Patent US4908027A successfully refreshed from Google Patents.
US4908027A
Expired / Lapsed
US
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Subsaturated transdermal therapeutic system having improved release characteristics
Assignee: Alza Corp
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Filing: 1986-09-12
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Granted: 1990-03-13
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Expires: 2006-09-12
Abstract
Abstract Rate-controlled transdermal delivery devices are disclosed which utilize an in-line adhesive to maintain the device on the skin and deliver an agent which is a solvent for the in-line adhesive. The initial equilibrated concentration of the agent in the agent reservoir and the adhesive is below saturation and the reservoir comprises the agent dissolved in a solvent with respect to which the rate controlling element of the device is substantially impermeable. In preferred embodiments the initial loading of the agent in reservoir is sufficient to prevent the activity of the agent in the reservoir from decreasing by more than about 50% and preferrably no more than about 25% during the predetermined period of administration; and the thicknesses of the adhesive, rate controlling membrane and reservoir layers are selected so that at least 50% and, preferrably at least 75% initial equilibrated agent loading is in the reservoir layer. The devices are usable to delivery oily non-polar agents which are liquid at body temperatures such as benztropine and secoverine.
Inventors
- 👤 David J. Enscore
- 👤 Patricia S. Campbell
- 👤 James L. Osborne
- 👤 Melinda K. Smart
- 👤 Su I. Yum
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-28 17:01
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/70; A61K9/7023; A61K9/703; A61K9/7084; A61K31/00; A61K31/33; A61K31/395; A61K31/435; A61K31/46
Claims Analysis
Total Claims: 33
Claim 1
Independent Claim
76 words
A method of producing a therapeutic effect which comprises placing a source of benztropine comprising a benztropine base permeable material having benztropine dissolved therein in benztropine transmitting relationship to an area of intact human skin and administering benztropine to the human subject from said source through said area of intact skin for an extended period of time at a therapeutically effective rate of approximately 10-40 μg/hr for a substantial portion of said extended period of time.
Claim 2
Independent Claim
76 words
A method of producing a therapeutic effect which comprises placing a source of benztropine comprising a benztropine base permeable material having benztropine dissolved therein in benztropine transmitting relationship to an area of intact human skin and administering benztropine to the human subject from said source through said area of intact skin for an extended period of time at a therapeutically effective rate of approximately 10-40 μg/hr for a substantial portion of said extended period of time.
Claim 3
Dependent Claim
16 words
The method of claim 1 wherein said extended period of time is at least 12 hours.
Claim 4
Independent Claim
75 words
A method for producing a therapeutic effect which comprises placing a source of dexsecoverine comprising a dexsecoverine permeable material having dexsecoverine dissolved therein in dexsecoverine transmitting relationship to an area of intact human skin and administering dexsecoverine to the human subject from such source through said area of intact skin for an extended period of time at a therapeutically effective rate of approximately 10-40 μg/hr for a substantial portion of said extended period of time.
Claim 5
Independent Claim
75 words
A method for producing a therapeutic effect which comprises placing a source of dexsecoverine comprising a dexsecoverine permeable material having dexsecoverine dissolved therein in dexsecoverine transmitting relationship to an area of intact human skin and administering dexsecoverine to the human subject from such source through said area of intact skin for an extended period of time at a therapeutically effective rate of approximately 10-40 μg/hr for a substantial portion of said extended period of time.
Claim 6
Dependent Claim
18 words
The method of claim 3 wherein said source of dexsecoverine is substantially free of the l-isomer of secoverine.
Claim 7
Dependent Claim
17 words
The method of claim 3 wherein said source of dexsecoverine comprises a racemic mixture of secoverine isomers.
Claim 8
Dependent Claim
16 words
The method of claim 3 wherein said extended period of time is at least 12 hours.
Claim 9
Dependent Claim
159 words
A medical device for the transdermal administration of dexsecoverine utilizing an in-line adhesive that is soluble in dexsecoverine, said device being adapted to deliver dexsecoverine at an antispasmolydically effective rate during a substantial portion of a predetermined administration period comprising, in combination: a. a dexsecoverine reservoir comprising dexsecoverine dissolved in an ethylene/vinyl acetate copolymer at a concentration less than saturation and at an initial dexsecoverine loading sufficient to prevent the thermodynamic activity of dexsecoverine in said ethylene/vinylacetate copolymer from decreasing by more than 50% during said administration period; b. dexsecoverine release rate controlling means disposed in the path of dexsecoverine migration from said reservoir to the skin, said rate controlling means being permeable to dexsecoverine and substantially impermeable to said solvent and being selected from the group consisting of polyethylene and ethylene/vinylacetate copolymers; and c. adhesive means disposed in the path of dexsecoverine migration from said release rate controlling means to the skin, said adhesive being soluble in dexsecoverine.
Claim 10
Dependent Claim
159 words
A medical device for the transdermal administration of dexsecoverine utilizing an in-line adhesive that is soluble in dexsecoverine, said device being adapted to deliver dexsecoverine at an antispasmolydically effective rate during a substantial portion of a predetermined administration period comprising, in combination: a. a dexsecoverine reservoir comprising dexsecoverine dissolved in an ethylene/vinyl acetate copolymer at a concentration less than saturation and at an initial dexsecoverine loading sufficient to prevent the thermodynamic activity of dexsecoverine in said ethylene/vinylacetate copolymer from decreasing by more than 50% during said administration period; b. dexsecoverine release rate controlling means disposed in the path of dexsecoverine migration from said reservoir to the skin, said rate controlling means being permeable to dexsecoverine and substantially impermeable to said solvent and being selected from the group consisting of polyethylene and ethylene/vinylacetate copolymers; and c. adhesive means disposed in the path of dexsecoverine migration from said release rate controlling means to the skin, said adhesive being soluble in dexsecoverine.
Claim 11
Dependent Claim
37 words
The device of claim 7 wherein said dexsecoverine is present at an initial equilibrated loading sufficient to permit delivery of said dexsecoverine at a therapeutically effective rate in the range of 10-40 mcg/hr throughout said administration period.
Claim 12
Dependent Claim
32 words
The device of claim 7 wherein the thickness of said reservoir and adhesive layers are selected such that at least 50% of the initial equilibrated loading of dexsecoverine is in the reservoir.
Claim 13
Dependent Claim
32 words
The device of claim 7 wherein the thickness of said reservoir and adhesive layers are selected such that at least 75% of the initial equilibrated loading of dexsecoverine is in the reservoir.
Claim 14
Dependent Claim
38 words
The device of claim 7 wherein the initial equilibrated loading of dexsecoverine in said reservoir is sufficient to prevent the thermodynamic activity of said dexsecoverine in said solvent from decreasing by more than 25% during said administration period.
Claim 15
Dependent Claim
38 words
The device of claim 10 wherein the initial equilibrated loading of dexsecoverine in said reservoir is sufficient to prevent the thermodynamic activity of said dexsecoverine in said solvent from decreasing by more than 25% during said administration period.
Claim 16
Dependent Claim
25 words
The device of claim 7 wherein the initial equilibrated thermodynamic activity of dexsecoverine in said reservoir and adhesive layers is no greater than about 0.15.
Claim 17
Dependent Claim
25 words
The device of claim 12 wherein the initial equilibrated thermodynamic activity of dexsecoverine in said reservoir and adhesive layers is no greater than about 0.15.
Claim 18
Dependent Claim
14 words
The device of claim 14 wherein said ethylene/vinylacetate copolymer solvent contains about 9% vinylacetate.
Claim 19
Dependent Claim
22 words
The device of claim 15 wherein said release rate controlling means comprises an ethylene/vinylacetate copolymer having a vinylacetate content of about 40%.
Claim 20
Dependent Claim
16 words
The device of claim 7 wherein the dexsecoverine in said device is present as racemic secoverine.
Claim 21
Dependent Claim
19 words
The device of claim 7 wherein said dexsecoverine in said device is substantially free of other stereoisomers of secoverine.
Claim 22
Dependent Claim
19 words
The device of claim 15 wherein said dexsecoverine in said device is substantially free of other stereoisomers of secoverine.
Claim 23
Dependent Claim
160 words
A medical device for the transdermal administration of benztropine utilizing an in-line adhesive that is soluble in benztropine, said device being adapted to deliver benztropine at an anticholinergically effective rate during a substantial portion of a predetermined administration period comprising, in combination: a. a benztropine reservoir comprising benztropine dissolved in an ethylene/vinyl acetate copolymer at a concentration less than saturation and at an initial equilibrated benztropine loading sufficient to prevent the thermodynamic activity of benztropine in said ethylene/vinylacetate copolymer from decreasing by more than 50% during said administration period; b. benztropine release rate controlling means disposed in the path of benztropine migration from said reservoir to the skin, said rate controlling means being permeable to benztropine and substantially impermeable to said solvent and being selected from the group consisting of polyethylene and ethylene/vinylacetate copolymers; and c. adhesive means disposed in the path of benztropine migration from said release rate controlling means to the skin, said adhesive being soluble in benztropine.
Claim 24
Dependent Claim
160 words
A medical device for the transdermal administration of benztropine utilizing an in-line adhesive that is soluble in benztropine, said device being adapted to deliver benztropine at an anticholinergically effective rate during a substantial portion of a predetermined administration period comprising, in combination: a. a benztropine reservoir comprising benztropine dissolved in an ethylene/vinyl acetate copolymer at a concentration less than saturation and at an initial equilibrated benztropine loading sufficient to prevent the thermodynamic activity of benztropine in said ethylene/vinylacetate copolymer from decreasing by more than 50% during said administration period; b. benztropine release rate controlling means disposed in the path of benztropine migration from said reservoir to the skin, said rate controlling means being permeable to benztropine and substantially impermeable to said solvent and being selected from the group consisting of polyethylene and ethylene/vinylacetate copolymers; and c. adhesive means disposed in the path of benztropine migration from said release rate controlling means to the skin, said adhesive being soluble in benztropine.
Claim 25
Dependent Claim
37 words
The device of claim 20 wherein said benztropine is present at an initial equilibrated loading sufficient to permit delivery of said benztropine at a therapeutically effective rate in the range of 10-40 mcg/hr throughout said administration period.
Claim 26
Dependent Claim
32 words
The device of claim 20 wherein the thickness of said reservoir and adhesive layers are selected such that at least 50% of the initial equilibrated loading of benztropine is in the reservoir.
Claim 27
Dependent Claim
32 words
The device of claim 20 wherein the thickness of said reservoir and adhesive layers are selected such that at least 75% of the initial equilibrated loading of benztropine is in the reservoir.
Claim 28
Dependent Claim
38 words
The device of claim 20 wherein the initial equilibrated loading of benztropine in said reservoir is sufficient to prevent the thermodynamic activity of said benztropine in said solvent from decreasing by more than 25% during said administration period.
Claim 29
Dependent Claim
38 words
The device of claim 23 wherein the initial equilibrated loading of benztropine in said reservoir is sufficient to prevent the thermodynamic activity of said benztropine in said solvent from decreasing by more than 25% during said administration period.
Claim 30
Dependent Claim
24 words
The device of claim 20 wherein the initial equilibrated thermodynamic activity of benztropine in said reservoir and adhesive layers is up to about 0.50.
Claim 31
Dependent Claim
24 words
The device of claim 25 wherein the initial equilibrated thermodynamic activity of benztropine in said reservoir and adhesive layers is up to about 0.50.
Claim 32
Dependent Claim
14 words
The device of claim 25 wherein said ethylene/vinylacetate copolymer solvent contains about 9% vinylacetate.
Claim 33
Dependent Claim
22 words
The device of claim 28 wherein said release rate controlling means comprises an ethylene/vinylacetate copolymer having a vinylacetate content of about 40%.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1993-03-12 | 1993-09-11 | 1994-03-13 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1997-03-12 | 1997-09-11 | 1998-03-13 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2001-03-12 | 2001-09-11 | 2002-03-13 | $7700.00 | Window Closed / Lapsed |