http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10463626-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eef6e8a72192a40f58c75e7330d59bf5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5089
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-495
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
filingDate 2016-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1868ee68de9100b5b839eb7611bece2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe4b5ed2ec9a9c96b12a5c6d900c80f1
publicationDate 2019-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10463626-B2
titleOfInvention Drug delivery composition comprising polymer-lipid hybrid microparticles
abstract 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 stabilizing 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.
priorityDate 2015-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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