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

Compositions and methods for enhanced drug delivery

Patent 5607691 Issued on March 4, 1997. Estimated Expiration Date: Icon_subject May 24, 2015. 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

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Inventor: Sipos

N,N,N-Trimethyl derivatives of polyene amphoteric antibiotics, process of producing same and pharmaceutical composition
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Water-soluble salts of trimethylammonium derivatives of polyene macrolide antibiotics and the preparation thereof
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Formyl-methionyl chemotatic peptide antibiotic conjugates useful in treating infections
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Issued on: 01/24/1984
Inventor: Schiffman ,   et al.

Oligopeptide prodrugs
Patent #: 4454065
Issued on: 06/12/1984
Inventor: Gilvarg ,   et al.

Transdermal administration of fentanyl and device therefor
Patent #: 4588580
Issued on: 05/13/1986
Inventor: Gale ,   et al.

Transdermal delivery of highly ionized fat insoluble drugs
Patent #: 4645502
Issued on: 02/24/1987
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Labile quaternary ammonium salts as prodrugs
Patent #: 4727151
Issued on: 02/23/1988
Inventor: Bodor

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Inventors

Assignee

Application

No. 449188 filed on 05/24/1995

US Classes:

424/449, Transdermal or percutaneous514/1, DESIGNATED ORGANIC ACTIVE INGREDIENT CONTAINING (DOAI)514/2, Peptide containing (e.g., protein, peptones, fibrinogen, etc.) DOAI514/26, Cyclopentanohydrophenanthrene ring system514/169, Cyclopentanohydrophenanthrene ring system DOAI514/183, Heterocyclic carbon compounds containing a hetero ring having chalcogen (i.e., O,S,Se or Te) or nitrogen as the only ring hetero atoms DOAI514/553, Radical -XH acid, or anhydride, acid halide or salt thereof (X is chalcogen) DOAI514/556, Inner quaternary ammonium salt (e.g., betaine, etc.)604/20Infrared, visible light, ultraviolet, X-ray or electrical energy applied to body (e.g., iontophoresis, etc.)

Examiners

Primary: Levy, Neil S.

Attorney, Agent or Firm

Foreign Patent References

  • 0031722 EP 07/13/1981
  • 0331391 EP 09/13/1989
  • 0351173 EP 01/13/1990
  • 0385610 EP 09/13/1990
  • 0559625 EP 09/13/1993
  • 8801615 WO 03/13/1988
  • 9008128 WO. 07/13/1990
  • 9106556 WO 05/13/1991
  • 9113631 WO 09/13/1991
  • 9114696 WO 10/13/1991
  • 9115259 WO 10/13/1991
  • 92/08459 WO. 05/13/1992
  • 9217180 WO 10/13/1992
  • 92/22530 WO. 12/13/1992
  • 9307883 WO 04/13/1993
  • 9317713 WO 09/13/1993

International Classes

A61K 009/70
A61K 031/00

Abstract

The present invention relates to methods of delivering pharmaceutical agents across membranes, including the skin layer or mucosal membranes of a patient. A pharmaceutical agent is covalently bonded to a chemical modifier, via a physiologically cleavable bond, such that the membrane transport and delivery of the agent is enhanced.

Other References

  • Bodor, et al. Int. J. Pharm, 35(1-2) 47-59 1987 Improved Delivery Through Biological Membranes
  • Pratt et al., 1990, Principles of drug action: The basis of pharmacology 203-227 Principles of drug action: The basis of pharmacology
  • Russell-Jones et al., 1988, Proceed Intern. Symp. Control. Rel. Bioact. Mater. 85: 142-143 Vitamin B12: A novel carrier for orally presented antigens
  • Bodde et al., 1989, Biochemical Society 17 (3): 197-199 Transdermal peptide delivery
  • Sanderson et al., 1989, J. of Pharm. Sci. 78 (5): 361-364. Iontophoretic delivery of nonpeptide drugs: Formulation optimization for maximum skin permeability
  • Harris, Physical Medicine Library vol. IV, Therapeutic electricity and ultraviolet radiation, pp. 146-149
  • Foder et al., 1991, Science 251: 767-773 Light-Directed, spatially addressable parallel chemical synthesis
  • Bioworld 29 Jan 92, 3 (20): p. 1 FDA approves Elan's nicotine patch
  • Chien et al., 1989, J. Pharm. Sci. 78 (5): 376-383 Direct current iontophoretic transdermal delivery of peptide and protein drugs
  • Srinivasan et al., 1989, J. of Pharm. Sci. 78(5): 370-375 Transdermal iontophoretic drug delivery : Mechanistic analysis and application to polypeptide delivery
  • West, Textbook of Biochemistry, Ch. 6: 169-170 Lipids
  • Chien et al., 5 May 1989, J. Pharm. Sci. 78 (5): 353-354 Iontophoretic (transdermal) delivery of drugs: Overview of historical development
  • Fix et al., 1986, The American Physiological Society: G332-G340 Acylccarnitines: drug absorption-enhancing agents in the gastrointestinal tract
  • Banga et al., 1988, J. Controlled Release 7: 1-24 Iontophoretic delivery of drugs: Fundamentals, developments and biomedical applications
  • Bernstein, 92, Bioworld 3 (105): p.1 Patch developers extinguish suits
  • Behl et al., 1989, J. of Pharm. Sci. 78 (5): 355-360 Iontophoretic drug delivery: Effects of physicochemical factors on the skin uptake of nonpeptide drugs
  • Benet et al., Pharmacokinetics: The dynamics of drug absorption, Distributuion, and elimination. Ch. 1: 3-10 Pharmacokinetics: The dynamics of drug absorption, distribution, and elimination
  • Phipps et al., 1989, J. of Pharm. Sci. 78 (5): 365-369 Iontophoretic delivery of model inorganic and drug ions
  • Ames et al., Feb. 1973, Proc. Natl. Acad. Sci. USA 70(2): 456-458 Illicit Transport: The Oligopeptide Permease
  • Bodor et al., 18 Sep. 1992, Science 257: 1698-1700 A strategy for delivering peptides into the central nervous system by sequential metabolism
  • Jacobson et al., 1986, Mol. Pharmacol. 29: 126-133 A fuctionalized congener approach to adenosine receptor antogonists: Amino Acid conjugates of 1,3-Dipropylxanthine
  • Jacobson et al., 1987, J. Med. Chem. 30: 1529-1532 Binary Drugs: Conjugates of purines and a peptide that binds to both adenosine and substance P receptor
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