The lack of a naturally occurring background signal from fluorine in m
agnetic resonance (MR) imaging makes fluorinated compounds potentially
attractive candidates for tissue-specific MR contrast agents. Problem
s associated with the in vivo use of fluorinated compounds are toxicit
y, which limits the amount of agent that can be used; multiple resonan
ce lines; and an excessively long T1, which leads to long sequence TRs
and consequently long imaging times. Many fluorinated agents also pos
sess complex MR spectra that result in chemical shift artifacts if not
corrected. The authors demonstrate the use of an extracellular fluori
nated agent with a single MR peak for selective imaging of a brain abs
cess in an animal model and show that the image signal per unit of acq
uisition time can be enhanced through the use of a T1 relaxation agent
, gadolinium diethylenetriamine-pentaacetic acid (DTPA). Trifluorometh
ylsulfonate was administered at a fluorine-19 dose of 4 mmol/kg, and f
luorine images of the induced abscess were acquired before and after t
he injection of a standard dose of Gd-DTPA (0.1 mmol/kg); non-section-
selected projection images were used. Typical imaging times were less
than 5 minutes. The signal enhancement factor achieved was approximate
ly four (4.0 +/- 0.8) with use of a 500/12 (TR msec/TE msec) spin-echo
sequence.