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Development of cellulosic material-based microchannel device capable of fluorescence immunoassay of microsamples.

Authors :
Shin J
Kasama T
Miyake R
Source :
Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2022 May; Vol. 414 (11), pp. 3419-3428. Date of Electronic Publication: 2022 Feb 15.
Publication Year :
2022

Abstract

Microfluidic immunoassay devices are a promising technology that can quickly detect biomarkers with high sensitivity. Recently, many studies implementing this technology on paper substrates have been proposed for improving cost and user-friendliness. However, these studies have identified problems with the large volume of sample required, low sensitivity, and a lack of quantitative accuracy and precision. In this paper, we report a novel structure implemented as a cellulosic material-based microchannel device capable of quantitative immunoassay using small sample volumes. We fabricated microfluidic channels between a transparent cellophane film and water-resistant paper to facilitate loading of small-volume samples and reagents, with a 40-μm-wide immunoreaction matrix constructed in the center of the microchannel using highly precise photolithography. A fluorescence sandwich immunoassay for C-reactive protein (CRP) was successfully implemented that required only a 1-μL sample volume and a 20-min reaction time. We confirmed that the limit of detection of the device was 10-20 ng/mL with a coefficient of variation under 5.6%, which is a performance level comparable to conventional plastic-based human CRP enzyme-linked immunosorbent assay (ELISA) kits. We expect that such devices will lead to the elimination of large amounts of medical waste from the use of ubiquitous diagnostics, a result that is consistent with environmental sustainability goals.<br /> (© 2022. Springer-Verlag GmbH Germany, part of Springer Nature.)

Details

Language :
English
ISSN :
1618-2650
Volume :
414
Issue :
11
Database :
MEDLINE
Journal :
Analytical and bioanalytical chemistry
Publication Type :
Academic Journal
Accession number :
35169907
Full Text :
https://doi.org/10.1007/s00216-022-03963-2