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Anal Chem ; 89(11): 5776-5783, 2017 06 06.
Article in English | MEDLINE | ID: mdl-28445636

ABSTRACT

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 specimens. The total test time from device initiation to result was approximately 35 min. Device performance for influenza A detection was ∼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.


Subject(s)
Influenza, Human/diagnosis , Specimen Handling/methods , Viral Proteins/analysis , Diagnostic Tests, Routine/instrumentation , Humans , Immunoassay/instrumentation , Influenza A virus/isolation & purification , Influenza B virus/isolation & purification , Nucleoproteins/analysis , Time Factors
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