Departamento de Química Farmacológica y Toxicológica, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago 8380494, Chile; Advanced Center for Chronic Diseases (ACCDiS), Sergio Livingstone 1007, Independencia, Santiago 8380494, Chile.
Departamento de Ingeniería Química, Biotecnología y Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Beauchef 851, Santiago 8370456, Chile.
Nanomedicine. 2022 Aug;44:102569. doi: 10.1016/j.nano.2022.102569. Epub 2022 May 17.
The β-amyloid (Aβ) peptide is one of the key etiological agents in Alzheimer's disease (AD). The in vivo detection of Aβ species is challenging in all stages of the illness. Currently, the development of fluorescent probes allows the detection of Aβ in animal models in the near-infrared region (NIR). However, considering future applications in biomedicine, it is relevant to develop strategies to improve detection of amyloid aggregates using NIR probes. An innovative approach to increase the fluorescence signal of these fluorophores is the use of plasmonic gold nanoparticles (surface-enhanced fluorescence effect). In this work, we improved the detection of Aβ aggregates in C. elegans and mouse models of AD by co-administering functionalized gold nanorods (GNRs-PEG-D1) with the fluorescent probes CRANAD-2 or CRANAD-58, which bind selectively to different amyloid species (soluble and insoluble). This work shows that GNRs improve the detection of Aβ using NIR probes in vivo.
β-淀粉样蛋白(Aβ)肽是阿尔茨海默病(AD)的关键病因之一。在疾病的所有阶段,体内检测 Aβ 物种都具有挑战性。目前,荧光探针的发展允许在近红外区域(NIR)检测动物模型中的 Aβ。然而,考虑到未来在生物医学中的应用,开发使用 NIR 探针改善淀粉样蛋白聚集物检测的策略是相关的。增加这些荧光团荧光信号的一种创新方法是使用等离子体金纳米粒子(表面增强荧光效应)。在这项工作中,我们通过与荧光探针 CRANAD-2 或 CRANAD-58 一起给予功能化的金纳米棒(GNR-PEG-D1),改善了秀丽隐杆线虫和 AD 小鼠模型中 Aβ 聚集物的检测,这些探针选择性地结合不同的淀粉样蛋白物种(可溶性和不溶性)。这项工作表明,GNR 提高了体内使用 NIR 探针检测 Aβ 的效果。