http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2190509-C

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filingDate 1995-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca523f7d8e5b767f93d31f20ad2671aa
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publicationDate 2008-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2190509-C
titleOfInvention Hepatocyte-selective oil-in-water emulsion
abstract A heat and shelf-stable oil-in-water emulsion useful as a tissue or cell- selective delivery vehicle. Radioactive or stable, synthetic or semi-synthet ic polyhalogenated triglycerides, such as 2-oleoylglycerol-1,3-bis[7-(3-amino- 2,4,6-triiodophenyl)heptanoate] or 2-oleoylglycerol-1,3-bis[.omega.-(3,5-bis - trifluoromethyl)-heptanoate] or phenyl acetate, can be incorporated into the lipophilic core of a lipoprotein-like emulsion particle. The lipophilic core is surrounded by a phospholipid membrane comprising cholesterol and apolipoproteins. For hepatocyte-selective delivery, the emulsion is chylomicron remnant-like by being in a size range of 50 to 200 nm as measure d by number weighting analysis with a narrow size distribution ( 2 % greater than 300 nm) and having a composition simulating naturally-occurring chylomicron remnants. Use of cholesterol in the emulsion formula facilitates association of apolipoproteins, especially Apo E which are recognized by liv er cells and necessary for binding and uptake. Stability and size constraints c an be achieved by ultra high energy mixing equipment, such as the MicroFluidize r (Microfluidics Corp., Newton, MA) to form the emulsion. In preferred embodiments, osmolality of the emulsion is controlled by glycerol rather tha n normal saline.
priorityDate 1994-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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