Contrast enhancement in liver MR can be achieved by a variety of funda
mentally different strategies. The published clinical literature regar
ding Gd DTPA (gadopentetate dimeglumine), Gd HP-DO3A (gadoteridol), Gd
BOPTA (gadobenate dimeglumine), Mn DPDP, and AMI-25 is reviewed, foll
owed by a brief discussion of two new iron particulate agents currentl
y in preclinical trials. Different imaging techniques also must be use
d for visualization of contrast enhancement depending on the specific
type of agent utilized. With both gadolinium and manganese chelates, T
1 weighted sequences are used to visualize the effect of the contrast
agent. There is positive enhancement (an increase in signal intensity)
of normal liver parenchyma post-contrast due to enhanced T1 relaxatio
n. With iron particulate agents, T2 weighted sequences are used. In th
is instance, there is negative enhancement (a decrease in signal inten
sity) of normal liver post-contrast due to enhanced T2 relaxation. Cli
nical use at present is limited to the extracellular gadolinium chelat
es, with bolus injection and dynamic imaging improving efficacy. Curre
nt research also supports the use of a high dose (0.3 mmol/kg) for imp
roved lesion detectability, a finding now clinically relevant due to t
he recent approval of Gd HP-DO3A at both standard and high doses.