免疫分析
多路复用
检出限
鼠疫耶尔森菌
色谱法
硝化棉
化学
分析物
再现性
膜
抗体
生物
生物化学
免疫学
基因
毒力
生物信息学
作者
Jasmine Pramila Devadhasan,Alexander J. Summers,Jian Gu,S. D. Smith,Baiju Thomas,Ali Fattahi,James Helton,Sujata G. Pandit,Marcellene A. Gates‐Hollingsworth,Derrick Hau,Kathryn J. Pflughoeft,Douglas C. Montgomery,Supriya Atta,Tuan Vo‐Dinh,David P. AuCoin,Frédéric Zenhausern
标识
DOI:10.1016/j.bios.2022.114796
摘要
This paper presents simple, fast, and sensitive detection of multiple biothreat agents by paper-based vertical flow colorimetric sandwich immunoassay for detection of Yersinia pestis (LcrV and F1) and Francisella tularensis (lipopolysaccharide; LPS) antigens using a vertical flow immunoassay (VFI) prototype with portable syringe pump and a new membrane holder. The capture antibody (cAb) printing onto nitrocellulose membrane and gold-labelled detection antibody (dAb) were optimized to enhance the assay sensitivity and specificity. Even though the paper pore size was relaxed from previous 0.1 μm to the current 0.45 μm for serum samples, detection limits as low as 0.050 ng/mL for LcrV and F1, and 0.100 ng/mL for FtLPS have been achieved in buffer and similarly in diluted serum (with LcrV and F1 LODs remained the same and LPS LOD reduced to 0.250 ng/mL). These were 40, 80, and 50X (20X for LPS in serum) better than those from lateral flow configuration. Furthermore, the comparison of multiplex format demonstrated low cross-reactivity and equal sensitivity to that of the singleplex assay. The optimized VFI platform thus provides a portable and rapid on-site monitoring system for multiplex biothreat detection with the potential for high sensitivity, specificity, reproducibility, and multiplexing capability, supporting its utility in remote and resource-limited settings.
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