http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101618222-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f447d8315e8cf777897a7544d3fc2b43
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-48
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filingDate 2009-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d52bb67d13f5b18170c9dc2e2448fb50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f365ab8ba8e31576d7450033ebf580cf
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab026858a7b341b5de5d630190454a21
publicationDate 2011-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101618222-B
titleOfInvention Anethol trithione and phospholipid compound and preparation method thereof
abstract The invention relates to a peroral anethol trithione preparation and a preparation method thereof, belonging to the field of pharmaceutical preparations, The preparation method comprises the following steps: dissolving anethol trithione and phospholipid in a compound mode to one or a plurality of fatty acid triglycerides to prepare soft capsules and/or palletizing the phospholipid compound and suitable pharmaceutical excipient to further prepare enteric-coated capsules. Compared with preparations sold in markets, animal experiment results show that the prepared new preparation of the phospholipid compound obviously improves the peroral bioavailability of the anethol trithione and the pharmaceutical concentration in the target tissue liver and predicts favorable liver protection efficacy and cholagogic efficacy.
priorityDate 2008-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID468046118

Total number of triples: 23.