会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明申请
    • FORMULATIONS DECREASING PARTICLE EXHALATION
    • 制剂减少颗粒物排放
    • US20150079173A1
    • 2015-03-19
    • US14058852
    • 2013-10-21
    • PULMATRIX, INC.
    • David A. EDWARDSJonathan Chun-Wah MANJeffrey P. KATSTRARobert W. CLARKE
    • A61K47/02A61K9/00
    • A61K47/02A61K9/0078A61K9/14A61K9/141A61K9/16A61M15/00
    • Formulations have been developed for pulmonary delivery to treat or reduce the infectivity of diseases such as viral infections, especially tuberculosis, SARS, influenza and respiratory synticial virus in humans and hoof and mouth disease in animals, or to reduce the symptoms of allergy or other pulmonary disease. Formulations for pulmonary administration include a material that significantly alters physical properties such as surface tension and surface elasticity of lung mucus lining fluid, which may be isotonic saline and, optionally, a carrier. The formulation may be administered as a liquid solution, suspension, aerosol, or powder where the particles consist basically of an osmotically active solute. Drugs, especially antivirals or antibiotics, may optionally be included with the formulation. These may be administered with or incorporated into the formulation.
    • 已经开发了用于肺部输送以治疗或降低人类感染病毒感染,特别是结核病,SARS,流感和呼吸道合成病毒以及动物蹄和口蹄疫等疾病或减轻过敏或其他肺部疾病症状的传染性的制剂 疾病。 用于肺部给药的制剂包括显着改变诸如等渗盐水和任选的载体的肺粘液衬里液体的表面张力和表面弹性的物理性质的材料。 制剂可以作为液体溶液,悬浮液,气雾剂或粉末施用,其中颗粒基本上由渗透活性的溶质组成。 药物,特别是抗病毒剂或抗生素,可以任选地包括在制剂中。 这些可以与制剂一起施用或掺入制剂中。
    • 8. 发明申请
    • TIOTROPIUM DRY POWDERS
    • 生物干粉
    • US20160120855A1
    • 2016-05-05
    • US14870736
    • 2015-09-30
    • Pulmatrix, Inc.
    • Jean C. SungDiana ManzanedoJason M. PerryWesley DehaanBrian Trautman
    • A61K31/439A61K31/57A61K9/00
    • A61K31/439A61K9/0075A61K9/1611A61K9/1617A61K31/57A61K31/58A61K45/06A61K2300/00
    • The present invention relates to respirable dry powder comprising respirable dry particles that comprise sodium chloride, leucine, and tiotropium bromide, wherein the sodium chloride is about 60% to about 90%, the leucine is about 10% to about 40%, the tiotropium bromide is about 0.01% to about 0.5%, and optionally one or more additional therapeutic agents up to about 20%, wherein all percentages are weight percentages on a dry basis and all the components of the respirable dry particles amount to 100%. The invention also relates to respirable dry powders that contain respirable dry particles that comprise sodium chloride, leucine, and tiotropium bromide, wherein the sodium chloride is 67% to 84%, the leucine is 12% to 28%, the tiotropium bromide is about 0.01% to about 0.5%, and optionally one or more additional therapeutic agents up to about 20%, wherein all percentages are weight percentages on a dry basis and all the components of the respirable dry particles amount to 100%. The invention also relates to respirable dry powders that contain respirable dry particles that comprise about 79.5% to about 80.5% (w/w) sodium chloride, about 19.5% to about 20.5% (w/w) leucine, and about 0.01% to about 0.5% (w/w) tiotropium bromide, and methods for treating a subject using the respirable dry powders.
    • 本发明涉及包含氯化钠,亮氨酸和噻托溴铵的可吸入干颗粒的可呼吸干粉,其中氯化钠为约60%至约90%,亮氨酸为约10%至约40%,噻托溴铵 约0.01%至约0.5%,以及任选的一种或多种另外的治疗剂至多约20%,其中所有百分比均为干基重量百分比,所有可呼吸干燥颗粒的组分均为100%。 本发明还涉及含有可吸入干颗粒的可呼吸干燥粉末,其包含氯化钠,亮氨酸和噻托溴铵,其中氯化钠为67%至84%,亮氨酸为12%至28%,噻托溴铵为约0.01 %至约0.5%,以及任选的一种或多种额外的治疗剂至多约20%,其中所有百分比均为干重的重量百分数,并且可呼吸干燥颗粒的所有组分均为100%。 本发明还涉及可吸入干粉,其含有可吸入干颗粒,其包含约79.5%至约80.5%(w / w)氯化钠,约19.5%至约20.5%(w / w)亮氨酸,和约0.01%至约 0.5%(w / w)噻托溴铵,以及使用可呼吸干粉治疗受试者的方法。