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Radical Dendrimers Based on Biocompatible Oligoethylene Glycol Dendrimers as Contrast Agents for MRI

机译:基于生物相容性低聚乙二醇树枝状大分子的根治性树枝状大分子作为MRI的造影剂

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摘要

Finding alternatives to gadolinium (Gd)-based contrast agents (CA) with the same or even better paramagnetic properties is crucial to overcome their established toxicity. Herein we describe the synthesis and characterization of entirely organic metal-free paramagnetic macromolecules based on biocompatible oligoethylene glycol dendrimers fully functionalized with 5 and 20 organic radicals (OEG Gn-PROXYL (n = 0, 1) radical dendrimers) with the aim to be used as magnetic resonance imaging (MRI) contrast agents. Conferring high water solubility on such systems is often a concern, especially in large generation dendrimers. Our approach to overcome such an issue in this study is by synthesizing dendrimers with highly water-soluble branches themselves. In this work, we show that the highly water-soluble OEG Gn-PROXYL (n = 0, 1) radical dendrimers obtained showed properties that convert them in good candidates to be studied as contrast agents for MRI applications like diagnosis and follow-up of infectious diseases, among others. Importantly, with the first generation radical dendrimer, a similar r1 relaxivity value (3.4 mM−1s−1) in comparison to gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA) used in clinics (3.2 mM−1s−1, r.t. 7T) has been obtained, and it has been shown to not be cytotoxic, avoiding the toxicity risks associated with the unwanted accumulation of Gd in the body.
机译:以相同甚至更好的顺磁性特性寻找钆(GD)的造林(CA)的替代品至关重要,以克服其既定的毒性至关重要。在此我们描述了基于用5和20个有机基团的生物相容的寡核苷树甘醇树枝状体(OEG GN-锂(n = 0,1)自由基树枝状大分子)完全官能化的完全有机金属甲基二氯二细胞的合成和表征。作为磁共振成像(MRI)造影剂。在这种系统上赋予高水力溶解度通常是一个问题,特别是在大代树枝状上。我们在本研究中克服这种问题的方法是通过合成具有高度水溶性分支的树枝状体。在这项工作中,我们表明,获得的高度水溶性OEG GN-巯基(n = 0,1)根的树枝状大分子显示出在良好的候选者中转化它们的性质,以进行诊断和后续的MRI应用的造影剂。传染病等。重要的是,与第一代自由基树枝状聚合物一起,与诊所(3.2mm-1s-1,RT 7T)使用的钆 - 二亚乙基三胺五乙酸(GD-DTPA)相比,具有类似的R1松弛率值(3.4mm-1s-1)已经获得,已被证明不是细胞毒性,避免与身体中Gd的不需要的积累相关的毒性风险。

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