http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102626387-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_84298b51a1fbdc3f0e2984520ae51c36
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-675
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filingDate 2012-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02699470eb521d5ad1dfdf7de21774c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54eed89d4deb18596724f650f8192e1d
publicationDate 2013-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102626387-B
titleOfInvention Clopidogrel bisulfate liposome solid preparation
abstract The invention discloses a clopidogrel bisulfate liposome solid preparation and a preparation method thereof. The method is to prepare liposome from an active ingredient clopidogrel bisulfate, and soybean lecithin, dioleoyl phosphatidylglycerole, cholesterol and tween 80 in a specific combination. The prepared liposome greatly improves stability, dissolution rate and bioavailability of a drug, andhas stable and lasting action and notable curative effect. The preparation provided by the invention improves product quality of a preparation and reduces toxic and side effects.
priorityDate 2012-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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