A variety of parenterally administered iron oxides have been developed
fur contrast-enhanced MRI of the liver. Two different classes of iron
oxides are currently clinically approved or in phase 3 trials: superp
aramagnetic iron oxides (SPIO) with a high R2/R1 relaxivity ratio and
short blood half-life (AMI-25 and SH U 555 A), and ultrasmall paramagn
etic iron oxides (USPIO) with a lower R2/R1 relaxivity ratio and longe
r blood half-life (AMI-227). All iron oxides significantly increase tu
mor-to-liver contrast and allow detection of more lesions than unenhan
ced MRI on T2-weighted images at a field strength of 0.2-1.5 T. Malign
ant lesions without phagocytic cells exhibit constant signal on T2-wei
ghted accumulation phase images with all three iron oxides. All iron o
xides cause a signal decrease of benign lesions with either phagocytic
cells or a significant blood pool on T2-weighted accumulation phase i
mages. The signal decrease of benign lesions is proportional to the Ku
pffer cell activity or tumor vascularity and is useful for lesion char
acterization. Another enhancement feature for the differentiation of b
enign from malignant lesions is ring enhancement of malignant lesions
(metastases) on T1-weighted enhanced images either during the perfusio
n phase with SH U 555 A or during the accumulation phase with AMI-227,
which is attributed to the blood pool effects of the compounds. Diffe
rentiation of lesions and vessels is easier on enhanced images with an
giographic effects than on unenhanced images. Iron oxides improve the
quality of two-dimensional MR angiography techniques of the portal ven
ous system by decreasing background signal (liver tissue with all iron
oxides) and increasing intravascular signal (AMI-227). The use of iro
n oxides for hepatic MRI provides an alternative to the existing multi
step diagnosis with CT, CT portography, MRI and biopsy.