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Supersaturated transdermal drug delivery systems, and methods for manufacturing the same

Patent 5906830 Issued on May 25, 1999. Estimated Expiration Date: Icon_subject September 4, 2016. 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

Transdermal release system for pharmaceutical preparation
Patent #: 4409206
Issued on: 10/11/1983
Inventor: Stricker

Transdermal medicament
Patent #: 4746509
Issued on: 05/24/1988
Inventor: Haggiage ,   et al.

Method for preventing the formation of a crystalline hydrate in a dispersion of a liquid in a monaqueous matrix
Patent #: 4832953
Issued on: 05/23/1989
Inventor: Campbell ,   et al.

Transdermal absorption dosage unit for estradiol and other estrogenic steroids and process for administration
Patent #: 4883669
Issued on: 11/28/1989
Inventor: Chien, et al.

Solid matrix system for transdermal drug delivery
Patent #: 5252334
Issued on: 10/12/1993
Inventor: Chiang, et al.

Compositions and methods for topical administration of pharmaceutically active agents
Patent #: 5332576
Issued on: 07/26/1994
Inventor: Mantelle

Transdermal device
Patent #: 5352457
Issued on: 10/04/1994
Inventor: Jenkins

Device and method for enhanced administration of physostigmine
Patent #: 5364629
Issued on: 11/15/1994
Inventor: Kochinke, et al.

Solubility parameter based drug delivery system and method for altering drug saturation concentration Patent #: 5474783
Issued on: 12/12/1995
Inventor: Miranda, et al.

Inventors

Application

No. 708389 filed on 09/04/1996

US Classes:

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

Examiners

Primary: Page, Thurman K.
Assistant: Shelborne, Kathryne E.

Attorney, Agent or Firm

Foreign Patent References

  • 0 144 486 A2 EP. 06/13/1985
  • 0 391 172 A1 EP. 10/13/1990
  • 0 497 626 A1 EP. 08/13/1992
  • 217 989 DE. 01/13/1985
  • 63093714 JP. 04/13/1988
  • WO 92 05811 WO. 04/13/1992
  • WO94/10984 WO. 05/13/1994
  • WO 97/09971 WO. 03/13/1997
  • WO 97/24148 WO. 07/13/1997

International Class

A61F 013/02

Abstract

Methods are provided for manufacturing transdermal drug delivery systems containing supersaturated drug reservoirs, such that higher drug fluxes are obtained. The methods involve heating the drug reservoir components to a predetermined temperature. Generally, this temperature is higher than the depressed melting temperature of the polymer-drug admixture which will serve as the drug reservoir. In an alternative embodiment, wherein heat treatment of the reservoir components results in a system having two liquid phases, the predetermined temperature is calculated so as to be higher than the melting temperature of the pure drug. Drug reservoirs and novel transdermal delivery systems prepared using the disclosed techniques are provided as well.

Other References

  • Akhtar et al., "The Influence of Crystalline Morphology and Copolymer Composition on Drug Release From Solution Cast and Melt-processed P(HB-HV) Copolymer Matrices," J. Controlled Release(1991) 17 (3):225-234 cript
  • Davis et al., "Effect of Supersaturation on Membrane Transport on Membrane Transport: 1. Hydrocortisone Actate," Intl. J. of Pharm. 76:1-8 (1991)
  • Pellet et al., "Effect of Supersaturation on Membrane Transport: 2. Piroxicam," Intl. J. of Pharm. 111:1-6 (1994
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