U.S. patents available from 1976 to present.
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Pharmaceutical formulations for parenteral use

Patent 5024998 Issued on June 18, 1991. Estimated Expiration Date: Icon_subject December 11, 2009. 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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Inclusion compound of p-hexadecylamino benzoic acid in cyclodextrin and method of use
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3,4-Di -isobutyryloxy-N-[3-(4-isobutyryloxyphenyl)-1-methyl-n-propyl]-beta-phene thylamine cyclodextrin complexes
Patent #: 4424209
Issued on: 01/03/1984
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3,4-Dih ydroxy-N-[3-(4-dihydroxyphenyl)-1-methyl-n-propyl]-beta-phenethylamine cyclodextrin complexes
Patent #: 4425336
Issued on: 01/10/1984
Inventor: Tuttle

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Inventor

Assignee

Application

No. 448655 filed on 12/11/1989

US Classes:

424/1.85, Halogen424/94.1, ENZYME OR COENZYME CONTAINING514/58, Dextrin or derivative514/777, Carbohydrate or lignin, or derivative514/937, DISPERSION OR EMULSION536/103Dextrin or derivative

Examiners

Primary: Griffin, Ronald W.

Attorney, Agent or Firm

Foreign Patent References

  • 0197571 EP. 10/13/1986
  • 58-213712 JP. 12/13/1983
  • 59-104556 JP. 06/13/1984
  • 60-054384 JP. 03/13/1985
  • 61-070996 JP. 04/13/1986
  • 61-197602 JP. 09/13/1986
  • 62-003795 JP. 01/13/1987
  • 62-106901 JP. 05/13/1987
  • 62-164701 JP. 07/13/1987
  • 61-236802 JP. 10/13/1987
  • 62-281855 JP. 12/13/1987
  • 63-027440 JP. 02/13/1988
  • 63-036793 JP. 02/13/1988
  • 63-135402 JP. 06/13/1988
  • 63-146861 JP. 06/13/1988
  • 63-218663 JP. 09/13/1988
  • 8303968 WO. 11/13/1983
  • 8502767 WO. 07/13/1985
  • 8503937 WO. 09/13/1985

International Classes

C08B 037/16
A61K 031/735

Foreign Application Priority Data

1988-12-13 CA

Abstract

Aqueous parenteral solutions of drugs which are insoluble or only sparingly soluble in water and/or which are unstable in water, combined with cyclodextrin selected from the group consisting of hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of ଲ- and γ-cyclodextrin, provide a means for alleviating problems associated with drug precipitation at the injection site and/or in the lungs or other organs following parenteral administration.

Other References

  • Chemical Abstracts, 110, 101775b (Abstract of Japanese Kokai 88/218,663, published Sep. 12, 1988)
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  • Yoshida et al., International Journal of Pharmaceutics, 46, 1988, 217-222
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  • Brewster et al., in Proceedings of the Fourth International Symposium on Cyclodextrins, Munich, 20th-22nd Apr., 1988, pp. 399-404, Kluwer Academic Publishers, Dordrecht, NL
  • Pitha et al., in Controlled Drug Delivery, ed. S. D. Bruck, vol. I, CRC Press, Boca Raton, Fla., 125-148 (1983)
  • Uekama, Pharm. Int., Mar. 1985, 61-65
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  • Estes et al. in Biological Approaches to the Controlled Delivery of Drugs, ed. R. L. Juliano, Annals of the New York Academy of Sciences, vol. 907, 1987, 334-33
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