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利用非共振旋转框架技术研究顺磁性造影剂的动力学

Dynamics of paramagnetic agents by off-resonance rotating frame technique.

作者信息

Zhang Huiming, Xie Yang

机构信息

Center for Basic MR Research, Evanston Northwestern Healthcare Research Institute, 1033 University Place, suite 100, Evanston, IL 60201, USA.

出版信息

J Magn Reson. 2006 Dec;183(2):213-27. doi: 10.1016/j.jmr.2006.08.008. Epub 2006 Sep 18.

Abstract

Off-resonance rotating frame technique offers a novel tool to explore the dynamics of paramagnetic agents at high magnetic fields (B0 > 3T). Based on the effect of paramagnetic relaxation enhancement in the off-resonance rotating frame, a new method is described here for determining the dynamics of paramagnetic ion chelates from the residual z-magnetizations of water protons. In this method, the dynamics of the chelates are identified by the difference magnetization profiles, which are the subtraction of the residual z-magnetization as a function of frequency offset obtained at two sets of RF amplitude omega(1) and pulse duration tau. The choices of omega(1) and tau are guided by a 2-D magnetization map that is created numerically by plotting the residual z-magnetization as a function of effective field angle theta and off-resonance pulse duration tau. From the region of magnetization map that is the most sensitive to the alteration of the paramagnetic relaxation enhancement efficiency R(1rho)/R1, the ratio of the off-resonance rotating frame relaxation rate constant R(1rho) verse the laboratory frame relaxation rate constant R(1), three types of difference magnetization profiles can be generated. The magnetization map and the difference magnetization profiles are correlated with the rotational correlation time tauR of Gd-DTPA through numerical simulations, and further validated by the experimental data for a series of macromolecule conjugated Gd-DTPA in aqueous solutions. Effects of hydration water number q, diffusion coefficient D, magnetic field strength B0 and multiple rotational correlation times are explored with the simulations of the magnetization map. This method not only provides a simple and reliable approach to determine the dynamics of paramagnetic labeling of molecular/cellular events at high magnetic fields, but also a new strategy for spectral editing in NMR/MRI based on the dynamics of paramagnetic labeling in vivo.

摘要

非共振旋转框架技术提供了一种新颖的工具,用于在高磁场(B0 > 3T)下探索顺磁性试剂的动力学。基于非共振旋转框架中顺磁性弛豫增强的效应,本文描述了一种从水质子的剩余z磁化强度确定顺磁性离子螯合物动力学的新方法。在该方法中,螯合物的动力学通过差分磁化轮廓来识别,差分磁化轮廓是在两组射频幅度ω(1)和脉冲持续时间τ下获得的作为频率偏移函数的剩余z磁化强度的差值。ω(1)和τ的选择由二维磁化图指导,该二维磁化图通过将剩余z磁化强度绘制为有效场角θ和非共振脉冲持续时间τ的函数进行数值创建。从对顺磁性弛豫增强效率R(1ρ)/R1的变化最敏感的磁化图区域,即非共振旋转框架弛豫速率常数R(1ρ)与实验室框架弛豫速率常数R(1)的比值,可以生成三种类型的差分磁化轮廓。通过数值模拟,磁化图和差分磁化轮廓与钆-二乙三胺五乙酸(Gd-DTPA)的旋转相关时间τR相关,并通过一系列大分子共轭Gd-DTPA在水溶液中的实验数据进一步验证。通过磁化图模拟探索了水合数q、扩散系数D、磁场强度B0和多个旋转相关时间的影响。该方法不仅提供了一种简单可靠的方法来确定高磁场下分子/细胞事件顺磁性标记的动力学,还提供了一种基于体内顺磁性标记动力学的核磁共振/磁共振成像(NMR/MRI)光谱编辑新策略。

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