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Drug delivery composition comprising polymer-lipid hybrid microparticles

机译:包含聚合物-脂质杂化微粒的药物递送组合物

摘要

A dry composition, comprising three-dimensional porous microparticles, wherein the microparticles comprise: (i) an active substance (eg a poorly water soluble drug), (ii) polymeric nanoparticles such as those composed of a biocompatible and/or biodegradable polymer (eg a PLGA polymer) (iii) lipid droplets (eg droplets of a medium chain triglyceride (MCT)), (iv) a nanoparticle stabilising agent such as PVA or DMAB, and optionally, (v) a cryoprotectant (eg mannitol); wherein said active substance is carried by said nanoparticles and/or lipid droplets. The composition of the present invention may be formulated into, for example, a medicament for the treatment and/or prevention of various diseases or disorders (eg human or veterinary therapeutics). The average diameter of the individual microparticles of the composition, may be in the order of 2.5-3.5 μm which are particularly suitable for administration to the lung.
机译:包含三维多孔微粒的干燥组合物,其中所述微粒包含:(i)活性物质(例如水溶性差的药物),(ii)聚合纳米颗粒,例如由生物相容性和/或可生物降解的聚合物组成的那些(例如PLGA聚合物)(iii)脂质液滴(例如中链甘油三酸酯(MCT)的液滴),(iv)纳米颗粒稳定剂(例如PVA或DMAB)和(v)冷冻保护剂(例如甘露醇);其中所述活性物质由所述纳米颗粒和/或脂质液滴携带。本发明的组合物可以配制成例如用于治疗和/或预防各种疾病或病症(例如人或兽医疗法)的药物。组合物的单个微粒的平均直径可以为2.5-3.5μm的量级,其特别适合于向肺给药。

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