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filingDate 2005-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2007-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007522238-A
titleOfInvention Preparation of microemulsion of high concentration propofol for anesthesia
abstract The present invention provides methods and compositions that enhance the dissolution and biocompatibility properties of propofol (2,6-diisopropylphenol) for use in anesthetics administered via mammalian veins. This method creates a self-emulsifiable base composition for use in the manufacture of water-based microemulsion preparations. In a preferred two-component base composition, the base composition consists of a surfactant containing polyethylene glycol and liquid propofol. The microemulsion is prepared by mixing the base composition with a carrier liquid to form a microemulsion containing a propofol concentration of up to about 4% by weight propofol relative to the volume of the microemulsion. In a quaternary base composition, the base composition is made of a surfactant containing polyethylene glycol, liquid propofol, a solvent that is not miscible with water, and ethanol. A microemulsion is prepared by mixing the base composition with a carrier liquid to form a microemulsion containing a propofol concentration of up to about 10% by weight propofol relative to the volume of the microemulsion. [Selection figure] None
priorityDate 2004-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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