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filingDate 2004-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8503aa586859237e56eca417a89dee90
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publicationDate 2012-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2388924-T3
titleOfInvention Method for preparing submicron particles of paclitaxel or docetaxel
abstract Method for preparing a pharmaceutical composition of submicron particles of paclitaxel or docetaxel, the solubility of paclitaxel or docetaxel being greater in a first solvent miscible in water than in a second solvent that is aqueous, including the method the steps of: i) mixing a first modifier surface comprising a phospholipid conjugated with a water-soluble or hydrophilic polymer in the first water miscible solvent or in the second solvent or both, the first water miscible solvent and the second solvent; ii) mixing a second surface modifier selected from the group consisting of anionic, cationic, non-ionic and biological modifying agents with surface activity, in the first water-miscible solvent or in the second solvent or in both, the first water-miscible solvent and the second solvent; iii) dissolve paclitaxel or docetaxel in the first water miscible solvent to form a solution; iv) mixing the solution with the second solvent to define a pre-suspension of particles; and v) homogenize the pre-suspension to form a suspension of small particles with an average effective particle size of less than about 1,000 nm.
priorityDate 2003-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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