<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang YY</submitter><funding>Ministry of Science and Technology, Taiwan</funding><pagination>e0217384</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6602418</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>[18F]T807 is a potent tau protein imaging agent. In order to fulfill the demand from preclinical and clinical studies, we developed an automated one-pot two-step synthesis of this potent tau imaging agent and studied its stability, and dosimetry in mice and monkeys. We also conducted a preliminary study of this imaging agent in humans. Using this one-pot two-step method, the radiochemical yield (RCY) of [18F]T807 was 20.5 ± 6.1% (n = 15) at the end of bombardment (EOB) in a synthesis time of 70±5 min. The chemical and radiochemical purities were >90% and the specific activities were 151 ± 52 GBq/μmol. The quality of [18F]T807 synthesized by this method met the U.S. Pharmacopoeia (USP) criteria. The stability test showed that the [18F]T807 injection was stable at room temperature for up to </pubmed_abstract><journal>PloS one</journal><pubmed_title>An one-pot two-step automated synthesis of [18F]T807 injection, its biodistribution in mice and monkeys, and a preliminary study in humans.</pubmed_title><pmcid>PMC6602418</pmcid><funding_grant_id>MOST 106-2321-B-002-018</funding_grant_id><pubmed_authors>Cheng CY</pubmed_authors><pubmed_authors>Ma KH</pubmed_authors><pubmed_authors>Huang YY</pubmed_authors><pubmed_authors>Chiu CH</pubmed_authors><pubmed_authors>Yen RF</pubmed_authors><pubmed_authors>Hsin LW</pubmed_authors><pubmed_authors>Tzen KY</pubmed_authors><pubmed_authors>Shiue CY</pubmed_authors><pubmed_authors>Wu CH</pubmed_authors><pubmed_authors>Chiu MJ</pubmed_authors><pubmed_authors>Tsai CL</pubmed_authors><pubmed_authors>Hsieh HY</pubmed_authors></additional><is_claimable>false</is_claimable><name>An one-pot two-step automated synthesis of [18F]T807 injection, its biodistribution in mice and monkeys, and a preliminary study in humans.</name><description>[18F]T807 is a potent tau protein imaging agent. In order to fulfill the demand from preclinical and clinical studies, we developed an automated one-pot two-step synthesis of this potent tau imaging agent and studied its stability, and dosimetry in mice and monkeys. We also conducted a preliminary study of this imaging agent in humans. Using this one-pot two-step method, the radiochemical yield (RCY) of [18F]T807 was 20.5 ± 6.1% (n = 15) at the end of bombardment (EOB) in a synthesis time of 70±5 min. The chemical and radiochemical purities were >90% and the specific activities were 151 ± 52 GBq/μmol. The quality of [18F]T807 synthesized by this method met the U.S. Pharmacopoeia (USP) criteria. The stability test showed that the [18F]T807 injection was stable at room temperature for up to </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-22T20:30:17.632Z</modification><creation>2019-07-25T07:01:33Z</creation></dates><accession>S-EPMC6602418</accession><cross_references><pubmed>31260447</pubmed><doi>10.1371/journal.pone.0217384</doi></cross_references></HashMap>