Abstract: Provided is a drug delivery system for control of initial burst of a drug. More particularly, there are provided a drug delivery formulation including: a granule containing a biodegradable polymer and a drug; and a temperature-sensitive hydrogel, and a method for preparing the same. The presently disclosed drug delivery formulation can be prepared via a relatively simple process and allows a drug to be released slowly at a constant rate without initial burst and thus maintains a constant blood level of the drug for a long period of time. Consequently, it is capable of preventing the initial burst of the existing injection-type drug delivery formulations and slow-release granules and providing a desired release profile, including sustained release with time.
Type:
Grant
Filed:
February 8, 2011
Date of Patent:
June 4, 2019
Assignee:
AJOU UNIVERSITY INDUSTRY-ACADEMIC COOPERATION FOUNDATION
Abstract: A combination of N-acetyl-L-cysteine, selenium in the form of selenomethionine and melatonin, and a medical product or pharmaceutical composition comprising such combination, useful for the treatment of a variety of diseases and conditions is described. The combination of N-acetyl-L-cysteine, selenium in the form of selenomethionine and melatonin is also useful for cosmetic treatment of skin and as an antibacterial agent.
Abstract: In one aspect, compositions and methods for the treatment of vulvovaginal atrophy (VVA) are provided. In one embodiment, the method comprises administering an estrogen to a subject having VVA by inserting a dosage form comprising a liquid pharmaceutical composition.
Type:
Grant
Filed:
February 9, 2018
Date of Patent:
April 16, 2019
Assignee:
TherapeuticsMD, Inc.
Inventors:
Sebastian Mirkin, Julia M. Amadio, Brian A. Bernick
Abstract: The present invention relates to a granular composition for oral suspension characterized by the presence of an insoluble resin and a silica gel.
Abstract: The present invention relates to an antimicrobial and antiviral polymeric drawn fiber and polymeric fiber-based materials comprising same, wherein the drawn fiber is a polymer fiber containing cuprous oxide particles dispersed therein, with particle size ranges from about 0.25 to about 0.65 micron. The invention also relates to processes for preparing the same.
Abstract: A guided bone regeneration material is disclosed. The guided bone regeneration material includes biodegradable fibers produced by an electrospinning method. The biodegradable fibers produced by the method include a silicon-releasing calcium carbonate and a biodegradable polymer. The silicon-releasing calcium carbonate is a composite of siloxane and calcium carbonate of vaterite phase. The biodegradable fibers may be coated with apatite. When the guided bone regeneration material is immersed in a neutral aqueous solution, silicon species ions are eluted from the calcium carbonate. The guided bone regeneration material excels in bone reconstruction ability.
Type:
Grant
Filed:
August 31, 2018
Date of Patent:
December 25, 2018
Assignees:
NATIONAL UNIVERSITY CORPORATION NAGOYA INSTITUTE OF TECHNOLOGY, YABASHI INDUSTRIES CO., LTD., YAMAHACHI DENTAL MFG., CO., ORTHOREBIRTH CO., LTD.
Abstract: The present invention relates to a method of pre-rinsing laundry and treating other surfaces employing a composition that can kill bedbug eggs. The composition includes an anionic compound and is at pH just above neutral, e.g., about 7 to about 9.
Type:
Grant
Filed:
November 20, 2012
Date of Patent:
December 4, 2018
Assignee:
Ecolab USA Inc.
Inventors:
Kim R. Smith, Erik Olson, Yvonne Killeen, Victor Man, Joelle Olson, Erin Loosbrock
Abstract: A drug delivery device comprising a non-erodible, non-porous housing member defining a reservoir is provided. The reservoir is loaded with a dry formulation of a selected salt of a neuroleptic agent. The housing member has one or more porous partitions, where the pores of the partitions are sufficiently small to retain the insoluble powder particles within the reservoir yet large enough to allow diffusion of the active agent once the device is hydrated. A therapeutic dose of the drug is released from the device at a constant rate over a period of approximately 2-6 months.
Abstract: Systems and methods for preparing synthetic osteoinductive bone grafts are provided in which a porous ceramic granule, which may be incorporated within a biocompatible matrix material, is loaded with an osteoinductive agent. Loading of granules is facilitated in some cases by the use of low-pH buffers and pre-treatments.
Type:
Grant
Filed:
December 29, 2015
Date of Patent:
November 20, 2018
Assignee:
Bioventus, LLC.
Inventors:
Eric Vanderploeg, Howard Seeherman, Christopher G. Wilson, John Wozney, Christopher T. Brown, John A. Kambouris
Abstract: A guided bone regeneration material is disclosed. The guided bone regeneration material includes biodegradable fibers produced by an electrospinning method. The biodegradable fibers produced by the method include a silicon-releasing calcium carbonate and a biodegradable polymer. The silicon-releasing calcium carbonate is a composite of siloxane and calcium carbonate of vaterite phase. The biodegradable fibers may be coated with apatite. When the guided bone regeneration material is immersed in a neutral aqueous solution, silicon species ions are eluted from the calcium carbonate. The guided bone regeneration material excels in bone reconstruction ability.
Type:
Grant
Filed:
May 5, 2014
Date of Patent:
October 9, 2018
Assignees:
National University Corporation, Nagoya Institute of Technology, Yabashi Industries Co., LTD, Yamahachi Dental Mfg., Co, Orthorebirth Co. Ltd.
Abstract: Drug delivery balloons have densely packed crystals of small particle size of the drug thereon. An amorphous drug coating is applied to a balloon surface and annealed to provide the crystals. The balloon surface is nucleated to induce formation of drug crystals in the annealing step to provide the crystals in high density with small size.
Type:
Grant
Filed:
June 14, 2010
Date of Patent:
September 25, 2018
Assignee:
BOSTON SCIENTIFIC SCIMED, INC.
Inventors:
Steve Kangas, Michael Sean Owens, Jon Patterson, Dave Ekberg, Erik Haun, Eric Henderson, Aaron Foss, Yen-Lane Chen
Abstract: The invention generally relates to dextran fibers which are preferably electrospun and devices formed from such fibers. In particular, such devices may include substances of interest (such as therapeutic substances) associated with the electrospun fibers. Upon exposure to a liquid the electrospun fibers dissolve immediately and the substances of interest are released into the liquid. Exemplary devices include bandages formed from electrospun dextran fibers and associated agents that promote hemostasis, such as thrombin and fibrinogen.
Type:
Grant
Filed:
July 29, 2014
Date of Patent:
August 14, 2018
Assignees:
The Henry M Jackson Foundation for the Advancement of Military Medicine, Inc., Virginia Commonwealth University
Inventors:
Gary Bowlin, David Simpson, James Bowman, Stephen Rothwell
Abstract: A system and method includes delivery of a redox gas solution to treat onychomycosis, wherein the redox gas solution comprises a reactive species dissolved in a perfluorocarbon liquid, and wherein the reactive species may include, alone or in combination, one or more of reactive oxygen, reactive nitrogen, reactive chlorine, or reactive bromine species, and the perfluorocarbon liquid may include perfluorodecalin.
Type:
Grant
Filed:
December 9, 2015
Date of Patent:
August 7, 2018
Assignee:
DeviceFarm, Inc.
Inventors:
Jeffrey N Roe, Timothy C Grammer, Michael P O'Neil
Abstract: Compositions and methods are described for a polymer hydrogel created by a cycloaddition reaction between an azide and an alkyne that proceeds rapidly without catalyst to produce the polymer hydrogel in less than ninety seconds. The polymer hydrogel can be used in in vivo applications for the localized delivery of therapeutic agent in aqueous solutions. An example of therapeutic delivery of a protein in a mouse model is demonstrated.
Type:
Grant
Filed:
March 19, 2012
Date of Patent:
August 7, 2018
Assignees:
Georgia Tech Research Corporation, Children's Healthcare of Atlanta, Inc.
Inventors:
Niren Murthy, Christopher Hermann, David Scott Wilson, Xinghai Ning, Barbara D. Boyan, Zvi Schwartz, Robert Guldberg, Tamim Diab
Abstract: A system and method includes delivery of a redox gas solution to treat onychomycosis, wherein the redox gas solution comprises a reactive species dissolved in a perfluorocarbon liquid, and wherein the reactive species may include, alone or in combination, one or more of reactive oxygen, reactive nitrogen, reactive chlorine, or reactive bromine species, and the perfluorocarbon liquid may include perfluorodecalin.
Type:
Grant
Filed:
March 21, 2017
Date of Patent:
August 7, 2018
Assignee:
DeviceFarm, Inc.
Inventors:
Jeffrey N Roe, Timothy C Grammer, Raul Ignacio Barrera-Barraza, Eric Tridas
Abstract: New liposomes are described, comprising: (i) phosphatidic acid and/or cardiolipin; (ii) apolipoprotein E (ApoE) or derivatives thereof. The so modified liposomes, administered systemically, obtain a dramatic in-vivo reduction of the amyloid plaque in the central nervous system, allowing an effective treatment of neurodegenerative diseases, in particular Alzheimer's disease.
Type:
Grant
Filed:
October 2, 2014
Date of Patent:
July 3, 2018
Assignee:
UNIVERSITA DEGLI STUDI DI MILANO-BICOCCA
Inventors:
Massimo Masserini, Francesca Re, Giulio Sancini, Gianluigi Forloni, Mario Salmona
Abstract: Oral pharmaceutical dosage form comprising tromethamine and a NSAID selected from the group comprising ibuprofen, naproxen and flurbiprofen, characterized in that it also comprises a compound selected from the group comprising glycine, vitamin B6 and mixtures thereof.
Type:
Grant
Filed:
December 16, 2004
Date of Patent:
May 15, 2018
Assignee:
AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F.S.p.A.
Abstract: A method of inhibiting HPV virus infection is disclosed. In one embodiment, the method involves exposing a papillomavirus to an effective amount of a compound selected from the group consisting of Compound 13, Compound 14, and analogs of Compounds 13 and 14. In another embodiment, the method involves administering an inhibitor selected from the group consisting of Compound 13, Compound 14, and analogs of Compounds 13 and 14 to a susceptible tissue or cell.
Type:
Grant
Filed:
June 2, 2015
Date of Patent:
April 24, 2018
Assignee:
Wisconsin Alumni Research Foundation
Inventors:
Paul F. Lambert, Paul G. Ahlquist, Dohun Pyeon, Hao Shun Huang
Abstract: Embodiments of the present invention provide a method for treatment of respiratory disorders such as asthma, chronic obstructive pulmonary disease, and chronic sinusitis, including cystic fibrosis, interstitial fibrosis, chronic bronchitis, emphysema, bronchopulmonary dysplasia and neoplasia. The method involves administration, preferably oral, nasal or pulmonary administration, of anti-inflammatory and anti-proliferative drugs (rapamycin or paclitaxel and their analogs) and an additive.
Abstract: A method for repairing an injury of cartilage in a patient by local administration of an organovanadium agent or use of an implantable device for delivery of an organovanadium agent. Implantable devices containing an organovanadium agent and methods of making these implantable devices are also disclosed.
Type:
Grant
Filed:
July 6, 2012
Date of Patent:
April 3, 2018
Assignee:
RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
Inventors:
Sheldon S. Lin, David N. Paglia, James P. O'Connor, Aaron Wey, Joseph Benevenia, Virak Tan