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Appl Radiat Isot ; 197: 110819, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37119703

RESUMO

This project focuses on the generation and evaluation of functional alternatives to radiometal-based pharmaceuticals supporting basic research and the in vitro developmental phase. Employing robust tritium chemistry and non-radioactive metal surrogates in two synthetic and labeling strategies resulted in ([ring-3H]Nal)PSMA-617 and ([α,ß-3H]Nal)PSMA-617. In particular, ([α,ß-3H]Nal)Lu-PSMA-617 exhibited high radiolytic as well as metal-complex stability and was compared to the clinically-established radiopharmaceutical [177Lu]Lu-PSMA-617. The cell-based assays confirmed the applicability of ([α,ß-3H]Nal)Lu-PSMA-617 as a substitute of [177Lu]Lu-PSMA-617 in pre-clinical biological settings.


Assuntos
Glutamato Carboxipeptidase II , Neoplasias de Próstata Resistentes à Castração , Masculino , Humanos , Trítio , Dipeptídeos , Compostos Radiofarmacêuticos , Compostos Heterocíclicos com 1 Anel , Preparações Farmacêuticas , Lutécio
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