US2002086905A1PendingUtilityA1
Gel for treatment of skin diseases and for disinfection of the skin
Priority: Mar 21, 1994Filed: Dec 12, 2001Published: Jul 4, 2002
Est. expiryMar 21, 2014(expired)· nominal 20-yr term from priority
A61P 31/04A61P 31/02A61K 47/38A61P 17/02A61P 17/00A61K 47/10A61P 17/16A61Q 17/02A61K 47/32A61K 9/0014A61K 8/731A61K 8/34
46
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Claims
Abstract
Gel for local treatment of skin diseases and for prophylaxis, characterized by containing more than 90% of a drying and/or protein coagulating, short-chained alcohol or alcohol mixture, primarily ethanol, and possibly adjuvants or additives and by containing a gelling agent, that possesses good skin-adhesive properties, that gives a matrix formation of alcohol or alcohol mixtures, that creates an evaporation inhibiting effect, gives a prolonged effect, and form a protective plaster when the gel has dried.
Claims
exact text as granted — not AI-modified1 . A method of treating a skin disorder caused by an insect bite or sting wherein a composition comprising more than 90% by weight alkanol selected from C 1-4 alkane-mono-ols, -diols and -triols and less than 10% by weight water, is applied to the area of skin affected by said disorder, and is retained in contact with the said area of skin for a period in the range 1 minute to 48 hours, whereby the sting or bite is cured.
2 . A method according to claim 1 wherein the said period is in the range 5 minutes to 6 hours.
3 . A method according to claim 1 in which a first dose of said composition is retained in contact with the skin for a period in the range 5 minutes to 6 hours and then a second dose of the composition is applied to the said area of skin and is retained in contact with the said area of skin for a further period in the range 5 minutes to 6 hours.
4 . A method according to claim 1 wherein the composition further comprises a polymeric gelling agent dispersed or dissolved in the alkanol.
5 . A method according to claim 4 wherein the active sting or bite curing ingredient consists essentially of said alkanol.
6 . A method according to claim 5 wherein the said active consists essentially only of said alkanol.
7 . A method according to claim 4 wherein said composition consists essentially only of alkanol, gelling agent and water.
8 . A method according to claim 1 wherein the alkanol is ethanol.
9 . A method of treating skin affected by an outbreak of herpes, wherein an antiviral composition consisting essentially of more than 90% by weight alkanol selected from C 1-4 alkane-mono-ols, -diols and -triols and less than 10% water, is contacted with the area of skin affected by said outbreak and is retained in contact with said area for a period of at least about 1 hour.
10 . A method according to claim 9 wherein a first dose of the said composition is retained in contact with said area for a first period of about 1 hour and then one or more further doses of said composition is (are) applied to and retained in contact with said area each for a further period of at least about 1 hour.
11 . A method according to claim 10 wherein, following said further doses, one or more follow-up doses of said composition is (are) applied to and retained in contact with said area each for a period of about 3 to about 5 hours until said outbreak is cured.
12 . A method according to claim 9 wherein the composition comprises an effective gelling amount of a polymeric gelling agent dissolved or dispersed in the alcohol.
13 . A method according to claim 12 wherein the polymeric gelling agent has a molecular weight of at least about 10 4 kDa and is -present in the composition in an amount in the range 0.1 to 10% by weight.
14 . A method according to claim 13 wherein the polymeric gelling agent is present in an amount in the range 0.5 to 2.0% by weight.
15 . A method according to claim 9 wherein the said outbreak is of herpes labialis or herpes genitalis.
16 . A method according to claim 9 wherein the composition is applied to and retained in contact with said area of skin from a cotton ball impregnated with said composition.
17 . A method according to claim 9 wherein the concentration of alkanol in the composition is at least 95%.
18 . A method according to claim 17 wherein said concentration is about 99%.
19 . A method according to claim 10 wherein said first period is about 1 hour.
20 . A method according to claim 10 wherein each said further period is about 1 hour and in which there are 2 to 4 said further periods.
21 . A method according to claim 1 wherein said concentration of alkanol is at least 95% by weight.
22 . A method according to claim 21 wherein said concentration is about 99% by weight.
23 . A method according to claim 9 in which said alkanol is ethanol.
24 . A method according to claim 16 in which said alkanol is ethanol.
25 . A method of treating a skin eruption caused by an intracellular infection of herpes virus by applying to the infected tissue an antiviral composition consisting essentially of more than 90% by weight from C 1-4 alkane-mono-ols and -diols, and less than 10% by weight of water.
26 . A method according to claim 25 in which the alkanol is selected from methanol, ethanol, n-propanol, isopropanol, n-butanol and mixtures thereof.
27 . A method according to claim 26 wherein the alkanol is selected from n-propanol and isopropanol and mixtures.
28 . A method according to claim 26 in which the alkanol is n-propanol.
29 . A method of treating a skin eruption caused by an intracellular infection of herpes virus by applying to the infected tissue a composition comprising at least 70% by weight n-propanol, and less than 30% by weight water.
30 . A method of treating a skin eruption caused by an intracellular infection of herpes virus by applying to the infected tissue a composition comprising at least 80% by weight alkanol, selected from C 3 - and C 4 -alkane mono-ols and mixtures and less than 20% by weight water.
31 . A composition for treating skin disorders comprising more than 90% by weight of an alkanol selected from isopropanol, n-propanol, mixtures of isopropanol and n-propanol, mixtures of propanol, selected from isopropanol, n-propanol and mixtures thereof, and ethanol in which the ratio of propanol to ethanol is in the range 10:1 to 1:10, a polymeric gelling agent in an amount in the range 0.1 to 10% by weight and less than 10% by weight water.
32 . A composition according to claim 31 comprising further an effective amount of an additional active ingredient selected from a local anaesthetic, an analgesic, an antihistamine and mixtures thereof.
33 . A composition for treating skin disorders comprising more than 90% by weight of an alkanol selected from C 1 , C 3 and C 4 alkanols, mixtures thereof and mixtures thereof with ethanol wherein the ratio of (C 1 C 3 and/or C 4 alkanol): ethanol is in the range 1:10 to 10:1, a polymeric gelling agent in an amount in the range 0.1 to 10% by weight and less than 10% by weight water.
34 . A composition according to claim 33 comprising further an effective amount of an additional active ingredient selected from a local anaesthetic, an analgesic, an anti-histamine and mixtures thereof.
35 . A composition according to claim 33 comprising further one or more vitamins dissolved or dispersed in the alcohol.
36 . A composition according to claim 33 wherein the gelling agent is present in an amount in the range 0.5 to 2.0% by weight.
37 . A method of treating a skin disorder by applying to the skin a composition comprising more than 90% by weight of an alkanol selected from isopropanol, n-propanol, mixtures of isopropanol and n-propanol, mixtures of propanol, selected from isopropanol, n-propanol and mixtures thereof, and ethanol in which the ratio of propanol to ethanol is in the range 10:1 to 1:10, a polymeric gelling agent in an amount in the range 0.1 to 10% by weight and less than 10% by weight water.
38 . A method of treating a skin disorder by applying to the skin a composition comprising more than 90% by weight of an alkanol selected from C 1 , C 3 and C 4 alkanols, mixtures thereof and mixtures thereof with ethanol wherein the ratio of (C 1 C 3 and/or C 4 alkanol): ethanol is in the range 1:10 to 10:1, a polymeric gelling agent in an amount in the range 0.1 to 10% by weight and less than 10% by weight water.
39 . A composition for treating skin disorders comprising at least 70% by weight n-propanol, less than 30% by weight water and 0.1 to 10% by weight polymeric gelling agent.
40 . A composition for treating skin disorders comprising at least 80% by weight of an alkanol selected from C 3 and C 4 alkane-mono-ols and mixtures thereof, 0.1 to 10% by weight of a polymeric gelling agent and less than 10% by weight water.Join the waitlist — get patent alerts
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