摘要:
Methods and compositions are provided for a broad-spectrum, bactericidal or bacteriostatic treatment of antibiotic-resistant bacteria in animals with a non-toxic agent. The teachings include bactericidal or bacteriostatic treatment of spore-forming, anaerobic antibiotic-resistant bacteria. And, the compositions and methods provided herein can at least inhibit the onset of, inhibit the growth of, inhibit the germination of, or kill the antibiotic-resistant bacteria. Suchantibiotic-resistant bacteria include, but are not limited to, Clostridium difficile , Enterococcus faecalis, Staphylococcus aureus , and Klebsiella pneumoniae.
摘要:
The present patent application relates to a method of treating allergic rhinitis in a subject (preferably a human) by administering a combination of mometasone or its salt and olopatadine or its salt.
摘要:
L'invention concerne une composition sous forme d'une solution aqueuse injectable, dont le pH est compris entre 6,6 et 7,8, comprenant au moins : a) une insuline basale dont le point isoélectrique pI est compris entre 5,8 et 8,5; b) un composé anionique porteur de charges carboxylates et de radicaux hydrophobes. Dans un mode de réalisation, les compositions selon l'invention comprennent en outre une insuline prandiale.
摘要:
The present invention relates to the field of drug abuse. More specifically, the present invention provides methods and compositions for treating drug abuse by preventing GAPDH nitrosylation. In one specific embodiment, a method for preventing the stimulant and neurotoxic effects of cocaine comprises the step of administering a compound that prevents the nitrosylation of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) by nitric oxide (NO). In another embodiment, a method for preventing the stimulant and neurotoxic effects of cocaine comprises the step of administering a compound that prevents the binding of GAPDH to Siah.
摘要:
The present invention relates to a bitter taste masked pharmaceutical formulation comprising: (i) corticosteroid or a pharmaceutically acceptable salt thereof; (ii) an antihistamine selected from the group consisting of olopatadine, azelastine and a pharmaceutically acceptable salt thereof; and (iii) stevia. The pharmaceutical formulation according to the present invention effectively blocks bitter taste of the active ingredients, thereby having improved taste and patient compliance, and thus can be efficiently used in the treatment of allergic rhinitis.
摘要:
This disclosure relates to a composition that may include frankincense resin and various combinations of essential oils, which combinations may be effective in promoting weight loss. The present disclosure further relates to a weight loss and satiation composition that may include frankincense resin and a flavorant. In some embodiments, the composition may include a gum base.
摘要:
La invención se relaciona con el uso de agonistas del receptor beta-3 adrenérgico en una terapia combinada para el tratamiento de enfermedades metabólicas como hiperglicemias, resistencia a la insulina, diabetes tipo 2 y dislipidemias. En dicha terapia se combina la administración de un agonista del receptor beta-3 adrenérgico con un agonista del receptor de GLP-1 o un agonista de PPARα, ambos compuestos capaces de reducir el apetito, reducir el incremento de peso e incrementar el gasto energético mediante la movilización de la grasa. La presente invención muestra que la administración combinada de dichos compuestos presenta un efecto sinérgico enla reducción de la grasa corporal.
摘要:
The present invention is directed to a stable formulation of a combination of ketorolac (non-steroidal anti-inflammatory drug) with olopatadine (anti-histaminic drug) intended for ophthalmic use. This pharmaceutical composition is used for treatment of ophthalmic diseases and conditions, particularly seasonal ocular surface allergy.
摘要:
Effective treatments of pain for extended periods of time are provided. Through the administration of an effective amount of mixed monoamine reuptake inhibitor locally at or near a target site, one can relieve pain caused by diverse sources, including but not limited to spinal disc herniation ( i.e. sciatica), spondilothesis, stenosis, discogenic back pain and joint pain, as well as pain that is incidental to surgery. When appropriate formulations are provided within biodegradable polymers, this relief can be continued for at least thirty days. In some embodiments, the relief can be for at least at least fifty days, at least one hundred days, at least one hundred and twenty days, at least one hundred and thirty, at least one hundred fifty days or at least one hundred and eighty days.