Certification of visinin-like protein-1 (VILIP-1) certified reference material by amino acid-based and sulfur-based liquid chromatography isotope dilution mass spectrometry

被引:0
作者
Zang, Yang [1 ,2 ]
Zhou, Xirui [1 ]
Pan, Mengyun [1 ]
Lu, Yanli [1 ,2 ]
Liu, Hangrui [1 ,3 ]
Xiong, Jinping [2 ]
Feng, Liuxing [1 ]
机构
[1] Natl Inst Metrol, Div Chem Metrol & Analyt Sci, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Technol, Beijing 100029, Peoples R China
[3] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Biomarker; Certified reference materials; VILIP-1; ID-MS; SI traceability; ABSOLUTE QUANTIFICATION; HUMAN SERUM; STRATEGIES;
D O I
10.1007/s00216-022-04401-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As an emerging neurodegenerative disease, Alzheimer's disease (AD) has become a leading cause of dementia in older adults. Visinin-like protein-1 (VILIP-1) is an increasingly used biomarker for AD besides the widely accepted A beta(1-40), A beta(1-42), and tau. However, significant variations exist in the commercial immuno-based assays for VILIP-1 quantification, underlining the necessity to establish a traceability chain. Certified reference materials (CRMs) located at the top of the traceability chain are traceability sources for relevant matrix standard materials. In this work, VILIP-1 solution CRM with a certified value and uncertainty of 39.82 +/- 1.52 mu g.g(-1) was developed and certified using amino acid-based isotope dilution mass spectrometry (AA-ID-MS) and sulfur-based isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS). Certified values from both strategies showed great consistency, with traceability to SI units. Moreover, the candidate VILIP-1 CRM shows excellent homogeneity and can be stable for at least 7 days at -20 degrees C and 12 months at -70 degrees C. The VILIP-1 CRM developed can be used in value assignment to secondary calibrators and clinical matrix CRMs, showing prospects in early diagnosis and disease monitoring for AD.
引用
收藏
页码:211 / 220
页数:10
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