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基于无标记量子点探针和侧向流测试条的禽流感病毒快速灵敏免疫分析。

A fast and sensitive immunoassay of avian influenza virus based on label-free quantum dot probe and lateral flow test strip.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Science, Huazhong Agricultural University, Wuhan 430070, PR China.

出版信息

Talanta. 2012 Oct 15;100:1-6. doi: 10.1016/j.talanta.2012.08.041. Epub 2012 Sep 3.

DOI:10.1016/j.talanta.2012.08.041
PMID:23141303
Abstract

A novel fluorescence immunoassay method for fast and ultrasensitive detection of avian influenza virus (AIV) was developed. The immunoassay method which integrated lateral flow test strip technique with fluorescence immunoassay used the label-free and high luminescent quantum dots (QDs) as signal output. By the sandwich immunoreaction performed on lateral flow test strip, the gold nanoparticle (NP) labels were captured in the test zone and further dissolved to release a large number of gold ions as a signal transduction bridge that was detected by the QDs-based fluorescence quenching method. Under the optimal conditions, the relative fluorescence intensity of QDs was linear over the range of 0.27-12 ng mL(-1) AIV, and the limit of detection was estimated to be 0.09 ng mL(-1) which was 100-fold greater than enzyme-linked immunosorbent assay (ELISA). The sensitive and specific response was also coupled with high reproducibility in the proposed method. A series of six parallel measurements produced reproducible fluorescent signals with a relative standard deviation of 4.7%. The proposed method can be used to directly detect clinical sample without any pretreatment, and showed high efficiency (90.0%), sensitivity (100.0%) and specificity (88.2%) compared with virus isolation (gold method). The new method shows great promise for rapid, sensitive, and quantitative detection of AIV in-field or point-of-care diagnosis.

摘要

一种用于快速和超灵敏检测禽流感病毒(AIV)的新型荧光免疫分析方法被开发出来。该免疫分析方法将横向流动测试条技术与荧光免疫分析相结合,使用无标记和高发光量子点(QDs)作为信号输出。通过在横向流动测试条上进行的夹心免疫反应,金纳米粒子(NP)标记物被捕获在测试区,并进一步溶解以释放大量金离子作为信号转导桥,该信号转导桥通过基于 QDs 的荧光猝灭法进行检测。在最佳条件下,QDs 的相对荧光强度在 0.27-12 ng mL(-1) AIV 的范围内呈线性,检测限估计为 0.09 ng mL(-1),比酶联免疫吸附测定(ELISA)高 100 倍。该方法还具有高重复性和良好的特异性。一系列六个平行测量产生了具有相对标准偏差为 4.7%的可重复荧光信号。与病毒分离(金方法)相比,该方法可直接用于临床样本的检测,无需任何预处理,具有高效(90.0%)、高灵敏度(100.0%)和特异性(88.2%)。新方法有望用于现场或即时诊断中快速、灵敏、定量检测 AIV。

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