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Improved radiosynthesis of the apoptosis marker 18F-ICMT11 including biological evaluation.

Abstract
We improved the specific radioactivity of the apoptosis imaging isatin derivative (18)F-ICMT11. We then evaluated (18)F-ICMT11 in EL4 tumor-bearing mice 24h after treatment with etoposide/cyclophosphamide combination therapy. Dynamic PET imaging demonstrated increased uptake in the drug-treated (0.115±0.011 SUV) compared to the vehicle-treated EL4 tumors (0.083±0.008 SUV). This effect correlated to the observed increases in apoptotic index.
AuthorsMatthias Glaser, Julian Goggi, Graham Smith, Matthew Morrison, Sajinder K Luthra, Edward Robins, Eric O Aboagye
JournalBioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 21 Issue 23 Pg. 6945-9 (Dec 01 2011) ISSN: 1464-3405 [Electronic] England
PMID22030029 (Publication Type: Journal Article)
CopyrightCopyright © 2011 Elsevier Ltd. All rights reserved.
Chemical References
  • (18)F-ICMT11
  • Azides
  • Biomarkers
  • Indoles
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • Isatin
Topics
  • Animals
  • Apoptosis
  • Azides (chemical synthesis, chemistry)
  • Biomarkers (chemistry)
  • Diagnostic Imaging
  • Disease Models, Animal
  • Fluorodeoxyglucose F18
  • Indoles (chemical synthesis, chemistry)
  • Isatin (chemistry)
  • Lymphoma (diagnostic imaging)
  • Mice
  • Molecular Structure
  • Positron-Emission Tomography
  • Radiopharmaceuticals (chemical synthesis, chemistry)

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