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用于体内生物正交点击化学预靶向正电子发射断层显像(PET)成像的低分子量(11)C标记四嗪的设计、合成与评价

Design, Synthesis, and Evaluation of a Low-Molecular-Weight (11)C-Labeled Tetrazine for Pretargeted PET Imaging Applying Bioorthogonal in Vivo Click Chemistry.

作者信息

Denk Christoph, Svatunek Dennis, Mairinger Severin, Stanek Johann, Filip Thomas, Matscheko Dominik, Kuntner Claudia, Wanek Thomas, Mikula Hannes

机构信息

Institute of Applied Synthetic Chemistry, Vienna University of Technology , 1040 Wien, Austria.

Health and Environment Department, Biomedical Systems, Austrian Institute of Technology , 2444 Seibersdorf, Austria.

出版信息

Bioconjug Chem. 2016 Jul 20;27(7):1707-12. doi: 10.1021/acs.bioconjchem.6b00234. Epub 2016 Jul 1.

Abstract

A low-molecular-weight tetrazine labeled with the short-lived positron emitter carbon-11 was developed as a bioorthogonal PET probe for pretargeted imaging. A method for efficient and fast synthesis of this imaging agent is presented using radiolabeling of a readily available precursor. High reactivity with trans-cyclooctenes was observed and in vivo investigations including PET/MR scanning showed homogeneous biodistribution, good metabolic stability, and rapid excretion in naive mice. These properties are key to the success of bioorthogonal (11)C-PET imaging, which has been shown in a simple pretargeting experiment using TCO-modified mesoporous silica nanoparticles. Overall, this (11)C-labeled tetrazine represents a highly versatile and advantageous chemical tool for bioorthogonal PET imaging and enables pretargeting approaches using carbon-11 for the first time.

摘要

一种用短寿命正电子发射体碳 - 11标记的低分子量四嗪被开发为用于预靶向成像的生物正交PET探针。本文介绍了一种使用易于获得的前体进行放射性标记来高效快速合成这种成像剂的方法。观察到其与反式环辛烯具有高反应性,包括PET/MR扫描在内的体内研究表明,在未处理的小鼠中具有均匀的生物分布、良好的代谢稳定性和快速排泄。这些特性是生物正交(11)C - PET成像成功的关键,这已在使用TCO修饰的介孔二氧化硅纳米颗粒的简单预靶向实验中得到证明。总体而言,这种(11)C标记的四嗪代表了一种用于生物正交PET成像的高度通用且有利的化学工具,并首次实现了使用碳 - 11的预靶向方法。

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