检出限
免疫分析
化学
荧光
银纳米粒子
肝细胞癌
临床诊断
色谱法
生物标志物
纳米技术
纳米颗粒
生物化学
癌症研究
免疫学
生物
物理
抗体
医学
材料科学
临床心理学
量子力学
作者
Zehui Sun,Xuanxuan Zhang,Duo Xu,Jie Liu,Ru‐Jia Yu,Chao Jing,Huanxing Han,Wei Ma
出处
期刊:Talanta
[Elsevier]
日期:2020-12-16
卷期号:225: 121963-121963
被引量:32
标识
DOI:10.1016/j.talanta.2020.121963
摘要
Development of simple, robust, and reliable detection strategy of disease biomarkers holds tremendous promise for early clinical diagnosis and prognosis of diseases. In this work, through combining a silver nanoparticle (AgNP) linked immunoassay and aggregation induced emission (AIE)-based fluorogenic Ag + probe, we developed a silver-amplified fluorescence immunoassay for the detection of disease biomarkers. This method overcame the intrinsic limitations of enzymes as the dissolution of AgNPs generated numerous Ag + , which could switch on the fluorogenic Ag + probe driven by tetrazolate-Ag + complexation. As a proof of concept, our method could be used for determining α-fetoprotein (AFP) with a linear relationship in concentrations ranging from 0.1 ng mL −1 to 5 μg mL −1 and a low limit of detection of 42 pg mL −1 . Our method was successfully confirmed for the detection of AFP in real serum samples from hepatocellular carcinoma (HCC) patients, demonstrating the great potential for clinical diagnosis. Schematic illustration of AgNPs amplified fluorescence immunoassay through an Ag + -tetrazolate aggregation-triggered AIE process for the detection of disease biomarkers. • A silver amplified fluorescence immunoassay was developed for detection of disease biomarkers without enzyme amplification. • Our method overcame the intrinsic limitations of enzyme as AgNPs generated numerous Ag + through particle-to-ions. • We demonstrated the feasibility of our assay for clinical diagnosis by detecting the disease biomarker in real serum samples.
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