http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2730405-T3

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filingDate 2013-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9839b98b06a3adb7e0273f6d916b8a8a
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publicationDate 2019-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2730405-T3
titleOfInvention Improved method for the preparation of vincristine encapsulated in liposomes for therapeutic use
abstract A method of preparing a pharmaceutically acceptable liquid composition comprising liposome-encapsulated vincristine that is free from substantial degradation products, the method comprising: (a) reconstituting in a single vial (i) a first solution comprising vincristine sulfate in a concentration from 1 mg / ml to 5 mg / ml, where the first solution has a pH of 3.5 to 5.5; and (ii) a second solution comprising sphingomyelin / cholesterol liposomes at a low pH; (b) raising the pH of the reconstitutive solution in the individual vial to a pH of 7.0 to 7.5; (c) heating the individual vial comprising the reconstitutive solution in a balanced dry thermoblock at 75 ° C for at least 13 to 18 minutes, wherein said thermoblock comprises one or more holes 1-5% greater than the length or diameter means of the individual vial to produce a reconstituted liposome encapsulated vincristine solution; and (d) equilibrate the reconstituted solution to room temperature.
priorityDate 2012-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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