Small particles of ferrite are used as superparamagnetic contrast medium in MR imaging (appearing predominantly dark on MRI). These agents exhibit strong T1 relaxation properties, and due to susceptibility differences to their surroundings also produce a strongly varying local magnetic field, which enhances T2 relaxation to darken the contrast media containing structures.
Superparamagnetic contrast agents are also known by the abbreviation SPIO's (small particle iron oxide or superparamagnetic iron oxide) and USPIO's (ultrasmall particle iron oxide or ultrasmall superparamagnetic iron oxide).
Two types of USPIO will be available on the market as blood pool agents, while SPIO's have been used as darkening contrast agents for liver imaging. As particulate matter they are taken up by the RES. Very small particles of less than 300 nanometers also remain intravascular for a prolonged period of time and thus can serve as blood pool agents.

See also the related poll result: 'The development of contrast agents in MRI is'

Short name: SHU 555 C, preliminary trade name: Supravistâ„¢
An ultrasmall superparamagnetic iron oxide under development as a positive enhancing blood pool agent (MRI contrast agent phase III, Bayer Schering Pharma AG). Supravist™ can be administered as an iv. bolus up to doses of 80 μmol/kg.

See also Ultrasmall Superparamagnetic Iron Oxide and Blood Pool Agents.

(VSOP = very small superparamagnetic iron oxide particles) This new class of contrast agents with smaller particle size than SPIO offers advantages for MR angiography. SPIO particles are usually coated with an organic polymer such as dextran, carboxydextran or polyethylene glycol, which limits the minimal overall particle size that can be obtained. VSOP-C184 consists of an aqueous solution of superparamagnetic iron oxide particles with a citrate coating and the overall particle size of 4-8 nm.
Short name: VSOP-C184, central moiety: Fe, concentration: 29 g Fe/l, relaxivity: R1=20.1, R2=37.1, B0=0.94 T.

A bolus is a rapid infusion of high dose contrast agent. Dynamic and accumulation phase imaging can be performed after bolus injection. Since the transit time of the bolus through the tissue is only a few seconds, high temporal resolution imaging can be required to obtain sequential images during the wash in and wash out of the contrast material and, therefore, resolve the first pass of the tracer.
For the same injected dose of contrast agent the injection rate (and, consequently, the total injected volume) modifies the bolus peak profile. Increasing the injection rate produces a sharpening of the peak (Cmax increase, Tmax decrease, peak length decrease). At a low injection rate, the first pass presents a plateau form. Substantial changes in the gadolinium concentrations during signal acquisition induce artifacts. Furthermore, the haemodynamic parameters (cardiac output, blood pressure) influence the bolus profile. The characteristics of gadolinium agents are favorable in the early bolus phase, whereas the advantages of large complexes (e.g. blood pool agents) and ultrasmall superparamagnetic iron oxide (USPIO) are most evident in the distribution phase.

An iron-based contrast agent with large molecular size, which prevents diffusion into body tissues and will be developed for MR imaging of the liver (taken up by macrophages), tumor microvasculature and microvessel permeability. The blood half live of the particles with 11-20 nm diameter is 3-4 hours.
At this time the development of Clariscanâ„¢ is discontinued.

See also NC100150 Injection and Ultrasmall Superparamagnetic Iron Oxide.