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Pharmaceutical composition containing acid addition salt of basic drug

Patent 6255502 Issued on July 3, 2001. Estimated Expiration Date: Icon_subject April 19, 2019. 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

Readily absorbable pharmaceutical compositions of per se poorly absorbable pharmacologically active agents and preparation thereof Patent #: 4722941
Issued on: 02/02/1988
Inventor: Eckert ,   et al.

Inventors

Assignee

Application

No. 225470 filed on 04/19/1999

US Classes:

552/549, Oxygen bonded directly at the 12-position (e.g., cholic acids, desoxycholic acids, dehydrocholic acids, etc.)424/550, Digestive system (e.g., salivary gland, etc.)424/551, Gastrointestinal system (e.g., intestine, stomach, gall bladder, etc.)424/553, Liver530/847, Bile552/550, Halogen, nitrogen, or sulfur containing (e.g., glycocholic acids, taurocholic acids, etc.)554/156Group IA or IIA metal containing reactant (e.g., forming a soap from fat and alkali, i.e., saponification, etc.)

Examiners

Primary: Carr, Deborah D.

Attorney, Agent or Firm

Foreign Patent References

  • 0 463 653 EP 01/13/1992
  • WO 94/16733 WO 08/13/1994
  • WO 96/33742 WO 10/13/1996

International Class

C07J 009/00

Foreign Application Priority Data

1996-07-11 ZA

Abstract

A pharmaceutical composition contains an acid addition salt of a basic drug and a fatty acid or bile acid. The acid addition salts thus formed exhibit enhanced transmucosal and transdermal penetration of the basic drug. The acid addition salts, an inclusion complex containing said salts and a use of said salts are also disclosed.

Other References

  • English Abstracts: JP 9278651; JP 9136835; JP 9136834; JP 9136828; JP 9104623; JP 9030965 and JP 8225448, (No date)
  • Chien, Y.W. ed., Novel Drug Deliver Systems, 2nd Edition, Marcel Dekker, 1992 pp. 183-188, 244-249
  • Walker et al, Advanced Drug Delivery Reviews, 18(1996) pp. 295-301
  • Lindmark et al, The Journal of Pharmacology and Experimental Therapeutics, vol. 275, No. 2, (1995), pp. 958-964
  • Yamamoto et al, International Journal of Pharmaceutics, 93 (1993), pp. 91-99
  • Tomita et al, Pharmaceutical Research, vol. 5, No. 6 (1988), pp. 341-346
  • Mishima et al, J. Pharmacobio-Dyn., 10 (1987), pp. 624-631
  • Aungst et al, Pharmaceutical Research, vol. 9, No.11 (1992), pp. 1507-1509
  • Ogiso et al, Journal of Pharmaceutical Sciences, vol. 79, No. 2 (Dec. 1990)
  • Ogiso et al, Chem. Pharm. Bull., 39(10), pp. 2657-2661 (1991)
  • Green et al, Pharmaceutical Research, vol. 6, No. 7 (1989), pp. 628-632
  • Jashnani et al, Journal of Pharmaceutical Sciences, vol. 82, No. 6 (Jun. 1993), pp. 613-616
  • Loftsson et al, International Journal of Pharmaceutics, 115 (1995), pp. 255-258
  • Vollmer et al, International Journal of Pharmaceutics, 99 (1993), pp. 51-58
  • Legendre et al, European Journal of Pharmaceutical Sciences, 3 (1995), pp. 311-322
  • Vollmer et al, J. Pharm. Pharmacol., vol. 46 (1994), pp. 19-22
  • Merkus et al, Pharmaceutical Research, vol. 8, No. 5 (1991), pp. 588-592
  • Shao et al, Pharmaceutical Research, vol. 9, No. 9 (1992), pp. 1157-1163
  • Salehian et al, Journal of Clinical Endoerinology and Metabolism, vol. 80, No. 12, pp. 3567-3575., (No date)
  • Gill et al, European Journal of Pharmaceutical Sciences, vol. 1 (1994), pp. 229-236
  • Szejtli, Cyclodextrin technology, Kluwer Academic Press, (1988), pp. 79-155
  • Szejtli et al, Cyclodextrins in Pharmacy, Kluwer Academic Press, pp. 19-32, (No date)
  • Stella et al, Pharmaceutical Research, vol. 12, No. 9 (1995) S205
  • Jashnani et al, J. Pharm. Sci., 82(6):13-24 (1996)
  • Nash et al, Skin Pharmacol., 5(3):160-170 (1992)
  • Elyan et al, J. Pharm. Sci., 85(1):101-105 (1996)
  • de Vries et al, Crit. Rev. Drug Carrier Systems, 8(3):290-298 (1991
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