A fully automated two-step synthesis of an 18F-labelled tyrosine kinase 
inhibitor for EGFR kinase activity imaging in tumors

Kobus, Diana; Giesen, Yvonne; Ullrich, Roland; Backes, Heiko; Neumaier, Bernd

doi:10.1016/j.apradiso.2009.07.018

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A fully automated two-step synthesis of an 18F-labelled tyrosine kinase inhibitor for EGFR kinase activity imaging in tumors

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Kobus, Diana
Radiochemistry, Scientific Services and Development, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Giesen, Yvonne
Radiochemistry, Scientific Services and Development, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Ullrich, Roland
Klinisches PET, Neurologische Abteilung, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Backes, Heiko
Multimodal Imaging of Brain Metabolism, Research Groups, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;
Gentherapie und Molekulare Bildgebung, Neurologische Abteilung, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Neumaier, Bernd
Radiochemistry, Scientific Services and Development, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Citation

Kobus, D., Giesen, Y., Ullrich, R., Backes, H., & Neumaier, B. (2009). A fully automated two-step synthesis of an 18F-labelled tyrosine kinase inhibitor for EGFR kinase activity imaging in tumors. Applied Radiation and Isotopes, 67(11), 1977-1984. doi:10.1016/j.apradiso.2009.07.018.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0026-D20B-C