Affiliation:
1. Universität Heidelberg Anorganisch-Chemisches Institut and Interdisciplinary Center for Scientific Computing, INF 270, D- 69120 Heidelberg Germany
2. Life Sciences Division TRIUMF 4004 Wesbrook Mall Vancouver V6T 2A3 British Columbia Canada
3. Medicinal Inorganic Chemistry Group University of British Columbia Department of Chemistry 2036 Main Mall Vancouver V6T 1Z1 British Columbia Canada
Abstract
AbstractThe synthesis of the octadentate bispidine ligand bearing two picolinic acid pendant arms (H2bispa2), and its coordination chemistry with radionuclides relevant for nuclear medicine, namely indium(III) (111In), lutetium(III) (177Lu), and lanthanum(III) (as surrogate for 225Ac), are reported. The non‐radioactive metal complexes of the N6O2‐type bispa ligand were characterized by 1H and 13C NMR spectroscopy, elemental analysis, mass spectrometry and single‐crystal X‐ray analysis. Experimental structural data, computational analysis, complex stabilities determined by potentiometric titration, and “radiostabilities” determined by competition studies in the presence of human serum reveal complex stabilities of H2bispa2 comparable to those of the macrocyclic “gold standard” DOTA. After an incubation time of 1 day, 86 and 87 % of [177Lu(bispa2)]+ and [177Lu(DOTA)]−, respectively, remain intact. Importantly, unlike DOTA, H2bispa2 is radiolabeled quantitatively with 111InIII and 225AcIII under ambient conditions, which is an essential aspect when working with heat‐sensitive antibodies as targeting vectors. In the case of 111InIII, room temperature radiolabeling of H2bispa2 yields molar activities as high as 70 MBq nmol−1 within 10 minutes. These are promising results for radiopharmaceutical applications of H2bispa2.
Funder
Universität Heidelberg
Natural Sciences and Engineering Research Council of Canada
Canada Council for the Arts
Alexander von Humboldt-Stiftung
Cited by
75 articles.
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