<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zajicek F</submitter><funding>Universiteit Antwerpen</funding><funding>CHDI Foundation</funding><funding>Research Foundation Flanders</funding><pagination>122-133</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11599348</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>52(1)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Positron emission tomography (PET) imaging of mutant huntingtin (mHTT) aggregates is a potential tool to monitor disease progression as well as the efficacy of candidate therapeutic interventions for Huntington's disease (HD). To date, the focus has been mainly on the investigation of &lt;sup>11&lt;/sup>C radioligands; however, favourable &lt;sup>18&lt;/sup>F radiotracers will facilitate future clinical translation. This work aimed at characterising the novel [&lt;sup>18&lt;/sup>F]CHDI-650 PET radiotracer using a combination of in vivo and in vitro approaches in a mouse model of HD.&lt;h4>Methods&lt;/h4>After characterising [&lt;sup>18&lt;/sup>F]CHDI-650 using in vitro autoradiography, we assessed in vivo plasma and brain radiotracer stability as well as kinetics through dynamic PET imaging in the heter</pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>Preclinical evaluation of the novel [&amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F]CHDI-650 PET ligand for non-invasive quantification of mutant huntingtin aggregates in Huntington's disease.</pubmed_title><pmcid>PMC11599348</pmcid><funding_grant_id>1229721N</funding_grant_id><funding_grant_id>FFB210050</funding_grant_id><funding_grant_id>A-11627</funding_grant_id><pubmed_authors>Munoz-Sanjuan I</pubmed_authors><pubmed_authors>Staelens S</pubmed_authors><pubmed_authors>Bertoglio D</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>De Lombaerde S</pubmed_authors><pubmed_authors>Verhaeghe J</pubmed_authors><pubmed_authors>Van Eetveldt A</pubmed_authors><pubmed_authors>Bard J</pubmed_authors><pubmed_authors>Dominguez C</pubmed_authors><pubmed_authors>Miranda A</pubmed_authors><pubmed_authors>Zajicek F</pubmed_authors><pubmed_authors>Khetarpal V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preclinical evaluation of the novel [&amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F]CHDI-650 PET ligand for non-invasive quantification of mutant huntingtin aggregates in Huntington's disease.</name><description>&lt;h4>Purpose&lt;/h4>Positron emission tomography (PET) imaging of mutant huntingtin (mHTT) aggregates is a potential tool to monitor disease progression as well as the efficacy of candidate therapeutic interventions for Huntington's disease (HD). To date, the focus has been mainly on the investigation of &lt;sup>11&lt;/sup>C radioligands; however, favourable &lt;sup>18&lt;/sup>F radiotracers will facilitate future clinical translation. This work aimed at characterising the novel [&lt;sup>18&lt;/sup>F]CHDI-650 PET radiotracer using a combination of in vivo and in vitro approaches in a mouse model of HD.&lt;h4>Methods&lt;/h4>After characterising [&lt;sup>18&lt;/sup>F]CHDI-650 using in vitro autoradiography, we assessed in vivo plasma and brain radiotracer stability as well as kinetics through dynamic PET imaging in the heter</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-22T14:24:11.324Z</modification><creation>2025-04-06T01:00:19.722Z</creation></dates><accession>S-EPMC11599348</accession><cross_references><pubmed>39190197</pubmed><doi>10.1007/s00259-024-06880-x</doi></cross_references></HashMap>