TY - JOUR
T1 - Label-free and Electrochemical Detection of Nucleic Acids Based on Isothermal Amplification in Combination with Solid-state pH Sensor
AU - Tabata, Miyuki
AU - Katayama, Yurika
AU - Mannan, Fahmida
AU - Seichi, Ayaka
AU - Suzuki, Koji
AU - Goda, Tatsuro
AU - Matsumoto, Akira
AU - Miyahara, Yuji
N1 - Publisher Copyright:
© 2016 The Authors.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016
Y1 - 2016
N2 - Label-free quantification methods for nucleic acids are attracting attention, since they provide potential tools in clinical applications such as disease diagnosis or prognosis observation. In this research, we developed a simpler and cost-effective electrical monitoring device of nucleic acid amplification, combining an isothermal amplification method and an Iridium/Iridium oxide (Ir/IrOx) electrode without labeling. The fabricated Ir/IrOx electrode showed ideal Nernstian response under the various pH buffer solutions, and its potential response was less affected even in the presence of charged proteins. Moreover, we successfully real-time monitored primer generation-rolling circle amplification (PG-RCA) at the 0, 10, 100, 1000 pM of target DNA by detection of released proton during amplification reaction at the constant reaction temperature. This label-free and portable device might be received considerable attention as a useful platform for a point-of-care testing in clinical use.
AB - Label-free quantification methods for nucleic acids are attracting attention, since they provide potential tools in clinical applications such as disease diagnosis or prognosis observation. In this research, we developed a simpler and cost-effective electrical monitoring device of nucleic acid amplification, combining an isothermal amplification method and an Iridium/Iridium oxide (Ir/IrOx) electrode without labeling. The fabricated Ir/IrOx electrode showed ideal Nernstian response under the various pH buffer solutions, and its potential response was less affected even in the presence of charged proteins. Moreover, we successfully real-time monitored primer generation-rolling circle amplification (PG-RCA) at the 0, 10, 100, 1000 pM of target DNA by detection of released proton during amplification reaction at the constant reaction temperature. This label-free and portable device might be received considerable attention as a useful platform for a point-of-care testing in clinical use.
KW - Biosensor
KW - iridium/iridium oxide
KW - isothermal nucleic acid amplification
UR - http://www.scopus.com/inward/record.url?scp=85009967841&partnerID=8YFLogxK
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U2 - 10.1016/j.proeng.2016.11.534
DO - 10.1016/j.proeng.2016.11.534
M3 - Conference article
AN - SCOPUS:85009967841
SN - 1877-7058
VL - 168
SP - 419
EP - 422
JO - Procedia Engineering
JF - Procedia Engineering
T2 - 30th Eurosensors Conference, Eurosensors 2016
Y2 - 4 September 2016 through 7 September 2016
ER -