Zhang Shanrong, Merritt Matthew, Woessner Donald E, Lenkinski Robert E, Sherry A Dean
Department of Chemistry, University of Texas at Dallas, P.O. Box 830688, Richardson, Texas 75083-0688, USA.
Acc Chem Res. 2003 Oct;36(10):783-90. doi: 10.1021/ar020228m.
Scientific interest in optimizing the properties of gadolinium (III) complexes as MRI contrast agents has led to many new insights into lanthanide ion coordination chemistry in the last two decades. Among these was the surprising observation that water exchange in lanthanide (III) derivatives of DOTA can be modulated dramatically by judicious choice of ligand side chain and Ln(3+) ionic radii. This resulted in the discovery of paramagnetic CEST agents for altering MRI image contrast based upon the chemical exchange saturation transfer mechanism. The goal of this article is to review the factors that govern water molecule and water proton exchange in these complexes and to compare the potential sensitivity of PARACEST agents versus Gd(3+)-based T(1) relaxation agents for altering tissue contrast.
在过去二十年中,对优化钆(III)配合物作为磁共振成像(MRI)造影剂性能的科学兴趣,为镧系离子配位化学带来了许多新见解。其中一个惊人的发现是,通过明智地选择配体侧链和Ln(3+)离子半径,可以显著调节DOTA的镧系(III)衍生物中的水交换。这导致了基于化学交换饱和转移机制来改变MRI图像对比度的顺磁性CEST造影剂的发现。本文的目的是回顾控制这些配合物中水分子和水质子交换的因素,并比较PARACEST造影剂与基于Gd(3+)的T(1)弛豫造影剂在改变组织对比度方面的潜在灵敏度。