http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2794581-T3

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filingDate 2016-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31ad8e8030b1251e0230267b96dd64ce
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publicationDate 2020-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2794581-T3
titleOfInvention Procedures and kits for preparing radionuclide complexes
abstract A process for preparing a complex comprising a gallium radioisotope for use in radiotherapy or in a medical imaging procedure, said process comprising adding a gallium radioisotope solution obtained directly from a gallium radionuclide generator to a composition comprising a pharmaceutically acceptable buffer, and optionally also a pharmaceutically acceptable basic reagent, in amounts sufficient to increase the pH to a level in the range of 3 to 8, wherein The composition further comprises a chelator that is capable of chelating radioactive gallium within said pH range and at a moderate temperature, said chelator being optionally linked to a target biological agent, wherein said chelator is selected from deferoxamine B (DFO), acid bis (2-hydroxybenzyl) ethylenediamine diacetic acid (HBED), 1,4,7-triacyclononane macrocycle substituted with phosph groups ionic in amines (NOTP), or a compound of formula (I) ** (See formula) ** or a salt thereof; wherein one of X and Y is C = 0 and the other is NR; wherein each m and p are independently selected from 0 to 6; wherein R1 is a chelating group capable of chelating a radionuclide and is selected from: ** (See formula) ** wherein R, R2, R3 and R4 are independently hydrogen or an optionally substituted C1-7 alkyl group; and where Z is hydrogen or a group of the formula -B'-H, -B'-A, or a group -B'-A * -T, where T is a target group capable of binding to a target of interest in a subject; A is a reactive group that allows coupling to group T, A * is a reactive group A that has reacted; B 'is a linking group to link the chelating group with a reactive group A, and is represented by the formula: ** (See formula) ** in which each Q is independently selected from a group consisting of -NR5- , -C (O) NR5-, -C (O) O, -NR5C (O) NR5-, -NR5C (S) NR5- and -0-, each R5 is independently hydrogen or an optionally substituted C1-7 alkyl group , each q and s are independently selected from 0 to 6 and each r is independently selected from 1 to 6.
priorityDate 2015-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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