Issue 16, 2014

Simultaneous concentration and detection of biomarkers on paper

Abstract

The lateral-flow immunoassay (LFA) is an inexpensive point-of-care (POC) paper-based diagnostic device with the potential to rapidly detect disease biomarkers in resource-poor settings. Although LFA is inexpensive, easy to use, and requires no laboratory equipment, it is limited by its sensitivity, which remains inferior to that of gold standard laboratory-based assays. Our group is the only one to have previously utilized various aqueous two-phase systems (ATPSs) to enhance LFA detection. In those studies, the sample was concentrated by an ATPS in a test tube and could only be applied to LFA after it had been extracted manually. Here, we bypass the extraction step by seamlessly integrating a polyethylene glycol–potassium phosphate ATPS with downstream LFA detection in a simple, inexpensive, power-free, and portable all-in-one diagnostic device. We discovered a new phenomenon in which the target biomarkers simultaneously concentrate as the ATPS solution flows through the paper membranes, and our device features a 3-D paper well that was designed to exploit this phenomenon. Studies with this device, which were performed at room temperature in under 25 min, demonstrated a 10-fold improvement in the detection limit of a model protein, transferrin. Our next-generation LFA technology is rapid, affordable, easy-to-use, and can be applied to existing LFA products, thereby providing a new platform for revolutionizing the current state of disease diagnosis in resource-poor settings.

Graphical abstract: Simultaneous concentration and detection of biomarkers on paper

Supplementary files

Article information

Article type
Paper
Submitted
05 May 2014
Accepted
12 Jun 2014
First published
12 Jun 2014

Lab Chip, 2014,14, 3021-3028

Author version available

Simultaneous concentration and detection of biomarkers on paper

R. Y.T. Chiu, E. Jue, A. T. Yip, A. R. Berg, S. J. Wang, A. R. Kivnick, P. T. Nguyen and D. T. Kamei, Lab Chip, 2014, 14, 3021 DOI: 10.1039/C4LC00532E

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