发明名称 DRUG DELIVERY COMPOSITION COMPRISING POLYMER-LIPID HYBRID MICROPARTICLES
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.
申请公布号 WO2016141413(A1) 申请公布日期 2016.09.15
申请号 WO2016AU00080 申请日期 2016.03.11
申请人 UNIVERSITY OF SOUTH AUSTRALIA 发明人 PRESTIDGE, Clive Allan;JOYCE, Paul Matthew
分类号 A61K9/50;B01J13/02 主分类号 A61K9/50
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