Carbohydrate Or Lignin, Or Derivative Patents (Class 514/777)
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Publication number: 20130302405Abstract: An object of the present invention is to provide a glucosamine-containing glucan, a modified product and a conjugate thereof. The glucosamine-containing glucan of the present invention is a glucosamine-containing glucan wherein the glucan has a plurality of non-reducing ends and at least one glucosamine residue is bound via an ?-1,4-bond to each of two or more non-reducing ends of the branched ?-1,4-glucan, but no glucosamine residue is present at a position other than the non-reducing ends of the branched ?-1,4-glucan, wherein the degree of polymerization of the glucan is 15 or more and 4×105 or less. The glucosamine-containing glucan of the present invention can be provided by allowing an ?-glucan phosphorylase to act on an aqueous solution comprising a branched ?-1,4-glucan and glucosamine-1-phosphate.Type: ApplicationFiled: November 7, 2011Publication date: November 14, 2013Applicant: EZAKI GLICO CO., LTD.Inventors: Takeshi Takaha, Akiko Kubo, Michiyo Yanase
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Publication number: 20130303632Abstract: The present invention is directed to a controlled release solid dosage form comprising a controlled release modifier and an active ingredient comprising at least one of a pharmaceutical, veterinary, or nutraceutical active ingredient, wherein the controlled release modifier comprises lambda carrageenan from the taxonomic order Halymeniales. The present invention is also directed to ethanol resistant controlled release solid dosage forms and methods for reducing the ethanol sensitivity of an active ingredient in a controlled release solid dose form.Type: ApplicationFiled: May 9, 2013Publication date: November 14, 2013Applicant: FMC CORPORATIONInventors: Christopher J. Sewall, William R. Blakemore, Bruno Leclercq
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Publication number: 20130295163Abstract: An object of the present invention is to provide a glucan containing at least one residue selected from an N-acetylglucosamine residue and a galactose residue, and a modified product. The branched glucan of the present invention is a branched glucan wherein the branched glucan has a plurality of non-reducing ends and at least one residue selected from an N-acetylglucosamine residue and a galactose residue is bound via an ?-1,4-bond to each of two or more non-reducing ends of the branched ?-1,4-glucan, but neither an N-acetylglucosamine residue nor a galactose residue is present at the position other than the non-reducing ends of the branched ?-1,4-glucan.Type: ApplicationFiled: November 7, 2011Publication date: November 7, 2013Applicant: EZAKI GLICO CO., LTD.Inventors: Takeshi Takaha, Michiyo Yanase, Akiko Kubo, Haruyo Sambe, Ryo Kakutani
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Publication number: 20130295184Abstract: Implantable medical devices having galvanic particulates are disclosed. The particulate may be coated onto at least part of a surface of the medical device. In addition, the galvanic particulates may be contained in the material used to manufacture the antimicrobial medical devices, or may be embedded into the surface of the medical devices. The present invention also provides novel coating methods and processing methods. The present invention further provides a combination of galvanic particulates with an aqueous gel, a method of making this combination, and a method of treatment using this combination. The devices and compositions may have advantageous characteristics and effects including anti-microbial, anti-inflammatory, tissue regeneration promoting, and pain reduction or elimination.Type: ApplicationFiled: July 9, 2013Publication date: November 7, 2013Inventors: Jennifer Hagyoung Kang Choi, Chunlin Yang, Ying Sun, Carrie H. Fang, James E. Hauschild, Abla A. Creasey
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Patent number: 8568777Abstract: The present invention relates to packaged orally consumable film dosage units for delivery of actives into the oral cavity. In particular, the packaged pharmaceutical product contains a complexate including a complexing agent and an active, an orally consumable film for delivery of the complexate and a package for containing the orally consumable film. The package includes indicia associated therewith. The indicia identifies the complexate as the active ingredient contained in the film, which is as a regulatory approvable chemical entity. The present invention also relates to methods of labeling, pricing, marketing and satisfying governmental regulations for such packaged pharmaceutical products.Type: GrantFiled: March 30, 2007Date of Patent: October 29, 2013Assignee: MonoSol Rx, LLCInventor: Richard C. Fuisz
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Publication number: 20130281548Abstract: Dispersible colorants that include a combination of a colorant and a polysaccharide are provided, wherein the weight ratio of total colorant to total polysaccharide is in the range of 5000:1 to 1:5000. In one aspect, the colorant is a synthetic or natural colorant. In one aspect, polysaccharide is interpreted very broadly and provides a colored precipitate upon the combination of the colorant with the polysaccharide.Type: ApplicationFiled: March 15, 2013Publication date: October 24, 2013Applicant: EPC (Beijing) Natural Products Co., Ltd.Inventors: Zhijin Jin, Jingang Shi
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Publication number: 20130280304Abstract: The present invention provides an improved method of administering a medicinal, dental or nutritional agent to a non-human animal, such as a domesticated dog or cat. The method comprises mixing a liquid composition in a mixer at various speeds and pressures for a period of time; pouring the liquid composition onto a conveyor belt propelled by polymer rollers, wherein the polymer rollers allow the components to advance on the conveyor belt without adhering to the belt; evenly distributing the composition on the belt with the use of a knife; heating the composition in one or more hot-air chambers; obtaining a film comprised of the composition; cutting the film into strips; and then administering one or more of the strips to the non-human animal by placing the strip under the tongue of the animal, i.e., by sub-lingual administration.Type: ApplicationFiled: October 22, 2012Publication date: October 24, 2013Inventor: Douglas Kramer
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Publication number: 20130281546Abstract: An intrabuccally rapidly disintegrating tablet which is manufactured by a simple method, has an enough practical hardness and is rapidly disintegrated in the buccal cavity and its production method. The intrabuccally rapidly disintegrating tablet is produced by growing a powder material into a granulated material with a fixed particle diameter, the powder material including a sugar alcohol or a saccharide as main ingredient, each of which is first particle having an average particle diameter of not more than 30 ?m, by mixing thus obtained granulated material with an active ingredient and a disintegrant, and by compressing the mixture into a predetermined shape.Type: ApplicationFiled: January 17, 2013Publication date: October 24, 2013Applicant: Kyowa Hakko Kirin Co., Ltd.Inventor: Kyowa Hakko Kirin Co., Ltd.
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Publication number: 20130281549Abstract: A sterile biofilm could be engineered to isolate the glue-like substance while eliminating the adverse properties of the bacteria. The resulting sterile glue-like substance would be used to help the cells stick to the support structure. The engineered biofilm could be added to the support structure in the laboratory that produces the support structure or just prior to the addition of the cells by the user. Alternatively, the biofilm and support structure could be combined intra-corporally. This biofilm also could be used as an independent polysaccharide based adhesive with mild to moderate adhesion forces. The biofilm could serve as a surgical adhesion or grouting for cells, for tissue fixation (soft tissue to soft tissue, soft tissue to bone, etc.) and as a sealant. The biofilm could be used in conjunction with other implants and devices. The biofilm could be used to coat a stent.Type: ApplicationFiled: June 7, 2013Publication date: October 24, 2013Inventor: Peter M. Bonutti
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Publication number: 20130274296Abstract: A method of preparing an orally ingestible hard boiled product, comprising: i) heating a sugar material to a first temperature sufficient to liquefy the sugar material; ii) cooling the liquefied sugar material to provide a cooled sugar material having a solid or semi-solid form; iii) heating the cooled sugar material to a second temperature, which is lower than the first temperature; iv) combining the sugar material with one or more temperature sensitive ingredients before, during, or after said heating step iii), but after said cooling step ii), such that an intimate mixture of the second liquefied sugar material and the one or more temperature sensitive ingredients is provided; and v) cooling the intimate mixture to form an orally ingestible product. Orally ingestible hard boiled products prepared according to this method are also provided.Type: ApplicationFiled: April 17, 2012Publication date: October 17, 2013Inventors: Thaddeus J. Jackson, Frank Kelley St. Charles
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Publication number: 20130273139Abstract: Disclosed are bupivacaine transdermal delivery systems, and related methods.Type: ApplicationFiled: March 13, 2013Publication date: October 17, 2013Inventors: Su Il Yum, Sung Yun Kwon, Xiaoping Song, James E. Brown
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Publication number: 20130274350Abstract: To develop a method for producing a novel sweetener containing glucose, fructose, and psicose, which is produced from glucose liquid sugar using an isomerase and an epimerase; use of the novel sweetener as a food or drink material; and a novel sweetener capable of preventing obesity caused by the intake thereof. An isomerase and an epimerase are allowed to act on glucose liquid sugar produced in a glucose liquid sugar production plant to thereby produce D-psicose, thereby providing a novel sweetener (product) that maintains the degree and quality of sweetness of a glucose-fructose mixed solution and never causes obesity, a method for producing the same, and use of the same.Type: ApplicationFiled: March 15, 2013Publication date: October 17, 2013Inventors: Kazuhiro Okuma, Koji Yamada, Koji Tsukuda, Tetsuo Iida, Hiroshi Oga, Ken Izumori, Yoshio Tsujisaka, Tsuyoshi Shimonishi, Takako Yamada, Iwao Okamoto
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Publication number: 20130274351Abstract: The invention relates to a process for producing highly soluble compositions containing purified steviol glycosides from Stevia rebaudiana Bertoni plant extract, more particularly Rebaudioside D. Obtained highly soluble compositions are useful as non-caloric sweeteners or in combination with sugar or high intensity sweeteners in edible and chewable compositions such as beverages, confectionaries, bakery products, chewing gums and the like.Type: ApplicationFiled: December 12, 2011Publication date: October 17, 2013Inventors: Avetik Markosyan, Siddhartha Purkayastha
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Publication number: 20130273115Abstract: Systems and method are disclosed for cosmetic augmentation by forming a biocompatible cross-linked polymer having a multi-phase mixture with a predetermined controlled release of a pharmaceutical substance to modulate soft tissue response to the polymer, the polymer having at least one phase cross-linked, glycosaminoglycan in a physiological buffer solution; and augmenting soft tissue with the biocompatible cross-linked polymer.Type: ApplicationFiled: January 18, 2012Publication date: October 17, 2013Inventors: Phi Nguyen, Loc Phan, Bao Tran
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Publication number: 20130273168Abstract: A solid, rapidly gelling oral pharmaceutical dosage form, as well as an aqueous formulation prepared thereof, comprising a) an acid sensitive proton pump inhibitor as active ingredient distributed in a multitude of enteric coated pellets, and b) a suspension modifying granulate. Furthermore, the invention relates to an improved process for the manufacture and the use of such formulation in medical treatment, including prevention of gastrointestinal disorders in humans.Type: ApplicationFiled: June 5, 2013Publication date: October 17, 2013Inventors: Eva PERSSON, Eva TROFAST
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Publication number: 20130251784Abstract: The present disclosure relates to a method for in vivo targeting of a nanoparticle via bioorthogonal copper-free click chemistry, more particularly to a method for in vivo targeting of a nanoparticle, including: injecting a precursor capable of being metabolically engineered in vivo when injected into a living system and having a first bioorthogonal functional group into the living system; and injecting a nanoparticle having a second bioorthogonal functional group which can perform a bioorthogonal copper-free click reaction with the first bioorthogonal functional group attached thereto into the living system. In accordance with the present disclosure, accumulation of nanoparticles at a target site in a living system can be increased remarkably and the biodistribution of the nanoparticles can be controlled since the nanoparticles bound to a cell surface are taken up into the cell with time.Type: ApplicationFiled: February 22, 2013Publication date: September 26, 2013Applicant: KOREA INSTITUTE OF SCIENCE AND TECHNOLOGYInventors: Kwang Meyung KIM, Ick Chan KWON, Kuiwon CHOI, Heebeom KOO, Sang-min LEE, Inchan YOUN
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Publication number: 20130253074Abstract: Disclosed herein is a hyaluronic acid epoxide derivative film comprises a polymer containing a hydroxyl (—OH) terminal group. The film is prepared by allowing an epoxy crosslinker to react with a mixture of hyaluronic acid and a polymer containing a hydroxyl (—OH) terminal group and has improved physical strength, in vivo stability, flexibility, adhesiveness to biological tissue, and biocompatibility.Type: ApplicationFiled: March 22, 2013Publication date: September 26, 2013Applicant: GENEWEL CO., LTDInventors: Young Woo Lee, Wan Jin Cho, Ji Yeon Jang
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Publication number: 20130251644Abstract: Described herein are cyclodextrin-stabilized microemulsion systems useful for increasing the solubility, stability, bioavailability, or safety of an active agent for delivery to the skin. The microemulsions may reduce the occurrence of skin irritation or odor upon application. In certain embodiments, the active agent is substantially insoluble in water. The microemulsions may be formulated as semi-solids, for example creams, or as aerosol or non-aerosol foams. Also described are methods of treating skin disorders, comprising the step of applying to an affected area of a subject in need thereof a therapeutically-effective amount of an inventive microemulsion.Type: ApplicationFiled: March 14, 2013Publication date: September 26, 2013Applicant: Precision Dermatology, Inc.Inventors: Pinaki Ranjan Majhi, Mark W. Trumbore
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Publication number: 20130253015Abstract: Described herein are cyclodextrin-stabilized microemulsion systems useful for increasing the solubility, stability, bioavailability, or safety of an active agent for delivery to the skin. The microemulsions may reduce the occurrence of skin irritation or odor upon application. In certain embodiments, the active agent is substantially insoluble in water.Type: ApplicationFiled: March 14, 2013Publication date: September 26, 2013Applicant: Precision Dermatology, Inc.Inventors: Pinaki Ranjan Majhi, Mark W. Trumbore
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Publication number: 20130253014Abstract: Described herein are cyclodextrin-stabilized microemulsion systems useful for increasing the solubility, stability, bioavailability, or safety of an active agent for delivery to the skin. The microemulsions may reduce the occurrence of skin irritation or odor upon application.Type: ApplicationFiled: March 14, 2013Publication date: September 26, 2013Applicant: Precision Dermatology, Inc.Inventors: Mark W. Trumbore, Pinaki Ranjan Majhi, Dinen Divyang Shah
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Publication number: 20130253075Abstract: The present invention provides derivatives of native lignin having a certain aliphatic hydroxyl content. Surprisingly, it has been found that consistent and predictable antioxidant activity may be provided by selecting for derivatives of native lignin having a certain aliphatic hydroxyl content.Type: ApplicationFiled: May 16, 2013Publication date: September 26, 2013Applicant: Lignol Innovations Ltd.Inventors: Mikhail Yurevich BALAKSHIN, Alex BERLIN, Humbert Thomas DELLICOLLI, Chadrick Adam Nathaniel Jordan GRUNERT, Vera Maximenko GUTMAN, Darwin ORTIZ, Edward Kendall PYE
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Patent number: 8541392Abstract: The present invention relates generally to a method of blunting the postprandial glycemic response in a human by feeding an induced viscosity fiber system. The invention also relates to an induced viscosity fiber system and the liquid products that incorporate the induced viscosity fiber system. Further, the invention relates to a method of incorporating soluble fiber into a liquid product without the typical negative organoleptic or physical stability issues. The invention also relates to a method of inducing the feeling of fullness and satiety by feeding the induced viscosity fiber system.Type: GrantFiled: September 30, 2009Date of Patent: September 24, 2013Assignee: Abbott LaboratoriesInventors: Bryan W. Wolf, Bruce B. Blidner, Keith A. Garleb, Chron-Si Lai, Timothy W. Schenz
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Publication number: 20130244972Abstract: A chitosan composition which forms a hydrogel at near physiological pH and 37° C., comprising at least one type of chitosan having a degree of acetylation in the range of from about 30% to about 60%, and at least one type of chitosan having a degree of deacetylation of at least about 70% is disclosed. Further disclosed is a chitosan composition which forms a hydrogel at near physiological pH and 37° C., that includes at least one type of chitosan having a degree of deacetylation of at least about 70% and a molecular weight of from 10-4000 kDa, and at least one type of a chitosan having a molecular weight of from 200-20000 Da. Further disclosed are methods of preparation and uses of the chitosan compositions.Type: ApplicationFiled: March 14, 2013Publication date: September 19, 2013Applicant: MOR RESEARCH APPLICATIONS LTD.Inventors: Noah Ben-Shalom, Zvi Nevo, Abraham Patchornik, Dror Robinson
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Patent number: 8535646Abstract: A method for blocking, neutralizing, or killing microorganisms that cause infectious disease in a mammal prior to or during the mammal encountering a contaminated environment or item includes: identifying a contaminated environment or item, wherein the contaminated environment or item is known or expected to be contaminated with harmful viral, fungal, or bacterial microorganisms; and administering a therapeutically effective amount of a barrier-forming composition to a mucosa of the mammal prior to or during the mammal encountering the contaminated environment or item. The barrier-forming composition provides a barrier on the mucosa that inhibits the microorganisms from contacting the mucosa. Other related methods are also included.Type: GrantFiled: April 17, 2012Date of Patent: September 17, 2013Assignee: ARMS Pharmaceutical LLCInventors: Brian Vincent Sokol, Afif Mahmoud Ghannoum
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Publication number: 20130237614Abstract: A kit for forming a bioerodible composition is provided with a first aliquot portion of a reaction mixture having an aldehydic polymer solution, and a second aliquot portion of a reaction mixture having solids which include a cross-linking hydrazide. When mixed, the first and second aliquot portions of the reaction mixture react at a pH of 4 to 6 to form a solidified bioerodible composition within about 1 to about 10 minutes, to form a hydrazide cross-linked aldehydic polymer matrix. The bioerodable composition may be usefully employed to seal and/or treat wounds (e.g., a surgical incision).Type: ApplicationFiled: April 22, 2013Publication date: September 12, 2013Applicant: ROYER BIOMEDICAL, INC.Inventor: Garfield P. ROYER
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Publication number: 20130237613Abstract: The present invention relates to a thermodynamically stable, biocompatible, environment friendly, and temperature-insensitive microemulsion containing various botanical essential oils, sugar based surfactants, polyhydric alcohols, and an aqueous phase.Type: ApplicationFiled: September 4, 2012Publication date: September 12, 2013Applicant: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCHInventor: Sanggu Kim
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Publication number: 20130237615Abstract: The subject of the present invention is a process of preparing a crosslinked gel of at least one polysaccharide or one of its salts, including at least the steps consisting in: a) providing, at a temperature below 35° C., an aqueous gel including at least one polysaccharide in an uncrosslinked form together with at least one difunctional or multifunctional epoxy crosslinking agent; b) maintaining the mixture of step a) at a temperature below 35° C. for at least one hour; c) stimulating the crosslinking reaction of the mixture obtained after step b), and if need be; d) recovering said crosslinked gel formed.Type: ApplicationFiled: December 6, 2011Publication date: September 12, 2013Applicant: TEOXANEInventors: Stephane Meunier, Francois Bourdon
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Publication number: 20130230491Abstract: The invention provides a method for forming an immobilized agent gradient within a 3-dimensional porous scaffold. A 3-dimensional scaffold formed from a biocompatible material is provided. The surface of the scaffold and/or the agent is activated so as to allow binding of the agent to the scaffold. The activated scaffold is contacted with a solution containing the agent. Contact with the solution is maintained for a sufficient period of time to allow diffusion of the solution through a portion of the scaffold, thereby forming a desired gradient of the agent through the 3-dimensional scaffold.Type: ApplicationFiled: February 25, 2013Publication date: September 5, 2013Applicants: MASSACHUSETTS INSTITUTE OF TECHNOLOGY, TRUSTEES OF TUFTS COLLEGEInventors: Charu Vepari, David L. Kaplan, Gordana Vunjak-Novakovic
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Patent number: 8524785Abstract: The present invention is directed to the use of one or more rebaudioside C polymorphs, or stereoisomers thereof, to enhance the sweet taste of a flavoring, such as glucosylated steviol glycoside, rebaudioside A, ammoniated glycyrrhizin, neohespherdin dihydrochalcone or thaumatin.Type: GrantFiled: December 21, 2011Date of Patent: September 3, 2013Assignee: International Flavors and Fragrances Inc.Inventors: Mark L. Dewis, Kenneth J. Kraut, Debra Merritt, Raymond F. Salemme
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Publication number: 20130224248Abstract: A formulation free of protein which stabilizes pharmaceutical active proteins, peptides, or mixtures thereof in large scale production processes comprising a mixture of a hydrophilic polymer and a non-ionic detergent, and a mixture of a polyalcohol and a sugar. In some embodiments the polyalcohol is absent.Type: ApplicationFiled: October 11, 2011Publication date: August 29, 2013Applicant: MERZ PHARMA GmbH & CO. KGaAInventors: Harold Victor Taylor, Gerd J. Mander, Markus Burger
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Publication number: 20130224300Abstract: The present invention provides therapeutic compositions including a therapeutic agent in a non-aqueous matrix having an absorption enhancer and therapeutic agent, as well as methods for administering such compositions and providing enhanced oral bioavailability.Type: ApplicationFiled: August 24, 2012Publication date: August 29, 2013Inventor: Edward T. Maggio
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Patent number: 8518381Abstract: The present invention is directed towards a process for making oral compositions comprising gel networks. The gel networks are formed from a fatty amphiphile dispersion and swelling surfactant. The fatty amphiphile dispersion comprises one or more fatty amphiphiles, one or more dispersing surfactants, and one or more solvents. A gel network is formed when the fatty amphiphile dispersion is combined with the swelling surfactant. A method of preparing the fatty amphiphile dispersion and oral composition is included.Type: GrantFiled: March 25, 2009Date of Patent: August 27, 2013Assignee: The Procter & Gamble CompanyInventors: Michael Jude LeBlanc, George Endel Deckner
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Publication number: 20130216623Abstract: Drug formulations, devices and methods are provided to deliver biologically active substances to the eye. The formulations are delivered into scleral tissues adjacent to or into the suprachoroidal space without damage to the underlying choroid. One class of formulations is provided wherein the formulation is localized in the suprachoroidal space near the region into which it is administered. Another class of formulations is provided wherein the formulation can migrate to another region of the suprachoroidal space, thus allowing an injection in the anterior region of the eye in order to treat the posterior region.Type: ApplicationFiled: March 15, 2013Publication date: August 22, 2013Applicant: ISCIENCE INTERVENTIONAL CORPORATIONInventor: ISCIENCE INTERVENTIONAL CORPORATION
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Publication number: 20130216592Abstract: The present invention relates to positively charged particles consisting of a chitosan polyelectrolyte complex and of an anionic polymer, characterized in that the chitosan has a degree of acetylation (DA) in the range of 35 to 49% and a mean molar mass by weight (Mw) in the range of 55 to 150 kg/mol, as well as to a method for preparing same.Type: ApplicationFiled: July 26, 2011Publication date: August 22, 2013Applicants: Universite Claude Bernard Lyon 1, Universite Jean Monnet Saint- Etienne, Institut National Des Sciences Appliquees De Lyon, Centre National De La Recherche ScientifiqueInventors: Thierry Delair, Bernard Verrier, Franck Gaudin
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Publication number: 20130210812Abstract: The present invention is an aqueous pharmaceutical composition that includes an ionized therapeutic agent, an ionic component and guar gum. The guar gum is present in the composition a concentration sufficient to limit interactions between the ionized therapeutic agent and the ionic component thereby imparting stability to the composition. The composition is preferably at or near physiologic pH. The aqueous pharmaceutical composition has been found particularly useful as an aqueous ophthalmic, otic or nasal composition. The pharmaceutical composition, due to its characteristics, is particularly suitable as an ophthalmic composition.Type: ApplicationFiled: February 8, 2013Publication date: August 15, 2013Applicant: Alcon Research, Ltd.Inventor: Alcon Research, Ltd.
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Patent number: 8507563Abstract: The composition disclosed is a pseudo-thermosetting neutralized chitosan composition, neutralized with a hydroxylated base, forming a phosphate-free transparent hydrogel at a temperature higher than 5° C. Said composition contains a homogeneously reacetylated chitosan derived from a chitosan having a deacetylation degree of 80-90%, having a molecular weight of not smaller than 200 kDa and a deacetylation degree of 30-60%, and may further contain a diol. Said composition may be used as a drug delivery system.Type: GrantFiled: December 29, 2009Date of Patent: August 13, 2013Assignee: Laboratoire Medidom S.A.Inventors: Jérôme Berger, Robert Gurny, Marianne Reist Oechslin
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Publication number: 20130203856Abstract: The present invention relates to a filler composition for tissue reinforcement, including hyaluronic acid and alkylene diamine crosslinked hydrogel. The filler composition exhibits the positive physical properties required for tissue reinforcement, such as biocompatibility and swelling ability, as well as useful effects in that the same can remain in vivo for a long time.Type: ApplicationFiled: July 11, 2011Publication date: August 8, 2013Applicants: Postech Academy-Industry Foundation, Shin Poon Pharmaceutical Co., Ltd.Inventors: Il Hwan Cho, Eui Jin Hwang, Moo Seok Seo, Young Soo Park, Byung Su Kim, Sei Kwang Hahn, Jung Kyu Park, Jun Seok Yeom, Eun Ju Oh
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Publication number: 20130203867Abstract: The invention provides a stevia formulation comprising a stevia sweetener with a rebaudioside A content of 95% or greater, and 0.25 to 5.15 parts by weight of a sugarcane-derived extract (a), 0.06 to 2.50 parts by weight of a sugarcane-derived extract (b) and 0.002 to 12.5 parts by weight of ?-aminobutyric acid with respect to 100 parts by weight of the stevia sweetener.Type: ApplicationFiled: February 17, 2012Publication date: August 8, 2013Applicant: MITSUI SUGAR CO., LTD.Inventors: Yumiko Tezuka, Takayuki Kiyofuji, Yukie Nagai, Toshiaki Sugitani
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Publication number: 20130203599Abstract: The present invention provides the agricultural chemical-spreading agent composition, containing: (A) a polysaccharide in an amount of 5 to 30% by weight; (B) a polyoxyalkylene sorbitan fatty acid ester in an amount of 5 to 40% by weight; and (C) at least one nonionic surfactant selected from polyoxyalkylene alkyl ethers, sorbitan fatty acid esters, and silicone surfactants in an amount of 5 to 40% by weight, wherein the component (A) has a viscosity of not less than 5000 mPa·s in the form of a 5% by weight aqueous solution at 25° C., and a weight ratio of contents of the component (A) to the sum of components (B) and (C), (A)/[(B)+(C)], is 10/90 to 40/60.Type: ApplicationFiled: September 1, 2011Publication date: August 8, 2013Applicant: KAO CORPORATIONInventors: Masaki Inoue, Masatoshi Kamei
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Publication number: 20130202582Abstract: The present invention provides a composition for selectively delivering an active agent to a portion of an organism. The composition comprises first and second polymer portions, having first and second functional groups attached as a side-chain thereto, respectively. The first and second functional groups form cross-links between the first and second polymer portions. The cross-links are capable of being broken by a substance of the organism, thereby resulting in release of the active agent. The composition provides a novel means for controlling the selective release of the active agent in the organism.Type: ApplicationFiled: August 10, 2012Publication date: August 8, 2013Applicants: Rutgers, The State University of New Jersey, Lucent Technologies Inc.Inventors: Noshir Langrana, David Lin, Bernard Yurke
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Patent number: 8501822Abstract: An ophthalmic composition that, despite containing alginic acid and/or a salt thereof, has improved tackiness during use and provides a satisfactory use feeling. The composition has an improved ability to remain on the eye mucosa. The ophthalmic composition contains (A) alginic acid and/or a salt thereof in combination with (B) hyaluronic acid and/or a salt thereof.Type: GrantFiled: March 27, 2012Date of Patent: August 6, 2013Assignee: Rohto Pharmaceutical Co., Ltd.Inventors: Eri Matsumoto, Yasuko Nishina, Kenichi Haruna, Harumasa Arita, Akiko Kita
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Publication number: 20130197104Abstract: A reduced sugar syrup having an advantageously low viscosity is prepared by hydrolysis of starch or starchy material using a particular type of alpha amylase enzyme which yields a saccharide distribution having a low DP1-2 and low DP11+ content. The DP4 content of the syrup may be favorably increased by using a maltotetragenic alpha amylase enzyme in combination with the aforementioned alpha amylase enzyme. The syrup is useful in the production of food, beverage, animal feed, animal health and nutrition, pharmaceutical, and cosmetic compositions and may be combined with a high intensity sweetener to provide a composition capable of being substituted for conventional corn syrups.Type: ApplicationFiled: January 29, 2013Publication date: August 1, 2013Applicants: Verenium Corporation, Tate and Lyle Ingredients Americas LLCInventors: Tate and Lyle Ingredients Americas LLC, Verenium Corporation
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Publication number: 20130197100Abstract: The invention “colloidal nanoscale carriers for active hydrophilic substances and method for producing same” pertains to the field of medical, odontological or hygiene preparations, and is characterized by structures formed by hydrophilic polymers that contain active hydrophilic substances coated with a non-hydrophilic phase and surfactants with affinity for the components, forming an invert emulsion that allows the incorporation and controlled delivery of active hydrophilic substances, conferring properties such as protection against degradation processes, improvement of compatibility with the other components of the formulation in the final product, increase in the availability and/or bioavailability of the active substance in the medium of interest (including improvements in permeation processes in biological materials, reduction of the exposure and volatilization of the active substance in the medium) and controlled release of the active substance(s).Type: ApplicationFiled: June 14, 2011Publication date: August 1, 2013Applicants: Instituto De Pesquisas Technologicas Do Estado De Sao Paulo, Rundacao De Amparo A Pesquisa Do Estado De Sao Paulo - FAPESP, Universidade De Sao Paulo - USPInventors: Natália Neto Pereira Cerize, Adriano Marim De Oliveira, Maria Inês Ré, Antônio Cláudio Tedesco
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Publication number: 20130195941Abstract: The present invention aims to provide a particulate composition containing pullulan, which can be produced without employing any complicated purification step such as solvent precipitation and, when formed into a film, exhibits a higher rupture strength compared to conventional ones; a process for producing the same; and uses thereof.Type: ApplicationFiled: June 17, 2011Publication date: August 1, 2013Applicant: HAYASHIBARA CO., LTD.Inventors: Takashi Shibuya, Seisuke Izawa, Toshio Miyake
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Publication number: 20130197103Abstract: The present invention relates to the enhancement of the efficacy of drugs, and more particularly, with overcoming the resistance of cells or organisms to drugs. In particular, the present invention provides a method for enhancing the effectiveness of a cytotoxic or anti-neoplastic agent, comprising the step of co-administering said agent with hyaluronan, wherein co-administration with hyaluronan enhances the agent's cancer cell-killing potential.Type: ApplicationFiled: December 14, 2011Publication date: August 1, 2013Applicant: Alchemia Oncology Pty LimitedInventor: Tracey J. BROWN
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Publication number: 20130195921Abstract: The present invention provides a method for preparing chitosan and xylan composite thereto-gelling solutions to allow regulating the conditions in which the chitosan and xylan solution will gel. The present invention also provides methods for using chitosan/xylan solutions as compositions and for using chitosan/xylan solutions in vitro and in vivo. A thermally-responsive composite hydrogel has been developed and synthesized from the natural polymers chitosan and xylan. The new material is a viscous liquid at room temperature, but turns to a solid gel at physiological temperature (37 C). Rate of gelation is controlled with addition of a salt solution. Applications are for tissue engineering and local delivery of therapeutic agents, including proteins and drugs, as wells as cells.Type: ApplicationFiled: November 30, 2010Publication date: August 1, 2013Applicant: UNIVERSITY OF VIRGINIA PATENT FOUNDATIONInventor: Joshua R. Bush
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Publication number: 20130195773Abstract: Compositions, comprising menthofuran and selected menthol compounds which feature improved flavour and odour properties, are provided and, in addition, the production of compositions, specifically, of emulsions with an improved storage stability.Type: ApplicationFiled: December 27, 2012Publication date: August 1, 2013Applicant: Symrise AGInventor: Symrise AG
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Publication number: 20130195769Abstract: The invention relates to stable oleaginous cosmetic or therapeutic foam compositions containing certain active agents, having unique therapeutic properties and methods of treatment using such compositions. The foamable composition includes at least one solvent selected from a hydrophobic solvent, a silicone oil, an emollient, a co-solvent, and mixtures thereof, wherein the solvent is present at a concentration of about 70% to about 96.5% by weight of the total composition, at least a non-ionic surface-active agent at a concentration of about 0.1% to less than about 10% by weight of the total composition; at least one gelling agent at a concentration of about 0.1% to about 5% by weight of the total composition; a therapeutically effective amount of at least one active agent; and at least one liquefied or compressed gas propellant, at a concentration of about 3% to about 25% by weight of the total composition.Type: ApplicationFiled: March 11, 2013Publication date: August 1, 2013Applicant: FOAMIX LTD.Inventor: Foamix Ltd.
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Publication number: 20130189304Abstract: This invention provides methods and compositions to preserve bioactive materials in a dried foam matrix. Methods provide non-boiling foam generation and penetration of preservative agents at temperatures near the phase transition temperature of the membranes.Type: ApplicationFiled: December 18, 2012Publication date: July 25, 2013Applicant: MEDIMMUNE, LLCInventor: MEDIMMUNE, LLC
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Publication number: 20130190839Abstract: An implantable drug-doped component, e.g., a cochlear implant, includes host material, a host-embedded drug and a sacrificial material integrated with the host. Upon exposure of the sacrificial material to a solvent, e.g., perilymph fluid, voids in the host are created which facilitate release of the drug. The host can be, e.g., polysiloxane or silicone rubber. The sacrificial material, e.g., can be a glucose monomer, sugar, cyclodextrin, a salt, a bioresorbable material, hyaluronic acid, polyurethane, polyester, polyamide, polyvinyl alcohol, polyacrylic acid, etc. Alternatively, the sacrificial material can be the host, and can facilitate release of the drug through changing a property of the sacrificial material, e.g., by exposing the component to an ethanol wash. For a cochlear implant, e.g., the drug doped material can be applied to a non-stimulating surface of the electrode array.Type: ApplicationFiled: January 20, 2012Publication date: July 25, 2013Inventors: Jane Rapsey, Martin Svehla, Peter Schuller, Christopher Robert Miller