http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2010331867-A1

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filingDate 2010-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f80467692dbf4472fb72c63335590d4
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publicationDate 2012-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2010331867-A1
titleOfInvention Composition comprising an amorphous non- crystalline glass form of azithromycin
abstract The invention relates to an amorphous non-crystalline glass form (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R) -2-ethyl-3,4, 10- trihydroxy- 3,5,6,8,10,12,14- heptamethyl-15-oxo- 11- {[3,4,6- trideoxy-3- (dimethylamino) -β-D-xylo- hexopyranosyl]oxy}-1-oxa- 6- azacyclopentadec-13-yl 2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo- hexopyranoside or azithromycin having an infra-red pattern displaying characteristic relatively broad peaks at approximately 3500 and 1727 cm and characteristic peaks at approximately 2970 and 2938 cm. The invention further relates to a preparation method of increasing the solubility of azithromycin including the steps of selecting anhydrous, monohydrated or dihydrated azithromycin; elevating the temperature of the azithromycin to above the melting point thereof; and reducing the temperature of the melt sufficiently to allow it to set into an amorphous non-crystalline glass form (Form-ll) of azithromycin having relatively increased solubility without decreasing the structural stability thereof.
priorityDate 2009-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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