Meeting Banner
Abstract #4347

Comparison of Three MRI Molecular Imaging Modalities: Application to Angiogenesis Imaging in a Brain Tumor Mouse Model

Cline Giraudeau1, Benjamin Marty1, Julien Flament1, Franoise Geffroy1, Christelle Mdina2, Philippe Robert2, Caroline Robic2, Marc Port2, Denis Le Bihan1,

1NeuroSpin, I2BM, Commissariat l'Energie Atomique, Gif-sur-Yvette, France; 2Guerbet, Research Division, Roissy-Charles de Gaulle, France

In the present work, three different contrast agents (CA) are evaluated: Gd-based emulsion, LipoCEST and fluorine emulsion. A comparison of the three modalities sensitivity and specificity is performed on a mouse model of brain tumor using CA grafted with RGD peptides to specifically target α ν β 3 integrins over-expressed in angiogenic vessels. CA are detected with a sub-nanomolar sensitivity by the three modalities. A higher contrast is systematically observed for RGD contrast agents inside the tumor. Each modality provides additional information, promising for multimodal investigation of brain diseases.

Keywords

acquisitions additional advantages agent agents allows animal animals application ascribed association asymmetric behavior best blue brain carried cells characteristics chem cohort commissariat compromise concentration concentrations conditions contrast contrasts course courses curve decrease derived detected detection development direct diseases division emulsion emulsions endogenous ensure evaluated even example exhibiting experimental expressed finally flowing fluorine grafted half hampered highlighting illustrated induced inhomogeneities injection insensitive inside investigation knowledge lack leads life limitations linearity lowest magnetization mapping maps materials mice modalities modality model molecular moreover mouse nevertheless nude offer opened optimized paramagnetic partial peak peptides plateau port preceded principles probably promising quantification quite rapidly reached recent remove resolution respectively rodent saturation scanner seems sensitive sensitivity shorter significantly slice sorted spatial specifically specificity specified suffers summarized surface systematically table target targeted thanks transfer tumor tumors untypical vessels vitro volume