Patents Represented by Attorney Geoffrey G. Dellenbaugh
  • Patent number: 4215112
    Abstract: There are disclosed new biological active polypeptides:A--X--Bwherein A is deamino-LYS or LYS; X is a suitable neutral aliphatic amino acid residue; e.g., one selected from the group consisting of SER, ALA, 2-Me-ALA, GLY, LEU, THR, D-SER, D-ALA, D-THR, allo-THR, D-LEU, and SAR; B is GLN-R', decarboxy-GLN, or ##STR1## and R' is a substituent which does not substantially affect the biological activity of the tripeptide.These polypeptides have the capability of inducing the differentiation of T-lymphocytes as measured by the acquisition of the thymic differentiation antigen Th-1, as well as B-lymphocytes as measured by the acquisition of the differentiation antigen Bu-1. The polypeptides are thus useful in thymic function and immunity areas such as in treatment for congenital absence of thymus. Also provided are therapeutic compositions and methods for use of the polypeptides.
    Type: Grant
    Filed: March 14, 1979
    Date of Patent: July 29, 1980
    Assignee: Ortho Pharmaceutical Corporation
    Inventors: Gideon Goldstein, George Heavner
  • Patent number: 4213963
    Abstract: Improved fluspirilene-containing compositions for intramuscular administration and a method of preparing the same.
    Type: Grant
    Filed: December 14, 1978
    Date of Patent: July 22, 1980
    Assignee: Janssen Pharmaceutica N.V.
    Inventors: Jean Mesens, Victor Haagen
  • Patent number: 4210420
    Abstract: A quantitative method and composition for precipitating fibrin monomers from plasma in the presence of fibrinogen, with only a small amount, if any, of fibrinogen being precipitated. A buffered precipitating agent is provided having a pH in the range of 6.5.+-.0.5, the buffer being one having a pKa in the range of 6 to 7 and protamine sulfate at a level of 0.025 to 0.2% by weight. Suitable buffers are 2-(N-morpholino)ethanesulfonic acid, sodium phosphate, histidine, maleic acid and imidazole. Analysis of the amount of fibrin present can be made by analyzing for protein using preferably a basic urea solution containing sodium hydroxide and measuring the absorbance at 282 nanometers.
    Type: Grant
    Filed: November 13, 1978
    Date of Patent: July 1, 1980
    Assignee: Ortho Diagnostics Inc.
    Inventors: D. Joe Baughman, Ann Lytwyn, Kurt Myrmel
  • Patent number: 4207890
    Abstract: A drug-dispensing device and method for controlled and prolonged internal administration of medicaments to warm-blooded animals comprising an outer polymer envelope containing an expanding agent, drug metering means, and the drug itself. The outer polymer envelope is permeable to both the drug and body fluids and expands when the expanding agent is contacted by body fluids when the device is in the environment of use (e.g., the stomach). This expansion maintains the device in the environment of use while the drug is administered by the metering means.
    Type: Grant
    Filed: September 21, 1978
    Date of Patent: June 17, 1980
    Assignee: McNeilab, Inc.
    Inventors: Ronald C. Mamajek, Ernest S. Moyer
  • Patent number: 4059583
    Abstract: Substituted thioindoles and their sulfoxide and sulfone derivatives, useful as cardiac rate lowering agents and for other pharmacological properties, and precursors therefor.
    Type: Grant
    Filed: October 13, 1976
    Date of Patent: November 22, 1977
    Assignee: McNeil Laboratories, Incorporated
    Inventors: David Fred McComsey, Michael John Zelesko
  • Patent number: 4055466
    Abstract: A chemically defined, protein-free culture medium embodying an anion-exchange resin and a water-soluble lipid source provides means for tissue culture.
    Type: Grant
    Filed: May 30, 1975
    Date of Patent: October 25, 1977
    Assignee: Johnson & Johnson
    Inventors: Harry L. Torney, Helen T. Torney, Dale E. Bordt
  • Patent number: 4048191
    Abstract: Halo-substituted 1-loweralkyl-5-aroylpyrrole-2-acetic acid compounds, useful for their anti-inflammatory activity.
    Type: Grant
    Filed: June 27, 1975
    Date of Patent: September 13, 1977
    Assignee: McNeil Laboratories, Incorporated
    Inventor: John Robert Carson
  • Patent number: 4046763
    Abstract: The compound 2,3-diphenyl-5-ethyl-pyrazine, useful as a precursor in the synthesis of those compounds of the class of pyrazine, arylpyrazine, diphenylpyrazine, and cycloalkylpyrazine malonates, acetates, acetamides, and acetic acids, useful for their ultraviolet light absorption properties.
    Type: Grant
    Filed: November 17, 1972
    Date of Patent: September 6, 1977
    Assignee: McNeil Laboratories, Incorporated
    Inventors: Norman Schwartz, Richard J. Mohrbacher
  • Patent number: 4024642
    Abstract: A dental appliance for removal of liquid from the mouth and for containment of solid debris which comprises a flat, flexible, generally hour glass-shaped shield attached to a bite block on one end. A suction tube for fluid removal connects with a system of suction channels within the shield terminating in apertures along only the edge of the shield. The appliance is placed in the mouth so that the narrow central portion of the shield is over the gum behind the subject lower tooth, the portion adjacent the bite block is on the lingual side thereof, the portion remote from the bite block is on the buccal side thereof, and the edge containing the suction apertures is lowermost.
    Type: Grant
    Filed: August 26, 1975
    Date of Patent: May 24, 1977
    Assignee: Johnson & Johnson
    Inventor: Dan Zorovich
  • Patent number: 4025517
    Abstract: Compounds of the class of 4-oxo-2-imidazolidinylidene ureas and 4-oxo-2-hexahydropyrimidinylidene ureas, useful as anti-secretory agents and central nervous system (CNS) depressants.
    Type: Grant
    Filed: June 7, 1976
    Date of Patent: May 24, 1977
    Assignee: McNeil Laboratories, Incorporated
    Inventor: Chris Royce Rasmussen
  • Patent number: 4021263
    Abstract: Polishing compositions for highly filled resin-bonded dental restorations comprising a dispersion of alumina having a particle size less than about 3.0 microns and for nonprecious metal used in dental construction comprising a dispersion of said alumina and diamond having a particle size at least equal to that of the alumina but less than about 3.0 microns.
    Type: Grant
    Filed: February 27, 1975
    Date of Patent: May 3, 1977
    Assignee: Johnson & Johnson
    Inventor: Marc Rosenblum
  • Patent number: 4020271
    Abstract: Alkali metal and ammonium salts of crosslinked phosphonoalkyl cellulose are described which have a phosphorous content of from about 1.5% to about 4.0% by weight and a degree of crosslinking sufficient to make the modified cellulose salts essentially insoluble in aqueous media. These crosslinked phosphonoalkyl cellulose salts have significantly increased fluid absorption capacities as compared to unmodified cellulose and may be incorporated alone or in combination with other absorbent materials into catamenial tampons, sanitary napkins, diapers, and like absorbent devices.
    Type: Grant
    Filed: January 13, 1975
    Date of Patent: April 26, 1977
    Assignee: Personal Products Company
    Inventor: Pronoy Kumar Chatterjee
  • Patent number: 4002643
    Abstract: A process for rearranging .alpha.-acyl pyrroles to .beta.-acyl pyrroles which comprises reacting the former with an excess of a strong, anhydrous, non-oxidizing acid, preferably with heating.
    Type: Grant
    Filed: June 27, 1975
    Date of Patent: January 11, 1977
    Assignee: McNeil Laboratories, Inc.
    Inventor: John Robert Carson