MRI and CT are modalities appropriate for liver imaging. To obtain hig
her sensitivity in diagnoses of focal lesions in the liver, contrast m
edia (CM) are used. Non-specific extracellular CM are not optimal as t
hey rapidly diffuse into both normal liver tissue and tumorous tissue.
By two different mechanisms, the hepatobiliary route and targeting to
the reticuloendothelial system, agents may accumulate in normal liver
tissue, thereby giving liver-specific CM. So far no such agents have
been approved for clinical use. In the present studies, animal models
were used to investigate the imaging efficacy of experimental liver-sp
ecific CM and answer the following questions: i) Do these new liver-sp
ecific CM result in enhancement of normal liver? ii) If enhancement in
normal liver is present, does this result in higher contrast of norma
l liver to tumorous tissue? iii) If higher contrast of normal liver to
tumorous tissue is present, does this result in higher tumour detecti
on-rates? Relative to non-enhanced and contrast-enhanced CT, what tumo
ur detection-rate is obtained using non-enhanced and contrast-enhanced
MRI? All the liver-specific CM studied possessed the ability to signi
ficantly alter the signal in normal liver tissue. Compared to precontr
ast values, the liver-specific CM studied in MRI (Mn-DPDP) and CT (IEE
C-particles and iodixanol-liposomes) were able to increase significant
ly the contrast of normal liver tissue to tumorous tissue and the tumo
ur detection-frequency in VX2-carcinoma liver tumour-bearing rabbits.
In CT using a non-specific extracellular CM, iohexol, no improvement i
n contrast or tumour detection-frequency was obtained. As reflected in
the values of contrast-to-noise obtained, MRI and CT have the same po
tential for tumour detection in the liver tumour model used in the pre
sent studies. Liver-specific CM have the property of improving the con
trast of normal liver tissue to tumorous tissue in MRI and CT, giving
higher tumour detection-rates. Permitting intravenous administration a
nd the use of long imaging-windows, liver-specific CM are easy to use.