Abstract: The present disclosure relates to rheology modified, low foaming aqueous antimicrobial compositions. The compositions are phase stable under acidic conditions, and do not need to be rinsed from the surface to which they are applied. The present disclosure further relates to methods of use thereof.
Type:
Grant
Filed:
May 20, 2011
Date of Patent:
February 18, 2020
Assignee:
Ecolab USA Inc.
Inventors:
Junzhong Li, Steven J. Lange, Richard K. Staub, David D. McSherry
Abstract: The subject matter of the present disclosure are agents for stabilizing keratin fibers, more particularly human hair, containing in a cosmetic carrier: (a) at least one compound of the formula (I) wherein X denotes oxygen (—O—), sulfur (—S—) or a grouping —NR5—.
Type:
Grant
Filed:
October 18, 2017
Date of Patent:
February 18, 2020
Assignee:
Henkel AG & Co. KGaA
Inventors:
Antje Gebert-Schwarzwaelder, Ralph Nemitz, Astrid Kroos
Abstract: Provided herein are long-acting, non-aqueous pharmaceutically acceptable compositions of active ingredients for subcutaneous injection, in particular analgesics such as buprenorphine.
Type:
Grant
Filed:
June 5, 2018
Date of Patent:
February 11, 2020
Assignee:
Piedmont Animal Health, LLC
Inventors:
Douglas I. Hepler, Gail L. Dempsey, Dorothea Erxleben
Abstract: A method and system for administering pharmaceutical agents to a subject is provided. The system includes a course of treatment regimen, which includes a prescribed order of medicine amounts for periodic administration to the subject in the prescribed order. The amount of medicine includes a dose of at least one active pharmacological agent (APA) and an amount of at least one non-active pharmacological agent (NPA). The NPA provides at least one non-visual sensory cue. The dosage amounts of the APA contained within the amounts of medicine periodically administered in the prescribed order are varied within the course of treatment regimen, and the amount of the NPA contained within the amounts of medicine periodically administered in the prescribed order are held constant within the course of treatment regimen.
Abstract: In the present invention, a new combination is disclosed comprising (i) 5-aminosalicylic acid (5-ASA) or a derivative thereof, or a pharmacologically acceptable salt thereof, and (ii) a group D vitamin, a derivative thereof, a metabolite or analogue, for use in the prevention and/or treatment of colorectal cancer (CRC). A further aspect of the invention is directed to pharmaceutical compositions comprising said combination together with at least one physiologically acceptable excipient and the use thereof in the prevention and/or in the treatment of the colorectal cancer.
Abstract: The present invention relates to dosage forms of gallium complexes suitable for oral delivery and methods of preparation thereof. Such dosage forms are useful for the treatment of diseases, including, but not limited to, cancer.
Type:
Grant
Filed:
February 9, 2018
Date of Patent:
February 4, 2020
Assignee:
Altum Pharmaceuticals Inc.
Inventors:
Rickey Roy Rhinebarger, Gina G. Stetsko
Abstract: The present invention relates to an ophthalmic solution comprising 0.00001 to 10.0 weight percent of a simple saccharide, at least 0.00001 weight percent of a preservative, and not more than about 0.2 percent by weight chloride. The simple saccharide is chosen from the group consisting of: inositol; mannitol; sorbitol; sucrose; dextrose; glycerin; propylene glycol; ribose; triose; tetrose; erythrose; threose; pentose; arabinose; ribulose; xylose; xylulose; lyxose; hexose; allose; altrose; fructose; galactose; glucose; gulose; idose; mannose; sorbose; talose; tagatose; adlose; ketose; heptose; sedoheptulose; monosaccharides; disaccharides; sugar alcohols; xylitol; and polyol.
Abstract: Several embodiments disclosed herein relate to formulations having antimicrobial and/or sanitizing effects, and uses of the same. In particular, the formulations and methods of using same provide, in several embodiments, an immediate and a persistent antimicrobial effect against a broad spectrum of microorganisms.
Type:
Grant
Filed:
June 18, 2018
Date of Patent:
January 7, 2020
Inventors:
Jesse Cozean, Colette Cozean, Susan Goldsberry
Abstract: The present invention provides stable liquid or semi-solid pharmaceutical compositions of apomorphine, more particularly composition comprising apomorphine and an organic acid, which are useful in treatment of neurological or movement diseases or disorders, e.g., Parkinson's disease, or conditions associated therewith.
Abstract: A method for treating a burn, lesion, lacuna, or wound comprising contacting the burn, lesion, or wound with a chitosan-functionalized silica sphere (“CHI-HSS”). Chitosan-functionalized silica spheres and pharmaceutical compositions containing them.
Abstract: This application discloses methods for treating or preventing an ophthalmic retinal vascular permeability, angiogenic or fibroproliferative disease, disorder or condition that involve administering to a patient in need thereof a composition that can inhibit mast cell migration into the vitreous or the retina, mast cell proliferation in the vitreous or the retina, or mast cell secretion into the vitreous or the retina.
Abstract: The present invention provides an aqueous ophthalmic composition comprising an alpha-2 adrenergic receptor agonist and a non-ionic cellulosic polymer, the solution having a pH less than 6.5. The present invention also provides an aqueous ophthalmic composition comprising an alpha-2 adrenergic receptor agonist and a benzododecinium halide. Also provided are methods of manufacture, use and method of reducing intraocular pressure in the patient in need thereof.
Abstract: A sunscreen composition having improved water resistance comprising (i) a sunscreen active agent; (ii) a water resistant agent comprising a natural wax having a Damping Factor of less than 1.0 in a linear viscoelastic range at body temperature; and (iii) an emulsifier or a surfactant capable of stabilizing an emulsion of components (i) to (iii), wherein said sunscreen composition maintains at least 75%, preferably at least 85%, and most preferably at least 99%, of its static SPF after water immersion for 4 hours.
Type:
Grant
Filed:
February 2, 2018
Date of Patent:
December 31, 2019
Assignee:
EDGEWELL PERSONAL CARE BRANDS, LLC
Inventors:
Hui-Ing Donna Hwang, Alexander Naranjo, Patricia Lynn Scott
Abstract: A ferment extract from a bacterial strain the Eupenicillium crustaceum species useful in the cosmetic treatment and/or care of the skin, mucous membranes, hair and/or nails and cosmetic uses of same.
Type:
Grant
Filed:
March 2, 2016
Date of Patent:
December 24, 2019
Assignee:
LUBRIZOL ADVANCED MATERIALS, INC.
Inventors:
Núria Almiñana Domènech, Albert Soley Astals, Nuria García Sanz, Gemma Mola Llobera, José Darias, Mercedes Cueto
Abstract: Amorphous solid dispersions suitable for oral delivery comprising fenretinide or an analog thereof and at least one matrix polymer, and processes for making the dispersions, are disclosed. Also disclosed are solid oral formulations comprising the amorphous solid dispersions, as well as uses thereof for the prevention and/or treatment of diseases or conditions treatable by fenretinide, including but not limited to cancers, conditions associated with a lipid imbalance, cystic fibrosis, osteoporosis, conditions associated with inflammation or opportunistic infections, and other diseases such as diabetes, obesity, dry-form age-related macular degeneration.
Type:
Grant
Filed:
October 26, 2018
Date of Patent:
December 24, 2019
Assignee:
LAURENT PHARMACEUTICALS
Inventors:
Aimesther Betancourt, Marc Lemieux, Roch Thibert
Abstract: A reflective skin-spread composition is provided. The composition comprises 80 to 90 w/w % reflective glass microspheres, and 10 to 20 w/w % carrier medium. The reflective glass microspheres have an average diameter of 30 to 80 microns. The carrier medium comprises an emollient ester, a plant emollient, a binder/stabilizer, and a water-resistant film-forming agent. The composition comprises the emollient ester at 3 to 6 w/w %, the plant emollient at 2 to 5 w/w %, the binder/stabilizer at 3 to 6 w/w %, and the water-resistant film-forming agent at 1 to 4 w/w %. An applicator for applying the composition to a surface also is provided. A method of enhancing visibility of a person comprising a step of applying the composition to an exposed skin surface of the person also is provided.
Abstract: The present invention relates to novel totally-mesoporous zirconium oxide nanoparticles as well as a sol-gel synthesis process thereof which include an innovative nanoparticles purification step. Said nanoparticles are characterized by a totally-mesoporous structure i.e. a distribution of pores within the so-called the mesoporous range uniformly distributed throughout the entire nanoparticle volume. Furthermore, said nanoparticles are non-cytotoxic and present a high surface area, which make particularly suitable in both biomedical and industrial applications (e.g. drug delivery, heavy metals ion sequestration). The manufacturing method is simple and advantageously allows for high control over the shape and diameter of the nanoparticles as well as over the nanoparticles pores.
Type:
Grant
Filed:
January 27, 2016
Date of Patent:
December 10, 2019
Assignee:
BRENTA S.R.L.
Inventors:
Gabriele Sponchia, Alvise Benedetti, Pietro Riello
Abstract: Gold(I) complexes and gold(I) dithiocarbamate polymers as anticancer therapeutics. The Au(I) ion within the gold(I) complexes is coordinated to two phosphine ligands. The repeating unit formed by Au(I) ion coordinating to dithiocarbamate ligands are connected by Au(I)—Au(I) interactions within the gold(I) dithiocarbamate polymers. Also disclosed are methods of synthesis, pharmaceutical compositions incorporating the gold(I) complexes, pharmaceutical compositions incorporating the gold(I) dithiocarbamate polymers, and methods of treating cancer.
Type:
Grant
Filed:
May 6, 2019
Date of Patent:
December 3, 2019
Assignee:
King Fahd University of Petroleum and Minerals
Inventors:
Anvarhusein A. Isab, Muhammad Altaf, Adam Ahmed Abdallah Seliman
Abstract: Disclosed are 1?,25-dihydroxy-24,24-difluoro-2-methylene-19-nor-vitamin D analogs and their pharmaceutical uses. These new vitamin D analogs are 19-nor-vitamin D analogs having two fluorine atom substitutions at the 24 position (C-24) in the side chain and optionally having a 2-methylene substituent.
Type:
Grant
Filed:
May 26, 2016
Date of Patent:
December 3, 2019
Assignee:
WISCONSIN ALUMNI RESEARCH FOUNDATION
Inventors:
Hector F. DeLuca, Agnieszka Flores, Lori A. Plum, Hazel Holden, James Thoden