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filingDate 2009-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2011-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2011514334-A
titleOfInvention Methods for preparing pharmaceutical formulations of contrast agents
abstract The present invention relates to a complex of a macrocyclic chelate compound and a lanthanide, between 0.002% and 0.4%, preferably between 0.02% and 0.3%, very preferably from 0.002%. The present invention relates to a method for preparing a liquid pharmaceutical formulation containing between 025% and 0.25% mol / mole of free macrocyclic chelate, preferably a macrocyclic chelate, preferably DOTA, NOTA , DOTAGA, DO3A, BT-DO3A, HP-DO3A and PCTA, preferably DOTA, wherein the method comprises the following sequential steps: b) First, a complex of a macrocyclic chelate compound and a lanthanide; Second, preparing a liquid pharmaceutical composition containing a free macrocyclic chelate compound and / or a free lanthanide; c) free large amount in the pharmaceutical preparation obtained in step b) Step measuring the concentration C ch 1 and / or concentration C lan 1 free lanthanide Jo chelate compound; d) wherein, C t ch 1 is at a target concentration of free macrocyclic chelate in the final liquid pharmaceutical formulation Adjusting C ch 1 and / or C lan 1 such that C ch 1 = C t ch 1 and C lan 1 = 0 are obtained.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11400172-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017535553-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018538358-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016117778-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016521275-A
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priorityDate 2008-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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