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    • 7. 发明申请
    • Compositions and methods for intranasal delivery of tricyclic cannabinoids
    • 用于鼻内输送三环大麻素的组合物和方法
    • US20070060639A1
    • 2007-03-15
    • US11515607
    • 2006-09-05
    • Daniel Wermeling
    • Daniel Wermeling
    • A61K31/353
    • A61K9/0043A61K31/00A61K31/353
    • A pharmaceutical composition for intranasal administration to a human or non-human subject is provided, comprising a therapeutically active component that comprises at least one tricyclic cannabinoid in a liquid to semi-solid medium that comprises a pharmaceutically acceptable solubilizing agent in an amount effective to solubilize the cannabinoid. An amount of the composition intranasally administrable as a single dose, upon intranasal administration in a rat model, provides a systemic plasma cannabinoid concentration (i) that, at least at one time point during a period from about 15 minutes to about 2 hours after said administration, is at least about 0.5 ng/ml, but (ii) that at no time exceeds about 100 ng/ml.
    • 提供了一种用于向人或非人受试者鼻内施用的药物组合物,其包含治疗活性成分,所述治疗活性成分在液体至半固体培养基中包含至少一种三环类大麻素,所述药物组合物包含有效溶解量的药学上可接受的增溶剂 大麻素。 在大鼠模型中鼻内给药时,鼻内给药作为单一剂量的组合物的量提供全身性血浆大麻素浓度(i)至少在所述第一个时间点之后约15分钟至约2小时的时间点 至少约0.5ng / ml,但(ii)在任何时候超过约100ng / ml。