http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-I262798-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1272
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-127
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-88
filingDate 2003-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ae4b7acbce77233b5ed37353f9e37c0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed93c3fe457af04eac9518756caa27e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebb09e6375d00e0fccbb0d87e4f8449b
publicationDate 2006-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-I262798-B
titleOfInvention Liposome and drug deliver system
abstract The present invention relates to a liposome comprising a phospholipid bilayer and a hydrophilic core, wherein the phospholipid dilayer contains TPGS (d-alpha tocopheryl polyethylene glycol 1000 succinate). The liposomes are first prepared by solvent injection and extrusion method, and then drug loading by ammonium sulfate gradient. The TPGS in the liposome composition can prolong the circulation time of liposomes and thus increase the chance for the drug composition to enter target sites so as to improve the efficiency of drug delivery.
priorityDate 2003-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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