http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105343031-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-51
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7048
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-51
filingDate 2015-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105343031-B
titleOfInvention A kind of ivermectin solid lipid nano granule and preparation method thereof
abstract The invention discloses a kind of ivermectin solid lipid nano granules, it includes the component of following parts by weight:0.75~3 part of 0.03~1 part of ivermectin, 5 parts of palmitic acid, 1~5 part of ten polyglycereol monolaurate and polyvinyl alcohol.Compared with prior art, ivermectin solid lipid nano granule produced by the present invention, for grain size between 230~350nm, potential value is preferable, polydispersity index<0.25, it is redissolved after freeze-drying, grain size, current potential are almost unchanged, can be preserved for a long time after freeze-drying.Electronic Speculum observes blank nanoparticle and drug-carrying nanometer particle in regular oblong, envelop rate, drugloading rate 0~12.9%.Meanwhile the Solid lipid of the invention screened and surfactant are biodegradable material, toxicity is low, has no stimulation of the skin;Matrix material used in the present invention can embedding medicinal reach the effect of sustained-release and controlled release.
priorityDate 2015-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 24.