Patents Issued in August 28, 2014
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Publication number: 20140242097Abstract: A method for promoting entry of an agent (introduced agent) into a cell, the method comprising the step of complexing the introduced agent in the presence of an entry-promoting agent and then exposing to cells, wherein the entry-promoting agent comprises a linear and/or branched or cyclic polymonoguanide/polyguanidine, polybiguanide, analogue or derivative thereof according to the following Formula 1a & b. The method also provides a means for formation of nanoparticles formed between the entry promoting agent and the introduced agent.Type: ApplicationFiled: October 11, 2012Publication date: August 28, 2014Applicant: THE ROYAL VETERINARY COLLEGEInventors: Liam Good, Kantaraja Chindera, Valentina Gburcik
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Publication number: 20140242098Abstract: Flexible film or strip dosing device and method for various therapeutic applications are disclosed. The device includes at least one film or strip and a packaging container for the film or strip. The film or strip normally include a polymer base with or without a therapeutic agent admixed with the polymer base. The film or strip is printed with doses, marks or calibrated lines to indicate different length of the film and therefore the different doses of the therapeutic agents. The packaging container or dispenser can have marks or calibrated lines similar to a ruler which measures the length of film and therefore the different doses of therapeutic agents. The packaging container may have a built-in cutter to conveniently cut the film or strips as needed for flexible dosing of therapeutic agents.Type: ApplicationFiled: February 24, 2014Publication date: August 28, 2014Applicant: MONMOUTH UNIVERSITYInventor: Xudong Yuan
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Publication number: 20140242099Abstract: The invention relates to certain compounds or pharmaceutically acceptable salts, solvates, clathrates, or prodrugs thereof, that are useful as immunosuppressive agents and for treating and preventing inflammatory conditions, allergic disorders, and immune disorders.Type: ApplicationFiled: October 26, 2012Publication date: August 28, 2014Inventors: Shoujun Chen, Junyi Zhang, Jun Jiang, Teresa Kowalczyk-Przewloka, Zhiqiang Xia, Shijie Zhang
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Publication number: 20140242100Abstract: The present invention features methods and compositions for the generation of conformation-specific antibodies.Type: ApplicationFiled: April 27, 2012Publication date: August 28, 2014Applicant: Beth Israel Deaconess Medical Center, Inc.Inventors: Kun Ping Lu, Xiao Zhen Zhou
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Publication number: 20140242101Abstract: The present invention relates to the field of prophylaxis and therapy of clinical conditions including cancer, autoimmune diseases and infectious diseases. In particular there is provided vaccine compositions comprising PD-L1 or peptide fragments thereof that are capable of eliciting immune responses useful in treatment of cancer, autoimmune diseases or infectious diseases.Type: ApplicationFiled: October 17, 2012Publication date: August 28, 2014Applicant: HERLEV HOSPITALInventor: Mads Hald Andersen
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Publication number: 20140242102Abstract: Polypeptides, polynucleotides, methods, compositions, and vaccines comprising influenza hemagglutinin and neuraminidase variants are provided.Type: ApplicationFiled: January 15, 2014Publication date: August 28, 2014Applicant: MEDIMMUNE, LLCInventors: Chin-Fen YANG, George KEMBLE, Chongguang LIU
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Publication number: 20140242103Abstract: The present invention provides a modified influenza virus wherein the RNA of the haemagglutinin gene has been modified such that the haemagglutinin signal sequence is not expressed and the virus produces a haemagglutinin protein that lacks a functional signal sequence. The invention further provides composition comprising the modified virus and uses of the modified virus.Type: ApplicationFiled: September 21, 2012Publication date: August 28, 2014Applicant: ISIS INNOVATION, LTD.Inventor: Alain Townsend
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Publication number: 20140242104Abstract: Self-assembling peptide nanoparticles (SAPN) incorporating T-cell epitopes and displaying the P domain of the norovirus protein VP1 are described. The nanoparticles of the invention consist of aggregates of a continuous peptide chain comprising two coiled coil oligomerization domains connected by a linker segment wherein one or both oligomerization domains incorporate T-cell epitopes within their peptide sequence. These nanoparticles are useful as vaccines and adjuvants for the prevention and treatment of norovirus infections.Type: ApplicationFiled: October 5, 2012Publication date: August 28, 2014Applicant: ALPHA-O PEPTIDES AGInventors: Peter Burkhard, Caroline Kulangara
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Publication number: 20140242105Abstract: The present invention relates to means and methods to protect against disease caused by bacteria belonging to the genus Chlamydia. In particular, the present invention relates to isolated B- and T-cell epitopes derived from the major outer membrane protein of Chlamydia psittaci which can be used against an infection with a species of the genus Chlamydia. More in particular, the invention provides a vaccine which can be used against chlamydiosis caused by Chlamydia psittaci in birds and man. In addition, the invention relates to a diagnostic method to diagnose the latter infections.Type: ApplicationFiled: June 15, 2012Publication date: August 28, 2014Applicant: UNIVERSITEIT GENTInventor: Daisy Vanrompay
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Publication number: 20140242106Abstract: The invention provides proteins from Staphylococcus aureus including amino acid sequences and the corresponding nucleotide sequences. The proteins are useful for vaccines, immunogenic compositions, diagnostics, enzymatic studies and also as targets for antibiotics.Type: ApplicationFiled: April 28, 2014Publication date: August 28, 2014Applicant: NOVARTIS AGInventors: Vega MASIGNANI, Mariarosa MORA, Maria SCARSELLI
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Publication number: 20140242107Abstract: The present invention relates to direct protein delivery with engineered micro vesicles.Type: ApplicationFiled: February 25, 2014Publication date: August 28, 2014Applicant: INSERM (Institut National de la Sante et de la Recherche Medicale)Inventors: Philippe Mangeot, Vincent Lotteau
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Publication number: 20140242108Abstract: A conjugated compound of Formula I: Q-Z—R4 wherein Q is a TLR7 and/or TLR8 agonist and Z—R4 is a TLR2 agonist, the conjugated compound being chosen among compounds of Formula II:Type: ApplicationFiled: February 22, 2013Publication date: August 28, 2014Applicant: CAYLAInventors: Thierry LIOUX, Daniel DROCOURT, Fabienne VERNEJOUL, Gerard TIRABY, Eric PEROUZEL
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Publication number: 20140242109Abstract: The objective of the present invention is to provide a method for cultivating an alga having ability to produce alginic acid industrially and effectively and a method for producing an alginic acid-containing composition industrially advantageously. The method for cultivating an alga according to the present invention is characterized in comprising the step of cultivating the alga heterotrophically, wherein the alga belongs to the genus Parachlorella and has ability to produce alginic acid.Type: ApplicationFiled: September 6, 2012Publication date: August 28, 2014Applicant: KANEKA CORPORATIONInventors: Noriyuki Kizaki, Takeshi Furuta, Taku Mouri, Naoaki Taoka
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Publication number: 20140242110Abstract: Formulations of and dosing protocols for the administration of botulinum toxin that maximize efficacy and specificity while minimizing the likelihood of overdosing and undesirable side effects of treatment. The formulations include positively charged carriers, such as cationic peptides, which otherwise have no inherent botulinum-toxin-like activity. The dosing regimen is based on the pattern, quantity, and location of neuromuscular junctions in the target tissue. Because the number of neuromuscular junctions in a target tissue remains generally stable throughout life and because the pharmacological effect of botulinum toxin is localized at the neuromuscular junction, dosing efficacy is unaffected by muscle mass, age of the patient, or body weight.Type: ApplicationFiled: February 28, 2013Publication date: August 28, 2014Inventor: L. Andrew Koman
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Publication number: 20140242111Abstract: Disclosed is an oral delivery system that overcomes major barriers encountered in the gastrointestinal tract, particularly rapid proteolytic degradation and low intestinal permeability. Provided is a method for oral delivery of an engineered microorganism to a mammal where the microorganism produces a macromolecule having a desired bioavailability outcome.Type: ApplicationFiled: March 8, 2012Publication date: August 28, 2014Applicant: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIAInventors: Casim Ali Sarkar, Ting Wun Ng
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Publication number: 20140242112Abstract: The present invention provides an immunogenic composition comprising one or more antigens and a Toll-like receptor (TLR) 7 agonist in an orally (e.g. sublingually) administered composition.Type: ApplicationFiled: April 25, 2014Publication date: August 28, 2014Applicant: GlaxoSmithKline Biologicals S.A.Inventors: Nadia Ouaked, Martin Plante, Daniel Larocque, Corey Patrick Mallett
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Publication number: 20140242113Abstract: This document provides methods and materials involved in making and using liquid vaccine preparations for oral administration. For example, methods and materials for making and using liquid vaccine preparations for oral administration that include a lyophilized or dried vaccine component (e.g., a lyophilized pathogenic agent such as a lyophilized rotavirus preparation) and a liquid edible oil composition (e.g., a liquid edible oil composition containing one or more medium chain triglycerides) are provided. In some cases, liquid vaccine preparations that include a buffer component (e.g., CaCO3) are provided.Type: ApplicationFiled: April 27, 2012Publication date: August 28, 2014Inventor: Leonard P. Ruiz, JR.
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Publication number: 20140242114Abstract: The invention concerns recombinant DNA's comprising cDNA of genomic RNA of a Salmonidae alphavirus preceded by a spacer sequence, under the control of a suitable promoter. Said recombinant DNAs are useful for obtaining expression vectors, producing recombinant Salmonidae alphavirus, and for obtaining vaccines.Type: ApplicationFiled: October 18, 2013Publication date: August 28, 2014Inventors: Monique Leberre, Coralie Moriette, Michel Bremont
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Publication number: 20140242115Abstract: The present disclosure provides methods for producing a vaccine composition containing a pathogen that is rendered noninfectious by exposure to hydrogen peroxide. The methods disclosed herein are suitable for the preparation of vaccines for a wide variety of pathogens, including viruses, bacteria and parasites. The disclosure also provides vaccine compositions (medicaments) containing a pathogen inactivated by exposure to hydrogen peroxide. Methods for eliciting an immune response in a subject by administering vaccine compositions containing a hydrogen peroxide inactivated pathogen are also provided.Type: ApplicationFiled: May 5, 2014Publication date: August 28, 2014Applicant: Oregon Health and Science UniversityInventors: Mark K. Slifka, Shirley Villadiego, Erika Hammarlund, Paul Yoshihara
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Publication number: 20140242116Abstract: Provided herein are insoluble particles that include polypeptides. The polypeptides may have immunogenicity that is greater than the immunogenicity of the same polypeptides when they are not present in the particle. The polypeptides may be soluble before incorporation into the particles and insoluble after incorporation into the particles. The particles may include lipopolysaccharide, wherein the lipopolysaccharide is insoluble. The particles may include a carrier. In one embodiment, a carrier is present at no greater than 0.001 mg carrier/mg particles. In one embodiment, a carrier is present at a ratio of carrier to polypeptide (weight:weight) of no greater than 0.05:1. In one embodiment, a carrier is not detectable in the particles.Type: ApplicationFiled: May 6, 2014Publication date: August 28, 2014Applicant: Life-Science Innovations, LLCInventors: Bobby Gene Poe, III, Jared Randall Huisinga
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Publication number: 20140242117Abstract: The present investigation relates to entrapment of carbohydrate antigen such as Vi polysaccharide of Salmonella typhi in poly (DL) lactide (PDLLA) and polylactide-co-glycolide (PLGA) polymer particles. The formulated product not only elicits primary antibody titers from single dose application but also evokes memory antibody titer against the T independent antigen.Type: ApplicationFiled: May 29, 2012Publication date: August 28, 2014Applicant: National Institute of ImmunologyInventors: Anish Chakkumkal, Amulya Kumar Panda
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Publication number: 20140242118Abstract: In one aspect, the present invention provides a method for treating cancer comprising tumor cell vaccination in combination with hematopoietic and immune cell transplantation. In some embodiments, the method involves autologous tumor cell vaccination prior to autologous hematopoietic and immune cell transplantation. In another aspect, the present invention provides a method of purifying tumor cells from a subject in preparation for vaccination.Type: ApplicationFiled: July 3, 2013Publication date: August 28, 2014Inventors: Samuel Strober, Alexander Filatenkov
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Publication number: 20140242119Abstract: The invention provides the use of compound of formula V or formula VI in the treatment of a demyelinating peripheral neuropathy: wherein X, R1, R2, R3, R4, R5, n, R1a, R2a, R3a, R4a, R5a, R6a, R7a, Xa and na are defined herein; or the N-oxide derivatives thereof or prodrugs thereof, or a pharmaceutically acceptable salt, solvate or hydrate thereof. The invention further provides combinations of a compound of Formula V or VI with one or more therapeutic agents and pharmaceutical composition thereof.Type: ApplicationFiled: April 18, 2014Publication date: August 28, 2014Applicant: NOVARTIS AGInventors: David LEPPERT, Erik WALLSTROEM, Barbara NUESSLEIN-HILDESHEIM
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Publication number: 20140242120Abstract: The invention relates to compounds of structural formula (I): or a pharmaceutically acceptable salt, solvate, clathrate, or prodrug thereof, wherein Y, L, A, W1, W2, and R?1 are defined herein. These compounds are useful as immunosuppressive agents and for treating and preventing inflammatory conditions, allergic disorders, and immune disorders.Type: ApplicationFiled: May 8, 2014Publication date: August 28, 2014Applicant: Synta Pharmaceuticals Corp.Inventors: Shoujun Chen, Lijun Sun, Yu Xie
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Publication number: 20140242121Abstract: The present invention relates to a compound of Formula I: or an enantiomer, diastereomer, tautomer, or pharmaceutically acceptable salt or solvate thereof, wherein the symbols are as defined in the specification; a pharmaceutical composition comprising the same; and a method for treating or preventing autoimmunity disease using the same.Type: ApplicationFiled: October 3, 2012Publication date: August 28, 2014Applicant: JANUS BIOTHERAPEUTICS, INC.Inventors: Grayson B. Lipford, Charles M. Zepp
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Publication number: 20140242122Abstract: Salts of glycopyrrolate, including solid forms thereof are herein disclosed. Methods of making glycopyrrolate salts and methods of treating hyperhidrosis with salts of glycopyrrolate are disclosed.Type: ApplicationFiled: September 11, 2013Publication date: August 28, 2014Applicant: Dermira, Inc.Inventors: John Allan STATLER, Anthony Adrian SHAW, Delphine Caroline IMBERT, Jennifer Leigh NELSON, Patricia ANDRES, Lisa Lynn McQUEEN, Stephan Xander Mattheus BOERRIGTER
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Publication number: 20140242123Abstract: The disclosure provides for saccharide-peptide based hydrogels, the functionalization of the saccharide-peptide based hydrogels with one or more biological agents, and the encapsulation of one or more biological materials and/or pharmaceutical agents in the hydrogels. The disclosure further provides for the use of the saccharide-peptide based hydrogels in treating a disease or disorder in a subject.Type: ApplicationFiled: February 21, 2014Publication date: August 28, 2014Inventors: Zhibin Guan, Yoko Mullen, Sophia W. Liao
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Publication number: 20140242124Abstract: This invention provides a method of colonic cleansing.Type: ApplicationFiled: February 25, 2014Publication date: August 28, 2014Inventors: Dennis Riff, Gary S. Jacob, Kunwar Shailubhai, Patrick H. Griffin
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Publication number: 20140242125Abstract: The invention is directed to methods and compositions for obtaining uniform sized muscle fiber fragments for transplantation. These muscle fiber fragments are able to reconstitute into long fibers that are oriented along native muscle. The implanted muscle cells integrate with native vascular and neural network, as confirmed by histology and immunohistochemistry. This invention is particularly advantageous because autologous muscle can be harvested from a donor site, processed and injected into target sites in the operating room. The fragmented muscle fibers can be readily integrated within the host.Type: ApplicationFiled: August 15, 2012Publication date: August 28, 2014Applicant: WAKE FOREST UNIVERSITY HEALTH SCIENCESInventors: Anthony Atala, James Yoo, In Kap Ko
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Publication number: 20140242126Abstract: The present invention includes a hydrogel and a method of making a porous hydrogel by preparing an aqueous mixture of an uncrosslinked polymer and a crystallizable molecule; casting the mixture into a vessel; allowing the cast mixture to dry to form an amorphous hydrogel film; seeding the cast mixture with a seed crystal of the crystallizable molecule; growing the crystallizable molecule into a crystal structure within the uncrosslinked polymer; crosslinking the polymer around the crystal structure under conditions in which the crystal structure within the crosslinked polymer is maintained; and dissolving the crystals within the crosslinked polymer to form the porous hydrogel.Type: ApplicationFiled: May 14, 2014Publication date: August 28, 2014Inventors: Scott Zawko, Christine Schmidt
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Publication number: 20140242127Abstract: Cosmetic compositions for topical application to the skin comprising at least one phase change material (PCM) in combination with a cosmetically compatible carrier, and methods for maintaining the skin of a wearer of a cosmetic product at a comfortable temperature, are provided.Type: ApplicationFiled: February 24, 2014Publication date: August 28, 2014Applicant: ELC Management LLCInventors: Akira Yokozeki, John R. Castro, Scott Miselnicky
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Publication number: 20140242128Abstract: An object of the present invention is to provide a composite powder that is stable even if it is present in water for a long time. A composite powder, comprising: an inorganic powder; a first coating layer containing a water-repellent organic compound on the surface of the inorganic powder; and a second coating layer which contains at least one compound selected from the group consisting of silicon oxide, silicon oxide hydrate, aluminum oxide, and aluminum hydroxide, and which is formed on the first coating layer.Type: ApplicationFiled: August 1, 2012Publication date: August 28, 2014Applicant: Sakai Chemical Industry Co., Ltd.Inventors: Takuro Ashida, Nanae Gouda
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Publication number: 20140242129Abstract: A photoprotective personal care composition. The invention to a photoprotective personal care composition. The invention more particularly relates to a sunscreen composition that not only provides high sun protection but does that with minimal or no amount of traditionally used organic sunscreens. It is thus objects of the present invention to obviate the drawbacks of the prior art and provide high SPF photo-protective sunscreen compositions. Another object of the present invention is to achieve the above object using negligible amounts or no amount of organic sunscreen agents, which are sometimes unstable with the added advantage that inclusion of low or no organic sunscreens enables low formulation cost.Type: ApplicationFiled: August 21, 2012Publication date: August 28, 2014Inventors: Kumar Gaurav, Praveen Kumar, Bharath Palanisamy
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Publication number: 20140242130Abstract: A cosmetic composition is disclosed for applying to skin. The composition includes a liquid and dispersed in the liquid: any amount or form of fucoidan, any amount or form of beta glucan; and any amount of a marine extract. When the cosmetic composition is applied to the skin, the appearance of the skin is improved.Type: ApplicationFiled: May 2, 2014Publication date: August 28, 2014Inventor: Gina Athwal
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Publication number: 20140242131Abstract: A sunscreen composition comprised of one or more sunscreen active agents encapsulated in a cellulose derived capsule wherein the composition can contain one or more additional agents. A sunscreen composition can be mixed with a bodywash, shampoo, conditioner, lotion, gel, soap, cream, hand sanitizer, spray or mousse and can be used by an individual during their normal hygiene processes, such as during a shower or bath or while applying a body product to their skin or hair.Type: ApplicationFiled: May 3, 2014Publication date: August 28, 2014Applicant: COLABS INTERNATIONAL CORPORATIONInventor: Laura E. Cohen
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Publication number: 20140242132Abstract: A sunscreen composition comprised of one or more sunscreen active agents encapsulated in a cellulose derived capsule wherein the composition can contain one or more additional agents. A sunscreen composition can be mixed with a bodywash, shampoo, conditioner, lotion, gel, soap, cream, hand sanitizer, spray or mousse and can be used by an individual during their normal hygiene processes, such as during a shower or bath or while applying a body product to their skin or hair.Type: ApplicationFiled: May 3, 2014Publication date: August 28, 2014Applicant: CoLabs International CorporationInventor: Laura E. Cohen
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Publication number: 20140242133Abstract: The present invention provides personal care compositions, as well as methods for protecting low viscosity hydrophobic liquid actives.Type: ApplicationFiled: May 8, 2014Publication date: August 28, 2014Inventors: David L. Malotky, Xiaodong Zhang
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Publication number: 20140242134Abstract: The invention relates to cosmetic compositions comprising a water-in-oil emulsion comprising hydrophobically modified particles, amino functionalized silicone and water; the cosmetic composition further comprising a viscosity modifying agent and optical light modifying agent. The invention further relates to a method of modifying the optical appearance of skin comprising the step of applying to the skin the cosmetic composition of the invention.Type: ApplicationFiled: October 16, 2012Publication date: August 28, 2014Applicant: CONOPCO, INC. D/B/A UNILEVERInventors: Ezat Khoshdel, Su Yuan, Qiqing Zhang
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Publication number: 20140242135Abstract: In one aspect, the invention relates to chemical modulators of insect olfactory receptors. In particular, compounds and compositions are provided that can inhibit sensory (e.g., host targeting) functions in airborne insects such as mosquitos. Method of employing such agents, and articles incorporating the same, are also provided. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.Type: ApplicationFiled: April 25, 2012Publication date: August 28, 2014Applicant: Vanderbilt UniversityInventors: Laurence Zwiebel, Gregory M. Pask, David C. Rinker, Ian M. Romaine, Gary A. Sulikowski, Paul R. Reid, Alex G. Waterson, Kwangho Kim, Patrick L. Jones, Robert W. Taylor
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Publication number: 20140242136Abstract: There is disclosed a spray apparatus for holding contents comprising diatomaceous earth and a compressed propellant for propelling the diatomaceous earth. There is also disclosed use of diatomaceous earth to control a population of bedbugs, wherein the diatomaceous earth comprises remains of pennate diatoms. There is also disclosed a method of controlling a population of insects, the method comprising causing a compressed propellant to propel diatomaceous earth on a surface. Method of manufacturing a spray apparatus and methods of preparing diatomaceous earth for use in controlling a population of insects are also disclosed.Type: ApplicationFiled: March 21, 2014Publication date: August 28, 2014Inventor: Roderick William Phillips
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Publication number: 20140242137Abstract: Compositions and methods for use in treating, in particular, lignocellulosic substrates such as lumber, are provided; wherein said compositions comprise a preservative or biocidal species, other than boron, in the form of a glycolate. The methods may be used for the purpose of, for example, preventing the growth of pest organisms, or for providing other specific properties to the substrate.Type: ApplicationFiled: July 27, 2012Publication date: August 28, 2014Applicant: Matterworks One LimitedInventor: Nigel Paul Maynard
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Publication number: 20140242138Abstract: Method for the preparation of microencapsulated essential oils or a formulation thereof for various non-agricultural applications.Type: ApplicationFiled: May 7, 2014Publication date: August 28, 2014Applicant: BOTANOCAP LTD.Inventors: Amnon Kritzman, Arie Markus, Pnina Strongin, Charles Linder
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Publication number: 20140242139Abstract: A medical device for placement in a body of a mammal is provided. The medical device comprises (1) a polymeric matrix forming the device and defining a lumen through the device, the matrix comprising polymer macromolecules and defining spaces between the polymer macromolecules; (2) a drug contained within at least some of the spaces of the matrix; and (3) a material contained within at least some of the spaces of the matrix to affect diffusion of the drug out of the polymeric matrix when the medical device is placed in the body of the mammal.Type: ApplicationFiled: February 26, 2014Publication date: August 28, 2014Applicant: Boston Scientific Scimed, Inc.Inventors: Jianmin Li, Weenna Bucay-Couto
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Publication number: 20140242140Abstract: Fabrication method for stratified and layered tissue to repair osteochondral defects. In a method of the present disclosure, the method comprises the step of applying a first direction magnetic field to a first quantity of a first collagen solution to align collagen within the first collagen solution in a first direction relative to the first direction magnetic field, forming a first layer of collagen. In a method of generating an aligned collagen layer of the present disclosure, the method comprises applying a first magnetic field at or greater than 0.1 Tesla to a layer of a first collagen solution defining a horizontal plane, within a temperature at or between 2° C. and 45° C., to generate an aligned collagen layer.Type: ApplicationFiled: February 28, 2014Publication date: August 28, 2014Applicant: Purdue Research FoundationInventors: Corey P. Neu, Tyler A. Novak, Garrett Shannon
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Publication number: 20140242141Abstract: In one aspect, the present invention provides composite coatings for implantable or insertable medical devices. These composite coatings comprise (a) an inorganic portion and (b) a polymeric portion that comprises a poly(vinyl pyrrolidone) (PVP) block.Type: ApplicationFiled: May 7, 2014Publication date: August 28, 2014Applicant: BOSTON SCIENTIFIC SCIMED, INC.Inventors: Liliana Atanasoska, Jan Weber, Robert W. Warner
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Publication number: 20140242142Abstract: The present invention relates to the use of secreted proteins from mesenchymal stem cells and other cells for the treatment of myocardial infarction. In particular, the invention provides compositions and methods based on secreted proteins from mesenchymal stem cells and the genes encoding them.Type: ApplicationFiled: June 25, 2012Publication date: August 28, 2014Applicant: National University of Ireland, GalwayInventors: Timothy O'Brien, Frank Barry, Claire Kavanagh
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Publication number: 20140242143Abstract: Three-dimensional tissue constructs are described, which may be created by isolating adipose-derived stromal vascular fraction (SVF) cells, plating the cells onto a polymer scaffold, and culturing the plated scaffold in a culture of DMEM with approximately 10% FBS.Type: ApplicationFiled: October 1, 2012Publication date: August 28, 2014Applicant: UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.Inventors: Amanda J. LeBlanc, James B. Hoying, Stuart K. Williams
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Publication number: 20140242144Abstract: Methods of treating renal cancers and other kidney-related inflammatory disorders with a bioabsorbable polymer scaffold (such as a stent) are described. The treatments are provided as alternative to complete or partial surgical removal of a diseased kidney.Type: ApplicationFiled: April 30, 2014Publication date: August 28, 2014Applicant: Abbott Cardiovascular Systems Inc.Inventors: Krishanankutty Sudhir, Joanne M. Ferguson
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Publication number: 20140242145Abstract: A chitosan nanofiber for delivering an anionic protein drug, a method of preparing the same, and a pharmaceutical preparation for transmucosal administration including the chitosan nanofiber are provided. The chitosan nanofiber including an anionic protein drug in a core and chitosan in a shell is prepared by coaxial electrospinning an aqueous solution of the anionic protein drug through an inner nozzle and a solution of the chitosan or a chitosan derivative through an outer nozzle.Type: ApplicationFiled: January 2, 2014Publication date: August 28, 2014Applicant: KNU-INDUSTRY COOPERATION FOUNDATIONInventors: Hyuk Sang YOO, Ji Suk CHOI, Younghee KIM, Jihyun KANG
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Publication number: 20140242146Abstract: The present invention relates to a method for preparing by wet spinning a continuous filament based on hyaluronic acid in free acid form, notably soluble in water. The preparation method according to the invention comprises the following steps: a) preparing a spinnable aqueous solution of hyaluronic acid or of a hyaluronic acid salt, preferably a sodium hyaluronate solution; b) extruding said solution to an extrusion die; c) forming the filament by passing the extruded solution into a bath of acetic acid, concentrated to more than 80%, drawing and drying. The invention also relates to a filament based on hyaluronic acid in free acid form, said filament having swelling properties in water and physiological liquids and moreover being solubilizable in water under certain conditions.Type: ApplicationFiled: May 5, 2014Publication date: August 28, 2014Applicants: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE, UNIVERSITE CLAUDE BERNARD LYON IInventors: Alain DOMARD, Laurent DAVID, Florence DUPASQUIER