http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103479653-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_653c418e41edbb4e1ce8bc5e53e70cec
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-616
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439
filingDate 2013-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df6f0fb4aa54d46486e8852f588485a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93683ae9d72a95385de56ab13f91ef80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4f62d2ae332af5c63aedb33739ec1bb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79a758f651c565705a60b84d753650e3
publicationDate 2014-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103479653-A
titleOfInvention Aspirin-esomeprazole compound enteric-coated pellet preparation and preparation method
abstract The invention relates to an aspirin-esomeprazole compound enteric-coated pellet preparation and a preparation method thereof. The ratio is 3-6:1. There are two types of compound enteric-coated pellets. One is aspirin pellets as the drug-containing pellet core, which is successively covered with isolation layer I, esomeprazole magnesium drug layer, isolation layer II, and enteric coating layer; The second is to prepare aspirin enteric-coated pellets and esomeprazole enteric-coated pellets respectively, and then mix them to obtain compound enteric-coated pellets. The invention has the advantages that the drug is released in the intestinal tract, avoiding the destruction of the acidic environment of the drug in the stomach; the compound preparation antagonizes the side effect of aspirin on gastrointestinal stimulation, so as to facilitate the long-term use of aspirin and exert its effect of inhibiting platelet aggregation; The pill form releases the drug, which has high bioavailability, less fluctuation of blood drug concentration, and lower side effects.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112190564-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107224585-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110478333-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111939139-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107224585-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110538165-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110538165-A
priorityDate 2013-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011293713-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002051814-A1
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID465927764
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164092777

Total number of triples: 28.