Abstract: Embodiments of the invention are generally directed to compositions useful for reducing pigmentation in the skin. The composition may further include other depigmenting agents such as nicotinamide and its melanasome transfer-inhibiting derivatives, 3,3?-thiodipropanoic acid and its tyrosinase-inhibiting derivatives, or resorcinol and its tyrosinase-inhibiting derivatives, in a topically acceptable vehicle.
Type:
Application
Filed:
January 31, 2017
Publication date:
May 18, 2017
Inventors:
Hong Hu, Sunghan Yim, Uma Santhanam, John W. Lyga
Abstract: Disclosed is a hair conditioning composition comprising: a cationic surfactant; a high melting point fatty compound; a cyclic compound selected from the group consisting of a vitamin B3 compound, a xanthine compound, a salicylic acid ester, and mixtures thereof; a compound having at least three large head groups; and an aqueous carrier. The composition of the present invention provides improved hair manageability.
Abstract: The present invention relates to a composition for pharmaceutical, nutritional or cosmetic use, suitable to preserve the physiological condition and health of skin and hair and to reestablish their regenerative functions, characterized in that it comprises a mixture of carnitine, caffeine and arginine as active principle, as such or as derivatives, such as pharmacologically acceptable salts. The effect of preserving the physiologic condition and health of skin and hair, and of reestablishing their regenerative functions is mainly achieved through an increase in ATP production by skin and hair cells.
Type:
Application
Filed:
June 25, 2015
Publication date:
May 18, 2017
Inventors:
Giammaria GIULIANI, Anna BENEDUSI, Barbara MARZANI, Antonio MASCOLO, Antonio LIMITONE
Abstract: Disclosed is a hair conditioning composition having a Max force peak value of at least about 58, and a Viscosity change value of at least about 800. The composition of the present invention provides reduced slimy feel on wet hair while providing conditioning to wet hair.
Abstract: The invention refers to novel dermatic and cosmetic compositions to protect against impaired pigmentation of the skin. Locally caring Ginkgoloides are selected out of pure, high quality products comprising phospholipids and lecithins to antagonize alkyl-acyl GPC. The Ginkgoloides are bound to one or more transport proteins, carrier proteins, peptides, amino acids and these carriers contain at least one acetyl group and/or Acetyl CoA. The entire transdermal compositions then endocrinologically equilibrate the skin and the skin cells whereby acetylating compounds locally act as sun screening agent.
Abstract: The present invention relates to a composition comprising isosorbide monooleate, a first surfactant selected from the group consisting of an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of more than 11, cocoamidopropyl betaine and mixtures thereof, a second surfactant which is an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of less than 11 and water. Furthermore it relates to a process for making this composition and to a cosmetic formulation, comprising this composition.
Type:
Application
Filed:
July 1, 2015
Publication date:
May 18, 2017
Inventors:
Claudia Stoer, Claus Nieendick, Markus Weissenegger, Daniela Prinz, Mirella Winzek, Jennifer Schoss, Markus Dierker, Norbert Boyxen, Ute Griesbach, Werner Seipel, Werner Mauer
Abstract: A method of improving the health of hair emerging from a scalp comprising application of a composition to reduce oxidative stress in the scalp causing reduced oxidative stress in pre-emergent hair resulting in healthier emergent hair having reduced water absorption and reduced surface energy
Type:
Application
Filed:
May 26, 2016
Publication date:
May 18, 2017
Inventors:
James Robert Schwartz, James Patrick Henry, Michael Joseph Flagler, Steven Hardy Page, Kathleen Marie Kerr, Kenneth Robert Wehmeyer, Lijuan Li, Nancy Lee Redman-Furey
Abstract: UV-photoprotective, topically applicable cosmetic/dermatological compositions contain: (a) at least one dibenzoylmethane compound, (b) at least one 1,3,5-triazine compound that is photosensitive in the presence of a dibenzoylmethane compound, and (c) at least one siliceous s-triazine compound substituted with two aminobenzoate or aminobenzamide groups, or a tautomeric form thereof, the 1,3,5-triazine compounds being improvedly photostable in such compositions.
Abstract: The present invention causes the tissues in the gingiva to be less permeable to the products of bacterial metabolism produced from dental plaque. In addition, chemicals derived from the ingestion of foods and beverages are blocked from entry into the gingival tissues. This results in the prevention of oral infections and, most importantly, the loss of teeth. In addition to the ingress of toxic chemicals, this mouth rinse results in cessation of gingival crevicular fluid, a medium for bacteria to thrive on. The overall result is a healthy periodontium which is free of infected tissues and inflammation and bodes well for optimum oral and systemic health.
Abstract: A dentifrice composition containing water, a calcium-containing abrasive, a fluoride ion source, and a thickening system providing a consumer preferred experience.
Abstract: A dentifrice composition containing water, a calcium-containing abrasive, a fluoride ion source, a zinc ion source, and a copolymer of maleic anhydride and methyl vinyl ether.
Abstract: Cationically-charged particulates and compositions containing the cationically-charged particulates for application to keratinous materials are provided. Methods of preparing the cationically-charged particulates are also disclosed.
Abstract: Cationically-charged particulates and compositions containing the cationically-charged particulates for application to keratinous materials are provided. Methods of preparing the cationically-charged particulates are also disclosed.
Abstract: Cationically-charged particulates and compositions containing the cationically-charged particulates for application to keratinous materials are provided. Methods of preparing the cationically-charged particulates are also disclosed.
Abstract: Cationically-charged particulates and compositions containing the cationically-charged particulates for application to keratinous materials are provided. Methods of preparing the cationically-charged particulates are also disclosed.
Abstract: Provided are polymeric nitrones comprising polymerized units of (a) acrylates of Formula I: wherein R1 and R2 are as defined herein; and (b) nitrone-pendant esters of Formula II: wherein R3 and R4 are as defined herein, and Z is a nitrone substituent of Formula III: wherein R5, R6, R7, R8, R9, R10, R11, R12, R13, and R14 are as defined herein, and wherein the sum of m+n is a number from 10 to 50, and the ratio of m to n is from 1:1 to 20:1.
Abstract: The present invention relates generally to compositions and methods of using them to treat keratin fibers. More particularly, the compositions according to the invention, such as mascaras and other cosmetics, comprise polyamide gelling agents and soft waxes, and are useful for imparting the appearance of enhanced length and volume to the treated keratin fibers.
Abstract: The present invention relates to a silicon dioxide-containing cosmetic composition for hair setting or for the temporary reshaping of keratinic fibers, in particular human hair, which depending on the use enables both a matte and a shiny look and which after application to the hair enables shaping and restructuring of the hairstyle for a long period of time and furthermore forms no visible residues.
Abstract: Disclosed is a hair conditioning composition comprising from about 0.1% to about 20% by weight of a silicone compound, and wherein the composition has a Silicone deposition amount of at least about 1,600, and Silicone deposition evenness value of at least 0.83. The composition of the present invention provides improved hair manageability.
Abstract: Cosmetic compositions for temporarily deforming keratinic fibers, cosmetic products, and methods for temporarily deforming keratinic fibers are provided herein. In one embodiment, a cosmetic composition for temporarily deforming keratinic fibers includes at least one uncrosslinked anionic polymer, at least one uncrosslinked cationic polymer, and water in a total amount of from about 80 to about 98% by weight, in relation to the total weight of the cosmetic composition.
Abstract: The present invention relates generally to compositions and methods of using them to treat keratin fibers. More particularly, the compositions according to the invention, such as mascaras and other cosmetics, comprise gelling agents and soft waxes, and are useful for imparting moldability to treated keratin fibers.
Abstract: A hair-applicable composition and method for visually identifying a single child amongst other children engaging in water-related activities or in another public setting. The composition includes a hair-application base and a waterproof hair dye. The hair-application base is the medium by which the waterproof hair dye is applied to the hair of a child. The waterproof hair dye includes a visually-vibrant pigmenting agent and a hydrophobic enabling agent. The visually-vibrant pigmenting agent alters the hair color of the child in order to allow a supervisor to easily identify him or her. The hydrophobic enabling agent ensures the color does not wash out with water when the child is engaging in water-related activities. The waterproof hair dye is homogeneously mixed into the topical base to create a latherable homogeneous composition.
Abstract: The present specification relates to a composition for a skin preparation for external use, containing an extract of bean leaves (danpung bean leaves) of a specific stage among the growth stages of beans as an active ingredient. The composition according to the present invention has an excellent antioxidant property, an excellent antiaging property and no skin irritation since natural-derived ingredients are contained in the composition, and thus is useful. The composition of the present specification can be widely used, by such characteristics, as an antioxidant or antiaging composition of an individual in the pharmaceutical or cosmetic field.
Type:
Application
Filed:
June 18, 2015
Publication date:
May 18, 2017
Inventors:
Young Gyu KANG, Ok Chan LEE, Yong Deog HONG, Myeong Hun YEOM, Jun Seong PARK
Abstract: The present disclosure relates to compositions containing a natural extract(s) and their fraction(s) and the use of such compositions for treatment of skin, hair and nail. For example, the present disclosure relates to compositions containing an aqueous extract of (i) Yacon leave, (ii) Amor Seco leave, or (iii) Porphyridium biomass, or a combination thereof and a pharmaceutically or cosmetically acceptable carrier use on hair skin and nails for cosmetic purposes.
Abstract: This invention relates to methods of improving the appearance of skin or hair. In particular, it relates to cosmetic products such as creams and serums comprising a subject's own platelet rich plasma (PRP). The invention also relates to kits that allow the user to apply the cosmetic products daily for several days.
Abstract: Compositions of and methods for formulating and delivering biologically active agent formulations having enhanced physical stability, and wherein deterioration from the presence of oxygen and/or water is minimized and/or controlled, to yield a stable formulation. The compositions of and methods for formulating and delivering biologically active agents of the present invention further facilitate their incorporation into a biocompatible coating which can be employed to coat a stratum-corneum piercing microprojection, or a plurality of stratum-corneum piercing microprojections of a delivery device, for delivery of the biocompatible coating through the skin of a subject, thus providing an effective means of delivering the biologically active agents.
Type:
Application
Filed:
January 30, 2017
Publication date:
May 18, 2017
Inventors:
Mahmoud Ameri, Michel J.N. Cormier, Scott Sellers, Yuh-Fun Maa
Abstract: The invention relates to a thermogelling composition comprising a chitosan having N-acetyl-glucosamine units, glucosamine units, and substituted glucosamine units other than the N-acetyl-glucosamine units, said substituted chitosan preferably having a degree of substitution of the glucosamine units ranging from 10 to 50%, expressed as a number of moles of the substituent based on the number of moles of total units, to its preparation and to its applications.
Abstract: Devices, systems, and methods for localized drug delivery. In at least one embodiment of a method of localized drug delivery, the method comprises the steps of placing a resorbable device within a tube, introducing the tube within a mammalian body at or near a tissue and/or organ within the mammalian body, and anchoring the resorbable device to the tissue and/or organ. Devices and systems useful for performing such a method are also disclosed herein, wherein an exemplary device comprises at least one drug release portion having at least one drug to be released over time and a binder intermixed with the at least one drug, and at least one resorbable anchor portion coupled to the at least one drug release portion.
Abstract: Residence devices as well as their related methods of manufacture and use are generally provided. In some embodiments, a residence device includes a plurality of self-assembling structures that assemble in vivo to form an aggregate structure. Each structure of the plurality of structures includes a first side and a first attachment point that attaches to a second attachment point on another structure of the plurality of structures. The aggregate structure may be sized and shaped to maintain an in vivo position relative to an internal orifice of a subject. The attachment between the first and second attachment points may degrade after a period of time.
Type:
Application
Filed:
June 11, 2015
Publication date:
May 18, 2017
Applicants:
Massachusetts Institute of Technology, The Brigham and Women's Hospital, Inc.
Inventors:
Andrew Bellinger, Shiyi Zhang, Carlo Giovanni Traverso, Robert S. Langer, Stacy Mo, Jiaqi Lin, Angela DiCiccio, Dean Liang Glettig, Lowell L. Wood, JR., Philip A. Eckhoff
Abstract: Provided are compositions and methods relating to hydrophobic agent loaded-micelle. The micelles comprise surfactant (such as poloxamer) and have hydrophobic agents incorporated therein. The compositions substantially lack surfactant that is not associated with the micelles. The compositions are able to achieve high hydrophobic agent:surfactant molar ratio. The compositions can be used for drug delivery and imaging applications.
Type:
Application
Filed:
July 2, 2015
Publication date:
May 18, 2017
Inventors:
Jonathan LOVELL, Yumiao ZHANG, Wentao SONG, Jumin GENG, Chulhong KIM, Mansik JEON
Abstract: The present disclosure relates to methods of preventing or treating parasite infection in a plurality of fish in need thereof, comprising administering to the fish an effective amount of a medicated fish feed. The medicated fish feed comprises fish feed granules or pellets coated with a composition comprising a neonicotinoid such as imidacloprid and a carrier having a high apparent digestibility coefficient such as a processed/cooked corn protein concentrate.
Abstract: Corticosteroid microparticle formulations are provided for use for treating pain, including pain caused by inflammatory diseases such as osteoarthritis or rheumatoid arthritis, and for slowing, arresting or reversing structural damage to tissues caused by an inflammatory disease, for example damage to articular and/or peri-articular tissues caused by osteoarthritis or rheumatoid arthritis. Corticosteroid microparticle formulations are administered locally as a sustained release dosage form (with or without an immediate release component) that results in efficacy accompanied by clinically insignificant or no measurable effect on endogenous cortisol production.
Type:
Application
Filed:
January 31, 2017
Publication date:
May 18, 2017
Inventors:
Neil Bodick, Robert C. Blanks, Anjali Kumar, Michael D. Clayman, Mark Moran
Abstract: The present invention includes compositions and methods for the use of an encapsulation additive having between about 0.1 to about 30 percent isolated and purified vitelline protein B to provide for mixed and extended release formulations.
Type:
Application
Filed:
January 26, 2017
Publication date:
May 18, 2017
Inventors:
Allison R. Ficht, Kenneth Carson, Cynthia Sheffield, John Herbert Waite
Abstract: The present invention relates to co-extruded pharmaceutical compositions and dosage forms comprising an adverse agent, such as an opioid antagonist, which can be sequestered. The pharmaceutical compositions and dosage forms diversion of a dosage form containing an active pharmaceutical agent, such as an opioid. The present invention also relates to methods of treating a patient with such a dosage form, as well as kits containing such a dosage form with instructions for using the dosage form to treat a patient. The present invention further relates to a process for the preparation of such pharmaceutical compositions and dosage forms comprising co-extrusion of a core comprising an adverse agent and a sheath.
Abstract: The present invention is a surface treated drug-loaded solid (e.g., non-porous) microparticle that aggregates in vivo to form a consolidated larger particle for medical therapy. In one embodiment, the particles are used for ocular therapy. Processes for producing the surface treated microparticle and injectable formulations which include the surface treated microparticle are also provided. When used in the eye, long-term consistent intraocular delivery can be achieved without disrupting vision and minimizing undesirable inflammatory responses.
Type:
Application
Filed:
November 11, 2016
Publication date:
May 18, 2017
Applicant:
GRAYBUG VISION, INC.
Inventors:
Yun Yu, Joshua Kays, Ming Yang, Jeffrey L. Cleland
Abstract: The invention provides a nanoparticle composition that is decorated with a urea-based small-molecule peptidomimetic inhibitor of prostate specific membrane antigen (PSMA), which is expressed by almost all solid tumors. This strategy takes advantage of both the avidity of the functionalized nanoparticle for binding to PSMA and the ability of the nanoparticle to be retained for longer periods of time in the tumor due to enhanced leakage via EPR into the tumor interstitium and poor clearance due to underdeveloped or non-existent lymphatics within the tumor.
Type:
Application
Filed:
July 13, 2016
Publication date:
May 18, 2017
Inventors:
Sachin S. Chandran, Sangeeta Ray, Martin G. Pomper, Samuel R. Denmeade, Ronnie C. Mease
Abstract: The instant invention provides for novel cationic lipids of Formula A that can be used in combination with other lipid components such as cholesterol and PEG-lipids to form lipid nanoparticles with oligonucleotides. It is an object of the instant invention to provide a cationic lipid scaffold that demonstrates enhanced efficacy along with lower liver toxicity as a result of lower lipid levels in the liver. The present invention employs low molecular weight cationic lipids with one short lipid chain coupled with inclusion of hydrolysable functionality in the lipid chains to enhance the efficiency and tolerability of in vivo delivery of siRNA.
Abstract: Biocompatible and biodegradable nanofibers are provided. The biocompatible and biodegradable nanofibers include an oil based polyesteramide, a protein/polysaccharide, and a pharmaceutical drug useful for wound healing and biomedical applications thereof.
Abstract: This invention relates to pharmaceutical composition and methods of using vitamin A and/or RAR? agonist for the treatment or prevention of diseases or conditions associated with high fat diet and/or vitamin deficiency.
Type:
Application
Filed:
January 24, 2017
Publication date:
May 18, 2017
Inventors:
LORRAINE J GUDAS, Yannick Benoit, Ronald Perez, Xiao-Han Tang, Steven Trasino
Abstract: Disclosed is an immediate release solution for oral administration of guaifenesin and at least one additional drug. In addition to water the solution comprises as solvents propylene glycol and glycerol in a concentration which significantly increases the bioavailability of guaifenesin in the human body.
Abstract: The present invention relates to feed supplements comprising vitamins and canthaxanthin and the use of such supplements for improving performance and health in poultry, in particular in poultry pullets. It has been found surprisingly that feed additive compositions as hereinafter defined improves immune status, bone and skeletal development, flock uniformity, growth and feed conversion of pullets. The feed additive composition according to the present invention comprises canthaxanthin, at least one vitamin selected from the group consisting of vitamin C and vitamin E, a trace mineral, in particular selenium, and optionally a mixture of at least two compounds selected from the group consisting of thymol, eugenol, vanillin and ?-terpinene.
Type:
Application
Filed:
January 27, 2017
Publication date:
May 18, 2017
Inventors:
Catherine HAMELIN, Rual LOPEZ ULIBARRI, Wolfgang SCHLIFFKA
Abstract: A solid pharmaceutical composition suitable for oral administration, comprising: (a) a SI P receptor modulator; (b) a filler, and (c) a cyclodextrin.
Abstract: Methods of storing and methods of stabilizing pharmaceutical compositions comprising cysteamine, or a pharmaceutically acceptable salt thereof, are provided. Methods of distributing pharmaceutical compositions comprising cysteamine, or a pharmaceutically acceptable salt thereof, and methods of treating cystinosis also are provided.
Abstract: The present invention generally relates to compositions and methods for topical or transdermal delivery, for promoting wound healing, reducing scarring, and/or promoting hair growth. Specifically, the present disclosure is directed to a topical arginine silicate formulation that demonstrates surprising improvement in wound healing time leading to more advantageous recovery and reducing hospital costs. Such formulations may also lessen scarring. The formulations may, for example, be applied to skin or to mucous membranes to facilitate wound healing.
Abstract: Methods and compositions comprising N-acetylcysteine amide (NAC amide) and derivatives thereof are used in treatments and therapies for human and non-human mammalian diseases, disorders, conditions and pathologies. Pharmaceutically or physiologically acceptable compositions of NAC amide or derivatives thereof are administered alone, or in combination with other suitable agents, to reduce, prevent, or counteract oxidative stress and free radical oxidant formation and overproduction in cells and tissues, as well as to provide a new source of glutathione.
Abstract: The present invention provides, in part, compositions and methods for treating cancer using a combination of C6-ceramide and other anti-cancer agents.
Abstract: Described herein are methods of inhibiting or reversing the progression of cataract formation or presbyopia in an eye by administering a bifunctional molecule comprising a substituted or unsubstituted amine, succinimide, carboxylic acid, isocyanate, isothiocyanate, sulfonyl chloride, aldehyde, carbodiimide, acyl azide, anhydride, fluorobenzene, carbonate, N-hydroxysuccinimide ester, imidoester, epoxide or fluorophenyl ester covalently linked to a molecular bristle. Both presbyopia and cataracts are caused by aggregation of the soluble crystalline lens proteins called the crystallins.
Abstract: Some embodiments of the present application are directed to oral formulations of L-ornithine phenylacetate and methods of using the same. These oral formulations offer alternative administration route than the standard intravenous administration of L-ornithine phenylacetate for treating hyperammonemia in patients having various acute and chronic liver diseases and disorders, for example, acute liver failure, liver cirrhosis, liver decompensation, portal hypertension, hepatic encephalopathy, or patients with urea cycle disorders.
Type:
Application
Filed:
November 11, 2016
Publication date:
May 18, 2017
Inventors:
Laurene Wang, Stan Bukofzer, Linda S. Grais
Abstract: Compositions comprising docosahexaenoic acid (DHA) and optionally one or more fatty acids selected from the group consisting of eicosapentaenoic acid (EPA), arachidonic acid (ARA), linoleic acid (LA), and ?-linoleic acid (ALA) are administered to felines for preventing or treating feline inflammatory bowel disease (IBD).
Type:
Application
Filed:
July 6, 2016
Publication date:
May 18, 2017
Applicant:
Hill's Pet Nutrition, Inc.
Inventors:
Christina Khoo, William David Schoenherr, Kathy Lynn Gross
Abstract: The invention relates to a composition comprising: i) one or more of uridine and cytidine, or salts, phosphates, acyl derivatives or esters thereof; ii) a lipid fraction comprising at least one of docosahexaenoic acid (22:6; DHA), eicosapentaenoic acid (20:5; EPA) and docosapentaenoic acid (22:5; DPA), or esters thereof, in which the lipid fraction comprises less than 2 weight % of ?-linolenic acid (ALA), calculated on the weight of all fatty acids; iii) choline, or salts or esters thereof; for use in the prevention or treatment of neurotrauma, traumatic brain injury, cerebral palsy and spinal cord injury.
Type:
Application
Filed:
January 27, 2017
Publication date:
May 18, 2017
Applicant:
N.V. Nutricia
Inventors:
Mattheus Cornelis DE WILDE, Johannes Wilhelmus Christina SIJBEN, Patrick Joseph Gerardus Hendrikus KAMPHUIS, Robert Johan Joseph HAGEMAN