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用于绝对 3D 温度磁共振成像的光开关对比剂。

Towards Photoswitchable Contrast Agents for Absolute 3D Temperature MR Imaging.

机构信息

Otto Diels Institute of Organic Chemistry, Christian Albrechts University, Otto Hahn Platz 4, 24118, Kiel, Germany.

Department of Electrical Engineering and Information Technology, South Westphalian University of Applied Sciences, Bahnhofsallee 5, 58507, Luedenscheid, Germany.

出版信息

Angew Chem Int Ed Engl. 2021 Apr 6;60(15):8220-8226. doi: 10.1002/anie.202015851. Epub 2021 Mar 3.

DOI:10.1002/anie.202015851
PMID:33606332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8048480/
Abstract

Temperature can be used as clinical marker for tissue metabolism and the detection of inflammations or tumors. The use of magnetic resonance imaging (MRI) for monitoring physiological parameters like the temperature noninvasively is steadily increasing. In this study, we present a proof-of-principle study of MRI contrast agents (CA) for absolute and concentration independent temperature imaging. These CAs are based on azoimidazole substituted Ni porphyrins, which can undergo Light-Driven Coordination-Induced Spin State Switching (LD-CISSS) in solution. Monitoring the fast first order kinetic of back isomerisation (cis to trans) with standard clinical MR imaging sequences allows the determination of half-lives, that can be directly translated into absolute temperatures. Different temperature responsive CAs were successfully tested as prototypes in methanol-based gels and created temperature maps of gradient phantoms with high spatial resolution (0.13×0.13×1.1 mm) and low temperature errors (<0.22 °C). The method is sufficiently fast to record the temperature flow from a heat source as a film.

摘要

温度可作为组织代谢以及炎症或肿瘤检测的临床标志物。使用磁共振成像(MRI)无创监测生理参数(如温度)的应用正在稳步增加。在这项研究中,我们提出了一种基于偶氮咪唑取代镍卟啉的 MRI 对比剂(CA)用于绝对和浓度无关的温度成像的原理验证研究。这些 CA 可以在溶液中进行光驱动配位诱导自旋态转变(LD-CISSS)。使用标准临床 MR 成像序列监测快速的顺式-反式异构化(cis 到 trans)的一级动力学,可确定半衰期,该半衰期可直接转化为绝对温度。不同的温度响应 CA 已成功作为原型在甲醇基凝胶中进行了测试,并以高空间分辨率(0.13×0.13×1.1 mm)和低温度误差(<0.22°C)生成了梯度体模的温度图。该方法足够快,可以记录热源的温度流动情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/6555a7f3b955/ANIE-60-8220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/62a672faa61f/ANIE-60-8220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/d727008afbfd/ANIE-60-8220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/85025afd54cb/ANIE-60-8220-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/f99ab96d404b/ANIE-60-8220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/a02d3e06a5b3/ANIE-60-8220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/45941e706bdb/ANIE-60-8220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/6555a7f3b955/ANIE-60-8220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/62a672faa61f/ANIE-60-8220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/d727008afbfd/ANIE-60-8220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/85025afd54cb/ANIE-60-8220-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/f99ab96d404b/ANIE-60-8220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/a02d3e06a5b3/ANIE-60-8220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/45941e706bdb/ANIE-60-8220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68f4/8048480/6555a7f3b955/ANIE-60-8220-g002.jpg

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