http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2834262-A1

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filingDate 2012-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70344f2594c6617e2aeabcbace78b648
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8c54bb16f2bd34d8ef9e30873a1c2d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76acd0261e60da2569de106ca6d14233
publicationDate 2012-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2834262-A1
titleOfInvention Improved parenteral formulations of lipophilic pharmaceutical agents and methods for preparing and using the same
abstract There may be provided compositions of lipophilic pharmaceutical agents with improved solubility and stability. For example, there may be provided a non-aqueous composition that comprises a lipophilic pharmaceutical agent, and an amphiphilic polymeric solvent such as PEG400 but essentially free of organic solvents and non-solubilized particles. The composition may be further diluted with a desired aqueous diluent such as an infusion fluid for parenteral administration to a subject such as a human. The compositions may be useful for the treatment for diseases or conditions that are sensitive to lipophilic agents, such as infectious diseases, malignant or autoimmune diseases.
priorityDate 2011-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1885.