Abstract: An equine dietary supplement which is fed to a horse to improve the health of the horse includes a mixture containing chia seeds, whey dextrose and bee pollen.
Abstract: The present invention relates to a preparation method for a traditional Chinese medicine drop pill and a traditional Chinese medicine micro drop pill prepared by using the method, and in particular, the present invention relates to a micro drop pill preparation method with high drug-loading capacity, simple preparation process and high production rate and a micro drop pill prepared by using the method. Specially, The drop pill preparation method used comprises the following steps: (1) material melting step: heat melting a medicine and a drop pill matrix to obtain a molten medicine liquid; (2) dropping step: delivering the molten medicine liquid to a dripper, and acquiring medicine drops of the molten medicine liquid by means of vibration dropping; and, (3) condensation step: cooling the medicine drops with a cooling gas to obtain micro drop pills.
Abstract: Compositions for treating non-cornified epithelial tissue of a female body, such as the labia, introitus, and the vagina are disclosed. Methods of regulating dryness in these tissues are also disclosed.
Type:
Grant
Filed:
August 10, 2018
Date of Patent:
May 11, 2021
Assignee:
The Procter & Gamble Company
Inventors:
Paul Robert Tanner, Larry Richard Robinson
Abstract: The composition of a set of formulations based on synthetic active ingredients and natural boosting additives, which provide repellent action against flying insects such as mosquitoes, flies and black-winged stilts, as well as crawling insects such as cockroaches and ants.
Type:
Grant
Filed:
February 15, 2017
Date of Patent:
May 11, 2021
Assignee:
IPEL-ITIBANYL PRODUTOS ESPECIAIS LTDA
Inventors:
Walter Piccirillo Pinto, Giovanni Caritá Júnior
Abstract: The present invention relates to an antibacterial dressing and a method for preparing the same. According to the present invention, there are provided an antibacterial dressing containing a rapid cell membrane-penetrating component that exhibits excellent bactericidal and antibacterial activities by disrupting the structure and synthesis of protein and nucleic acid, and a method for preparing the same.
Type:
Grant
Filed:
March 25, 2016
Date of Patent:
April 27, 2021
Assignee:
Genewel Co., Ltd.
Inventors:
Hyun Jung Kim, Il Kyu Park, Seung Moon Lee, Yong Soo Kim
Abstract: The invention relates to an oral pharmaceutical composition in the form of a sustained-release tablet comprising an active ingredient capable of being misused, which composition makes it possible to combat misuse by injection.
Abstract: Provided is low-substituted hydroxypropyl cellulose from which a granulation product having an adequate particle size can be obtained in a wet granulation method and a tablet having excellent compactibility and disintegrability can be obtained. More specifically, provided is low-substituted hydroxypropyl cellulose having a hydroxypropoxyl content of from 5 to 16% by weight and a water-soluble content of less than 2% by weight, wherein a weight ratio of water to the low-substituted hydroxypropyl cellulose giving a maximum torque is from 3 to 5 as determined while adding one part by weight of water per minute to one part by weight of the low-substituted hydroxypropyl cellulose under mixing with biaxial mixing blades. Also provided are a solid preparation including the low-substituted hydroxypropyl cellulose, and the like.
Abstract: The invention is directed to pharmaceutical compositions such as tablets that exhibit delayed release properties when administered as either whole or half tablets. The invention is also directed to delayed release tablets comprising deferiprone for oral administration, for which twice daily administration is bioequivalent to the same daily dose of an immediate release tablet administered thrice daily. The invention is also directed to methods of making and using the same.
Abstract: The invention is directed to pharmaceutical compositions such as tablets that exhibit delayed release properties when administered as either whole or half tablets. The invention is also directed to delayed release tablets comprising deferiprone for oral administration, for which twice daily administration is bioequivalent to the same daily dose of an immediate release tablet administered thrice daily. The invention is also directed to methods of making and using the same.
Abstract: The present disclosure is directed to topical dermatological formulations, dermatological cleansing compositions, and bathwater conditioners designed to acidify the skin, and their use for restoring epidermal acidity, restoring a the epidermal barrier, inhibiting inflammation, establishing an environment appropriate for maintaining a balanced symbiotic microbiome, and inhibiting the growth of pathogenic microorganisms in the epidermis—the outer layer of mammalian skin.
Abstract: Described herein are methods and formulations for treating, inhibiting, or ameliorating vaginitis, including bacterial vaginosis. Aspects described herein relate to formulations including a reactive oxygen species, a rheology agent, and a silicone polymer and methods of using these formulations for treating, ameliorating, or inhibiting a vaginitis, including bacterial vaginosis.
Abstract: Compositions of the invention contain, in a cosmetically acceptable aqueous medium, a) a cationic polyelectrolyte, b) at least one surfactant; and (c) from about 0.01 to about 1.2 weight percent of an anionic polyelectrolyte, where the weight ratio of the anionic polyelectrolyte to the cationic polyelectrolyte is from about 0.05 to about 1.2, and where the composition exhibits a viscosity change that is below a minimum significant-change-threshold (??min) and exhibits no measurable yield stress or increase in yield stress value when compared to a substantially identical composition that does not contain from about 0.01 to about 1.2 weight percent of the anionic polyelectrolyte, at a weight ratio of anionic polyelectrolyte to cationic polyelectrolyte of from about 0.05 to about 1.2.
Type:
Grant
Filed:
November 30, 2018
Date of Patent:
February 9, 2021
Assignee:
Johnson & Johnson Consumer Inc.
Inventors:
Michael J. Fevola, Tobias J. Fuetterer, Matthew A. Lohr
Abstract: This document relates to methods and materials for reducing the risk of infection after a shoulder surgery or medical procedure. For example, this document relates to methods and materials for using a topical composition containing clindamycin or erythromycin to reduce the risk of or to prevent infection associated with shoulder surgeries or medical procedures.
Type:
Grant
Filed:
December 27, 2018
Date of Patent:
November 17, 2020
Assignee:
Mayo Foundation for Medical Education and Research
Abstract: Methods of reducing hepatitis delta virus (HDV) viral loads in a patient are provided. In some embodiments, the method comprises treating the patient with lonafarnib-ritonavir co-therapy. In some embodiments, the method further comprises treating the patient with an interferon.
Type:
Grant
Filed:
August 1, 2018
Date of Patent:
November 10, 2020
Assignee:
Eiger Biopharmaceuticals, Inc.
Inventors:
David A. Cory, Ingrid Choong, Jeffrey S. Glenn
Abstract: An in situ gel formulation comprising poly lactide-co-?-caprolactone (PLCL), a surfactant with a hydrophilic-lipophilic balance value of 14-15, a plasticizer, and a statin is provided. Methods of treating hyperlipidemia by parenterally administering the in situ gel formulation are also provided.
Type:
Grant
Filed:
December 6, 2019
Date of Patent:
October 27, 2020
Assignee:
KING ABDULAZIZ UNIVERSITY
Inventors:
Tarek A. Ahmed, Mohammed M. Mussari, Abdelsattar M. Omar, Khalid M. El-Say
Abstract: A cosmetic product includes a container main body that has an opening at one end thereof and contains a cosmetic therein, and a lid that has an application tool provided with an application element at a tip portion thereof and inserted into the opening part. When the lid is attached to the container main body, the application element and the cosmetic are brought into contact with each other and the cosmetic is hermetically sealed. The cosmetic contains (A) wax which is solid at 25° C., (B) powder, (C) film-forming agent, and (D) volatile oil agent, and a content of the (C) film-forming agent is 10% to 40% by mass based on a total amount of the cosmetic.
Abstract: The present invention generally relates to dietary supplement and pharmaceutical formulations comprising layered acid protective oral dosage formulations comprising probiotics and provided as single unified or cohesive dosage form units. Each individual acid protective layer of the cohesive dosage form provides one of a different probiotic payload, a different release profile to target delivery of probiotic to a particular region in the gastrointestinal tract, or both different probiotic payloads and release profiles to target delivery of different probiotics to particular regions in the gastrointestinal tract.
Abstract: This disclosure concerns compounds which are useful as inhibitors of protein kinase C (PKC) and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of PKC. This disclosure also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
Type:
Grant
Filed:
March 12, 2018
Date of Patent:
October 6, 2020
Assignee:
Rigel Pharmaceuticals, Inc.
Inventors:
Rajinder Singh, Matthew Duncton, Jing Zhang, Salvador Alvarez, Kin Tso, Sacha Holland, Rose Yen, Rao Kolluri, Thilo Heckrodt, Yan Chen, Esteban Masuda, Hui Li, Donald G. Payan
Abstract: The present invention relates to a polyacrylamide hydrogel for use in prevention and/or treatment of synovitis or pain associated with synovitis in a mammal by formation of an extra layer to the synovial membrane i.e. a sub-synovial layer and a novel synovial lining layer. Synovitis may occur in association with arthritis, such as osteoarthritis or rheumatoid arthritis, lupus, or gout, and the mammal suffering from synovitis is a preferably a human, a racing animal or a companion animal.
Type:
Grant
Filed:
March 30, 2017
Date of Patent:
September 15, 2020
Assignee:
Contura International A/S
Inventors:
Ieva Ankorina-Stark, Lise Hanne Christensen