Amplified fluorogenic immunoassay for early diagnosis and monitoring of Alzheimer’s disease from tear fluidopen access
- Authors
- 이소정; Kim, Eunjung; Moon, Chae-Eun; Park, Chaewon; Lim, Jong-Woo; Baek, Minseok; Shin, Moo-Kwang; Ki, Jisun; Cho, Hanna; Ji, Yong Woo; Haam, Seungjoo
- Issue Date
- Dec-2023
- Publisher
- Nature Publishing Group
- Citation
- Nature Communications, v.14, no.1
- Journal Title
- Nature Communications
- Volume
- 14
- Number
- 1
- URI
- https://yscholarhub.yonsei.ac.kr/handle/2021.sw.yonsei/22989
- DOI
- 10.1038/s41467-023-43995-5
- ISSN
- 2041-1723
- Abstract
- <jats:title>Abstract</jats:title><jats:p>Accurate diagnosis of Alzheimer’s disease (AD) in its earliest stage can prevent the disease and delay the symptoms. Therefore, more sensitive, non-invasive, and simple screening tools are required for the early diagnosis and monitoring of AD. Here, we design a self-assembled nanoparticle-mediated amplified fluorogenic immunoassay (SNAFIA) consisting of magnetic and fluorophore-loaded polymeric nanoparticles. Using a discovery cohort of 21 subjects, proteomic analysis identifies adenylyl cyclase-associated protein 1 (CAP1) as a potential tear biomarker. The SNAFIA demonstrates a low detection limit (236 aM), good reliability (R<jats:sup>2</jats:sup> = 0.991), and a wide analytical range (0.320–1000 fM) for CAP1 in tear fluid. Crucially, in the verification phase with 39 subjects, SNAFIA discriminates AD patients from healthy controls with 90% sensitivity and 100% specificity in under an hour. Utilizing tear fluid as a liquid biopsy, SNAFIA could potentially aid in long-term care planning, improve clinical trial efficiency, and accelerate therapeutic development for AD.</jats:p>
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