| Literature DB >> 19027307 |
E B de Araújo1, J S Caldeira Filho, L T Nagamati, E Muramoto, M T Colturato, R M Couto, P B Pujatti, J Mengatti, C P G Silva.
Abstract
This work analysed the influence of the chelating group and radioligand on somatostatin analogues in vivo and in vitro properties. The presence of DOTA in the radioiodinated peptide produced a labeled analogue with similar blood kinetics and biodistribution to (177)Lu-DOTATATE and with lower abdominal uptake than (131)I-TATE. In addition, (131)I-DOTATATE showed significative tumour uptake, despite not so persistent after 24h. (131)I-DOTATATE can represent a cost-effective alternative to lutetium labeled peptide for neuroendocrine tumours therapy.Entities:
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Year: 2008 PMID: 19027307 DOI: 10.1016/j.apradiso.2008.09.009
Source DB: PubMed Journal: Appl Radiat Isot ISSN: 0969-8043 Impact factor: 1.513