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Preclinical evaluation of (177)lu-nimotuzumab: a potential tool for radioimmunotherapy of epidermal growth factor receptor-overexpressing tumors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F11%3A00003553" target="_blank" >RIV/00216208:11120/11:00003553 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389005:_____/11:00365501 RIV/00216208:11160/11:10100351

  • Result on the web

    <a href="http://dx.doi.org/10.1089/cbr.2010.0916" target="_blank" >http://dx.doi.org/10.1089/cbr.2010.0916</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1089/cbr.2010.0916" target="_blank" >10.1089/cbr.2010.0916</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Preclinical evaluation of (177)lu-nimotuzumab: a potential tool for radioimmunotherapy of epidermal growth factor receptor-overexpressing tumors

  • Original language description

    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. 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. Radioimmunoconjugates stability was tested in 2-[bis[2-[bis(carboxymethyl)amino]ethyl]amino]acetic acid (DTPA) excess and human serum. In vitro studies were performed intumor model cell lines. Receptor-specific binding was tested by competitive inhibition. (177)Lu-Nimotuzumab in vivo studies were conducted in healthy and xenograft animals. (177)Lu-Nimotuzumab was obtained with high purity and specific a

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/OE08018" target="_blank" >OE08018: Radionuclide precursors and radiopharmaceuticals for targeted radionuclide imaging and therapy</a><br>

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Cancer Biotherapy and Radiopharmaceuticals

  • ISSN

    1084-9785

  • e-ISSN

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    287-297

  • UT code for WoS article

    000292447100005

  • EID of the result in the Scopus database