TY - JOUR
T1 - Paper Microfluidics and Tailored Gold Nanoparticles for Nonenzymatic, Colorimetric Multiplex Biomarker Detection
AU - Pinheiro, Tomás
AU - Marques, Ana Carolina
AU - Carvalho, Patrícia
AU - Martins, Rodrigo
AU - Fortunato, Elvira
N1 - info:eu-repo/grantAgreement/EC/H2020/787410/EU#
The authors acknowledge funding from the project UID/CTM/50025/2019 by FCT-MCTES, I.P.. A.C.M. acknowledges funding from FCT-MCTES, I.P., through the Ph.D. Grant SFRH/BD/115173/2016. The authors acknowledge the Norwegian Research Council for the support to the NorFab (245963/F50) and NorTEM (197405/F50) research infrastructures. This work is part of the Master Thesis in Biomedical Engineering defended by T.P. at FCT NOVA titled “Multiplex, Enzyme-free, Colorimetric Paper-based Device for the Measurement of Glucose, Uric Acid and Cholesterol”.
PY - 2021/1/27
Y1 - 2021/1/27
N2 - The plasmonic properties of gold nanoparticles (AuNPs) are a promising tool to develop sensing alternatives to traditional, enzyme-catalyzed reactions. The need for sensing alternatives, especially in underdeveloped areas of the world, has given rise to the application of nonenzymatic sensing approaches paired with cellulosic substrates to biochemical analysis. Herein, we present three individual, low-step, wet-chemistry, colorimetric assays for three target biomarkers, namely, glucose, uric acid, and free cholesterol, relevant in diabetes control and their translation into paper-based assays and microfluidic platforms for multiplexed analysis. For glucose determination, an in situ AuNPs synthesis approach was applied into the developed μPAD, giving semiquantitative measures in the physiologically relevant range. For uric acid and cholesterol determination, modified AuNPs were used to functionalize paper with a gold-on-paper approach with the optical properties changing based on different aggregation degrees and hydrophobic properties of particles dependent on analyte concentration. These paper-based assays show sensitivity ranges and limits of detection compatible for target analyte level determination and detection limits comparable to those of similar enzymatic, colorimetric systems, relying only on plasmonic transduction without the need for enzymatic activity or other chromogenic substrates. The resulting paper-based assays were integrated into a single 3D, multiplex paper-based device using paper microfluidics, showing the capability for performing different colorimetric assays with distinct requirements in terms of sample flow and sample uptake in test zones using a combination of both horizontal and vertical flows inside the same device. The presented device allows for multiparametric, colorimetric measures of different metabolite levels from a single complex sample matrix drop using digital color analysis, showing the potential for development of low-cost, low-complexity tools for diagnostics toward the point-of-care.
AB - The plasmonic properties of gold nanoparticles (AuNPs) are a promising tool to develop sensing alternatives to traditional, enzyme-catalyzed reactions. The need for sensing alternatives, especially in underdeveloped areas of the world, has given rise to the application of nonenzymatic sensing approaches paired with cellulosic substrates to biochemical analysis. Herein, we present three individual, low-step, wet-chemistry, colorimetric assays for three target biomarkers, namely, glucose, uric acid, and free cholesterol, relevant in diabetes control and their translation into paper-based assays and microfluidic platforms for multiplexed analysis. For glucose determination, an in situ AuNPs synthesis approach was applied into the developed μPAD, giving semiquantitative measures in the physiologically relevant range. For uric acid and cholesterol determination, modified AuNPs were used to functionalize paper with a gold-on-paper approach with the optical properties changing based on different aggregation degrees and hydrophobic properties of particles dependent on analyte concentration. These paper-based assays show sensitivity ranges and limits of detection compatible for target analyte level determination and detection limits comparable to those of similar enzymatic, colorimetric systems, relying only on plasmonic transduction without the need for enzymatic activity or other chromogenic substrates. The resulting paper-based assays were integrated into a single 3D, multiplex paper-based device using paper microfluidics, showing the capability for performing different colorimetric assays with distinct requirements in terms of sample flow and sample uptake in test zones using a combination of both horizontal and vertical flows inside the same device. The presented device allows for multiparametric, colorimetric measures of different metabolite levels from a single complex sample matrix drop using digital color analysis, showing the potential for development of low-cost, low-complexity tools for diagnostics toward the point-of-care.
KW - biomarker detection
KW - colorimetric
KW - gold nanoparticles
KW - nonenzymatic
KW - paper microfluidics
UR - http://www.scopus.com/inward/record.url?scp=85099965375&partnerID=8YFLogxK
U2 - 10.1021/acsami.0c19089
DO - 10.1021/acsami.0c19089
M3 - Article
C2 - 33449630
AN - SCOPUS:85099965375
SN - 1944-8244
VL - 13
SP - 3576
EP - 3590
JO - ACS Applied Materials & Interfaces
JF - ACS Applied Materials & Interfaces
IS - 3
ER -