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Pharmacokinetics of [18F]FETNIM: A Potential Hypoxia Marker for PET

Tove Grönroos, Olli Eskola, Kaisa Lehtiö, Heikki Minn, Päivi Marjamäki, Jörgen Bergman, Merja Haaparanta, Sarita Forsback and Olof Solin

Medicity Research Laboratory and Radiopharmaceutical Chemistry Laboratory, Turku PET Centre, Turku; and Department of Oncology and Radiotherapy, Turku University Central Hospital, Turku, Finland



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FIGURE 1. Radiochemical synthesis of [18F]FETNIM from 1-(2'-nitro-1'-imidazolyl)-2,3-O-isopropylidene-4-tosyloxybutane.

 


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FIGURE 2. Typical chromatograms of rat and human tissues as detected by radio-TLC and digital autoradiography. Human plasma sample was analyzed at 30 min after injection of [18F]FETNIM, whereas rat tumor and liver samples were analyzed at 60 min. Radiochromatograms of rat and human plasma were qualitatively and quantitatively similar. arb. = arbitrary.

 


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FIGURE 3. Relationship between percentage of unchanged [18F]FETNIM and uptake in DMBA-induced rat tumors. Poor correlation was observed at early times (A and B), but, at later time, significant inverse correlation was found (C).

 





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