<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Khosravifarsani M</submitter><pubmed_abstract>To overcome resistance to chemotherapy for colorectal cancer, we propose to validate &lt;i>in vivo&lt;/i> a novel terpyridine-platinum (TP) compound radiolabeled with the radio-theranostic isotope &lt;sup>64&lt;/sup>Cu. &lt;i>In vivo&lt;/i> stability, biodistribution, PET imaging, tumor growth delay, toxicity and dosimetry of [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP were determined. The current experimental studies show that [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP is stable &lt;i>in vivo&lt;/i>, rapidly eliminated by the kidneys and has a promising tumor uptake ranging from 1.8 ± 0.4 to 3.0 ± 0.2 %ID/g over 48 h. [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP retarded tumor growth by up to 6 ± 2.0 days and improved survival relative to vehicle and non-radioactive [&lt;sup>Nat&lt;/sup>Cu]NOTA-C3-TP over 17 days of tumor growth observation. This effect was obtaine</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>975213</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9549809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>In vivo&lt;/i> behavior of [&lt;sup>64&lt;/sup>Cu]NOTA-terpyridine platinum, a novel chemo-radio-theranostic agent for imaging, and therapy of colorectal cancer.</pubmed_title><pmcid>PMC9549809</pmcid><pubmed_authors>Ait-Mohand S</pubmed_authors><pubmed_authors>Paquette B</pubmed_authors><pubmed_authors>Sanche L</pubmed_authors><pubmed_authors>Khosravifarsani M</pubmed_authors><pubmed_authors>Guerin B</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>In vivo&lt;/i> behavior of [&lt;sup>64&lt;/sup>Cu]NOTA-terpyridine platinum, a novel chemo-radio-theranostic agent for imaging, and therapy of colorectal cancer.</name><description>To overcome resistance to chemotherapy for colorectal cancer, we propose to validate &lt;i>in vivo&lt;/i> a novel terpyridine-platinum (TP) compound radiolabeled with the radio-theranostic isotope &lt;sup>64&lt;/sup>Cu. &lt;i>In vivo&lt;/i> stability, biodistribution, PET imaging, tumor growth delay, toxicity and dosimetry of [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP were determined. The current experimental studies show that [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP is stable &lt;i>in vivo&lt;/i>, rapidly eliminated by the kidneys and has a promising tumor uptake ranging from 1.8 ± 0.4 to 3.0 ± 0.2 %ID/g over 48 h. [&lt;sup>64&lt;/sup>Cu]NOTA-C3-TP retarded tumor growth by up to 6 ± 2.0 days and improved survival relative to vehicle and non-radioactive [&lt;sup>Nat&lt;/sup>Cu]NOTA-C3-TP over 17 days of tumor growth observation. This effect was obtaine</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T21:41:13.435Z</modification><creation>2025-04-04T21:41:13.435Z</creation></dates><accession>S-EPMC9549809</accession><cross_references><pubmed>36226156</pubmed><doi>10.3389/fmed.2022.975213</doi></cross_references></HashMap>