Affiliation:
1. Department of Chemistry University of Wisconsin‐Madison Madison Wisconsin USA
2. Department of Medical Physics University of Wisconsin‐Madison Madison Wisconsin USA
3. School of Pharmacy University of Wisconsin‐Madison Madison Wisconsin USA
4. Department of Radiology University of Iowa Iowa City Iowa USA
Abstract
AbstractMagnetic resonance imaging (MRI) is a routine diagnostic modality in oncology that produces excellent imaging resolution and tumor contrast without the use of ionizing radiation. However, improved contrast agents are still needed to further increase detection sensitivity and avoid toxicity/allergic reactions associated with paramagnetic metal contrast agents, which may be seen in a small percentage of the human population. Fluorine‐19 (19F)‐MRI is at the forefront of the developing MRI methodologies due to near‐zero background signal, high natural abundance of 100%, and unambiguous signal specificity. In this study, we have developed a colloidal nanoemulsion (NE) formulation that can encapsulate high volumes of the fluorous MRI tracer, perfluoro‐[15‐crown‐5]‐ether (PFCE) (35% v/v). These nanoparticles exhibit long‐term (at least 100 days) stability and high PFCE loading capacity in formulation with our semifluorinated triblock copolymer, M2F8H18. With sizes of approximately 200 nm, these NEs enable in vivo delivery and passive targeting to tumors. Our diagnostic formulation, M2F8H18/PFCE NE, yielded in vivo 19F‐MR images with a high signal‐to‐noise ratio up to 100 in a tumor‐bearing mouse model at clinically relevant scan times. M2F8H18/PFCE NE circulated stably in the vasculature, accumulated in high concentration of an estimated 4–9 × 1017 19F spins/voxel at the tumor site, and cleared from most organs over the span of 2 weeks. Uptake by the mononuclear phagocyte system to the liver and spleen was also observed, most likely due to particle size. These promising results suggest that M2F8H18/PFCE NE is a favorable 19F‐MR diagnostic tracer for further development in oncological studies and potential clinical translation.
Funder
National Institutes of Health
National Science Foundation