6533b831fe1ef96bd1298c7d

RESEARCH PRODUCT

Bimodal tracers synthesis for medical imaging PET/MRI

Sybille Kennel

subject

Chimie «click» catalysée au ruthéniumFluorine 18Fluor 18GadoliniumBimodal TracerDO3APETTEP[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingGallium 68Traceurs bimodauxRuthenium catalyzed « click » chemistryMRIIRM

description

Today physicians can use a wide variety of medical imaging techniques to establish early and accurate diagnosis. Nevertheless, each modality has its own advantages and drawbacks. This is why bi- or multimodality approach seems interesting. Among them, PET/MRI combination seems very promising because it can bring complementary informations. It is therefore necessary to inject to patients tracers specific to each imaging modality. This work described the synthesis of molecular platforms for MRI and PET imaging, according to 2 different strategies. The first one consisted in the synthesis of a DO3A macrocycle allowing the chelation of both gadolinium for MRI and gallium 68 for PET. The aim here is to have a bimodal probe, with a mixture of each compound. The second strategy was the preparation of a single molecule that can be simultaneously labeled by both gadolinium for MRI and fluorine 18 for PET. The final goal is to introduce onto these platforms a biomolecule in a versatile and easy way, to be able to target a specific pathophysiological process. ‘‘Click’’ chemistry seems to be an attractive methodology to achieve this goal. However, this reaction, usually catalyzed with copper is not suitable to DO3A macrocyles due to the copper affinity with those azamacrocycles. This issue has been circumvent by the use of ruthenium catalyzed ‘‘click’’ chemistry. We were then able to access to both macrocycles platforms.

https://theses.hal.science/tel-01249613