Patents Examined by R DeWitty
  • Patent number: 6592860
    Abstract: A polymerized hydrogel composition and applicator for hydrating or dehydrating a surface, particularly a dermatological surface, to which it is applied and a method for forming the composition. The composition is comprised of a mixture of two polymerizable materials, a two-part redox catalyst system and a two-part polymerization medium. The percentage by weight of each element in the composition may be varied within stated percentage ranges. The rate at which hydration or dehydration occurs may be controllably altered by varying the percentages of certain of the composition elements. The applicator includes a thermoplastic center section and two reservoir sections each having a reservoir storage area for holding moisture and/or medicaments. The composition is mechanically bonded onto each of the reservoir sections and then hydrated. The applicator is designed for insertion into a human mouth after hydration and is used for treating xerostomia.
    Type: Grant
    Filed: May 30, 2000
    Date of Patent: July 15, 2003
    Assignee: Soluble Systems, LLC
    Inventors: Guy Glickson Levy, Carl Anthony Williams, James David Rancourt, Christine June Gerdon
  • Patent number: 6461646
    Abstract: The invention provides a pharmaceutical composition for preventing and/or curing digestive disorders such as digestive ulcers, gastritis, etc. The pharmaceutical composition contains, as the active ingredient, an aluminosilicate having silver and zinc ions, and it has an excellent effect for protecting gastric mucous membrane and an excellent effect of promoting the curing of a gastric ulcer.
    Type: Grant
    Filed: July 30, 2001
    Date of Patent: October 8, 2002
    Assignees: Lintec Corporation, Sinanen Zeomic Co., Ltd.
    Inventor: Mikio Ito
  • Patent number: 6413549
    Abstract: This invention is directed to an oral solid, rapidly disintegrating, freeze-dried dosage form containing coarse particles of a pharmaceutically active material which are uncoated or coated with a polymer or lipid material. Preferably, the oral dosage form comprises coarse particles having a size in the range of 50 micron to 400 micron. The oral solid rapidly disintegrating dosage form according to the present invention preferably disintegrates in the oral cavity in less than 10 seconds.
    Type: Grant
    Filed: June 17, 1999
    Date of Patent: July 2, 2002
    Assignee: R. P. Scherer Corporation
    Inventors: Richard Green, Patrick Kearney