Disposable Autonomous Device for Swab-to-Result Diagnosis of Influenza

被引:30
作者
Huang, Shichu [1 ]
Abe, Koji [1 ]
Bennett, Steven [1 ]
Liang, Tinny [1 ]
Ladd, Paula D. [1 ]
Yokobe, Lindsay [2 ]
Anderson, Caitlin E. [1 ]
Shah, Kamal [1 ]
Bishop, Josh [1 ]
Purfield, Mike [1 ]
Kauffinan, Peter C. [1 ]
Paul, Sai [1 ]
Welch, AnneMarie E. [1 ]
Strelitz, Bonnie [3 ]
Follmer, Kristin [3 ]
Pullar, Kelsey [3 ]
Sanchez-Erebia, Luis [3 ]
Gerth-Guyette, Emily [2 ]
Domingo, Gonzalo [2 ]
Klein, Eileen [3 ]
Englund, Janet A. [3 ]
Fu, Elain [4 ]
Yager, Paul [1 ]
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[2] PATH, Seattle, WA 98121 USA
[3] Seattle Childrens Hosp, Ctr Clin & Translat Res, Seattle, WA 98105 USA
[4] Oregon State Univ, Chem Biol & Environm Engn, Corvallis, OR 97331 USA
基金
美国国家科学基金会;
关键词
TESTS; VIRUSES; MALARIA; SYSTEM; IMPACT; ASSAYS;
D O I
10.1021/acs.analchem.6b04801
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A prototype of a self-contained, automated, disposable device for chemically amplified protein-based detection of influenza virus from nasal swab specimens was developed and evaluated in a clinical setting. The device required only simple specimen manipulation without any dedicated instrumentation or specialized training by the operator for interpretation. The device was based on a sandwich immunoassay for influenza virus nucleoprotein; it used an enzyme-labeled antibody and a chromogenic substrate to provide an amplified visible signal, in a two-dimensional paper network format. All reagents were stored within the device. Device performance was assessed at Seattle Children's Hospital; clinical staff collected nasal-swab samples from 25 patients and then operated test devices on site to detect influenza A and B in those specithens. The total test time from device initiation to result was approximately 35 min. Device performance for influenza A detection was similar to 70% accurate using in-house qRT-PCR influenza A as a gold-standard comparison. The ratio of valid to total completed device runs yielded a success rate of 92%, and the negative predictive value for both the influenza A and B assay was 81%. The ability to diagnose respiratory infections rapidly and close to the patient was well received by hospital staff, inspiring further optimization of device function.
引用
收藏
页码:5777 / 5784
页数:8
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