Abstract
Tryptophan (Trp)-based radiotracers have excellent potential for imaging many different types of brain pathology because of their involvement with both the serotonergic and kynurenine (KYN) pathways. However, radiotracers specific to the kynurenine metabolism pathway are limited. In addition, historically Trp-based radiopharmaceuticals were synthesized with the short-lived isotope carbon-11. A newer generation of Trp-based imaging agents using the longer half-lived and commercially available isotopes, such as fluorine-18 and iodine-124, are being developed. The newly developed amino acid-based tracers have been demonstrated to have favorable radiochemical and imaging characteristics in pre-clinical studies. However, many barriers still exist in the clinical translation of KYN pathway-specific radiotracers.
Funding Information
  • Diagnostic & Research PET/MRI Center, Department of Research, and Department of Radiology at Nemours Children’s Health, Wilmington, Delaware (P20GM103446, P20GM103446-23S6, EB032025, R01 CA263216)
  • National Institutes of Health (P20GM103446, P20GM103446-23S6, EB032025, R01 CA263216)
  • National Institute of Biomedical Imaging and Bioengineering (NIBIB) (P20GM103446, P20GM103446-23S6, EB032025, R01 CA263216)
  • NIH (P20GM103446, P20GM103446-23S6, EB032025, R01 CA263216)

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