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filingDate 1993-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6186e3f17d7020a015b62c4bca2300b
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publicationDate 1994-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9407537-A1
titleOfInvention Pharmaceutical composition for site-specific release of a clot-dissolving protein
abstract A pharmaceutical composition for the treatment of blood clots as well as a diagnostic composition for the detection of blood clots are described, which composition comprises a liposome or another biodegradable colloidal carrier, which has a plasminogen bonded to it as targeting device and has a plasminogen activator, in particular a tissue-type plasminogen activator (tPA), as clot-dissolving protein, or a diagnostic agent. A method is also described for the preparation of a composition having blood clot-decomposing properties, in which method: a) plasminogen is bound to liposomes, the affinity of the plasminogen for fibrin being essentially maintained; and b) a plasminogen activator is incorporated in the liposomes, under conditions such that the interaction of the plasminogen with the plasminogen activator is reduced. A method is also described for bonding plasminogen to liposomes, a substantially purified plasminogen being used as starting material.
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