Bach-Gansmo T. 1993. Ferrimagnetic susceptibility contrast agents. Con
trast, agents based on superparamagnetic particles have been in clinic
al development for more than 5 years, and the complexity of their effe
cts is still not elucidated, The relaxivities are frequently used to g
ive an idea of their efficacy, but these parameters can only be used i
f they are concentration independent for large superparamagnetic syste
ms, the evolution of the transverse magnetization is biexponential, af
ter an initial loss of magnetization. Both these characteristics of la
rge superparamagnetic systems should lead to prudence in using the rel
axivities as indicators of contrast medium efficacy. Susceptibility in
duced artefacts have been associated with the use of superparamagnetic
contrast agents since the first imaging evaluation took place. The ra
nge of concentrations where good contrast effect was achieved without
inducing artefacts, as well as blurring and metal artefacts were evalu
ated. The influence of motion on the induction of artefacts was studie
d, and compared to the artefacts induced by a paramagnetic agent subje
ct to motion. With a suitable concentration of a negative contrast age
nt, a signal void could be achieved in the region prone to motion, and
no artefacts were induced. If the concentration was too high, a displ
acement of the region close to the contrast agent was observed. The ar
tefacts occurred in a volume surrounding the contrast agent, i.e., als
o outside the imaging plane. In comparison a positive, paramagnetic co
ntrast agent induced heavy artefacts in the phase encoding direction,
appearing as both high intensity regions and black holes, in a mosaic
pattern. Clinical trials of the oral contrast agent OMP for abdominal
MR imaging showed this agent to be safe and efficacious. OMP increased
the diagnostic efficacy of abdominal MR imaging in 2 of 3 cases exami
ned, with a significant decrease in motion artefacts. Susceptibility c
ontrast agents may also be of use in the evaluation of small lesions i
n the liver. Particulate material injected i.v. will be targeted to th
e liver and spleen by way of the mononuclear phagocyte system (MPS). S
mall particles, without specific receptor affinities were targeted to
the hepatocytes and the MPS. The distribution correlated with a high e
fficiency as a contrast agent, whereas no correlation to in vitro rela
xation rates and relaxivities could be found. Superparamagnetic partic
les have important possibilities as contrast agents. The identificatio
n of in vitro properties of these agents may help the comparison of va
rious agents before in vivo imaging.