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用于阿尔茨海默病小鼠模型中淀粉样β成像的多模式治疗性氰基-钆(III)配合物。

Multimodal Theranostic Cyanine-Conjugated Gadolinium(III) Complex for Imaging of Amyloid-β in an Alzheimer's Disease Mouse Model.

机构信息

Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong SAR China.

ICMUB (UMR CNRS 6302), Université Bourgogne Franche-Comté, 21000 Dijon, France.

出版信息

ACS Appl Mater Interfaces. 2021 Apr 28;13(16):18525-18532. doi: 10.1021/acsami.1c01585. Epub 2021 Apr 14.

DOI:10.1021/acsami.1c01585
PMID:33852279
Abstract

Despite the wide use of magnetic resonance imaging (MRI) as a clinical diagnostic tool, there are still no clinically approved MRI contrast agents that can be applied for cerebral Alzheimer's disease (AD) biomarker imaging. We report here the design and development of the first amyloid-β (Aβ)-targeted, blood-brain barrier (BBB) penetrable theranostic Gd(DOTA)-cyanine dyad, which was synthesized by the conjugation of Gd(DOTA) complex and carbazole-based cyanine dye by the copper(I)-catalyzed azide-alkyne cycloaddition click reaction for imaging of Aβ and in AD mouse models. This dyad, as a multimodal probe, possesses desirable multifunctional properties, including good biocompatibility, low cytotoxicity, high Aβ selectivity, strong fluorescence enhancement upon binding with Aβ species, good paramagnetic properties, high stability, good BBB penetrability, and fast elimination from the mouse. The longitudinal relaxivity () of the dyad was found to be 4.42 mM s at 3 T, suggesting it to be promising as a -weighted MRI contrast agent. The probe has been successfully demonstrated to be able to be applied for one- and two-photon excited fluorescence and magnetic resonance (MR) imaging of Aβ in transgenic mouse models of AD. In addition, it can inhibit Aβ aggregation, protect against toxicity induced by Aβ, and suppress Aβ-induced reactive oxygen species (ROS) production. Our results demonstrate the highly promising theranostic capability of the dyad for diagnosis and therapy of AD and extraordinary potential for MRI of Aβ in humans.

摘要

尽管磁共振成像(MRI)已被广泛用作临床诊断工具,但仍没有经过临床批准的 MRI 对比剂可用于脑阿尔茨海默病(AD)生物标志物成像。我们在此报告首例淀粉样蛋白-β(Aβ)靶向、血脑屏障(BBB)可穿透的治疗性 Gd(DOTA)-菁染料二联体的设计和开发,该二联体是通过铜(I)催化的叠氮-炔环加成点击反应将 Gd(DOTA)配合物和咔唑基菁染料连接而成,用于 AD 小鼠模型中 Aβ和的成像。该二联体作为一种多模态探针,具有理想的多功能特性,包括良好的生物相容性、低细胞毒性、对 Aβ的高选择性、与 Aβ结合时荧光强度的强增强、良好的顺磁性、高稳定性、良好的 BBB 穿透性和从小鼠体内快速消除。该二联体的纵向弛豫率()在 3T 下为 4.42mM s,表明其有望成为 T1 加权 MRI 对比剂。该探针已成功应用于 AD 转基因小鼠模型中 Aβ的单光子和双光子激发荧光和磁共振(MR)成像。此外,它可以抑制 Aβ聚集,防止 Aβ诱导的毒性,并抑制 Aβ诱导的活性氧(ROS)产生。我们的结果表明,该二联体在 AD 的诊断和治疗方面具有很高的治疗潜力,并且在人类 Aβ的 MRI 中具有非凡的潜力。

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