Patents Examined by Lakshmi Channavajjala
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Patent number: 9675530Abstract: Personal cleansing compositions comprise (A) a cleansing phase containing a surfactant and water; and (B) a separate benefit phase containing a hydrophobic material; wherein the cleansing and benefit phases are packaged together and are in physical contact. The two phases are packaged in physical contact and remain separate and stable at ambient conditions for at least 180 days. These compositions and corresponding methods provide improved cosmetics, skin feel, and/or skin benefit efficacy.Type: GrantFiled: September 18, 2003Date of Patent: June 13, 2017Assignee: The Procter & Gamble CompanyInventors: Heather Lynn Focht, Christopher Dean Putman, Cheyne Pohlman Thomas, Karl Shiqing Wei
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Patent number: 9675539Abstract: A method for treating hair loss in mammals uses compositions containing 2-decarboxy-2-phosphinico prostaglandin derivatives. The compositions can be applied topically to the skin. The compositions can arrest hair loss, reverse hair loss, and promote hair growth. Compositions containing 2-decarboxy-2-phosphinico prostaglandin derivatives can also be used to lower intraocular pressure and treat bone disorders.Type: GrantFiled: April 14, 2016Date of Patent: June 13, 2017Assignee: Duke UniversityInventors: Mitchell A. deLong, John M. McIver, Robert S. Youngquist
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Patent number: 9649272Abstract: A nail compositions comprising at least one photo-curable polymer dispersed in water (latex), at least one polyurethane non-photo-curable polymer dispersed in water (latex), at least one photo-initiator, optionally at least one plasticizer, optionally a colorant, and water are provided. Also provided are nail composition systems and kits comprising the nail compositions of the invention together with a base coat composition and/or a top coat composition.Type: GrantFiled: October 13, 2014Date of Patent: May 16, 2017Assignee: L'ORÉALInventors: Aline Aude Guimont, Chunhua Li, Xianzhi Zhou, Hy Si Bui, Jean-Thierry Simonnet
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Patent number: 9636322Abstract: The present invention is directed to formulations of genistein and methods for making and using the same. In particular embodiments, the formulations described herein include suspension formulations of nanoparticulate genistein.Type: GrantFiled: March 1, 2016Date of Patent: May 2, 2017Assignee: Humanetics CorporationInventors: Edmund Joseph Elder, Jr., Mark Joseph Sacchetti, Randall Joseph Tlachac, John L. Zenk
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Patent number: 9636293Abstract: A nail compositions comprising at least one photo-curable polymer dispersed in water (latex), at least one non-photo-curable polymer dispersed in water (latex), at least one photo-initiator, optionally at least one plasticizer, optionally a colorant, and water are provided. Also provided are nail composition systems and kits comprising the nail compositions of the invention together with a base coat composition and/or a top coat composition.Type: GrantFiled: October 13, 2014Date of Patent: May 2, 2017Assignee: L'ORÉALInventors: Aline Aude Guimont, Chunhua Li, Xianzhi Zhou, Hy Si Bui, Jean-Thierry Simonnet
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Patent number: 9629944Abstract: The present invention provides an implantable device having a coating including a slow dissolving polymer or material and the methods of making and using the same.Type: GrantFiled: May 20, 2016Date of Patent: April 25, 2017Assignee: Abbott Cardiovascular Systems Inc.Inventors: O. Mikael Trollsas, Michael H. Ngo, David J. Sherman, Syed F. A. Hossainy
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Patent number: 9617409Abstract: The present invention describes methods for preparing a pigment particle dispersion. Specifically, a premix composition including pigments, dispersants and a liquid carrier is milled by a solid milling agent to predetermined particle size. The solid milling agent is solubilized in the liquid carrier which eliminates the need for separating the solid milling agent from the dispersion.Type: GrantFiled: December 13, 2011Date of Patent: April 11, 2017Assignee: Sun Chemical CorporationInventor: Mark Ortalano
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Patent number: 9592197Abstract: A pharmaceutical dosage form which comprises diphenhydramine and/or a pharmaceutically acceptable salt thereof and at least one second drug. The dosage form provides a plasma concentration within the therapeutic range of the at least one second drug over a period which is coextensive with a substantial part of the period over which the dosage form provides a plasma concentration within the therapeutic range of diphenhydramine or salt thereof. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.Type: GrantFiled: December 16, 2004Date of Patent: March 14, 2017Assignee: SOVEREIGN PHARMACEUTICALS, LLCInventors: Viswanathan Srinivasan, Juan Carlos Menendez, Venkatesh Balasubramanian, Somphet Peter Suphasawud, Ralph Brown, David Brown
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Patent number: 9592200Abstract: An abuse-deterrent pharmaceutical composition has been developed to reduce the likelihood of improper administration of drugs, especially drugs such as opioids. In a preferred embodiment, a drug is modified to increase its lipophilicity. In some embodiments the modified drug is homogeneously dispersed within spherical microparticles composed of a material that is either slowly soluble or not soluble in water. In some embodiments the drug containing microparticles or drug particles are coated with one or more coating layers, where at least one coating is water insoluble and/or organic solvent insoluble. The abuse-deterrent composition retards the release of drug, even if the physical integrity of the formulation is compromised (for example, by chopping with a blade or crushing) and the resulting material is placed in water, snorted, or swallowed. However, when administered as directed, the drug is slowly released from the composition as the composition is passes through the GI tract.Type: GrantFiled: November 19, 2015Date of Patent: March 14, 2017Assignee: COLLEGIUM PHARMACEUTICAL, INC.Inventors: Roman V. Rariy, Alison B. Fleming, Jane Hirsh, Alexander M. Klibanov
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Patent number: 9561249Abstract: The present invention relates to pharmaceutical compositions of nitrites such as inorganic nitrites, or any pharmaceutically acceptable salts, solvates, or prodrugs thereof, and the medical use of these compositions. The pharmaceutical compositions, which can be formulated for oral administration, can provide immediate release or extended release of the nitrite ion (NO2?). The pharmaceutical compositions of the invention are useful, for example, for modulating brain function, in particular improving mood and/or psychological state, in the treatment of disorders of brain development, and in the treatment and/or reduction of pain.Type: GrantFiled: February 19, 2015Date of Patent: February 7, 2017Assignee: TheraVasc Inc.Inventors: Christopher Kevil, Kyle Chan, Amol Soin
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Patent number: 9554945Abstract: A wound care bandage for treating a wound is provided. The bandage includes an SIS layer to be placed on the wound surface and a cover to placed over the wound. The bandage further includes a structure to provide a vacuum space. A method for promoting wound healing is further provided. The method includes applying the above-mentioned wound care bandage to the wound and creating a vacuum in the vacuum space to draw blood controllably from the wound into the SIS layer.Type: GrantFiled: December 30, 2015Date of Patent: January 31, 2017Assignee: KCI Medical Resources Unlimited CompanyInventor: Arthur C. Coffey
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Patent number: 9549893Abstract: The invention provides compositions, methods and kits for the removal of harmful or irritating substances from bodily surfaces. Kits may include a composition containing capsaicin and a capsaicin-cleansing composition, e.g., a composition in which capsaicin is soluble.Type: GrantFiled: November 14, 2014Date of Patent: January 24, 2017Assignee: Acorda Therapeutics, Inc.Inventors: Arturo J. Angel, Larry W. Litle, Keith R. Bley, Allan L. Wilcox, Gene C. Jamieson, Naweed Muhammad
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Patent number: 9522158Abstract: The present invention relates to the field of viral disorders, and in particular to the use of natural compounds to inhibit viruses and viral infection. Compositions comprising NGNA are provided for treating or preventing viral infections, such as those causing the common cold.Type: GrantFiled: January 13, 2014Date of Patent: December 20, 2016Assignee: LIFE SCIENCE NUTRITION ASInventors: Jan Remmereit, Dan Edwall, Anders Struksnes
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Patent number: 9521841Abstract: A process for producing aqueous chlorous acid solution in which chlorous acid, which is safe for the human body, is easy to handle, and less generates chlorine dioxide, is yielded and used as a disinfectant for a pretreatment in food processing. To an aqueous sodium chlorate solution is added sulfuric acid or an aqueous solution thereof in such an amount and concentration that the pH of the aqueous solution can be kept at 2.3-3.4 to thereby react them and generate chloric acid. Subsequently, hydrogen peroxide is added to the chloric acid in an amount which is equal to or larger than the amount necessary for a reduction reaction to thereby yield chlorous acid. Any one of inorganic acids, inorganic acid salts, organic acids, and organic acid salts, or two or more thereof, or a combination or these is added to the aqueous solution containing chlorous acid yielded, whereby the chlorous and acid can be present for long and the pH of the aqueous solution is regulated to regulated to 3.2-7.0.Type: GrantFiled: July 16, 2015Date of Patent: December 20, 2016Assignee: Honbu Sankei Co., Ltd.Inventor: Hisataka Goda
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Patent number: 9517210Abstract: A method for producing a microcapsule powder includes a concentration step. In the concentration step, an aqueous dispersion of a microcapsule is supplied into a cyclone, and the aqueous dispersion is then concentrated. The concentration step includes an aqueous dispersion-supplying step and a concentrated dispersion-recovering step. In the aqueous dispersion-supplying step, the aqueous dispersion is supplied into a cylindrical member inlet. In the concentrated dispersion-recovering step, a microcapsule dispersion is recovered. The microcapsule dispersion is discharged through a conical member outlet.Type: GrantFiled: July 10, 2013Date of Patent: December 13, 2016Assignee: TAKEDA PHARMACEUTICAL COMPANY LIMITEDInventors: Seitaro Mizukami, Naoki Choda
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Patent number: 9517205Abstract: Influenza vaccines are administered using solid biodegradable microneedles. The microneedles are fabricated from the influenza vaccine in combination with solid excipient(s) and, after penetrating the skin, they dissolve in situ and release the vaccine to the immune system. The influenza vaccine is (i) a purified influenza virus surface antigen vaccine, rather than a live vaccine or a whole-virus or split inactivated vaccine (ii) an influenza vaccine prepared from viruses grown in cell culture, not eggs, (iii) a monovalent influenza vaccine e.g. for immunizing against a pandemic strain, (iv) a bivalent vaccine, (v) a tetravalent or >4-valent vaccine, (vi) a mercury-free vaccine, or (vii) a gelatin-free vaccine.Type: GrantFiled: August 19, 2011Date of Patent: December 13, 2016Assignee: Seqirus UK LimitedInventors: Derek O'Hagan, Manmohan Singh, Sung-Yun Kwon
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Patent number: 9516878Abstract: A process for producing aqueous chlorous acid solution in which chlorous acid, which is safe for the human body, is easy to handle, and less generates chlorine dioxide, is yielded and used as a disinfectant for a pretreatment in food processing. To an aqueous sodium chlorate solution is added sulfuric acid or an aqueous solution thereof in such an amount and concentration that the pH of the aqueous solution can be kept at 2.3-3.4 to thereby react them and generate chloric acid. Subsequently, hydrogen peroxide is added to the chloric acid in an amount which is equal to or larger than the amount necessary for a reduction reaction to thereby yield chlorous acid. Any one of inorganic acids, inorganic acid salts, organic acids, and organic acid salts, or two or more thereof, or a combination or these is added to the aqueous solution containing chlorous acid yielded, whereby the chlorous and acid can be present for long and the pH of the aqueous solution is regulated to regulated to 3.2-7.0.Type: GrantFiled: December 8, 2014Date of Patent: December 13, 2016Assignee: Honbu Sankei Co., Ltd.Inventor: Hisataka Goda
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Patent number: 9511018Abstract: Effective treatments of pain for extended periods of time are provided. Through the administration of an effective amount of clonidine in a matrix at or near a target site, one can relieve pain caused by diverse sources, including but not limited to spinal disc herniation (i.e. sciatica), spondilothesis, stenosis, discogenic back pain and joint pain, as well as pain that is incidental to surgery. When appropriate matrix formulations are provided within biodegradable polymers, this pain relief can be continued for at least three days. In some embodiments, the relief can be for at least twenty-five days, at least fifty days, at least one hundred days, at least one hundred and thirty-five days or at least one hundred and eighty days.Type: GrantFiled: April 5, 2012Date of Patent: December 6, 2016Assignee: Warsaw Orthopedic, Inc.Inventors: Danielle L. Clay, Nicholas A. Moore
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Patent number: 9492371Abstract: A cosmetic composition, comprising the following components (A), (B), (C), and (D): (A) from 0.01 to 48 % by mass of a fluorine-modified silicone having a polysiloxane unit represented by the following formulae (1) and (2): wherein, Rf represents a linear or branched perfluoroalkyl group having 6 carbon atoms; R1, R2, and R3 are the same or different and each represent a linear or branched hydrocarbon group having 1 to 6 carbon atoms; m represents a number of 2 to 6; n represents a number of 1 to 6; p represents a number of 3 to 50; s represents a number of 1 to 5; and a ratio between p and s satisfies 0.66?p/(p+s)?0.9, (B) from 0.01 to 40 % by mass of a powder having been subjected to a surface treatment with tridecafluoro octyltriethoxysilane, (C) from 0.Type: GrantFiled: February 25, 2013Date of Patent: November 15, 2016Assignee: KAO CORPORATIONInventors: Hirohisa Suzuki, Yoshiaki Matsui, Takashi Kodate
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Patent number: 9486286Abstract: The medical laser user interface of the present invention generally comprises a medical laser unit and a control system. The medical laser unit includes an optical probe for delivering laser light to a patient's tissue. The control system controls operation of the medical laser unit. Specifically, the control system provides a foot pedal system that enables the user to switch between the delivery of a first wavelength of laser light and a second wavelength of laser light through depression of a foot pedal. In a first embodiment, a single foot pedal can be used to toggle the wavelengths, where as in a second embodiment two foot pedals can be use, i.e., one for the first wavelength and one for the second wavelength. The two wavelengths provided include a wavelength for vaporization of tissue and a wavelength for coagulation.Type: GrantFiled: May 14, 2008Date of Patent: November 8, 2016Assignee: Boston Scientific Scimed, Inc.Inventors: Michael R. Hodel, Terry J. Smith