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高弛豫率而无配位水:纳米凝胶中[Gd(DOTP)]的看似矛盾行为。

High Relaxivity with No Coordinated Waters: A Seemingly Paradoxical Behavior of [Gd(DOTP)] Embedded in Nanogels.

机构信息

Dipartimento di Scienze e Innovazione Tecnologica, Università del Piemonte Orientale "A. Avogadro", Viale Teresa Michel 11, Alessandria 15121, Italy.

Molecular Imaging Centre, Department of Molecular Biotechnology and Health Sciences, University of Torino, Via Nizza 52, Torino 10126, Italy.

出版信息

Inorg Chem. 2022 Apr 4;61(13):5380-5387. doi: 10.1021/acs.inorgchem.2c00225. Epub 2022 Mar 22.

Abstract

Nanogels (NGs) obtained by electrostatic interactions between chitosan and hyaluronic acid and comprising paramagnetic Gd chelates are gaining increasing attention for their potential application in magnetic resonance bioimaging. Herein, the macrocyclic complexes [Gd(DOTP)], lacking metal-bound water molecules ( = 0), were confined or used as a cross-linker in this type of NG. Unlike the typical behavior of Gd complexes with = 0, a remarkable relaxivity value of 78.0 mM s was measured at 20 MHz and 298 K, nearly 20 times greater than that found for the free complex. A careful analysis of the relaxation data emphasizes the fundamental role of second sphere water molecules with strong and long-lived hydrogen bonding interactions with the complex. Finally, PEGylated derivatives of nanoparticles were used for the first magnetic resonance imaging study of this type of NG, revealing a fast renal excretion of paramagnetic complexes after their release from the NGs.

摘要

纳米凝胶(NGs)是通过壳聚糖和透明质酸之间的静电相互作用获得的,包含顺磁 Gd 螯合物,由于其在磁共振生物成像中的潜在应用而受到越来越多的关注。在此,大环配合物[Gd(DOTP)]被限制或用作这种 NG 的交联剂,其中不含配位水分子( = 0)。与典型的 = 0 的 Gd 配合物的行为不同,在 20 MHz 和 298 K 下测量到 78.0 mM s 的显著弛豫率,几乎比游离配合物高 20 倍。对弛豫数据的仔细分析强调了第二水合层水分子的基本作用,这些水分子与配合物具有强且持久的氢键相互作用。最后,纳米颗粒的聚乙二醇化衍生物首次用于该类型的 NG 的磁共振成像研究,表明在从 NGs 释放后,顺磁配合物的快速肾脏排泄。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4c3/8985129/01e144861e33/ic2c00225_0002.jpg

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