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Preclinical Evaluation of (177)Lu-Nimotuzumab: A Potential Tool for Radioimmunotherapy of Epidermal Growth Factor Receptor-Overexpressing Tumors

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    SYSNO ASEP0365501
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitlePreclinical Evaluation of (177)Lu-Nimotuzumab: A Potential Tool for Radioimmunotherapy of Epidermal Growth Factor Receptor-Overexpressing Tumors
    Author(s) Beckford, Denis R. (UJF-V) RID
    Eigner, Sebastian (UJF-V) RID
    Beran, Miloš (UJF-V)
    Eigner-Henke, Kateřina (UJF-V) RID
    Lázníček, M. (CZ)
    Melichar, František (UJF-V) RID
    Chinol, M. (IT)
    Number of authors7
    Source TitleCancer Biotherapy and Radiopharmaceuticals - ISSN 1084-9785
    Roč. 26, č. 3 (2011), s. 287-297
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    KeywordsEGFR ; (177)Lu ; monoclonal antibodies ; Nimotuzumab
    Subject RIVFR - Pharmacology ; Medidal Chemistry
    R&D ProjectsOE08018 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z10480505 - UJF-V (2005-2011)
    UT WOS000292447100005
    DOI10.1089/cbr.2010.0916
    AnnotationBackground: The humanized monoclonal antibody Nimotuzumab (h-R3) has demonstrated an exceptional and better clinical profile than other monoclonal antibodies for immunotherapy of epidermal growth factor receptor-overexpressing tumors. This work deals with the preparation and radiolabeling optimization of (177)Lu-Nimotuzumab and their preclinical evaluation. Methods: Nimotuzumab was conjugated with S-2-(4-isothiocyanatobenzyl)-1,4,7,10-tetraazacyclododecane tetraacetic acid (p-SCN-Bn-DOTA), testing different molar ratios. The immunoconjugates were characterized. The radiolabeling with (177)Lu was optimized.
    WorkplaceNuclear Physics Institute
    ContactMarkéta Sommerová, sommerova@ujf.cas.cz, Tel.: 266 173 228
    Year of Publishing2012
Number of the records: 1  

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