http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2612032-T3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-4866
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
filingDate 2008-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dff8c42c228e473a042275502406e516
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d80a1c387854e2127239e0aaad566642
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publicationDate 2017-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2612032-T3
titleOfInvention Oral pharmaceutical forms based on inviolable lipids for opioid agonists
abstract An inviolable drug delivery system comprising at least one lipid, at least one gelling agent and at least one active drug principle, in which the gelling agent quickly gels in the presence of water in about 10 seconds or less and the active drug substance is released. in the digestive system, in which the weight ratio between gelling agent and lipid is in the range between 1: 2 and 1: 7, and in which the lipid is a solid at room temperature and is present in the delivery system between approximately 20% by weight and 50% by weight.
priorityDate 2007-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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