Biological Physics Department, University of Mons-UMONS, 20 Place du Parc, 7000 Mons, Belgium.
MAGMA. 2012 Dec;25(6):467-78. doi: 10.1007/s10334-012-0326-7. Epub 2012 Jul 12.
Paramagnetic nanoparticles, mainly rare earth oxides and hydroxides, have been produced these last few years for use as MRI contrast agents. They could become an interesting alternative to iron oxide particles. However, their relaxation properties are not well understood.
Magnetometry, (1)H and (2)H NMR relaxation results at different magnetic fields and electron paramagnetic resonance are used to investigate the relaxation induced by paramagnetic particles. When combined with computer simulations of transverse relaxation, they allow an accurate description of the relaxation induced by paramagnetic particles.
For gadolinium hydroxide particles, both T(1) and T(2) relaxation are due to a chemical exchange of protons between the particle surface and bulk water, called inner sphere relaxation. The inner sphere is also responsible for T(1) relaxation of dysprosium, holmium, terbium and erbium containing particles. However, for these latter compounds, T(2) relaxation is caused by water diffusion in the field inhomogeneities created by the magnetic particle, the outer-sphere relaxation mechanism. The different relaxation behaviors are caused by different electron relaxation times (estimated by electron paramagnetic resonance).
These findings may allow tailoring paramagnetic particles: ultrasmall gadolinium oxide and hydroxide particles for T(1) contrast agents, with shapes ensuring the highest surface-to-volume ratio. All the other compounds present interesting T(2) relaxation performance at high fields. These results are in agreement with computer simulations and theoretical predictions of the outer-sphere and static dephasing regime theories. The T(2) efficiency would be optimum for spherical particles of 40-50 nm radius.
近年来,顺磁纳米粒子(主要为稀土氧化物和氢氧化物)已被用于 MRI 对比剂,它们可能成为氧化铁粒子的替代品。然而,其弛豫特性尚未得到很好的理解。
使用磁强计、不同磁场下的 (1)H 和 (2)H NMR 弛豫结果以及电子顺磁共振研究顺磁粒子引起的弛豫。与横向弛豫的计算机模拟相结合,它们可以准确描述顺磁粒子引起的弛豫。
对于氢氧化镝粒子,T1 和 T2 弛豫均归因于粒子表面和体相水分子之间的质子化学交换,称为内球弛豫。内球也是含镝、钬、铽和铒粒子的 T1 弛豫的原因。然而,对于这些后一种化合物,T2 弛豫是由磁场不均匀性中水分子扩散引起的,这是外球弛豫机制。不同的弛豫行为是由不同的电子弛豫时间(通过电子顺磁共振估计)引起的。
这些发现可能使顺磁粒子的定制成为可能:超小的氧化镝和氢氧化镝粒子用于 T1 对比剂,其形状确保了最高的表面积与体积比。所有其他化合物在高磁场下都具有有趣的 T2 弛豫性能。这些结果与外球和静态相消理论的计算机模拟和理论预测一致。对于 40-50nm 半径的球形粒子,T2 效率将达到最佳。