US2002058068A1PendingUtilityA1
Compositions and methods for drug delivery
Priority: Jan 14, 1999Filed: May 14, 2001Published: May 16, 2002
Est. expiryJan 14, 2019(expired)· nominal 20-yr term from priority
A61K 8/0208A61K 9/7061A61Q 19/00A61K 31/4439A61K 2800/594A61K 8/8147A61K 31/445A61K 2800/54A61K 8/8152
53
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Claims
Abstract
A dermal composition for administration of a drug comprising a blend of two or more acrylic-based polymers having differing functionalities so as to modulate the drug solubility in the polymer matrix and the delivery rate of the drug, and methods therefor.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A dermal composition comprising a blend of:
(a) a polymer composition of two or more polymers which includes:
(I) a first acrylic-based polymer having a first functionality and solubility parameter; and
(ii) a second acrylic-based polymer having a second functionality and solubility parameter, wherein the first and second functionalities differ in the amount and type of functional groups to provide an acrylic-based polymer combination having a net functionality proportional to the ratio of the first and second acrylic-based polymers used, and are present in proportions to provide a net solubility parameter; and
(b) a therapeutically effective amount of one or more drugs incorporated into the polymer composition.
2 . A dermal composition as claimed in claim 1 , wherein the first acrylic-based polymer has a functionality which provides a lower drug solubility than the second acrylic-based polymer.
3 . A dermal composition as claimed in claim 2 , wherein the first acrylic-based polymer is present in an amount to provide a flux of the one or more drugs in the dermal drug delivery composition which is greater than a composition based solely on the second acrylic-based polymer.
4 . A dermal composition as claimed in claim 2 , wherein the amount of the second acrylic-based polymer is in the range of 5-95 weight % and the amount of the first acrylic-based polymer is in the range of 95 to 5% by weight, all based on the total dry weight of the polymer.
5 . A dermal composition as claimed in claim 2 , wherein the amount of the second acrylic-based polymer is in the range of 20-75 weight % and the amount of the first acrylic-based polymer is in the range of 75 to 20% by weight, all based on the total dry weight of the polymer.
6 . A dermal composition as claimed in claim 2 , wherein the first acrylic-based polymer has substantially no functional groups and the second acrylic-based polymer has functional groups.
7 . A dermal composition as claimed in claim 6 , wherein the second acrylic-based polymer has carboxyl and/or hydroxy functional groups.
8 . A dermal composition as claimed in claim 6 , wherein the second acrylic-based polymer is present in an amount to provide a increased saturation concentration in the dermal drug delivery composition which is greater than a composition based solely on the first acrylic-based polymer.
9 . A dermal composition as claimed in claim 6 , wherein the functional groups are provided by monomer units containing functional groups which are incorporated into the second acrylic-based polymer in an amount of from 0.1 to 20% by weight, based on the dry weight of the second acrylic-based polymer.
10 . A dermal composition as claimed in claim 9 , wherein the functional monomers are incorporated into the second acrylic-based polymer in an amount of from 0.1 to 8% by weight, based on the dry weight of the second acrylic-based polymer.
11 . A dermal composition as claimed in claim 1 , wherein the at least two polymer polymers contain substantially only the first and second acrylic-based polymers.
12 . A dermal composition as claimed in claim 7 , wherein the second acrylic-based polymer includes carboxyl functional groups.
13 . A dermal composition as claimed in claim 12 , wherein the one or more drug includes haloperidol.
14 . A dermal composition as claimed in claim 13 , wherein the carboxyl functional acrylic-based polymer includes 0.1 to 10% by weight of carboxyl functional monomer units.
15 . A dermal composition as claimed in claim 14 , wherein the carboxyl functional acrylic-based polymer is a crosslinked vinyl acetate acrylic-based polymer.
16 . A dermal composition as claimed in claim 12 , wherein the one or more drug includes nicotine.
17 . A dermal system as claimed in claim 16 , wherein the carboxyl functional acrylic-based polymer includes 0.1 to 12% by weight of carboxyl functional monomer units.
18 . A dermal system as claimed in claim 16 , wherein the carboxyl functional monomer units are acrylic acid.
19 . A pressure-sensitive dermal drug delivery composition as claimed in claim 3 , wherein the first acrylic-based polymer includes a first functional group and the second acrylic-based polymer includes a second functional group, wherein the first and second functional groups are different.
20 . A pressure-sensitive dermal drug delivery composition as claimed in claim 19 , wherein the first functional group is a hydroxy functional monomer unit and the second functional group is a carboxyl functional monomer unit.
21 . A dermal composition as claimed in claim 20 , wherein the one or more drug includes clonidine.
22 . A dermal system as claimed in claim 21 , wherein the carboxyl functional acrylic-based polymer includes 0.1 to 12% by weight of carboxyl containing monomer units and the hydroxy functional acrylic-based polymer includes 0.1 to 10% by weight of hydroxy containing monomer units.
23 . A dermal system as claimed in claim 21 , wherein the carboxyl containing functional monomer units are acrylic acid, and the hydroxy containing monomer units are 2-hydroxy ethyl acrylate.
24 . A dermal system as claimed in claim 6 , wherein the drug includes scopolamine.
25 . A dermal system as claimed in claim 24 , wherein the second acrylic includes carboxyl groups and the first acrylic includes no or substantially no functional groups.
26 . A method of producing a dermal composition, comprising the steps of:
(1) producing a blend of:
(a) a polymer composition of two or more polymers which includes:
(I) a first acrylic-based polymer having a first functionality and solubility parameter; and
(ii) a second acrylic-based polymer having a second functionality and solubility parameter,
wherein the first and second functionalities differ in the amount and type of functional groups to provide an acrylic-based polymer combination having a net functionality proportional to the ratio of the first and second acrylic-based polymers used, and are blended in proportions to provide a net solubility parameter; and
(b) a therapeutically effective amount of one or more drugs incorporated into the polymer composition;
(2) forming the blend into a polymer matrix; and
(3) drying the polymer matrix to remove the solvent system to form the dermal composition.
27 . A method as claimed in claim 26 , wherein the first acrylic-based polymer has a functionality which provides a lower solubility parameter than the second acrylic-based polymer.
28 . A method as claimed in claim 26 , further comprising the step of applying a backing material to one side of the composition, the backing material being substantially impermeable to the drug contained therein.
29 . A method as claimed in claim 28 , further comprising the step of applying a release liner to a surface of the composition opposite said backing material.
30 . A method of controlling the flux of a drug from a dermal drug delivery composition, comprising the steps of:
(a) selecting at least two polymer polymers which includes:
(I) a first acrylic-based polymer having a first functionality and solubility parameter; and
(ii) a second acrylic-based polymer having a second functionality and solubility parameter,
wherein said first and second functionalities differ in the amount and type of functional groups to provide a polymer combination having a net solubility of one or more drugs within the composition proportional to the ratio of the first and second acrylic-based polymers used;
(b) combining the at least two acrylic-based polymers with a therapeutically effective amount of one or more drugs to form the dermal drug delivery composition, wherein the one or more drugs have a flux which is determined by the net solubility in the composition and is different than the flux of a composition produced solely from said first or second acrylic-based polymers alone.Join the waitlist — get patent alerts
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