Patents by Inventor Ronald Pero

Ronald Pero has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20090258937
    Abstract: Methods and pharmaceutical compositions for modulating tumor growth or metastasis are provided.
    Type: Application
    Filed: November 7, 2008
    Publication date: October 15, 2009
    Inventors: Francis Y. Lee, Ronald Peck, David Chaplin, Ronald Pero, Klaus Edvardsen
  • Publication number: 20060194770
    Abstract: Methods and pharmaceutical compositions for modulating tumor growth or metastasis are provided.
    Type: Application
    Filed: May 1, 2006
    Publication date: August 31, 2006
    Inventors: Francis Lee, Ronald Peck, David Chaplin, Ronald Pero, Klaus Edvardson
  • Publication number: 20060100179
    Abstract: Treatment of warm-blooded animals having a tumor or non-malignant hypervascularation, by administering a sufficient amount of a cytotoxic agent formulated into a phosphate prodrug form having substrate specificity for microvessel phosphatases, so that microvessels are destroyed preferentially over other normal tissues, because the less cytotoxic prodrug form is converted to the highly cytotoxic dephosphorylated form.
    Type: Application
    Filed: April 22, 2005
    Publication date: May 11, 2006
    Inventors: Ronald Pero, David Sherris, David Chaplin, George Pettit, John Lippert
  • Publication number: 20060068035
    Abstract: A method for isolating the bioactive component of the water-soluble extract of Uncaria tomentosa known as C-MED-100®, comprising (i) precipitating the spray drying carrier from C-MED-100®; (ii) using the resulting C-MED-100® to obtain a spotting mixture for thin layer chromatography (TLC); (iii) spotting the C-MED-100® spotting mixture on pre-run TLC plates and eluting the plates to obtain the fluorescing band with Rf=0.2-0.3; (iv) scraping off the Rf=0.2-0.3 band, eluting it in ammonia and freeze drying the eluted band to form a powder; and (v) extracting the powder with methanol to remove solubilized silica gel, concentrating the methanol solution and crystalizing the concentrated solution to obtain the bioactive component. The isolated bioactive component is a quinic acid analog, preferably quinic acid lactone. A pharmaceutical composition comprising a pharmaceutically effective amount of the bioactive component and a nontoxic inert carrier or diluent.
    Type: Application
    Filed: November 9, 2005
    Publication date: March 30, 2006
    Inventor: Ronald Pero
  • Publication number: 20050287227
    Abstract: A supplement for administering to a human, or other mammals, includes a carotenoid material, a nicotinamide material, a zinc source material, and a water soluble extract material of an Uncaria species. The supplement can be in a form for oral administration, particularly in a form of nutritional drink, or in a formulation for parenteral administration. Also disclosed is a method of treating a human including administering to an individual the supplement daily in amounts effective, in combination, to improve the individual's resistance to DNA damage, enhance DNA repair capacity, stimulate immune cell function, and inhibit tumor cell growth.
    Type: Application
    Filed: April 14, 2005
    Publication date: December 29, 2005
    Inventors: Ronald Pero, Vincent Giampapa
  • Publication number: 20050202105
    Abstract: A process for producing a composition of water-soluble phytomedicinal compounds is provided comprising combining plant material with water, in a ratio of plant material to water within a range of about 1:5 to about 1:50, at a temperature between about 75° C. and about 100° C. for a period of time to solubilize a substantial portion of thermal aqueous extractable phytocompounds present in the plant material, to produce a first extract; and removing substantially all entities having a molecular weight greater than about 10 kd from the extract to produce a composition of water-soluble phytomedicinal compounds. Compositions of water-soluble phytomedicinal compounds are provided that exhibit improved efficacy and reduced toxicity.
    Type: Application
    Filed: March 16, 2005
    Publication date: September 15, 2005
    Inventor: Ronald Pero
  • Publication number: 20050176825
    Abstract: A method for isolating the bioactive component of the water-soluble extract of Uncaria tomentosa known as C-MED-100®, comprising (i) precipitating the spray drying carrier from C-MED-100®; (ii) using the resulting C-MED-100® to obtain a spotting mixture for thin layer chromatography (TLC); (iii) spotting the C-MED-100® spotting mixture on pre-run TLC plates and eluting the plates to obtain the fluorescing band with Rf=0.2-0.3; (iv) scraping off the Rf=0.2-0.3 band, eluting it in ammonia and freeze drying the eluted band to form a powder; and (v) extracting the powder with methanol to remove solubilized silica gel, concentrating the methanol solution and crystalizing the concentrated solution to obtain the bioactive component. The isolated bioactive component in vitro is a quinic acid analog, preferably quinic acid lactone. By contrast, the isolated bioactive component in vivo is quinic acid, whether as free acid or as a quinic acid salt, including quinic acid ammonium salt.
    Type: Application
    Filed: October 21, 2004
    Publication date: August 11, 2005
    Inventor: Ronald Pero