Nanoparticles in magnetic resonance imaging: from simple to dual contrast agents

Abstract

Magnetic resonance imaging (MRI) has become one of the most widely used and powerful tools for noninvasive clinical diagnosis owing to its high degree of soft tissue contrast, spatial resolution, and depth of penetration. MRI signal intensity is related to the relaxation times (T₁, spin–lattice relaxation and T₂, spin–spin relaxation) of in vivo water protons. To increase contrast, various inorganic nanoparticles and complexes (the so-called contrast agents) are administered prior to the scanning. Shortening T₁ and T₂ increases the corresponding relaxation rates, 1/T₁ and 1/T₂, producing hyperintense and hypointense signals respectively in shorter times. Moreover, the signal-to-noise ratio can be improved with the acquisition of a large number of measurements. The contrast agents used are generally based on either iron oxide nanoparticles or ferrites, providing negative contrast in T₂-weighted images; or complexes of lanthanide metals (mostly containing gadolinium ions), providing positive contrast in T₁-weighted images. Recently, lanthanide complexes have been immobilized in nanostructured materials in order to develop a new class of contrast agents with functions including blood-pool and organ (or tumor) targeting. Meanwhile, to overcome the limitations of individual imaging modalities, multimodal imaging techniques have been developed. An important challenge is to design all-in-one contrast agents that can be detected by multimodal techniques. Magnetoliposomes are efficient multimodal contrast agents. They can simultaneously bear both kinds of contrast and can, furthermore, incorporate targeting ligands and chains of polyethylene glycol to enhance the accumulation of nanoparticles at the site of interest and the bioavailability, respectively. Here, we review the most important characteristics of the nanoparticles or complexes used as MRI contrast agents.

Keywords:

• gadolinium
• iron oxide nanoparticles
• magnetoliposomes
• paramagnetic nanoparticles
• superparamagnetic nanoparticles
• relaxivity

Acknowledgments

The authors are grateful to the Spanish Ministerio de Economía y Competitividad (MINECO) for financial support of the project MAT2012-36270-C04-03.

Disclosure

The authors report no conflicts of interest in this work.