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作为用于电子顺磁共振波谱和成像的生物相容性自旋探针的葡聚糖共轭四硫代三芳基甲基自由基

Dextran-conjugated tetrathiatriarylmethyl radicals as biocompatible spin probes for EPR spectroscopy and imaging.

作者信息

Poncelet Martin, Driesschaert Benoit, Tseytlin Oxana, Tseytlin Mark, Eubank Timothy D, Khramtsov Valery V

机构信息

In Vivo Multifunctional Magnetic Resonance center, Robert C. Byrd Health Science Center, West Virginia University, Morgantown, WV 26506, United States; Department of Biochemistry, West Virginia University School of Medicine, Morgantown, WV 26506, United States.

In Vivo Multifunctional Magnetic Resonance center, Robert C. Byrd Health Science Center, West Virginia University, Morgantown, WV 26506, United States; Department of Pharmaceutical Sciences, West Virginia University, School of Pharmacy, Morgantown, WV 26506, United States.

出版信息

Bioorg Med Chem Lett. 2019 Jul 15;29(14):1756-1760. doi: 10.1016/j.bmcl.2019.05.017. Epub 2019 May 13.

Abstract

Tetrathiatriarylmethyl (TAM) radicals represent soluble paramagnetic probes for biomedical electron paramagnetic resonance (EPR)-based spectroscopy and imaging. There is an increasing demand in the development of multifunctional, biocompatible and targeted trityl probes hampered by the difficulties in derivatization of the TAM structure. We proposed a new straightforward synthetic strategy using click chemistry for the covalent conjugation of the TAM radical with a water-soluble biocompatible carrier exemplified here by dextran. A set of dextran-grafted probes varied in the degrees of Finland trityl radical loading and dextran modification by polyethelene glycol has been synthesized. The EPR spectrum of the optimized macromolecular probe exhibits a single narrow line with high sensitivity to oxygen and has advantages over the unbound Finland trityl of being insensitive to interactions with albumin. In vivo EPR imaging of tissue oxygenation performed in breast tumor-bearing mouse using dextran-grafted probe demonstrates its utility for preclinical oximetric applications.

摘要

四硫代三芳基甲基(TAM)自由基是用于基于生物医学电子顺磁共振(EPR)的光谱学和成像的可溶性顺磁探针。在多功能、生物相容性和靶向性三苯甲基探针的开发方面需求日益增加,但TAM结构的衍生化困难阻碍了这一进程。我们提出了一种新的直接合成策略,利用点击化学将TAM自由基与水溶性生物相容性载体(此处以葡聚糖为例)进行共价连接。合成了一组葡聚糖接枝探针,其芬兰三苯甲基自由基负载程度和聚乙二醇对葡聚糖的修饰程度各不相同。优化后的大分子探针的EPR光谱呈现出一条单一的窄线,对氧气具有高灵敏度,并且相对于未结合的芬兰三苯甲基具有优势,即对与白蛋白的相互作用不敏感。使用葡聚糖接枝探针在荷乳腺肿瘤小鼠中进行的组织氧合的体内EPR成像证明了其在临床前血氧测定应用中的效用。

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