<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31(2)</volume><submitter>Xu X</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Epidermal growth factor receptor (EGFR) is overexpressed in a wide variety of solid tumors, serving as a well-characterized target for cancer imaging or therapy. In this study, we aimed to design and synthesize a radiotracer, &lt;sup>64&lt;/sup>Cu-NOTA-C225, targeting EGFR for tumor positron emission tomography (PET) imaging.&lt;h4>Methods&lt;/h4>Cetuximab (C225) was conjugated to a bifunctional chelator, p-isothiocyanatobenzyl-1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA), and further radiolabeled with copper-64 for PET imaging. &lt;sup>64&lt;/sup>Cu-NOTA-IgG and Cy5.5-C225 were also synthesized as control probes. A431 and A549 mouse models were established for micro-PET and/or near-infrared fluorescence (NIRF) imaging.&lt;h4>Results&lt;/h4>&lt;sup>64&lt;/sup>Cu-NOTA-C225 exhibited stability &lt;i</pubmed_abstract><journal>Chinese journal of cancer research = Chung-kuo yen cheng yen chiu</journal><pagination>400-409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6513748</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and evaluation of &lt;sup>64&lt;/sup>Cu-radiolabeled NOTA-cetuximab (&lt;sup>64&lt;/sup>Cu-NOTA-C225) for immuno-PET imaging of EGFR expression.</pubmed_title><pmcid>PMC6513748</pmcid><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Xia L</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Xie Q</pubmed_authors><pubmed_authors>Liu F</pubmed_authors><pubmed_authors>Li N</pubmed_authors><pubmed_authors>Xin Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and evaluation of &lt;sup>64&lt;/sup>Cu-radiolabeled NOTA-cetuximab (&lt;sup>64&lt;/sup>Cu-NOTA-C225) for immuno-PET imaging of EGFR expression.</name><description>&lt;h4>Objective&lt;/h4>Epidermal growth factor receptor (EGFR) is overexpressed in a wide variety of solid tumors, serving as a well-characterized target for cancer imaging or therapy. In this study, we aimed to design and synthesize a radiotracer, &lt;sup>64&lt;/sup>Cu-NOTA-C225, targeting EGFR for tumor positron emission tomography (PET) imaging.&lt;h4>Methods&lt;/h4>Cetuximab (C225) was conjugated to a bifunctional chelator, p-isothiocyanatobenzyl-1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA), and further radiolabeled with copper-64 for PET imaging. &lt;sup>64&lt;/sup>Cu-NOTA-IgG and Cy5.5-C225 were also synthesized as control probes. A431 and A549 mouse models were established for micro-PET and/or near-infrared fluorescence (NIRF) imaging.&lt;h4>Results&lt;/h4>&lt;sup>64&lt;/sup>Cu-NOTA-C225 exhibited stability &lt;i</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2026-06-01T06:32:31.43Z</modification><creation>2026-04-08T10:01:33.95Z</creation></dates><accession>S-EPMC6513748</accession><cross_references><pubmed>31156310</pubmed><doi>10.21147/j.issn.1000-9604.2019.02.14</doi></cross_references></HashMap>