating solvent for transporting said at least said member through the skin.
2. The medicament as set forth in Claim 1, said substance being present at a level of up to about 50% by volume.
3. The medicament as set forth in Claim 2, said level being about 15% by volume.
4. The medicament as set forth in Claim 1, said amount being from about 5 to 90% by volume.
5. The medicament as set forth in Claim 4, said amount being about 1 5% by volume.
6. The medicament as set forth in Claim 1, said member being present at a level of up to about 10% by volume.
7. The medicament as set forth in Claim 6, said level being about .5% by volume.
8. The medicament as set forth in Claim 1, including at least one suspending agent.
9. The medicament as set forth in Claim 8, said agent being selected from the group consisting of sodium lauryl sulfate, stearyl alcohol, cetyl alcohol, glycerol monostearate, the polyethylene glycols, bentonite, tragacanth, and mixtures thereof.
10. The medicament as set forth in Claim 8, said agent being present at a level of up to about 15% by volume.
11. The medicament as set forth in Claim 1, including a rubefacient.
12. The medicament as set forth in Claim 11, said rubefacient being camphor.
13. The medicament as set forth in Claim 11, said rubefacient being present at a level of up to about 5% by volume.
14. The medicament as set forth in Claim 1, said member being selected from the group consisting of the hydrocortisones and derivatives thereof.
1 5. The medicament as set forth in Claim 1, said solvent being dimethyl sulfoxide.
16. The medicament as set forth in Claim 1, said solvent being a lower alcohol.
17. A penetrating topical medicament, comprising:
a quantity of dimethyl sulfoxide; and
a member selected from the group consisting of methyl salicylate, triethanolamine salicylate, salicyamide and mixtures thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB08222494A GB2124485B (en) | 1982-08-04 | 1982-08-04 | Penetrating topical medicament |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB08222494A GB2124485B (en) | 1982-08-04 | 1982-08-04 | Penetrating topical medicament |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2124485A true GB2124485A (en) | 1984-02-22 |
GB2124485B GB2124485B (en) | 1986-06-04 |
Family
ID=10532108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08222494A Expired GB2124485B (en) | 1982-08-04 | 1982-08-04 | Penetrating topical medicament |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2124485B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
GB2180750B (en) * | 1985-09-26 | 1989-09-06 | Shionogi & Co | Topical analgesic anti-inflammatory composition |
US5130139A (en) * | 1990-07-06 | 1992-07-14 | Alza Corporation | Reduction or prevention of skin irritation by drugs |
US5160741A (en) * | 1990-07-06 | 1992-11-03 | Alza Corporation | Reduction or prevention of skin irritation by drugs |
WO2009048841A1 (en) * | 2007-10-09 | 2009-04-16 | Humco Holding Group, Inc. | Antifungal treatment of nails |
-
1982
- 1982-08-04 GB GB08222494A patent/GB2124485B/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
GB2180750B (en) * | 1985-09-26 | 1989-09-06 | Shionogi & Co | Topical analgesic anti-inflammatory composition |
US5130139A (en) * | 1990-07-06 | 1992-07-14 | Alza Corporation | Reduction or prevention of skin irritation by drugs |
US5160741A (en) * | 1990-07-06 | 1992-11-03 | Alza Corporation | Reduction or prevention of skin irritation by drugs |
WO2009048841A1 (en) * | 2007-10-09 | 2009-04-16 | Humco Holding Group, Inc. | Antifungal treatment of nails |
US8333981B2 (en) | 2007-10-09 | 2012-12-18 | Humco Holding Group, Inc. | Antifungal treatment of nails |
Also Published As
Publication number | Publication date |
---|---|
GB2124485B (en) | 1986-06-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |