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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-704
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-704
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-127
filingDate 2004-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4ddf58cf4d95cff3429a31f35561ecd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b441b42e4d2d0f538da861792ff304d
publicationDate 2006-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20060134952-A
titleOfInvention How to load drugs in liposomes
abstract The present invention discloses liposome compositions having therapeutic agents protonable in the form of salts with glucuronic anion. The present invention also discloses a process for preparing the composition using an ammonium ion dura mater gradient with glucuronic acid ions as the counterion. In one embodiment where the protonable agent is doxorubicin, the method of the invention is comparable to loading efficiency, faster release without compromising therapeutic efficacy when compared to loading with an ammonium ion gradient with sulfate ions as the counterion. Have speed.
priorityDate 2003-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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