| Literature DB >> 28197310 |
Ai-Yan Ji1, Qiao-Mei Jin2, Dong-Jian Zhang2, Hua Zhu3, Chang Su1, Xing-Hua Duan1, Li Bian4, Zi-Ping Sun5, Yi-Cheng Ni6, Jian Zhang2, Zhi Yang3, Zhi-Qi Yin7.
Abstract
Rapid detection and precise evaluation of myocardial viability is necessary to aid in clinical decision making whether to recommend revascularization for patients with myocardial infarction (MI). Three novel 18F-labeled 1-hydroxyanthraquinone derivatives were synthesized, characterized, and evaluated as potential necrosis avid imaging agents for assessment of myocardial viability. Among these tracers, [18F]FA3OP emerged as the most promising compound with best stability and highest targetability. Clear PET images of [18F]FA3OP were obtained in rat model of myocardial infarction and reperfusion at 1 h after injection. In addition, the possible mechanisms of [18F]FA3OP for necrotic myocardium were discussed. The results showed [19F]FA3OP may bind DNA to achieve targetability to necrotic myocardium by intercalation. In summary, [18F]FA3OP was a more promising "hot spot imaging" tracer for rapid visualization of necrotic myocardium.Entities:
Keywords: 18F; Myocardial infarction; anthraquinone; necrosis avid agents; positron emission tomography
Year: 2016 PMID: 28197310 PMCID: PMC5304286 DOI: 10.1021/acsmedchemlett.6b00398
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345