Department of Chemistry, University of Texas at Dallas, Richardson, Texas, USA.
J Magn Reson Imaging. 2009 Dec;30(6):1240-8. doi: 10.1002/jmri.21966.
Gadolinium is widely known by all practitioners of magnetic resonance imaging (MRI) but few appreciate the basic solution chemistry of this trivalent lanthanide ion. Given the recent linkage between gadolinium contrast agents and nephrogenic systemic fibrosis, some basic chemistry of this ion must be more widely understood. This short primer on gadolinium chemistry is intended to provide the reader the background principles necessary to understand the basics of chelation chemistry, water hydration numbers, and the differences between thermodynamic stability and kinetic stability or inertness. We illustrate the fundamental importance of kinetic dissociation rates in determining gadolinium toxicity in vivo by presenting new data for a novel europium DOTA-tetraamide complex that is relatively unstable thermodynamically yet extraordinarily inert kinetically and also quite nontoxic. This, plus other literature evidence, forms the basis of the fundamental axiom that it is the kinetic stability of a gadolinium complex, not its thermodynamic stability, that determines its in vivo toxicity. J. Magn. Reson. Imaging 2009;30:1240-1248. (c) 2009 Wiley-Liss, Inc.
镝在磁共振成像(MRI)的所有从业者中广为人知,但很少有人了解这种三价镧系离子的基本溶液化学。鉴于最近镝对比剂与肾源性系统性纤维化之间的联系,必须更广泛地了解这种离子的一些基本化学知识。本镝化学简介旨在为读者提供必要的背景原理,以了解螯合化学、水合配位数以及热力学稳定性和动力学稳定性或惰性之间的区别。我们通过呈现新型铕 DOTA-四酰胺络合物的新数据来说明动力学离解速率在确定体内镝毒性方面的重要性,该络合物在热力学上相对不稳定,但在动力学上非常惰性且毒性极低。这一点,再加上其他文献证据,构成了一个基本公理的基础,即决定镝配合物体内毒性的是其动力学稳定性,而不是热力学稳定性。J. Magn. Reson. Imaging 2009;30:1240-1248。(c)2009 Wiley-Liss,Inc.