dc.contributor.author |
Fani, M |
en |
dc.contributor.author |
Bouziotis, P |
en |
dc.contributor.author |
Harris, AL |
en |
dc.contributor.author |
Psimadas, D |
en |
dc.contributor.author |
Gourni, E |
en |
dc.contributor.author |
Loudos, G |
en |
dc.contributor.author |
Varvarigou, AD |
en |
dc.contributor.author |
Maecke, HR |
en |
dc.date.accessioned |
2014-03-01T01:26:33Z |
|
dc.date.available |
2014-03-01T01:26:33Z |
|
dc.date.issued |
2007 |
en |
dc.identifier.issn |
0033-8230 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/18133 |
|
dc.subject |
Angiogenesis |
en |
dc.subject |
DOTA |
en |
dc.subject |
DTPA |
en |
dc.subject |
Lutetium-177 |
en |
dc.subject |
Monoclonal antibodies |
en |
dc.subject |
VEGF |
en |
dc.subject.classification |
Chemistry, Inorganic & Nuclear |
en |
dc.subject.classification |
Nuclear Science & Technology |
en |
dc.subject.other |
ENDOTHELIAL GROWTH-FACTOR |
en |
dc.subject.other |
CANCER-THERAPY |
en |
dc.subject.other |
NUDE-MICE |
en |
dc.subject.other |
RADIOIMMUNOTHERAPY |
en |
dc.subject.other |
BIODISTRIBUTION |
en |
dc.subject.other |
VEGF |
en |
dc.subject.other |
Y-90 |
en |
dc.subject.other |
BEVACIZUMAB |
en |
dc.subject.other |
INHIBITION |
en |
dc.subject.other |
STABILITY |
en |
dc.title |
177Lu-labeled-VG76e monoclonal antibody in tumor angiogenesis: A comparative study using DOTA and DTPA chelating systems |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1524/ract.2007.95.6.351 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1524/ract.2007.95.6.351 |
en |
heal.language |
English |
en |
heal.publicationDate |
2007 |
en |
heal.abstract |
Vascular Endothelial Growth Factor (VEGF) is one of the molecules which regulate angiogenesis, a phenomenon observed in many diseases, including cancer. VG76e, an anti-VEGF monoclonal antibody, was labeled with 177Lu via p-SCN-Bz-DOTA and CHX-A″-DTPA chelating systems, in order to investigate its possible therapeutic use. Labeling was performed by a 30 min incubation of 177LuCl3 and each immunoconjugate, at 37°C. Radiochemical analysis showed the formation of a single radioactive species, at a yield higher than 98%, for both immunoconjugates. Kits have been formulated for both VG76e-DOTA and VG76e-DTPA. Stability studies, in the presence of a competitor excess, showed that both radiolabeled species remained sufficiently stable (95%) for at least 48 h. Biodistribution results in normal mice were similar for both radioimmunoconjugates, with no significant bone uptake. Gamma camera images of tumor-bearing mice showed satisfactory visualization of the tumor 24 h p.i., while a higher uptake was observed at 48 h p.i. Our findings indicate that both the bifunctional chelating agents p-SCN-Bz-DOTA and CHX-A″-DTPA can be used for the labeling of VG76e with 177Lu, with high labeling yield and stability. Their in vivo behaviour in normal and tumor-bearing mice looks promising and they can be successfully used for tumor imaging studies. © by Oldenbourg Wissenschaftsverlag. |
en |
heal.publisher |
OLDENBOURG VERLAG |
en |
heal.journalName |
Radiochimica Acta |
en |
dc.identifier.doi |
10.1524/ract.2007.95.6.351 |
en |
dc.identifier.isi |
ISI:000247310700008 |
en |
dc.identifier.volume |
95 |
en |
dc.identifier.issue |
6 |
en |
dc.identifier.spage |
351 |
en |
dc.identifier.epage |
357 |
en |