Abstract

Paper-based biosensors are considered simple and cost-efficient sensing platforms for analytical tests and diagnostics. Here, a paper-based electrochemical biosensor was developed for the rapid and sensitive detection of microRNAs (miRNA-155 and miRNA-21) related to early diagnosis of lung cancer. Hydrophobic barriers to creating electrode areas were manufactured by wax printing, whereas a three-electrode system was fabricated by a simple stencil approach. A carbon-based working electrode was modified using either reduced graphene oxide or molybdenum disulfide nanosheets modified with gold nanoparticle (AuNPs/RGO, AuNPs/MoS2) hybrid structures. The resulting paper-based biosensors offered sensitive detection of miRNA-155 and miRNA-21 by differential pulse voltammetry (DPV) in only 5.0 µL sample. The duration in our assay from the point of electrode modification to the final detection of miRNA was completed within only 35 min. The detection limits for miRNA-21 and miRNA-155 were found to be 12.0 and 25.7 nM for AuNPs/RGO and 51.6 and 59.6 nM for AuNPs/MoS2 sensors in the case of perfectly matched probe-target hybrids. These biosensors were found to be selective enough to distinguish the target miRNA in the presence of single-base mismatch miRNA or noncomplementary miRNA sequences.

Highlights

  • Introduction iationsThe use of paper in chemical analysis started as early as the 1930s [1,2], and the first paper-based glucose sensor was fabricated in the 1950s [3]

  • Characterization Studies of the Paper Electrode Modified with Gold Nanoparticles/Reduced

  • The measurements were achieved by using a 10X objective with a laser spot size of 7.5 μm

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Summary

Introduction

The use of paper in chemical analysis started as early as the 1930s [1,2], and the first paper-based glucose sensor was fabricated in the 1950s [3]. Paper-based sensors have received increased interest because they are easy to use and disposable with low-cost fabrication [6,7,8]. They provide benefits, such as short analysis time and usage of a small volume of sample [9]. Two- or three-electrode systems can be fabricated using various

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