Cited 8 times in

Amplified fluorogenic immunoassay for early diagnosis and monitoring of Alzheimer’s disease from tear fluid

DC Field Value Language
dc.contributor.author조한나-
dc.contributor.author지용우-
dc.date.accessioned2024-02-15T06:48:26Z-
dc.date.available2024-02-15T06:48:26Z-
dc.date.issued2023-12-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198046-
dc.description.abstractAccurate 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 (R2 = 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. © 2023, The Author(s).-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Pub. Group-
dc.relation.isPartOfNATURE COMMUNICATIONS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAlzheimer Disease* / metabolism-
dc.subject.MESHAmyloid beta-Peptides-
dc.subject.MESHBiomarkers / metabolism-
dc.subject.MESHEarly Diagnosis-
dc.subject.MESHHumans-
dc.subject.MESHImmunoassay-
dc.subject.MESHProteomics-
dc.subject.MESHReproducibility of Results-
dc.titleAmplified fluorogenic immunoassay for early diagnosis and monitoring of Alzheimer’s disease from tear fluid-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorSojeong Lee-
dc.contributor.googleauthorEunjung Kim-
dc.contributor.googleauthorChae-Eun Moon-
dc.contributor.googleauthorChaewon Park-
dc.contributor.googleauthorJong-Woo Lim-
dc.contributor.googleauthorMinseok Baek-
dc.contributor.googleauthorMoo-Kwang Shin-
dc.contributor.googleauthorJisun Ki-
dc.contributor.googleauthorHanna Cho-
dc.contributor.googleauthorYong Woo Ji-
dc.contributor.googleauthorSeungjoo Haam-
dc.identifier.doi10.1038/s41467-023-43995-5-
dc.contributor.localIdA03920-
dc.contributor.localIdA03967-
dc.relation.journalcodeJ02293-
dc.identifier.eissn2041-1723-
dc.identifier.pmid38071202-
dc.contributor.alternativeNameCho, Hanna-
dc.contributor.affiliatedAuthor조한나-
dc.contributor.affiliatedAuthor지용우-
dc.citation.volume14-
dc.citation.number1-
dc.citation.startPage8153-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, Vol.14(1) : 8153, 2023-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.