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177Lu-labeled-VG76e monoclonal antibody in tumor angiogenesis: A comparative study using DOTA and DTPA chelating systems

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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


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