Meeting Banner
Abstract #4221

In Vivo Detection of ParaCEST Contrast Agents at 9.4T

Nevin McVicar1, Alex Li2, Mojmir Suchy, 23, Robert H.E Hudson3, Robert Bartha, 12

1Medical Biophysics, University of Western Ontario, London, ON, Canada; 2Imaging Research Group, Robarts Research Insitute, London, ON, Canada; 3Chemistry, University of Western Ontario, London, ON, Canada

In vitro properties are characterized for four paraCEST contrast agents. Each paraCEST agent was then individually injected directly into a mouse leg prior to immediate acquisition of CEST spectra. All four agents were detected in vivo. Using the properties measured in vitro along with the paraCEST contrast measured in vivo, it is concluded that in vivo performance can be predicted based on in vitro characterization of the MR properties of each agent.

Keywords

according achieved achieving acquisition agent agents alto amide anatomical animal appear appeared appears applications approved aqueous audience began biophysics bore bound built capabilities caused characterization chemical chemistry chemists clear coil compatible constants containing content contrast custom decrease described detected detection developing directly dissolved either endogenous equipped especially evaluate exchange expected experiment fast finding forward frequencies generate generated generation greater healthy horizontal identical in vivo included injected injection insight interestingly inversion john lifetime lifetimes limited local long macromolecules magnetization maps measured medical medicine mice millipede minutes motion mouse muscle noise omega optimization paramagnetic performance phantoms physicists pixels plots post powers preceded precession predicted prepared previously probability procedures produce properties protocol protons pulse real reasonable recovery reduced relatively representative represents resolution restrict saturation scanner scientists secured sensitivity sherry short significantly site slice sons spectra spectrum spin stage steady step studies subcommittee suggests superimposed surface synthesis table target transfer vary vitro volume water wave western whether