U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Transdermal drug delivery system and method

Patent 4810499 Issued on March 7, 1989. Estimated Expiration Date: Icon_subject February 5, 2008. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Percutaneous absorption enhancer dispenser for use in coadministering drug and percutaneous absorption enhancer
Patent #: 4460372
Issued on: 07/17/1984
Inventor: Campbell ,   et al.

Skin permeation enhancer compositions
Patent #: 4568343
Issued on: 02/04/1986
Inventor: Leeper ,   et al.

Method of transdermal drug delivery Patent #: 4624665
Issued on: 11/25/1986
Inventor: Nuwayser

Inventor

Assignee

Application

No. 07/152940 filed on 02/05/1988

US Classes:

424/448, Pressure sensitive adhesive means424/449Transdermal or percutaneous

Examiners

Primary: Page, Thurman K.
Assistant: Horne, Leon R.

Attorney, Agent or Firm

International Class

A61K 9/70 (20060101)

Abstract

A transdermal drug delivery system which system comprises an impervious backing sheet and face membrane, the backing sheet and membrane secured together to form an intermediate reservoir. The face membrane is a macroporous membrane which has pores of sufficient size to avoid any rate control of the drug to be transdermally delivered to the user. The reservoir contains a viscous liquid base material selected to exude from the membrane to form a film and to occlude the skin of the user to force hydration of the stratum corneum with water from the lower layers of the epidermis of the user. The liquid base material contains an effective, therapeutic amount of the drug for transdermal delivery, such as the contraceptive steroid, which drug is highly soluble in the liquid base material. In use, the liquid base material exuded from the macroporous membrane face forms a thermodynamically stable, thin film layer in intimate contact with the skin, while the drug is released from the base material and transdermally into the user.

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