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

Supported drugs with increased dissolution rate, and a process for their preparation

Patent 5449521 Issued on September 12, 1995. Estimated Expiration Date: Icon_subject February 28, 2014. 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

3079303

3089824

3328256

3499784

Method of treatment of medicines
Patent #: 3966899
Issued on: 06/29/1976
Inventor: Nakai ,   et al.

Injectable compositions, nanoparticles useful therein, and process of manufacturing same
Patent #: 4107288
Issued on: 08/15/1978
Inventor: Oppenheim ,   et al.

Granulation process
Patent #: 4111371
Issued on: 09/05/1978
Inventor: Melliger

Pharmaceutical composition
Patent #: 4639370
Issued on: 01/27/1987
Inventor: Carli

Compositions containing ibuprofen Patent #: 4837031
Issued on: 06/06/1989
Inventor: Denton

Inventor

Assignee

Application

No. 203034 filed on 02/28/1994

US Classes:

424/489, Particulate form (e.g., powders, granules, beads, microcapsules, and pellets)424/490, Coated (e.g., microcapsules)424/491, Containing proteins and derivatives424/493, Containing polysaccharides (e.g., sugars)424/497, Containing solid synthetic polymers424/500, Contains natural gums and resins424/501Contains solid synthetic resin

Examiners

Primary: Kishore, Gollamudi S.

Attorney, Agent or Firm

Foreign Patent References

  • 001268 EP. 05/13/1980
  • 0129893 EP. 02/13/1985
  • 0049428 JP. 03/13/1983

International Class

A61K 009/14

Foreign Application Priority Data

1988-11-28 IT

Abstract

Supported drugs with an increased dissolution rate, prepared by a process comprising mixing the drug with the support material under dry conditions, co-grinding the mixture in a mill with its grinding chamber saturated with the vapour of one or more solvents able to solubilize the drug or to be adsorbed on the surface of the support material, vacuum-drying the product obtained, and sieving. The drugs obtained in this manner have a reduced heat of fusion, a reduced melting point, an increased dissolution rate and an increased solubilization kinetics.

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