TY - JOUR
T1 - Graphene-based rapid and highly-sensitive immunoassay for C-reactive protein using a smartphone-based colorimetric reader
AU - Vashist, Sandeep Kumar
AU - Marion Schneider, E.
AU - Zengerle, Roland
AU - von Stetten, Felix
AU - Luong, John H.T.
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2015/4/5
Y1 - 2015/4/5
N2 - A novel immunoassay (IA) has been developed for human C-reactive protein (CRP), an important biomarker and tissue preserving factor for infection and inflammation. Graphene nanoplatelets (GNP) and 3-aminopropyltriethoxysilane (APTES) were admixed and covalently attached to a polystyrene based-microtiter plate (MTP), pretreated with KOH. The resulting surface served as a stable layer for the covalent attachment of the anti-human CRP antibody. The IA procedure was based on the one-step kinetics-based sandwich IA employing a minimum number of process steps, whereas the enzymatic reaction solution was monitored by a smartphone-based colorimetric reader. With a limit of detection and a limit of quantification of 0.07ngmL-1 and 0.9ngmL-1, it precisely detected CRP spiked in diluted human whole blood and plasma as well as the CRP levels in clinical plasma samples. The results obtained for "real-world" patient samples agreed well with those of the conventional immunosorbent assay and the clinically-accredited analyzer-based IA. The antibody-bound GNP-functionalized MTPs retained its original activity after 6 weeks of storage in 0.1M PBS, pH 7.4 at 4°C.
AB - A novel immunoassay (IA) has been developed for human C-reactive protein (CRP), an important biomarker and tissue preserving factor for infection and inflammation. Graphene nanoplatelets (GNP) and 3-aminopropyltriethoxysilane (APTES) were admixed and covalently attached to a polystyrene based-microtiter plate (MTP), pretreated with KOH. The resulting surface served as a stable layer for the covalent attachment of the anti-human CRP antibody. The IA procedure was based on the one-step kinetics-based sandwich IA employing a minimum number of process steps, whereas the enzymatic reaction solution was monitored by a smartphone-based colorimetric reader. With a limit of detection and a limit of quantification of 0.07ngmL-1 and 0.9ngmL-1, it precisely detected CRP spiked in diluted human whole blood and plasma as well as the CRP levels in clinical plasma samples. The results obtained for "real-world" patient samples agreed well with those of the conventional immunosorbent assay and the clinically-accredited analyzer-based IA. The antibody-bound GNP-functionalized MTPs retained its original activity after 6 weeks of storage in 0.1M PBS, pH 7.4 at 4°C.
KW - C-reactive protein
KW - Graphene
KW - One-step kinetics-based sandwich immunoassay
KW - Smartphone-based colorimetric reader
UR - https://www.scopus.com/pages/publications/84918518473
U2 - 10.1016/j.bios.2014.11.017
DO - 10.1016/j.bios.2014.11.017
M3 - Article
C2 - 25460898
AN - SCOPUS:84918518473
SN - 0956-5663
VL - 66
SP - 169
EP - 176
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -