http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102697765-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e328f3403a32b1dbb56db1d343f262f5
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-341
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-194
filingDate 2012-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5162cebd8e673a9e453a73eb340a9deb
publicationDate 2013-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102697765-B
titleOfInvention Ranitidine hydrochloride/bismuth potassium citrate pharmaceutical composition solid lipid nanoparticles preparation
abstract The invention discloses a ranitidine hydrochloride/bismuth potassium citrate pharmaceutical composition solid lipid nanoparticles preparation and a preparation method thereof. The preparation method includes dissolving water-insoluble lipid in organic solvent to constitute oil phase; taking aqueous solution of ranitidine hydrochloride and hydrophilic surfactant as water phase; loading ranitidine hydrochloride in solid lipid nanoparticles by combining stirring emulsification and high-pressure emulsion homogenizing; mixing with bismuth potassium citrate to obtain ranitidine hydrochloride/bismuth potassium citrate pharmaceutical composition solid lipid nanoparticles; and formulating into solid preparation by conventional method. The preparation is high in drug loading rate, uniform in particle size, and long in drug retention time in blood circulation, and has better sustained-release and controlled-release effects; and facilitates release of bismuth potassium citrate so as to cover on gastrointestinal ulcer surface to exert effect of ulcer isolator. The preparation method is simple in preparation device and easy in operation, improves preparation product quality, reduces toxic and side effects, and is suitable for industrialized production.
priorityDate 2012-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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