http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015328164-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c485186959750ae94211c8abce29b5a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-4891
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-4858
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-48
filingDate 2014-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44bb85f7988c705cf6a99ccca05d5c88
publicationDate 2015-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2015328164-A1
titleOfInvention Physically dispersed, molecularly dissolved and/or chemically bound drug(s) in an empty, hard capsule shell composition
abstract The present invention proposes a design to incorporate drug(s) in the hard capsule shells (body and cap) composition. Drug(s) in the cap and body of the capsule shell may be the same or may be different. Other drug(s) in the form of granules, beads etc. can be filled into the capsules as a core material. The drug(s) in the capsule core material may be the same as in the shell-composition or may be different. Thus, the same capsule may contain different drug(s) as the core material and in the shell. The key advantages of incorporation of drug in the capsule shell compositions are to minimize drug-drug interaction and to obtain a desired rate of release of the drug(s), mainly for potent ones. The concept can be applied to the hard gelatin, and hard non-gelatin capsules.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020254401-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10357461-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2018256671-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2018116970-A1
priorityDate 2005-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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