There are many things in life everybody wants more of, and this is particularly true for magnetic resonance imaging (MRI). The major challenge in the daily life of an MRI professional is gaining maximal image signal and contrast in a reasonable amount of time. The application of gadolinium (Gd)-based MR contrast material has offered contrast features in MRI that have been used and appreciated for almost 20 years in both neurological and whole-body MRI. For example, state-of-the-art MRI is not possible in brain tumours, vascular pathologies or focal liver disease without the use of Gd. Cardiac MRI has also benefited enormously from Gd enhancement; indeed, some of the most important and established cardiac MRI applications are based on the use of Gd contrast. 1,2 Although there are strong data in support of the superiority of dedicated contrast-enhanced MRI techniques over other modalities in many clinical indications, there is still a need for improvements in image quality and stability, whether in terms of the hardware, software or 'wetware' (contrast agents). In terms of cardiac MRI, in general more contrast would be preferable since many cardiac pathologies are difficult to distinguish from normal myocardium. Therefore, the use of higher-concentration Gd compounds could improve the reliability of cardiac MRI. The aim of this article is to summarise recent knowledge about gadobutrol, the only approved 1.0-molar Gd contrast agent, in MR angiography (MRA) and neurological and whole-body MRI, and to provide an outlook on expected future developments in cardiac MRI.
Gadobutrol
Chemistry and Safety ProfileMost MR contrast media are based on Gd as a paramagnetic ion. The Gd 3+ ion has strong magnetic properties, which lead primarily to a T1-relaxation shortening of protons and the production of a high signal in T1-weighted MR sequences. However, the free Gd 3+ ion has to be bound in chelates to reduce unwanted side effects and create desirable pharmacokinetic properties. 3 Many Gd-based contrast agents have been clinically approved and commercially available for more than a decade. Typically, Gd agents are extracellular, non-tissue-specific, non-protein-binding, water-soluble compounds such as gadopentetate dimeglumine (Gd-DTPA), gadoteridol (Gd-HPDO3A), gadoterate (Gd-DOTA), gadoversetamide (Gd-DTPABMEA) and gadodiamide (Gd-DTPA-BMA). 4 Gadobenate dimeglumine (Gd-BOPTA) and gadofosveset, on the other hand, interact with serum albumin, resulting in a higher in vivo relaxivity and longer plasma half-lives. All of the abovementioned compounds are prepared at a concentration of 0.5mol/l.