US5064654A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Mixed solvent mutually enhanced transdermal therapeutic system
Assignee: Novartis Corp
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Filing: 1990-04-20
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Granted: 1991-11-12
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Expires: 2010-04-20
Abstract
Abstract The invention relates to the art of transdermal administration of drug substances, particularly those drug substances having a greater solubility in ethanol than in water and those drug substances having cationic or anionic substituent groups. It is especially useful for the administration of nitroglycerin.
Inventors
- 👤 Bret Berner
- 👤 Charles Ebert
- 👤 Gerard C. Mazzenga
- 👤 John H. Otte
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-04 03:20
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/70; A61K9/7023; A61K9/703; A61K9/7084
Claims Analysis
Total Claims: 13
Claim 1
Independent Claim
216 words
A transdermal drug delivery system comprising (i) an occlusive, impermeable polymeric backing layer; (ii) a drug depot on one side thereof; (iii) a removable, occlusive covering layer over said drug depot; and (iv) an adhesive means by which said delivery system, absent said removable covering layer may be affixed to an intended patient; said drug depot containing a drug formulation comprising a transdermally administrable pharmaceutically acceptable pharmaceutically active agent or a precursor thereof, water and ethanol said active agent or precursor thereof being present in a pharmaceutically effective amount; said ethanol and said water being present in a volume:volume ratio of from 30:70 up to less than 95:5 such that said ethanol, water and drug are delivered to a patient's skin, which patient has applied said system absent said removable covering layer to said patient's skin, in amounts that said drug is delivered in a transdermally administrable efficacious amount, said water has an activity at said patients skin of about 0.4 to about 0.95 and said ethanol, at said patient's skin, has an activity of 0.3 to about 0.9, and wherein, once applied to said patient's skin, said ethanol has a flux from said system to said skin of at least 1500 mcg/cm 2 /hr and through said skin of at least 1500 mcg/cm 2 /hr.
Claim 2
Dependent Claim
216 words
A transdermal drug delivery system comprising (i) an occlusive, impermeable polymeric backing layer; (ii) a drug depot on one side thereof; (iii) a removable, occlusive covering layer over said drug depot; and (iv) an adhesive means by which said delivery system, absent said removable covering layer may be affixed to an intended patient; said drug depot containing a drug formulation comprising a transdermally administrable pharmaceutically acceptable pharmaceutically active agent or a precursor thereof, water and ethanol said active agent or precursor thereof being present in a pharmaceutically effective amount; said ethanol and said water being present in a volume:volume ratio of from 30:70 up to less than 95:5 such that said ethanol, water and drug are delivered to a patient's skin, which patient has applied said system absent said removable covering layer to said patient's skin, in amounts that said drug is delivered in a transdermally administrable efficacious amount, said water has an activity at said patients skin of about 0.4 to about 0.95 and said ethanol, at said patient's skin, has an activity of 0.3 to about 0.9, and wherein, once applied to said patient's skin, said ethanol has a flux from said system to said skin of at least 1500 mcg/cm 2 /hr and through said skin of at least 1500 mcg/cm 2 /hr.
Claim 3
Dependent Claim
20 words
The system of claim 1 wherein said composition further comprises at least one further transdermal drug delivery device acceptable adjuvant.
Claim 4
Dependent Claim
17 words
The system of claim 1 wherein said volume:volume ratio is from 45:55 up to and including 85:15.
Claim 5
Dependent Claim
17 words
The system of claim 5 wherein said volume:volume ratio is from 65:35 up to and including 75:25.
Claim 6
Dependent Claim
28 words
The system of claim 1 wherein said water and ethanol are delivered to said patient's skin so as to result in an ethanol activity of at least 0.5.
Claim 7
Dependent Claim
59 words
The system of claim 1 wherein, once applied to a patient's skin, said alkanol ethanol has a potential flux through said skin of at least 1500 mcg/cm 2 /hr, and an actual flux from said system through said skin of at least 900 mcg/cm 2 /hr, and at least 50% of the diffusional resistance is provided by said system.
Claim 8
Dependent Claim
99 words
A dosage form for transdermally administering a pharmaceutically active agent which dosage form comprises a) an impermeable backing, b) a rate-controlling membrane of polyurethane or ethylene/vinylacetate of greater than 20% vinyl acetate and from 0.5 to 10.0 mils thick, c) a silicone-based or acrylic-based pressure-sensitive adhesive on said rate controlling membrane distal from said backing, d) a reservoir formed by a and b, e) an aqueous pharmaceutically acceptable lower alkanol reservoir composition having a volume fraction of said ethanol of from 0.35 to 0.9 calculated based on said ethanol alkanol and water only, and f) said pharmaceutically active agent.
Claim 9
Dependent Claim
99 words
A dosage form for transdermally administering a pharmaceutically active agent which dosage form comprises a) an impermeable backing, b) a rate-controlling membrane of polyurethane or ethylene/vinylacetate of greater than 20% vinyl acetate and from 0.5 to 10.0 mils thick, c) a silicone-based or acrylic-based pressure-sensitive adhesive on said rate controlling membrane distal from said backing, d) a reservoir formed by a and b, e) an aqueous pharmaceutically acceptable lower alkanol reservoir composition having a volume fraction of said ethanol of from 0.35 to 0.9 calculated based on said ethanol alkanol and water only, and f) said pharmaceutically active agent.
Claim 10
Dependent Claim
22 words
The dosage form of claim 7 further comprising a salt of said pharmaceutically active agent or a buffering agent in said adhesive.
Claim 11
Dependent Claim
16 words
A dosage form of claim 7 wherein the membrane is microporous and the adhesive is pressure-sensitive.
Claim 12
Dependent Claim
38 words
A dosage form of claim 7 where the membrane allows said ethanol to permeate therethrough between 1.5 and 12 mg/cm 2 /hr and water to permeate therethrough at between 0.5-10 mg/cm 2 /hr and the adhesive is pressure-sensitive.
Claim 13
Dependent Claim
26 words
A unit dosage form according to claim 7 wherein said membrane is impermeable to said pharmaceutically active agent and said adhesive contains said pharmaceutically active agent.
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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) | 1994-11-11 | 1995-05-13 | 1995-11-12 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1998-11-11 | 1999-05-13 | 1999-11-12 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2002-11-11 | 2003-05-13 | 2003-11-12 | $7700.00 | Window Closed / Lapsed |