Tes David, Kratkiewicz Karl, Aber Ahmed, Horton Luke, Zafar Mohsin, Arafat Nour, Fatima Afreen, Avanaki Mohammad Rn
Department of Biomedical Engineering, College of Engineering, Wayne State University, Detroit, MI, USA.
School of Health and Related Research, University of Sheffield, Sheffield, UK.
Biomed Eng Comput Biol. 2018 Jun 18;9:1179597218781081. doi: 10.1177/1179597218781081. eCollection 2018.
Alzheimer disease is the most common form of dementia, affecting more than 5 million people in the United States. During the progression of Alzheimer disease, a particular protein begins to accumulate in the brain and also in extensions of the brain, ie, the retina. This protein, amyloid-β (Aβ), exhibits fluorescent properties. The purpose of this research article is to explore the implications of designing a fluorescent imaging system able to detect Aβ proteins in the retina. We designed and implemented a fluorescent imaging system with a range of applications that can be reconfigured on a fluorophore to fluorophore basis and tested its feasibility and capabilities using Cy5 and CRANAD-2 imaging probes. The results indicate a promising potential for the imaging system to be used to study the Aβ biomarker. A performance evaluation involving ex vivo and in vivo experiments is planned for future study.
阿尔茨海默病是最常见的痴呆形式,在美国影响着超过500万人。在阿尔茨海默病的发展过程中,一种特定的蛋白质开始在大脑以及大脑的延伸部位即视网膜中积累。这种蛋白质,β-淀粉样蛋白(Aβ),具有荧光特性。这篇研究文章的目的是探讨设计一种能够检测视网膜中Aβ蛋白的荧光成像系统的意义。我们设计并实现了一种具有一系列应用的荧光成像系统,该系统可以在不同荧光团之间进行重新配置,并使用Cy5和CRANAD-2成像探针测试了其可行性和能力。结果表明该成像系统在用于研究Aβ生物标志物方面具有广阔的前景。计划在未来的研究中进行涉及离体和体内实验的性能评估。