Evaluation of the influence of the conjugation site of the chelator agent HYNIC to GLP1 antagonist radiotracer for insulinoma diagnosis
dc.contributor.author | FAINTUCH, BLUMA L. | |
dc.contributor.author | SEO, DANIELE | |
dc.contributor.author | OLIVEIRA, ERICA A. de | |
dc.contributor.author | TARGINO, ROSELAINE C. | |
dc.contributor.author | MORO, ANA M. | |
dc.coverage | Internacional | pt_BR |
dc.date.accessioned | 2017-08-14T17:09:36Z | |
dc.date.available | 2017-08-14T17:09:36Z | |
dc.date.issued | 2017 | pt_BR |
dc.description.abstract | Background and Objective: Radiotracer diagnosis of insulinoma, can be done using somatostatin or glucagon-like peptide 1 (GLP-1). Performance of GLP-1 antagonists tends to be better than of agonists. Methods: We investigated the uptake of the antagonist exendin (9-39), radiolabeled with technetium-99m. Two different sites of the biomolecule were selected for chelator attachment. Results: HYNIC-beta Ala chelator attached to serine (C-terminus) of exendin, was associated with higher tumor uptake than to aspartate (N-terminus). Conclusion: The chelator position in the biomolecule influenced receptor uptake. | pt_BR |
dc.format.extent | 65-72 | pt_BR |
dc.identifier.citation | FAINTUCH, BLUMA L.; SEO, DANIELE; OLIVEIRA, ERICA A. de; TARGINO, ROSELAINE C.; MORO, ANA M. Evaluation of the influence of the conjugation site of the chelator agent HYNIC to GLP1 antagonist radiotracer for insulinoma diagnosis. <b>Current Radiopharmaceuticals</b>, v. 10, n. 1, p. 65-72, 2017. DOI: <a href="https://dx.doi.org/10.2174/1874471010666170126143636">10.2174/1874471010666170126143636</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/27705. | |
dc.identifier.doi | 10.2174/1874471010666170126143636 | pt_BR |
dc.identifier.fasciculo | 1 | pt_BR |
dc.identifier.issn | 1874-4729 | pt_BR |
dc.identifier.percentilfi | Sem Percentil | en |
dc.identifier.uri | http://repositorio.ipen.br/handle/123456789/27705 | |
dc.identifier.vol | 10 | pt_BR |
dc.relation.ispartof | Current Radiopharmaceuticals | pt_BR |
dc.rights | closedAccess | pt_BR |
dc.subject | tracer techniques | |
dc.subject | insulin | |
dc.subject | glucagon | |
dc.subject | peptide hormones | |
dc.subject | technetium 99 | |
dc.title | Evaluation of the influence of the conjugation site of the chelator agent HYNIC to GLP1 antagonist radiotracer for insulinoma diagnosis | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dspace.entity.type | Publication | |
ipen.autor | DANIELE SEO | |
ipen.autor | ERICA APARECIDA DE OLIVEIRA | |
ipen.autor | BLUMA LINKOWSKI FAINTUCH | |
ipen.codigoautor | 6400 | |
ipen.codigoautor | 9158 | |
ipen.codigoautor | 51 | |
ipen.contributor.ipenauthor | DANIELE SEO | |
ipen.contributor.ipenauthor | ERICA APARECIDA DE OLIVEIRA | |
ipen.contributor.ipenauthor | BLUMA LINKOWSKI FAINTUCH | |
ipen.date.recebimento | 17-08 | pt_BR |
ipen.identifier.fi | Sem F.I. | pt_BR |
ipen.identifier.ipendoc | 23933 | pt_BR |
ipen.identifier.iwos | WoS | pt_BR |
ipen.identifier.ods | 3 | |
ipen.type.genre | Artigo | |
relation.isAuthorOfPublication | c96def2e-d2f1-4481-8209-ed17f2ffc2e6 | |
relation.isAuthorOfPublication | 5389c24b-46b6-429c-9901-ced453124943 | |
relation.isAuthorOfPublication | e86aa86f-0601-4b44-aa7a-3ad168745a77 | |
relation.isAuthorOfPublication.latestForDiscovery | e86aa86f-0601-4b44-aa7a-3ad168745a77 | |
sigepi.autor.atividade | FAINTUCH, BLUMA L.:51:110:S | pt_BR |
sigepi.autor.atividade | SEO, DANIELE:6400:110:N | pt_BR |
sigepi.autor.atividade | OLIVEIRA, ERICA A. DE:9158:-1:N | pt_BR |
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