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基于三氮杂环壬烷的亮单 Aqua 铕配合物,可与阴离子可逆结合并有效地穿透细胞。

Bright mono-aqua europium complexes based on triazacyclononane that bind anions reversibly and permeate cells efficiently.

机构信息

Department of Chemistry, Durham University, South Road, Durham, DH1 3LE, UK.

出版信息

Chemistry. 2013 Jul 15;19(29):9511-7. doi: 10.1002/chem.201301273. Epub 2013 Jun 6.

Abstract

A series of five europium(III) complexes has been prepared from heptadentate N5O2 ligands that possess a brightness of more than 10 mM(-1) cm(-1) in water, following excitation over the range λ=330-355 nm. Binding of several oxy anions has been assessed by emission spectral titrimetric analysis, with the binding of simple carboxylates, lactate and citrate involving a common ligation mode following displacement of the coordinated water. Selectivity for bicarbonate allows the rapid determination of this anion in human serum, with K(d)=37 mM (295 K). The complexes are internalised quickly into mammalian cells and exhibit a mitochondrial localisation at early time points, migrating after a few hours to reveal a predominant lysosomal distribution. Herein, we report the synthesis and complexation behaviour of strongly emissive europium (III) complexes that bind oxy-anions in aqueous media with an affinity and selectivity profile that is distinctively different from previously studied systems.

摘要

已制备了一系列具有七齿 N5O2 配体的五铕(III)配合物,在 λ=330-355nm 范围内激发后,其在水中的亮度超过 10mM(-1)cm(-1)。通过发射光谱滴定分析评估了几种含氧阴离子的结合情况,简单的羧酸根、乳酸盐和柠檬酸盐的结合涉及到配位水置换后的常见配位模式。对碳酸氢盐的选择性允许快速测定人血清中的这种阴离子,K(d)=37mM(295K)。这些配合物很快被内吞到哺乳动物细胞中,并在早期表现出线粒体定位,几个小时后迁移,显示出主要的溶酶体分布。在此,我们报告了强发光铕(III)配合物的合成和配位行为,该配合物在水相中与含氧阴离子结合,其亲和力和选择性与以前研究的系统明显不同。

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